人工合成芸薹属异源六倍体与诸葛菜属间杂种的细胞学及分子生物学研究
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摘要
在芸苔属与诸葛菜(Orychophragmus violaceus(L.)O.E.Schulz,2n=24)的属间杂交中发现亲本种染色体组分开的新细胞学现象及其遗传控制;芸苔属6个栽培种与诸葛菜属间杂种中的染色体行为受芸苔属亲本种含有的染色体组的影响;3个四倍体种与诸葛菜杂种中的不同染色体行为及差异,可由3个二倍体种与诸葛菜杂种中的不同染色体行为解释或预测。这是继假配生殖(Pseudogamy)、半配生殖(Semigamy)和染色体消除(Chromosome elimination)之后,植物远缘杂交中观察到的新染色体行为,丰富了植物遗传学的内容。为了更深入研究染色体组分开现象的遗传和发生机制,本研究拟进行诸葛菜与人工合成的芸苔属异源六倍体(2n=54,AABBCC)的杂交。利用普通细胞学、基因组原位杂交(Genomic in situ hybridization,GISH)、扩增片段长度多态性(Amplified fragment length polymorphism,AFLP)及单链构象多态性分析(single-stranded DNA conformation polymorphism,SSCP)对杂种及其后代作系统的研究,探讨来源于三个不同基因组的芸薹属染色体在杂种细胞有丝分裂及减数分裂时的染色体行为。为此我们合成了三个不同来源的三基因组杂种,分别为埃塞俄比亚芥“G0-11”(B.carinata A.Braun,2n=34,BBCC)×白菜“上海青”(B.camprists,2n=20,AA)(组合BC.A),甘蓝型油菜“中油821”(B.napus,2n=38,AACC)×黑芥(B.nigra(L.)Koch,2n=16)(组合AC.B),人工合成的甘蓝型油菜×黑芥(组合A.C.B)的杂种一代。通过加倍获得三个不同来源的六倍体(分别表示为六倍体Ⅰ,Ⅱ,Ⅲ),在细胞学观察的基础上以确认为六倍体的植株为母本与诸葛菜杂交。主要结果如下:
     1.普通细胞学分析表明三个三基因组杂种在减数分裂过程中均有较高数目的二价体形成。组合BC.A、AC.B、A.C.B分别有88.2%,96.8%和91.2%的细胞包含有6—10个二价体。同时包含有少于8个单价体的细胞比例在组合间有较大的差异,分别为14.7%,24.5%和29.8%。GISH分析表明三个组合的杂种在减数分裂过程中,均有相当比例的B基因组染色体参与了异源的染色体配对。三个组合中分别有31.9%,45.4%和50%的细胞包含有至少一条B基因组染色体参与了异源配对;在AC.B、A.C.B组合中同一个细胞中最多有三条B基因组染色体参与了异源的配对,而在组合BC.A最多只有两条。同时,分别有10.9%,16.6%和9.4%的花粉母细胞细胞至少形成一对B基因组染色体间的二价体。三个组合中,同一细胞中均出现了最多有两个二价体完全由B基因组染色体形成。上述结果进一步验证了芸薹属三个基因组在基因组间及基因组内存在的同源性。
     2.六倍体Ⅰ、Ⅱ、Ⅲ与诸葛菜杂交分别获得30,4及3株杂种单株,每个单株均来自不同的胚。杂种一代在表型上与母本的六倍体及六倍体自交后代有较大的差别,在苗期的叶形及成年植株茎杆颜色上表现有父本的特征。普通细胞学观察表明,所有单株的体细胞均由具不同数目染色体的细胞组成,即均为混倍体。体细胞最高的染色体数目为46,最低为20。杂种单株体细胞中出现频率最高的染色体数目有三种,一是44,有32株;二是42,有4株;三是36,有1株。可能的是杂种植株在合子细胞形成后的发育过程中经历了染色体组加倍和部分染色体消除的过程。
     3.GISH分析表明,所有杂种细胞中均未检测到诸葛菜的整条或者染色体的片段。同时根据B基因组DNA为探针的GISH结果,以细胞中B基因组染色体的数目及减数分裂时的配对及分离的方式,将所有杂种植株分为三大类:Ⅰ类具有16条B基因组染色体,以8Ⅱ的方式配对,以8:8分离,共32株;Ⅱ类具有14条B基因组染色体,以6Ⅱ+2Ⅰ方式配对,以7:7或者6:8的方式分离,共4株:Ⅲ类植株包含有上述两种细胞类型类型,共1株。GISH结果同时表明,六倍体Ⅰ中一对带有rDNA位点的A基因组染色体在所有杂种中均只有一条。GISH的结果表明所有的诸葛菜染色体在合子的发育过程中被全部消除。
     4.杂种一代的AFLP分析表明,六倍体Ⅰ与诸葛菜的杂种中具有较多诸葛菜的特异带,诸葛菜特异带占该单株的总带数的百分比在4.8%到7.1%之间。同时杂种单株中出现了母本的缺失带和双亲均无的新带,表明外源遗传物质的进入引起受体基因组结构的变化。六倍体Ⅱ、Ⅲ与诸葛菜的所有杂种中,25对引物中只有3对引物能够扩出诸葛菜的特异带,但是母本缺失带和新带的数量较多。
     5.六倍体与诸葛菜杂种及后代的AFLP,普通细胞学,表型及杂交分析表明,杂种及后代在基因组组成上更偏向于芥菜型油菜。由于B基因组染色体在绝大多数的杂种植株中均是完整的,说明所有杂种一代单株种中C基因组被消除或者说丢失的染色体要多于A基因组染色体,即在杂种细胞中三个基因组染色体表现出B>A>C的稳定性关系。
     6.SSCP分析发现在三种六倍体及六倍体与诸葛菜的杂种中,A/C来源的rRNA基因只在一个杂种植株中表达,而B基因组来源的rRNA基因在所有单株中均表达。A/C来源的rRNA基因表达的单株中B基因组染色体为14条,我们认为缺少的染色体上载有rDNA位点,该染色体的缺失导致核仁显性关系的变化。
     7.在六倍体Ⅰ和诸葛菜杂种一代的两个单株中,减数分裂四分体时期,当且仅当四分体形成时,小孢子中的染色质重新收缩呈染色体状,染色体随后随机的分到两极或者多极,同时在这些细胞中发现了两极和多极的纺锤体。随后细胞质分裂,单个的小孢子被分成了大小不等的几个微小孢子。原位杂交分析表明,染色体分离前没有经历复制的过程;染色体的两极或者多极分离是完全随机的,没有基因组的特异性。在另外一些细胞中,四分体形成后,四个小孢子逐渐融合成为一个大的细胞,染色体数目随之上升。这两种异常情况是相伴发生的,但是细胞额外分裂的频率要远高于融合的频率。这两种小孢子发育的异常只发生在两个植株的部分四分体中,甚至于同一个四分体的个别细胞中。
     8.六倍体Ⅲ和诸葛菜杂种的一个单株中,减数分裂粗线期之前未见异常,粗线期之后,染色体缺少配对的过程,单价体聚集在一起。聚在一起的染色体总是出现在细胞的边缘。随后这些染色体随机的分向两极,但是细胞质并不分裂,导致双核细胞的形成,双核细胞停止了进一步的发育。这些细胞在后期形成外壁,染色深,似成熟的花粉,但是细胞内空洞无物。在这些异常分裂的花粉母细胞中未发现纺锤体的出现。
     最后,我们认为芸薹属六倍体与诸葛菜杂种的染色体行为不同于二倍体或者四倍体与诸葛菜杂种的染色体行为。我们推测合子细胞在发育过程中经历了染色体组的加倍与双亲染色体组的部分分开。在染色体组部分分开的过程中,母本染色体的分开具有基因组的特异性,可能的是较多的C基因组染色体分到了诸葛菜染色体的一极,而包含有较多诸葛菜染色体的细胞最后被消除导致有较多C基因组染色体的消除。而B基因组染色体、较多的A基因组染色体、部分的C基因组及少量的诸葛菜染色体分到了同一极,但诸葛菜染色体在随后的细胞分裂过程中被消除。由于染色体的稳定性关系与核仁显性的一致性,我们认为基因组特异性rRNA基因的表达有助于该基因组染色体的稳定存在。诸葛菜染色体在消除的过程中亦可能与其他基因组的染色体发生交换和重组导致其遗传物质渗入。外源遗传物质的进入导致受体基因组结构及基因表达的改变,例如,杂种AFLP新带型的出现和小孢子发育的异常等。
The phenomenon of complete and partial parent genome separation was found inhybrids between six Brassica species and Orychophragmus violaceus (L.) O.E.Schulz(2n=24). Results from the hybridization also indicated that the different chromosomebehavior in different combinations might be arised by differetn maternal parent genome.The different chromosome behavior of hybrids with three Brassica diploids (B. rape, B.nigra and B. oleracea) might contribute to the different cytogenetics of hybrids with threetetraploids (B. napus, B. juncea and B. carinata). Those findings are new chromosomebehaviors in plant wide hybridization beside pseudogamy, semigamy and chromosomeelimination and enriched the knowledge of plant genetics. To further study the mechanismbehind the phenomenon, we synthesized Brassica allohexaploid from differentcombinations and cross with O.violaceus as maternal parent. Cytology, genomic in situhybridization (GISH), amplified fragment length polymorphisms (AFLP) andsingle-strand DNA conformation polymorphisms (SSCP) analyses were applied tohybrids. To obtain different allohexaploid, three different tri-genomic hybrids (ABC,2n=27) from crosses BC.A: B.carinata (G0-11, BBCC, 2n=34)×B.camprists (shanghaiqin,AA, 2n=20), AC. B: B. napus (zhong you 821, AACC, 2n=38)×B. nigra (Koch, BB, 2n=16),A. C. B: artificial B. napus×B. nigra were used for chromosome double. Three typeallohexaploids were named hexaploidⅠ,Ⅱ,Ⅲrespectively. Main results were describedas follows:
     1. A relatively high proportion of bivalents were formed in all tri-genomic hybridsfrom different combinations. Hybrids from combination of BC. A, AC. B, A. C. B had88. 2%, 96. 8% and 91. 2% PMCs (Pollen Mother Cells) with 6-10 bivalents, 14.7%, 24.5%and 9.8% PMCs with univalents less than 8 respectively. GISH analyses also revealed thateach type of hybrids had 31. 9%, 45. 4% and 50% PMCs contained at least one B-genomechromosome paired with A/C chromosomes and maximally three B-chromosomes inallosyndesis per cell observed in AC.B and A.C.B combinations. Each type of hybrids had10.9%, 16.6% and 9.4% PMCs with at least one bivalent formed by B chromosomes. Amaximum of two bivalents formed by autosyndesis within B genome at diakinesisappeared in all combinations. The accurate analyses of auto- and allo-syndetic pairing forB genome in trigenomic combinations provided further evidence for the hypothesis thatthree basic genomes of the cultivated Brassica species were secondary polyploids andderived from one common ancestral genome with a lower chromosome number.
     2. 30, 4 and 3 hybrid plants were produced from crosses hexaploidⅠ,Ⅱ,Ⅲ×O.violaceus respectively. All hybrids were different from the hexaploid or self progeniesof hexaploid on phenotype. Young leaves and stem of adult plants showed some traits ofO.violaceus. Cytology observation revealed that all hybrids contained cells with differentchromosomes which indicated the mixploidy of the F_1 plants. The highest chromosomenumber was 46, and the lowest was 20. Cells with 44 chromosomes were found withhighest frequency in 32 hybrid plants, 42 in 4 hybrid plants and 36 in only hybrid plant.
