性别相关基因在牙鲆性腺分化和性别表型形成中的遗传学分析
详细信息    本馆镜像全文|  推荐本文 |  |   获取CNKI官网全文
摘要
本文首先克隆了牙鲆(Paralichthys olivaceus)dmrt1、dmrt4和sox9基因,连同已知的P450arom,研究了这4个基因在成鱼各组织的表达差异谱,明确了它们的两性差异表达模式,进一步定量和定位分析了这些基因在性腺分化和发育过程中的表达;并在体外对dmrt1基因进行了原核重组表达,同时从表观遗传学水平上研究了从头DNA甲基化转移酶基因dnmt3基因的表达差异图式以及性腺中性别相关基因启动子CpG岛的甲基化水平与这些基因两性表达差异的相关性。研究表明:
     牙鲆dmrt1基因cDNA全长3373bp,其5’UTR中存在与性别相关的转录因子Sry、Sox9和Sox5的结合位点,编码蛋白含有保守的DM结构域;dmrt4基因包含2个外显子和1个内含子,其5’UTR中有性别相关的转录因子Sox9的结合位点,编码产物含有保守的DM结构域和特有的DMA结构域;sox9基因包含3个外显子和2个内含子,在其5’UTR中发现了转录因子Ftz、Foxd3和Oct1的结合位点,编码蛋白含有保守的HMG结构域。牙鲆P450arom基因5’UTR中具有性别相关的转录因子Foxl2和Sf1的结合位点以及DM结构域的结合位点。
     组织特异表达研究显示,牙鲆dmrt1、dmrt4、sox9和P450arom均为两性差异表达的性别相关基因。dmrt1基因在牙鲆性腺中特异表达,且在精巢中的表达强于卵巢;dmrt4和sox9基因的表达范围相对较广,在性腺、脾脏、鳃、脑和胃等组织中都有不同程度的表达,且也都是在精巢的表达较卵巢的表达强;而P450arom基因在卵巢中的表达明显强于精巢,在其它一些组织中有强弱不同的表达。
     根据real-time RT-PCR结果可以看出,dmrt1基因在牙鲆原始性腺和性腺分化期间的表达都很低,在分化的精巢中表达强度迅速上升,而在卵巢中的表达却依然很弱。dmrt4则在原始性腺中高表达,其后的性腺分化期间表达降到很低的水平,然后在分化的精巢中强表达。sox9基因在牙鲆原始性腺中高表达,之后在性腺分化期间的表达呈现上下浮动的模式,在分化的精巢卵巢中具有不同程度的表达。P450arom在原始性腺中开始表达,其表达量在性腺分化期间有向上向下浮动的变化趋势,其后在分化的卵巢早期发育阶段表达很强。
     这4个基因在牙鲆各期性腺中的表达也各有不同,dmrt1在牙鲆I期性腺中表达很弱,II期精巢中表达量迅速上升,到了IV期精巢,其表达量有所下降,V期精巢中的表达量又上升而达到峰值;dmrt1在II期到V期卵巢的表达量却都极低。dmrt4基因在I期和II期精巢中表达很强,且呈上升趋势,其后在III、IV期精巢中的表达急剧下降,到了V期精巢,其表达量又略有回升;而其在各期的卵巢中表达一直很低。sox9在牙鲆I期精巢的表达量较卵巢的低,之后精巢中的表达开始上升,II期到V期精巢中该基因的表达量均较卵巢中的高,II期卵巢达到峰值,III到V期卵巢却几乎不表达。P450arom基因在I到V期卵巢的表达量均高于同期精巢的表达量,其中I期和II期的差异较大,这两个时期卵巢中的表达量很高,其后各期卵巢中的表达有所降低,而精巢中的表达量一直处于较低水平。
     性腺组织切片原位杂交定位表达分析可知,dmrt1、dmrt4和sox9基因的转录本主要定位于牙鲆精巢的精母细胞和Sertoli细胞,且在精母细胞中的表达强于Sertoli细胞的表达;在卵巢中,这3个基因的杂交信号都很弱。牙鲆P450arom基因则主要在卵巢的滤泡细胞和卵母细胞中表达,且滤泡细胞的表达强于卵母细胞中的表达,在精巢的精母细胞中却弱表达。整体原位杂交定位表达研究结果显示,在牙鲆胚胎发育过程中,dmrt4在外胚层来源的嗅基板,以及神经外胚层来源的前脑、端脑和耳基板中表达。从神经胚期