     3. GISH analyses found no intact chromosome or chromosome fragments fromO.violaceus in all three type hybrids. According to the number and behavior of B genomechromosomes, all hybrid plants were classified into three types. All somatic cells of TypesⅠplants contained 16 B genome chromosomes which formed 8Ⅱat diakinesis and shown8:8 segregation at anaphase; TypesⅡcontained 14 B genome chromosomes whichformed 6Ⅱ+2Ⅰat diakinesis and showed 6:8 or 7:7 segregation at anaphase. TypesⅢcontained above two chromosomes number and behavior. GISH analyses also found thatone chromosome from A genome with rDNA locus was eliminated in all hybrids betweenhexploidⅠand O.violaceus. Obviously, complete O.violaceus chromosomes and partialmaternal chromosomes were eliminated.
     4. AFLP analyses revealed that all hybrids contained bands specific for O.violaceus,especially for hybrids between hexaploid I and O.violaceus which contained 4.8%-7.1%bands specific for O.violaceus. Deleted bands for maternal parent and novel bands werealso found in all hybrids. Possilably, introgressinon of O.violaceus chromatin disturbedthe maternal genome.
     5. Cytology, morphology, AFLP and cross analyses indicated that the genome ofhybrids and their self progenies resembled B.juncea. For intact B-genome chromosomeswere found in most of the hybrids, more chromosomes from C genome were eliminatedthan from A genome which indicated that the stability of three genome showingrelationships with B>A>C.
     6. RT-PCR SSCP analyses revealed that rRNA genes from A/C genome had beentranscripted in only hybrid but rRNA genes from B genome were transcripted in allhybrids. The plant contained 14 chromosomes which indicated that the deleted twochromosomes might have rDNA locus.
     7. Here extra divisions and nuclei fusions were observed to occur in microsporenuclei of partial hybrids between synthetic Brassica hexaploid I and O.violaceus.
     Abnormal spindle were formed and chromosomes were separated into several nuclei ofvariable sizes after bi-, or multi-polar divisions in the four cells of tetrads. As aconsequence, more than eight mini-microspores of different sizes were produced by onetetrad. Genomic in situ hybridization results indicated that no chromosome replicationoccurred during such divisions. In some tetrads, the four nuclei were fused to form onelarge cell with increased chromosome number. The extra divisions or fusions appearedonly in some flower buds of one plant, some anthers in the same buds, or even inindividual cells of tetrads. The possible mechanisms behind these cytological phenomenawere discussed.
     8. In meiosis of one hybrid between hexaploidⅢand O.violaceus, no chromosomepairing was found at diakinesis. Univalents then congregated which were found always atedge of the cell. Congregated chromosomes then separated randomly to two poles.However, cytoplasm did not divide. Cells with two nuclei then stopped development butformed thick ektexine which were dyed darkly. No spindle was found when specific dyefor spindle was used for those cells.
     Finally, chromosome behavior of hybrids between Brassica hexaploid andO.violaceus was different from that of hybrids between diploid or tetraploid andO.violaceus. Probably, zygote cells experienced chromosome double and partial parentgenome separation during development. More C genome chromosomes were divided intocells with more O.violaceus chromosomes and those cells were eliminated later. Thespecific genome rRNA gene expression might help to stabilize its chromosomes.O.violaceus chromatin introgression lead to alternation of maternal genome structure anddisturbed gene expression, such as new AFLP bands emergence and abnormal meiosis.
引文
1.陈纯贤,孙敬三,朱立煌.导入小麦加倍单倍体植株的玉米DNA在后代中的遗传及序列同源性分析[J].植物学报,2000,42(7):728-731
    2.陈纯贤,孙敬三,朱立煌.由小麦×玉米获得的普通小麦加倍单倍体后代的RFLP变异[J].植物学报,1999,41(1):55-59
    3.陈纯贤,朱立煌,孙敬三.玉米特异DNA通过有性杂交导入小麦DH后代的分子证据[J].中国科学(C),1997,27(5):432-437
    4.胡琼,李云昌.体细胞杂交在油菜细胞质雄性不育创建和改良中的应用[J].作物学报,2006,1:138-143
    5.华玉伟.诸葛菜与芸薹属三个四倍体栽培种杂种的分子细胞遗传学研究.[博士学位论文].武汉:华中农业大学图书馆,2005
    6.胡婷婷.甘蓝型油菜和诸葛菜的体细胞杂交研究.[硕士学位论文].武汉:华中农业大学图书馆,2006
    7.李大玮,欧阳平,姚庆筱.普通小麦与鸭茅状摩擦禾的远缘杂交Ⅱ.未成熟胚的培养[J].遗传学报,1994,21(6):474—478
    8.李再云.甘蓝型油菜与诸葛菜属间杂交新材料的染色体行为及其进化意义[J].自然科学进展,2003,13(8):807—813
    9.李再云,华玉伟,葛贤宏,徐传远.植物远缘杂交中的染色体行为及其遗传与进化意义[J].遗传,2005,27(2):315—324
    10.李柱刚,崔崇士,马荣才,曹鸣庆,王广.芸墓属植物基因组学研究进展[J].中国生物工程杂志,2005,,25(8):30—34
    11.栗茂腾,张椿雨,刘列钊,余龙江.芸薹属A,B和C基因组之间关系研究进展[J].遗传,2005,27(4):671—676
    12.栗茂腾.甘蓝型油菜新类型创建及油菜亚基因组间杂种优势研究.[博士学位论文].武汉:华中农业大学图书馆,2003
    13.栗茂腾,张椿雨,李宗芸,孟金陵.埃塞俄比亚芥与白菜型油菜间六倍体杂种的获得及其生物学特性研究[J].作物学报,2005,12:1579—1585
    14.刘曼.白菜和白菜型油菜与诸葛菜杂种及后代的遗传研究.[硕士学位论文].武汉:华中农业大学图书馆,2005
    15.吕世友,李彦舫,陈祖铿,林金星.花粉发育的研究进展[J].植物学通报,2001,18(3):340—346
    16.马霓.高油酸的甘蓝型油菜与诸葛菜属间杂交新材料的细胞学和遗传学研究.[博士学位论文].武汉:华中农业大学图书馆,2006
    17.牛应泽,汪良中,刘玉贞,郭世星.利用人工合成甘蓝型油菜创建人工合成种[J].中国油料作物学报,2003,25(4):11—15
    18.孙敬三,方仁.利用小麦×玉米获得小麦单倍体[J].1992,植物学报,34:817—821
    19.孙敬三,王景林.莜麦与玉米的远缘杂交[J].植物学报,1995,37:255—258
    20.孙敬三等,路铁刚.小麦×高梁的受精率和小麦单倍体的诱导(简报)[J].实验生物学报,1996,29:191~194
    21.王汉中.发展油菜生物柴油的潜力、问题与对策[J].中国油料作物学报,2005,27(2):74—76
    22.吴征镒,路安民,汤彦承.中国被子植物科属综论[M].北京:科学出版社,2003
    23.伊增芳,樊汝汶.花粉发育的电镜研究进展[J].南京林业大学学报,1993,17(1):91—95
    24.周清元,李加纳,崔翠,殷家明,谌利,唐章林.芥菜型油菜×羽衣甘蓝种间杂种的获得及其性状表现[J].作物学报,2005,131(18):1058—1063
    25.周清元,殷家明,崔翠,林呐,谌利,唐章林,李加纳.白菜型油菜×羽衣甘蓝种间杂种的性状表现[J].西南农业大学学报(自然科学版),2006,28(1):1—7
    26. Albertsen M C and Phillips R L. Developmental cytology of 13 genetic male sterile loci in maize[J]. Can. J. Genet.Cytol, 1981, 25:195-208
    27. Alves E R, Carneiro V T, Araujo A C. Direct evidence of pseudogamy in apomictic Brachiaria brizantha (Poaceae) [J]. Sexual Plant Reproduction, 2001, 14(4): 207-212
    28. Apel P, Bauwe H, Ohle H. Hybrids between Brassica alboglabra and Moricandia arvensis and their photosynthetic properties [J]. Biochem Physiol Pflanz, 1984, 179:793-797
    29. Armstrong K C, Keller W. A Chromosomes pairing in haploid of Brsssica campestris [J]. Theor Appl Genet, 1981, 59:49-52
    30. Armstrong K C, Keller W A. Chromosomes pairing in haploid of Brsssica oleracea [J]. Can J Genet Cytol, 1982, 24:735-739
    31. Armstrong S J, Caryl A P, Jones G H, Franklin F C H. Asyl, a protein required for meiotic chromosome synapsis, localizes to axis-associated chromatin in Arabidopsis and Brassica [J]. J Cell Sci, 2002, 115:3645-3655
    32. Armstrong S J, Franklin F C H, Jones G H. Nucleolusassociated telomere clustering and pairing precede meiotic chromosome synapsis in Arabidopsis thaliana [J]. J Cell Sci, 2001, 114: 4207-4217
    33. Ar-Rushdi A H. The cytogenetics of variegation in a species hybrid in Nicotiana [J]. Genetics, 1957, 42:312-325
    34. Atria T, Busso C, RObbelen G. Dignomic triploids for an assessment of chromosome relationships in the cultivated diploid Brassica species [J]. Genome, 1987, 29:326-330
    35. Attia T, RObbelen G. Cytogenetic relationship within cultivated Brassica analyzed in amphihaploids from the three diploid ancestors [J]. Can J Genet Cytol, 1986, 28:323-329
    36. Bai X, Peirson B N, Dong F, Xue C, Makaroff C A. Isolation and characterization of SYN1, a RAD21-like gene essential for meiosis in Arabidopsis [J]. The Plant Cell, 1999,11: 417-430
    
    37. Bang S W, Kaneko Y, Matsuzawa Y. Production of intergeneric hybrids between Raphanus and Moricandia [J]. Plant Breed, 1996,115: 385-390
    
    38. Banga S S, Bhaskar P B, Ahuja I. Synthesis of intergeneric hybrids and establishment of genomic affinity between Diplotaxis catholica and crop Brassica species [J]. Theor Appl Genet, 2003,106:1244-1247
    
    39. Bannerot T. L, Boulidard L, Cauderon Y, Tempe J. Transfer of cytoplasmic male sterility from Raphanus sativus to Brassica oleracea [C]. Eucarpia Meeting on Cruciferae. Dundee. Scotland, 1974,52-54.
    
    40. Barclay I R. A study of the genetics and mechanism of genome and chromosome loss in cereals. PhD Thesis, Cambridge, 1976
    
    41. Barclay, I. R. High frequencies of haploid production in wheat (Triticum aestivum) by chromosome elimination [J]. Nature, 1975,256:410—411
    
    42. Bass H W, Marshall W F, Sedat J W, Agard D A and Cande W Z. Telomeres cluster de novo before the initiation of synapsis: A three-dimensional spatial analysis of telomere positions before and during meiotic prophase [J]. J Cell Biol, 1997,137: 5-18.
    
    43. Bassam B J, Caetano-Anolles G, Gresshoff P M. Fast and sensitive silver staining of DNA in polyacrylamide gels [J]. Analytical Biochemistry, 1991,196: 80-83.
    
    44. Bennett M D, Finch R A, Barclay I R. The time rate andmechanism of chromosome elimination in Hordeum hybrids [J]. Chromosoma, 1976,54:175-200
    
    45. Bhatt A M, Lister C, Page T, Fransz P, Findlay K, Jones G H, Dickinson HG and Dean C. The DIF1 gene of Arabidopsis is required for meiotic chromosome segregation and belongs to the REC8/RAD21 cohesin gene family [J]. Plant J, 1999,19: 463-472.
    
    46. Bishop J D, Han Z, Schumacher J M The Caenorhabditis elegans Aurora B kinase AIR-2 phosphorylates and is required for the localization of a BimC kinesin to meiotic and mitotic spindles [J]. Mol Biol Cell, 2005,16: 742-56
    
    47. Blangy A, Lane HA, d'Herin P, Harper M, Kress M, Nigg EA Phosphorylation by p34cdc2 regulates spindle association of human Eg5, a kinesin-related motor essential for bipolar spindle formation in vivo [J]. Cell, 1995,83:1159-1169
    
    48. Brewbaker J L. The distribution and phylogenetic significance of binucleate and trinucleate pollen grains in the angiosperms [J]. Am J Bot, 1967,54:1069-1083
    
    49. Brewer E P,. Saunders J A, Scott Angle J, Chaney R L, McIntosh M S. Somatic hybridization between the zinc accumulator Thlaspi caerulescens and Brassica napus [J]. Theor Appl Genet, 1999, 99: 761-771
    
    50. Busso C, Attia T, Robbelen G Trigenomic combinations for the analysis of meiotic control in the cultivated Brassica species [J]. Genome, 1987, 29: 331-333
    
    51. Caetano-Pereira C M and Pagliarini M S. A new meiotic abnormality in Zea mays: Multiple spindles associated with abnormal cytokinesis in both divisions [J]. Genome, 2001,44: 865-871
    
    52. Cai X, Makaroff C A. The dsy10 mutation of Arabidopsis results in desynapsis and a general breakdown in meiosis [J]. Sexual Plant Reproduction, 2001,14: 63-67
    
    53. Caryl A P, Armstrong S J, Jones G H and Franklin F C H. A homologue of the yeast HOP1 gene is inactivated in the Arabidopsis meiotic mutant asyl [J]. Chromosoma, 2000,109: 62-71.
    
    54. Catchside DG The chromosomal relationship in the Swede and turnip groups Brassica [J]. Ann Bot, 1934,48: 601-633
    
    55. Chaudhury AM, Lavithis M, Taylor PE, Graig S, Singh MB, Signer ER, Knox RB, Dennis ES. Genetic control of male fertility in Arabidopsis thaliana; structural analysis of premeiotic developmental mutants [J]. Sex Plant Reprod, 1994,7:17-28
    
    56. Chen A, Cande W Z. Maize meiotic spindles assemble around chromatin and do not require paired chromosomes [J]. J Cell Sci, 1998, 111: 3507-3515
    
    57. Chen B Y, Cheng B F, Jurgensen R B, Heneen W K. Production and cytogenetics of Brassica campestris-alboglabra chromosome addition lines [J]. Theor Appl Genet, 1997,94: 633-640.
    
    58. Chen B Y, Heneen W K, Jφnsson R. Resynthesis of Brassica napus L. through interspecific hybridization between B. alboglabra Bailey and B. campestris L. with special emphasis on seed colour [J]. Plant Breed, 1988,101: 52-59
    
    59. Chen C, Marcus A, Li W, Hu Y, Calzada J P V, Grossniklaus U, Cyr R J, Ma H. The Arabidopsis ATK1 gene is required for spindle morphogenesis in male meiosis [J]. Development, 2002,129:2401-2409
    
    60. Chen Y C, McCormick S. sidecar pollen, an Arabidopsis thaliana male gametophytic mutant with aberrant cell divisions during pollen development [J]. Development, 1996, 122: 3243-3253
    
    61. Chen Z J, Pikaard C S, Transcriptional analysis of nucleolar dominance in polyploid plants: Biased expression/silencing of progenitor rRNA genes is developmentally regulated in Brassica [J]. Proc Natl Acad Sci USA, 1997a, 94: 3442-3447
    
    62. Chen Z J, Pikaard C S. Epigenetic silencing of RNA polymerase I transcription: a role for DNA methylation and histone modification in nucleolar dominance [J]. Genes & Development, 1997b, 11: 2124-2136
    
    63. Chen Z J, Comai L, Pikaard, CS. Gene dosage and stochastic effects determine the severity and direction of uniparental rRNA gene silencing (nucleolar dominance) in Arabidopsis allopolyploids [J]. Proc Natl Acad Sci, USA, 1998,95:14891-14896
    
    64. Cheng B F, Seguin-Swartz G, Somers D J. Cytogenetic and molecular characterization of intergeneric hybrids between Brassica napus and Orychophragmus violaceus [J]. Genome, 2002,45:110-115
    
    65. Choudhary B R, Joshi P, Ramarao S. Interspecific hybridization between Brassica carinata and Brassica rape [J]. Plant Breed, 2000, 119: 417-420
    
    66. Chyi Y S, Hoenecke M., Sernyk J L. A genetic linkage map of restriction fragment length polymorphism loci for Brassica rapa [J]. Genome, 1992, 35: 746-757
    
    67. Comeau A, Nadeau P, Plourde A, Simard R, Maes O, Kelly S, Harper L, Lettre J, Landry B, St-Pierre C-A. Media for the in ovulo culture of proembryos of wheat and wheat-derived inter-specific hybrids and haploids [J]. Plant Sci, 1992, 81:117-125
    
    68. Davies D R. Male parthenogenesis in barley [J]. Heredity, 1958,12:493-498
    
    69. Davies D R. Chromosome elimination in inter-specific hybrids [J]. Heredity, 1974, 32: 267-270
    
    70. Dell KR, Turck CW, Vale RD. Mitotic phosphorylation of the dynein light intermediate chain is mediated by cdc2 kinase [J]. Traffic, 2000,1: 38-44
    
    71. Dellaporta S L, Wood J, Hicks J B A. plant DNA mini preparation [J]: version II. Plant Mol Biol Rep, 1983,1:19-21
    
    72. Dernburg A F, Sedat J W, Cande W Z, Bass H W. Cytology of telomeres [M]. In, E.H. Blackburn and C.W. Grieder, eds. Telomeres. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press, 1995, 295-338
    
    73. Donini P, koebner R M D, Ceoloni C. Cytogenetic and molecular mapping of the wheat-Aegilops longissima chromatin breakpoints in powdery mildew-resistant introgression lines [J]. Theor Appl Genet, 1996, 9-1: 738-743
    
    74. Dunaway M. A transcription factor, TFIS, interacts with both the promoter and enhancer of the Xenopus rRNA genes [J]. Genes Dev, 1989,3:1768-1778
    
    75. Durbarry A, Vizir I, Twell D. Male germ line development in Arabidopsis. duo pollen mutants reveal gametophytic regulators of generative cell cycle progression [J]. Plant Physiol, 2005,137(1): 297-307
    
    76. Eady C, Lindsey K, Twell D. The significance of microspore division and division symmetry for vegetative cell-specific transcription and generative cell differentiation [J]. The Plant Cell, 1995,7:65-74
    
    77. Earley K, Lawrence RJ, Pontes O, Reuther R, Enciso AJ, Silva M, Neves N, Gross M, Viegas W, Pikaard CS. Erasure of histone acetylation by Arabidopsis HDA6 mediates large-scale gene silencing in nucleolar dominance [J]. Genes Dev. 2006,20(10): 1283-1293
    
    78. Endow SA. Microtubule motors in spindle and chromosome motility [J]. Eur J Biochem, 1999, 262(1):12-8
    
    79. Fahleson J, Eriksson I and Glimelius K. Intertribal somatic hybrids between Brassica napus and Barbarea vulgaris-production of in vitro plantlets [J]. Plant Cell Rep, 1994a, 13: 411-416
    
    80. Fahleson J, Eriksson I, Landgren M, Stymne S and Glimelius K. Intertribal somatic hybrids between Brassica napus and Thlaspi perfoliatum with high content of the T perfoliatum-specific nervonic acid [J]. Theor. Appl. Genet, 1994b, 87: 795-804
    
    81. Fahleson J, Lagercrantz U, Mouras A, Glimelius K Characterization of somatic hybrids between Brassica napus and Eruca sativa using species-specific repetitive sequences and genomic in situ hybridization [J]. Plant Sci, 1997,123: 133-142
    
    82. Fahleson J, Rahlen L, Glimelius K. Analysis of plants regenerated from protoplast fusions between Brassica napus and Eruca sativa. [J]. Theor Appl Genet, 1988,76: 507-512
    
    83. Falk D E, Kasha K J. Genetic studies of the crossability of hexaploid wheat with rye and Hordeum bulbosum [J]. Theor Appl Genet, 1983,64: 303-307
    
    84. Faure N, Serieys H, Berville A, Cazaux E, Kaan F. Occurrence of partial hybrids in wide crosses between sunflower (Helianthus annuus) and perennial species H. mollis and H. orgyalis [J]. Theor Appl Genet, 2002a, 104: 652-660
    
    85. Faure N, Serieys H, Cazaux E, Kaan F, Berville A. Partial hybridization in wide crosses between cultivated sunflower and the perennial Helianthus species H. mollis and H. orgyalis [J]. Ann Bot (Lond), 2002b, 89(1): 31-39
    
    86. Ferreira M E, Williams P H, Osborn T C. RFLP mapping of Brassica napus using doubled haploid lines [J]. Theor Appl Genet, 1994,89: 615-621
    
    87. Filho R J, Mendes-Bonato A B, Pagliarini M S, Bione N C, Valle C B, Penteado M I. Absence of microspore polarity, symmetric divisions and pollen cell fate in Brachiaria decumbens (Gramineae) [J]. Genome, 2003,46: 83-88
    
    88. Finch RA. Tissue-specific elimination of alternative whole parental genomes in one barley hybrid [J]. Chromosoma, 1983,88: 386-393
    
    89. Finch R A, Bennett M D The mechanism of somatic chromosome elimination in Hordeum [C]. In: Brandham P E, ed. Kew Chromosome Conference II: Proceedings of the Second Chromosome Conference, London: Allen & Unwin, 1983,146-153
    
    90. Flavell RB. The structure and control of expression of ribosomal RNA genes [J]. Oxford Surv. Plant Mol Cell Biol, 1986,3:252-274
    
    91. Flavell RB, O"Dell M. The genetic control of nucleolus formation in wheat [J]. Chromosoma, 1979,71:135-152
    
    92. Foisset N, Delourme R,Barret P, Hubert N, Landry B S, Renard. Molecular-mapping analysis in Brassica napus using isozyme, RAPD and RFLP markers on a doubled-haploid progeny [J]. Theor Appl Genet, 1996,93:1017-1025
    
    93. Franklin A E and Cande W Z. Nuclear Organization and Chromosome Segregation [J]. The Plant Cell, 1999,11: 523-534
    
    94. Furusho M, Suenaga K, Nakajima K. Production of haploid barley plants from barley ×maize and barley ×ltalian ryegrass crosses [J]. Jpn J Breed, 1991, 41:175-179
    
    95. Gernand D, Rutten T, Varshney A, Rubtsova M, Prodanovic S, Bruss C, Kumlehn J, Matzk F, Houben A. Uniparental chromosome elimination at mitosis and interphase in wheat and pearl millet crosses involves micronucleus formation, progressive heterochromatinization, and DNA fragmentation [J]. Plant Cell, 2005,17(9): 2431-2438
    
    96. Glover J, Grelon M, Craig S, Chaudhury A, Dennis E. Cloning and characterization of MS5 from Arabidopsis: a gene critical in male meiosis [J]. Plant J, 1998,15: 345- 356
    
    97. Golubovskaya I N. Genetic control of meiosis [J]. Int Rev Cytol, 1979, 58: 247-290
    
    98. Gupta SB Duration of mitotic cycle and regulation of DNA replication in Nicotiana plumbaginifolia and a hybrid derivative of N. tabacum showing chromosome instability [J]. Can J Genet Cytol, 1969,11,133-142
    
    99. Grummt I, Roth E, Paule M R. rRNA transcription in vitro is species-specific [J]. Nature, 1982, 296:173-174
    
    100. Haga T. Relationship of genome to secondary pairing in Brassica (a preliminary note) [J]. Jpn J Genet, 1938,13:177-284
    
    101. Hagimori M, Nagaoka M, Kato N, Yoshikawa H. Production and characterization of somatic hybrids between the Japanese radish and cauliflower [J]. Theor Appl Genet, 1992, 82: 819-824
    
    102. Hansen L N, Intertribal somatic hybridization between rapid cycling Brassica oleracca L. and Camelina sativa (L,) Crantz [J]. Euphytica, 1998,104,173-179
    
    103. Hansen L N, Earle E D. Somatic hybridization between Brassica kleracea L. and Sinapis alba L. with resistance to Alternaria brassicae (Berk.) Sacc [J]. Theor Appl Genet, 1997, 94: 1078-1085
    
    104. Heitz E. Nukleolen und Chromosomen in der Gattung Vicia [J]. Planta, 1931,15:495-505
    
    105. Heslop-Harrison J S, Schwarzacher T. Genomic Southern and in situ hybridization for plant genome analysis. In: Jauhar PP, ed., Methods of genome analysis in plants [J]. Boca Raton, Fla. CRC Press, 1996, pp. 163-179
    
    106. Heyn F W. Transfer of restorer genes from Raphanus to cytoplasmic male sterile Brassica napus [J]. Cruciferae Newsl, 1976,1:15-16
    
    107. Hohmann U, Graner A, Endo T R. Comparison of wheat physical maps with barley linkage maps for group 7 chromosomes [J]. Theor Appl Genet, 1995,91(5): 618-626
    
    108. Hu Q, Andersen S B, Dixelius C, Hansen L N. Production of fertile intergeneric somatic hybrids between Brassica napus and Sinapis arvensis for the enrichment of the rapeseed gene pool [J]. Plant Cell Rep, 2002b, 21 (2): 147-152
    
    109. Hu Q, Hansen L N, Laursen J, Dixelius C, Andersen S B. Intergeneric hybrids between Brassica napus and Orychophragmus violaceus containing traits of agronomic importance for oilseed rape breeding [J]. Theor Appl Genet, 2002a, 105: 834-840
    
    110. Hua Y W, Liu M, Li Z Y. Parental genome separation and elimination of cells and chromosomes revealed by AFLP and GISH analyses in a Brassica carinata ×Orychophragmus violaceus cross [J]. Ann Bot, 2005,97: 993-998
    
    111. Hulskamp M, Parekh N S, Grini P, Schneitz K, Zimmermann I, Lolle S J and Pruitt R E. The STUD gene is required for male-specific cytokinesis after telophase II of meiosis in Arabidopsis thaliana [J]. Dev Biol, 1997, 187: 114-124
    
    112. Hatsumi M, Endow S. Mutants of the microtubule motor protein, nonclaret disjunctional, affect spindle structure and chromosome movement in meiosis and mitosis [J]. J Cell Sci,1992, 101: 547-559
    
    113. Inagaki M, Tahir M. Comparison of haploid production frequencies in wheat varieties Crossed with Hordeum Bulbosum L. and maize [J]. Jpn J Breed, 1990, 40: 209-216
    114. Inomata N. Embryo rescue techniques for wide hybridization. In: K S Labana S S. Banga K Banga Shashi, eds. Breeding Oilseed Brassicas [J] Monogr Theor Appl Genet, 1993, 19; 94-105
    
    115. Islam A K M R, Shepherd, K W, Sparrow, D H B. Isolation and characterization of euplasmic wheat-barley chromosome. addition lines [J]. Heredity, 1981,46:161-174
    
    116. Jauhar P P, Dogramaci M, Peterson T S. Synthesis and cytological characterization of trigeneric hybrids of durum wheat with and without ph1 [J]. Genome, 2004,47:1173-1181
    
    117. Jenczewski E, Eber F, Grimaud A Huet S, Lucas M O, Monod H, Chevre A M. PrBn, a major gene controlling homeologous pairing in oilseed rape (Brassica napus) haploids [J]. Genetics, 2003,164: 645-653
    
    118. Jin W W, Melo J R, Nagaki K, Talbert PB, Henikoff S, Dawe R K, Jiang JM. Maize centromeres: Organization and functional adaptation in the genetic background of oat [J]. Plant Cell, 2004,16: 571-581
    
    119. Kaneko Y, Matsuzawa Y, Sarashima M. Breeding of the chromosome addition lines of radish with single kale chromosome [J]. Jpn J Breed, 1987,37,438-452
    
    120. Kao Ko N, Kasha K J. Haploidy from interspecific crosses with tetraploid barley [C]. Proc. 2nd Int. Barley Genet, Symp, II. 1969,82-88
    
    121. Kasha K J, Reinbergs E. Recent developments in the production and utilization of haploids in barley [C]. In: Asher MJC (ed), Barley genetics, IV. Proc 4th Intern Barley Genet Symp, Edinbrugh, 1981,655-665
    
    122. Kasha K J, Kao K N. High frequency haploid production in barley (Hordeum vulgare L.) [J]. Nature, 1970,225: 874-876
    
    123. Kianian S F, Quiros C F. Generation of a Brassica oleracea composite RFLP map: linkage arrangements among various populations and evolutionary implications [J]. Theor Appl Genet, 1992, 84: 544-554
    
    124. Kim N S, Armstrong K C, Fedak G, Ho K, Park N I.A microsatellite sequence from the rice blast fungus (Magnaporthegrisea) distinguishes between the centromeres of Hordeum vulgare and H. bulbosum in hybrid plants [J]. Genome, 2002, 45,165-174
    
    125. Kirti P B, Baldev A, Gaikwad K, Bhat S, Dineshkumar V, Prakash S, Chopra V L. Introgression of a gene restoring fertility to the CMS (Trachystoma) Brassica juncea and the genetics of restoration [J]. Plant Breed, 1997,116:259-262
    
    126. Kirti P B, Banga S S, Prakash S, Chopra V L. Transfer of Ogu cytoplasmic male-sterile line of Brassica juncea and improvement of the male sterile through somatic cell fusion [J]. Theor Appl Genet, 1995a, 91: 517-521
    
    127. Kirti P B, Narasimhulu S B, Prakash S, Chopra V L. Somatic hybridization between Brassica juncea and Moricandia arvensis by protoplast fusion [J]. Plant Cell Rep, 1992a, 11: 318-321
    
    128. Kirti PB, Mohapatra T, Khanna H, Prakash S and Chopra VL. Diplotaxis catholica + Brassica juncea somatic hybrids: molecular and cytogentic characterization [J]. Plant Cell Rep, 1995b. 14,593-597
    
    129. Kirti P B, Narasimhulu S B, Prakash S, Chopra V L. Production and characterization of intergeneric somatic hybrids of Trachystoma ballii and Brassica juncea [J]. Plant Cell Rep, 1992b, 11: 90-92
    
    130. La Cour LF. Nuclear differentiation in the pollen grain. Heredity, 1949,3: 319-337
    
    131. Labhart P, Reeder RH. Enhancer-like properties of the 60/81 bp elements in the ribosomal gene spacer of Xenopus laevis [J]. Cell, 1984, 37: 285-289
    
    132. Lagercrantz U, Lydiate D. Comparative genome mapping in Brassica [J]. Genetics, 1996,144: 1903-1910
    
    133. Lagercrantz U, Lydiate D J. RFLP mapping in Brassica nigra indicates differing recombination rates in male and female meioses [J]. Genome, 1995,38(2): 255-264
    
    134. Lanaud C. Origin of haploids and semigamy in Theobroma cacao L [J]. Euphytica, 1988, 38(3):221-228
    
    135. Landry B S, Hubert N, Crete R, Chang M S, Lincoln S E, Etho T. A genetic map of Brassica oleracea based on RFLP markers detected with expressed DNA sequences and mapping of resistance genes to race 2 of Plasmodiophora brassicae (Woronin) [J]. Genome, 1992, 35: 409-420
    
    136. Lange W. Crosses between Hordeum vulgare L. and H. bulbosum L. II. Elimination of chromosomes in hybrid tissues [J]. Euphytica, 1971,20:181-194
    
    137. Laurie D A, Bennett M D. The effect of the cross ability loci Kr1 and Kr2 on fertilization frequency in hexaploid wheat×maize crosses [J]. Theor Appl Genet, 1988a,76: 393~397
    
    138. Laurie D A. The frequency of fertilization in wheat × pearl millet crosses [J]. Genome, 1989, 32:1063-1067
    
    139. Laurie D A, Bennett M D. The effect of the crossability loci Kr1 and Kr2 on fertilization frequency in hexaploid wheat ×maize crosses [J]. Theor Appl Genet, 1987,73:403—409
    
    140. Laurie D A, Bennett M D. Early post-pollination events in hexaploid wheat × maize crosses [J]. Sex Plant Reprod, 1990a, 3:70-76
    
    141. Laurie D A, Bennett M D. The timing of chromosome elimination in hexaploid wheat×maize crosses [J]. Plant Breed, 1991,106:182-189
    
    142. Laurie D A, O'Donoughue L S, Bennett M D. Wheat × maize and other wide sexual hybrids: their potential for genetic manipulation and crop improvement [M]. In: J. P. Gustafson, ed. Gene Manipulation in Plant Improvement. Plenum Press, New York, USA, 1990b, Vol. 2, 95-126
    
    143. Laurie D A, Bennett M D. Wheat × maize hybridization [J]. Can J Genet Cytol, 1986, 28: 313-316
    
    144. Laurie D A, Bennett M D. Cytological evidence for fertilization in hexaploid wheat × sorghum crosses [J]. Plant Breed, 1988b, 100: 73-82
    
    145. Laurie D A, Bennett M D. The timing of chromosome elimination in hexaploid wheat × maize crosses [J]. Genome, 1989, 32: 953-961
    146. Lawrence R J, Earley K, Pontes O, Silva M, Chen Z J, Neves N, Viegas W, Pikaard C S. A concerted DNA methylation/histone methylation switch regulates rRNA gene dosage control and nucleolar dominance [J]. Mol Cell, 2004, 13: 599-609
    147. Leino M, Teixeira R, Landgren M, Glimelius K. Brassica napus lines with rearranged Arabidopsis mitochondria displays CMS and a range of developmental aberrations [J]. Theor Appl Genet, 2003, 106: 1156-1163
    148. Leino M, Thyselius S, Landgren M, Glimelius K. Arabidopsis thaliana chromosome Ⅲ. restores fertility in a cytoplasmic male-sterile Brassica napus line with A. thaliana mitochonddal DNA [J]. Theor Appl Genet, 2004, 109: 272-279
    149. Leitch A R, Schwarzacher T, Jackson D, Leitch I J. In situ hybridization: a practical guide [M]. In: Microscopy Handbook No.27. Oxford: Bios Scientific, 1994
    150. Li M, Qian W, Meng J, Li Z. Construction of novel Brassica napus genotypes through chromosomal substitution and elimination using interploid species hybridization [J]. Chromosome Res, 2004, 12: 417-426
    151. Li M T, Li Z Y, Zhang C Y, Qian W, Meng J L. Reproduction and cytogenetic characterization of interspecific hybrids derived from crosses between Brassica carinata and B. rapa [J]. Theor Appl Genet, 2005, 110: 1284-1289
    152. Li Z, Heneen W K. Production and cytogenetics of intergeneric hybrids between the three cultivated Brassica diploids and Orychophragmus violaceus [J]. Theor Appl Genet, 1999, 99: 694-704
    153. Li Z, Liu H L, Luo P. Production and cytogenetics of intergenedc hybrids between Brassica napus and Orychophragmus violaceus [J]. Theor Appl Genet, 1995, 91: 131-136
    154. Li Z, Wu J G, Liu Y, Liu H L, Heneen W K. Production and cytogenetics of intergeneric hybrids Brassica juncea ×Orychophragmus violaceus and B. carinata×O. violaceus [J]. Theor Appl Genet, 1998, 96: 251-265
    155. Linde-Laursen I, Bothmer R von. Elimination and duplication of particular Hordeum vulgate chromosomes in aneuploid interspecific Hordeum hybrids [J]. Theor Appl Genet, 1988, 76: 897-908
    156. Linde-Laursen I, yon Bothmer R. Orderly arrangement of the chromosomes within barley genomes of chromosome-eliminating Hordeum lechleri x barley hybrids [J]. Genome, 1999, 42: 225-236
    157. Liu B, Wendel J F. Retrotransposon activation followed by rapid repression in introgressed rice plants [J]. Genome, 2000, 43(5): 874-80
    158. Liu M, Li Z Y. Genome doubling and chromosome elimination with fragment recombination leading to the formation of Brassica rapa-type plants with genomic alterations in crosses with Orychophragmus violaceus [J]. Genome, 2007, In Press
    159. Liu Q, Golubvskaya I, Cande W Z. Abnormal cytoskeletal and chromosome distribution in po, ms4 and ms6: mutant alleles of polymitotic that disrupt the cell cycle progression from meiosis to mitosis in maize [J]. J Cell Sci, 1993,106:1169-1178
    
    160. Liu Z, Adamczyk K, Manzanares-Dauleux M, Eber F, Lucas M O, Delourme R, Chevre A M, Jenczewski E. Mapping PrBn and Other Quantitative Trait Loci Responsible for the Control of Homoeologous Chromosome Pairing in Oilseed Rape (Brassica napus L.) Haploids [J]. Genetics, 2006, in press
    
    161. Liu Z, Wang Y, Shen Y, Guo W, Hao S, Liu B. Extensive alterations in DNA methylation and transcription in rice caused by introgression from Zizania latifolia [J]. Plant Mol- Biol, 2004, 54(4): 571-582
    
    162. Liu B, Piao H M, Zhao F S, Zhao JH, Zhao R. Production and molecular characterization of rice lines with introgressed traits from a wild species of Zizania latifolia Griseb [J]. J Genet Breed, 1999,53: 279-284
    
    163. Lukaszewski A J. Physical distribution of translocation break-.points in homoeologous recombinants induced by the absence of the Ph1 gene in wheat and triticale [J]. Theor Appl Genet, 1995,90: 714-719
    
    164. Lydiate, D J; Sharpe, A G; Lagercrantz, U; Parkin, I A P. Mapping the Brassica Genome [J]. Outlook on Agriculture, 1993, 22: 85-92.
    
    165. Manton I. Introduction to the general cytology of the Cruciferae [J]. Ann Bot, 1932, 46: 509-556
    
    166. Mariani C, Beckeleer M D, Truettner J, Leemans J and Goldberg R B. Induction of male sterility in plant by a chimaeric ribonuclease gene [J]. Nature, 1990,347: 737-741
    
    167. Martin A, Jouve N. In: Kallo G, Chowdury J B (eds). Distant Hybridization of Crop Plants [M]. Monog Theor Appl Genet 16. Springer-Verlag, Berlin Heidelberg New York ,1992, 94-105
    
    168. Martini G, O'Dell M, Flavell RB. Partial inactivation of wheat nucleolus organizers by the nucleolus organizer chromosomes from Aegilops umbellulata [J]. Chromosoma, 1982, 84: 687-700
    
    169. McClintock B. The relationship of a particular chromosomal element to the development of the nucleoli in Zea mays. Z Zellforsch Mikr [J]. Anat, 1934, 21: 294-328
    
    170. McCormick S. Control of Male Gametophyte Development [J]. Plant Cell, 2004, 16: S142-S153
    
    171. McGrath J M, Quiros C F, Harada J J, Landry B S. Identification of Brassica oleracea monosomic alien chromosome addition lines with molecular markers reveals extensive gene duplication [J]. Mol Gen Genet, 1990, 223: 198-204
    
    172. McStay B. Nucleolar dominance: a model for rRNA gene silencing [J]. Genes Dev. 2006, 20(10): 1207-1214
    
    173. Mendes-Bonato AB, Pagliarini MS, Forli F, Valle CB, Penteado MIO. Chromosome number and microsporogenesisi in Brachiaria brizantha (Gramineae) [J]. Euphytica, 2002, 125: 419-425
    
    174. Meng J, Yan Z, Tian Z, Huang R, Huang B. Somatic hybrids between moricandia nitens and three Brassica species [C]. Proc. 10th Intl. Rapeseed Congr., Australia. Contribution, 1999, No.6
    
    175. Meng J L, Gan L, Zhun Y. Hybridization and hybrids between Moricandia arvensis, M. nitens and three Brassica napus [J]. Cruciferae Newslerr. Eucarpia, 1997,19: 25-26
    
    176. Mercier R, Armstrong S J, Horlow C, Jackson N P, Makaroff C A, Vezon D, Pelletier G, Jones G H, Franklin F C. The meiotic protein SWI1 is required for axial element formation and recombination initiation in Arabidopsis [J]. Development, 2003,130: 3309-3318
    
    177. Mercier R, Vezon D, Bullier E, Motamayor JC, Sellier A, Lefevre F, Pelletier G and Horlow C. SWITCH1 (SWI1): a novel protein required for the establishment of sister chromatid cohesion and for bivalent formation at meiosis [J]. Genes Dev, 2001,15(14): 1859-1871
    
    178. Miesfeld R, Arnheim N. Species-specific rDNA transcription is due to promoter-specific binding factors [J]. Mol Cell Biol, 1984,4:221-227
    
    179. Mishima Y, Financsek I, Kominami R, Muramatsu M. Fractionation and reconstitution of factors required for accurate transcription of mammalian ribosomal RNA genes: identification of a species-dependent initiation factor [J]. Nucl Acids Res, 1982,10: 6659-6670
    
    180. Mizushima U. Karyogenetic studies of species and genus hybrids in the tribe Brassiceae of Cruciferae [J]. Tohoku J Agric Res, 1950,1:1-14
    
    181. Mizushima U. Genome analysis in Brassica and allied genera [M]. In: Tsunoda S, Hinata K, C.Gomez-Campo C, eds. Brassica Crops and Wild Allies, Biology and Breeding. Tokyo: Japan Scientific Soc. Press, 1980,89-106
    
    182. Mochida K, Tsujimoto H, Sasakuma T. Confocal analysis of chromosome behavior in wheat × maize zygotes [J]. Genome, 2004,47:199-205
    
    183. Morinaga T. Interspecific hybridization in Brassica. I. The cytology of F1 hybrids of B .napella and various other species with 10 chromosomes [J]. Cytologia, 1929,1:16-27
    
    184. Morinaga T. Interspecific hybridization in Brassica. VI The cytology of Fl hybrids of B. juncea and B. nigra [J]. Cytologia, 1934, 6:62-67
    
    185. Naumova T N, der Laak J V, Osadtchiy J, Matzk F, Kravtchenko A, Bergervoet J, Ramulu K S, Boutilier K. Reproductive development in apomictic populations of Arabis holboellii (Brassicaceae) [J]. Sexual Plant Reproduction, 2001,14(4): 195-200
    
    186. Navashin, M.S. Amphiplastie, eine neue karyologische Erscheinung [J]. Proc Int Conf. Genet, 1928,5:1148-1152
    
    187. O'Donoughue L S, Bennett M D. Comparative responses of tetraploid wheats pollinated with Zea mays L. and Hordeum bulbosum L [J]. Theor Appl Genet, 1994a, 87: 673- 680
    
    188. O'Donoughue L S, Bennett M D. Durum wheat haploid production using maize wide-crossing [J].Theor Appl Genet, 1994b, 89: 559-566
    
    189. O'Neill C M, Bancroft I. Comparative physical mapping of segments of the genome of Brassica oleracea var alboglabra that are homoeologous to sequenced regions of the chromosomes 4 and 5 of Arabidopsis thaliana [J]. Plant J, 2000, 23: 233-243
    190. O'Neill C M, Murata T, Morgan C L and Mathias RJ. Expression of the C3-C4 intermediate character in somatic hybrids between Brassica napus and the C3-C4 species Moricandia arvensis [J]. Theor Appl Genet, 1996,93,1234-1241
    
    191. Olssong, Hagberg A. Investigation on haploid rape [J]. Hereditas, 1955,41: 227-237
    
    192. Olsson G Species crossing with in the genus Brassica. I .Artificial Brassica napus [J]. Hereditas, 1960,46:351-366
    
    193. Park J Y, Koo D H, Hong C P, Lee S J, Jeon J W, Lee S H, Yun P Y, Park B S, Kim H R, Bang J W, Plaha P, Bancroft I, Lint Y P. Physical mapping and microsynteny of Brassica rapa ssp. pekinensis genome corresponding to a 222 kb gene-rich region of Arabidopsis chromosome 4 and partially duplicated on chromosome 5 [J]. Mol Genet Genomics, 2005,274:579-588
    
    194. Park S K, Howden R, Twell D. The Arabidopsis thaliana gametophytic mutation gemini pollenl disrupts microspore polarity, division asymmetry and pollen cell fate [J]. Development, 1998, 125: 3789-3799
    
    195. Pathania A, Bhat S R, Dinesh Kumar V, Kirti P B Ashutosh, Prakash S, Chopra V L. Cytoplasmic male sterility in alloplasmic Brassica juncea carrying Diplotaxis catholica cytoplasm: molecular characterization and genetics fertility restoration [J]. Theor Appl Genet, 2003,107:455-461
    
    196. Pelletier G, Primard C, Vedel F, Chetrit P, Remy R, Rousselle, Renard M. Intergeneric cytoplasmic hybridization in cruciferae by protoplast fusion [J]. Mol Gen Genet, 1983, 191: 244-250
    
    197. Peterka H, Budahn H, Schrader O, Ahne, Schutze W. Transfer of resistance against the beet cyst nematode from radish (Raphanus sativus) to rape (Brassica napus) by monosomic chromosome addition [J]. Theor Appl Genet, 2004,109: 30-41
    
    198. Pikaard C S. Nucleolar dominance: uniparental gene silencing on a multi-megabase scale in genetic hybrids [J]. Plant Mol Biol, 2000,43(2-3): 163-77
    
    199. Pikaard CS, McStay B, Schultz M C, Bell S P, Reeder R H. The Xenopus ribosomal gene enhancers bind an essential polymerase I transcription factor, xUBF [J]. Genes Dev, 1989, 3: 1779-1788
    
    200. Pikaard C S, Pape L K, Henderson S L, Ryan K, Paalman M H, Lopata M A, Reeder R H, Sollner-Webb B. Enhancers for RNA polymerase I inmouse ribosomal DNA [J]. Mol Cell Biol, 1990,10: 4816-4825
    
    201. Prakash S. Haploidy in Brassica nigra Koch. [J] Euphytica, 1973, 22: 613-614
    
    202. Prakash S. Probable basis of diploidization of Brassica juncea cross [J]. Can J Genet Cytol, 1974,16: 232-234
    
    203. Prakash S, Hinata K. taxonomy, cytogenetics and origin of crop Brassicas, a review [J]. Opera Bot, 1980, 55: 1-57
    
    204. Prakash S. Utilization of wild germplasm of Brassica allies in developing cytoplasmic male sterility -fertility restoration systems in Indian mustard Brassica juncea [C]. In: Liu, Fu T (eds). Proc Int Symp Rapeseed Sci, Science Press, New York, 2001,63-67
    
    205. Preuss D, Rhee S Y, Davis R W. Tetrad analysis possible in Arabidopsis with mutation of the QUARTET (QRT) genes [J]. Science, 1994,264:1458-1460
    
    206. Quiros C F, Ochoa O, Kianian S F, Douches D. Analysis of the Brassica oleracea genome by the generation of B. campestris-oleracea chromosome addition lines: Characterization by isozymes and rDNA genes [J]. Theor Appl Genet, 1987,74,758-766
    
    207. Quiros C F. Genome structure and mapping. In: Gomez-Campo C, ed., Biology of Brassica coenospecies [M]. Amsterdam: Elsevier, 1999,217-246
    
    208. Quiros C F, Ochoa O, Douches D S. Exploring the role of n=7 species in Brassica evolution: Hybrdization with B. nigra and B. oleracea [J]. J Hered, 1988,79: 351-358
    
    209. Rana D, van den Boogaart T, O'Neill CM, Hynes L, Bent E, Macpherson L, Park J Y, Lim Y P, Bancroft I. Conservation of the microstructure of genome segments in Brassica napus and its diploid relatives [J]. Plant J, 2004,40: 725-733
    
    210. Rawsthome S, Morgan C L, O'Neill C M, Hylton C M, Jones D A, Frean M L. Cellular expression pattern of the glycine decarboxylase P protein in leaves of an intergeneric hybrid between the C3-C4 intermediate species Moricandia nitens and the C3 species Brassica napus [J]. Theor Appl Genet, 1998,96: 922-927
    
    211. Riera-Lizarazu O, A. Mujeeb-Kazi. Polyhaploid production in the Triticeae: wheat × Tripsacum crosses [J]. Crop Sci, 1993,33: 973-976
    
    212. Riera Lizarazu O, Rines H W, Phillips R L. Cytological and molecular characterization of oat × maize partial hybrids [J]. Theor Appl Genet, 1996,93:123-135
    
    213. Rines H W, Dahleen L S. Haploid oat plants produced by application of maize pollen to emasculated oat florets [J]. Crop Sci, 1990,30:1073-1078
    
    214. Risso-Pascotto C, Pagliarini MS, do Valle CB. A mutation in the spindle checkpoint arresting meiosis II in Brachiaria ruziziensis [J]. Genome, 2003, 46(4): 724-728
    
    215. Risso-Pascotto C, Pagliarini MS, Valle CB, Jank L. Asynchronous meiosis in an interspecific hybrid of Brachiaria ruziziensis and B. brizantha [J]. Plant Cell Rep, 2004, 23: 304-310
    
    216. Risso-Pascotto C, Pagliarini MS, do Valle CB. Multiple spindles and cellularization during microsporogenesis in an artificially induced tetraploid accession of Brachiaria ruziziensis (Gramineae) [J]. Plant Cell Rep, 2005,23: 522-527
    
    217. RObbelen, G Beitrage zur analyse des Brassica-Genoms [J]. Chromosoma, 1960,11: 205-228
    
    218. Ross K J, Fransz P, Armstrong S J, Vizir I, Mulligan B, Franklin F C H and Jones G H. Cytological characterization of four Meiotic mutants of Arabidopsis 37 meiotic mutants of Arabidopsis isolated from T-DNA transformed lines [J]. Chromosome Research, 1997, 5: 551-559
    
    219. Saez-Vasquez J, Pikaard C S. Extensive purification of a putative RNA polymerase I holoenzyme from plants that accurately initiates rRNA gene transcription in vitro [J]. Proc. Natl. Acad Sci USA, 1997, 94:11869-11874
    220. Sakai T, Imamura J. Intergeneric transfer of cytoplasmic male sterility between Raphanus sativus CMS) and Brassica napus through cytoplast-protoplast fusion [J]. Theor Appl Genet, 1990,80: 421-427
    
    221. Sakai T, Iwabuchi M, Kohno-Murase J. Liu H J, Imamura J. Transfer of radish CMS-restorer gene into Brassica napus by intergeneric protoplast fusion [C]. Proc 9th int. Rapeseed Congress, Cambridge, UK, 1995,3-5
    
    222. Sanchez I and Dynlacht B D. New insights into cyclins, CDKs, and cell cycle control [J]. Seminars in Cell& Developmental Biology, 2005,16: 311-321
    
    223. Sareen P K, Chowdhury J B, Chowdhury V K. Amphidiploids/synthetic crop species [M]. In: Kalloo G, Chowdhury J B (eds). Distant hybridization of crop plants. Springer, Berlin Heidelberg New York, 1992,62-69
    
    224. Sari-Gorla M, Gatti E, Villa M, Pe M E. A multi-nucleate male-sterile mutant of maize with gametophytic expression [J]. Sex Plant Reprod, 1997,10: 22-26
    
    225. Scherthan H, Weich S, Schwegler H, Heyting C, Haerle M and Cremer T. Centromere and telomere movements during early meiotic prophase of mouse and man are associated with the onset of chromosome pairing [J]. J Cell Biol, 1996,134:1109-1125
    
    226. Schiefthaler U, Balasubramanian S, Sieber P, Chevalier D, Wisman E & Schneitz K. Molecular analysis of NOZZLE, a gene involved in pattern formation and early sporogenesis during sex organ development in Arabidopsis thaliana [J]. Proc Natl Acad Sci USA, 1999, 96: 11664-11669
    
    227. Schnable P S and Wise R P. The molecular basis of cytoplasmic male sterility and fertility restoration [J]. Trends in Plant Science, 1998,3:175-180
    
    228. Schnapp A, Rosenbauer H, Grummt I. Trans-acting factors involved in species-specificity and control of mouse ribosomal gene transcription [J]. Mol Cell Biochem, 1991,104:137-147
    
    229. Schroder-Pontoppidan M, Skarzhinskaya M, Dixelius C, Stymne S, Glimelius K. Very long chain and hydroxylated fatty acids in offspring of somatic hybrids between Brassica napus and Lesquerella fendler. [J]. Theor Appl Genet, 1999,99:108-114
    
    230. Scott R J, Spielman M and Dickinson H G Stamen Structure and Function [J]. Plant Cell, 2004, 16: S46-S60
    
    231. Sernyk J L, Stefansson B R. White flower color in rape (Brassica napus) associated to with a rasish (Raphanus sativus) chromosome [J]. Can J Genet Cytol, 1982, 24: 729-734
    
    232. Sharma A, Mohatopara T, Sharma. Molecular mapping and character tagging in B.juncea. I Degree, nature and linkage relationships of RFLPs and their associations with quantitative traits [J]. J Plant Biochem, Biotch, 1994, 3: 85-89
    
    233. Sheridan W F, Avalkina N A, Shamrov II, Batygina T B, Golubovskaya I N. The mac1 gene: controlling the commitment to the meiotic pathway in maize [J]. Genetics, 1996, 142: 1009-1020
    
    234. Sikka S M. Cytogenetics of Brassica hybrids and species [J]. Genet, 1940, 40: 441-509
    235. Skarzhinskaya M, Landgren M and Glimelius K. Production of intertribal somatic hybrids between Brassica napus L. and Lesquerella fendleri (Gray) Wars [J]. Theor Appl Genet, 1996, 93:1242-1250
    236. Slocum M K. In: Helentjaris T, Burr B (eds), Development Application of Molecular Markers to Problems in Plant Genetics [M]. Gold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. 1989, 73-80
    237. Slocum M K, Figdore S S, Kennard W, Suzuki J Y, Osbom T C. RFLP linkage map of Brassica oleracea [J]. Thero Appl Genet, 1990, 80:57-64
    238. Snape J W, Chapman V, Moss J, Blanchard C E, Miller T E. The crossabilities of wheat varieties with Hordeum bulbosum [J]. Heredity, 1979, 42:291-298
    239. Snowdon R J, Kohler W, Friedt W, Kohler A. Genomic in situ hybridization in Brassica amphidiploids and interspecific hybrids[J]. Theor Appl Genet, 1997, 95:1320-1324
    240. Snowdon R J, Winter H, Diestel A Development and characterization of Brassica napus-Sinapis arvensis addition lines exhibiting resistance to Leptosphaeria maculans [J]. Theor Appl Genet, 2000, 101:1008-1014
    241. Song K M, Osborn T C, Williams P H. Brassica taxonomy based on nuclear restriction fragment length polymorphisms (RFLPs)—3. Genome relationship in Brassica and related genera and the origin of B. oleracea and B. rapa (syn. campestris) [J]. Theor Appl Genet, 1990, 79: 497-506.
    242. Song K M, Suzuki J Y, Slocum M K, Williams P H, Osborn T C. A linkage map of Brassica rapa (syn. campestris) based on restriction fragment length polymorphism loci [J]. Theor Appl Genet, 1991, 82:296-304
    243. Spielman M, Preuss D, Li F L, Browne W E, Scott R J. Dickinson H G. TETRASPORE is required for male meiotic cytokinesis in Arabidopsis thaliana [J]. Development, 1997, 124: 2645-2657
    244. Srinivasan K, Malathi V G, Kirti P B, Prakash S and. Chopra V L Generation and characteristics of monosomic chromosome addition lines of Brassica campestris-B.oxyrrhina [J]. Theor Appl Genet, 1998, 97:976-981
    245. Struss D, Bellin U, Rrbbelen G. Development of B-genome chromosome addition lines of B.napus using different interspecific Brassica hybrids [J]. Plant Breed, 1991, 106:219-214
    246. Struss D, Quiros C F, Plieske J, Robbelen G. Construction of Brassica B genome synteny groups based on chromosomes extracted from three different sources by phenotypic, isozyme and molecular markers [J]. Theor Appl Genet, 1996, 93:1026-1031
    247. Sari-Gorla M, Ferrario S, Villa M, Pe M E. gaMS-1, a gametophytic expressed male sterile mutant of maize[J]. Sex Plant Reprod, 1996, 9:215-220
    248. Subrahmanyam N C, Kasha K J. Selective chromosomal elimination during haploid formation in barley following interspecific hybridization [J]. Chromosoma, 1973, 42:111-125
    249. Tai W Multipolar meiosis in diploid crested wheatgrass Agropirum cristatum [J]. Am J Bot,1970, 57:1160-1169
    250. Takahata Y, Takeda T. Intergeneric (intersuctribe) hybridization betweem Moricandia arvensis and Brassica A and B genome species by ovary culture [J]. Theor Appl Genet, 1990, 80:38-42
    251. Taketa S, Kato J, Taketa K. High crossability of wild barley. (Hordeum spontaneum C. Koch) with bread wheat and the differential elimination of barley chromosomes in the hybrids [J]. Theor Appl Genet, 1995, 91:1203-1209
    252. Tanaka I, Ito M. Control of division patterns in explanted microspores of Tulipa gesnerian [J]. Protoplasma, 1981, 108:329-340
    253. Taschetto O M, pagliarini M S. Description of a new type of meiotic abnormality in maize (Zea Mays L) [J]. Maydia, 1993, 38:47-50
    254. Terasaka O, Niitsu T. Unequal cell division and chromatin differentiation in pollen grain cells. I. Centrifugal, cold and caffeine treatments [J]. Bot. Mag. Tokyo 100, 1987, 205-216
    255. Thompson K F. Production of haploid plants of narrow stem kale [J]. Nature, 1956, 178: 748.
    256. Tilquin JP, Brower KD, Horvat F. Unsusal cytological patterns in microsporogenesis in a cultivar of Fuchsia [J]. Theor Appl Genet,1984, 67:413-417
    257. Toriyama K, Hinata K. and Kameya T. Production of somatic hybrid plants, 'Brassicomoricandia', through protoplast fusion between Moricandia arvensis and B. oleracea [J]. Plant Sci, 1987, 48:123-128
    258. Town C D, Cheung F, Maiti R, Crabtree J, Haas B J, Wortman J R, Hine E E, Althoff R, Arbogast T S, Tallon L J, Vigouroux M, Trick M, Bancroft I. Comparative genomics of Brassica oleracea and Arabidopsis thaliana reveal gene loss, fragmentation, and dispersal after polyploidy [J]. Plant Cell, 2006, 18:1348-1359
    259. Truco M J, Hu J, Sadowski J, Quiros C F. Inter-genomic and intra-genomic homology of Brassica genomes: implications for their origin and evolution [J]. Theor Appl Genet, 1996, 93: 1225-1233
    260. Truco M J, Quiros C F. Structure and organization of the B genome based on a linkage map of Brassica nigra [J]. TheorAppl Genet, 1994, 89:590-598
    261. Turcotte E L, Feaster C V. Semigamy in cotton [J]. Heredity, 1967, 58: 54-57
    262. Twell D, Park S K and Lalanne E. Asymmetric division and cell fate determination in developing pollen [J]. Trends Plant Sci, 1998, 3:305-310
    263. U N. Genome analysis in Brassica with special reference to the experimental formation of B. napus and peculiar mode of fertilization [J]. Jpn J Bot, 1935, 7:389-452
    264. van Heemst D, Heyting C. Sister chromatid cohesion and recombination in meiosis [J]. Chromosoma, 2000, 109(1-2):10-26
    265. Vantard M, Cowling R, Delichere C Cell cycle regulation of the microtubular cytoskeleton [J]. Plant Mol Biol, 2000;43(5-6): 691-703
    266. Vos P, Hogers R, Bleeker M, Reijans M, van de Lee T, Homes M, Freijters A, Pot J, Peleman J, Kuiper M and Zabeau M. AFLP: a new technique for DNA fingerprinting [J]. Nucl Acid Res, 1995, 21: 4407-4414
    267. Venkateswarlu J, Kamala T. Pachytene chromosome complements and genome analysis in Brassica [J]. Ind. Bot Soc, 1971, 50:442-449
    268. Wallace H, Langridge W H R. Differential amphiplasty and the control of ribosomal RNA synthesis [J]. Heredity, 1971, 27:1-13
    269. Wang Y M, Dong Z Y, Zhang Z J, Lin X Y, Shen Y, Zhou D, Liu B. Extensive de Novo genomic variation in rice induced by introgression from wild rice (Zizania latifolia Griseb.) [J]. Genetics, 2005, 170(4): 1945-1956
    270. Wang Y P, Zhao X X, Sonntag K, Wehling P, Snowdon R J. Behaviour of Sinapis alba chromosomes in a Brassica napus background revealed by genomic in situ hybridization [J]. Chromosome Res, 2005, 13:819-826
    271. Wang Y P, Sonntag K, Rudloff E. Development of rapeseed with high erucic acid content by asymmetric somatic hybridization between Brassica napus and Crambe abyssinica [J]. Theor Appl Genet, 2003, 106:1147-1155
    272. Warwick S I, Black L D. Molecular systematics of Brassica and allied genera (subtribe Brassicinae, Brassiceae)-chloroplast genome and cytodeme congruence [J]. Theor Appl Genet, 1991, 82: 81-92
    273. Wittmann T, Hyman A, Desai A. The spindle: a dynamic assembly of microtubules and motors [J]. Nat Cell Biol, 2001, 3(1): E28-34
    274. Wilson Z A, Yang C. Plant gametogenesis: conservation and contrasts in development [J]. Reproduction, 2004, 128: 483-492
    275. Wolfe K W, Liu O. The maize mutant polymitotic affects cell cycle events during microspore development [J]. Planta, 1999, 210:27-33
    276. Worrall D, Hird D L. Premature dissolution of the microsporocyte callose wall causes male sterility in transgenic tobacco [J]. The Plant Cell, 1992, 4:759-771
    277. Yamagishi H, Glimelius K. Somatic hybrids between Arabidopsis thaliana and cytoplasmic male-sterile radish (Raphanus sativus) [J]. Plant cell Rep, 2003, 22:52-58
    278. Yan Z, Tian Z, Huang R, Huang B, Meng J. Production of somatic bybrids between Brassica oleracea and the C3-C4 intermediate species Moricandia nitens [J]. Theor Appl Genet, 1999, 99:1281-1286
    279. Yang S L, Xie L F, Mao H Z, Puah C S, Yang W C, Jiang L, Sundaresan V, Ye D. TAPETUM DETERMINANT1 is required for cell specialization in the Arabidopsis anther[J]. The Plant Cell, 2003, 15:2792-2804
    280. Yang W C, Ye D, Xu J and Sundaresan V. The SPOROCYTELESS gene of Arabidopsis is required for initiation of sporogenesis and encodes a novel nuclear protein [J]. Genes and Development, 1999, 13:2108-2117
    281. Zenkteler M, Nitzsche W. Wide hybridization experiments in cereals [J]. Theor Appl Genet, 1984, 68:311-315
    282. Zhang J F, Stewart J M. Semigamy Gene Is Associated with Chlorophyll Reduction in Cotton [J]. Crop Science, 2004,44(6): 2054-2062
    
    283. Zhong X B, de Hans J J, Zabel P. Preparation of tomato meiotic pachytene and mitotic metaphase chromosomes suitable for fluorescence in situ hybridization (FISH) [J]. Chromosome Res, 1996,4: 24-28

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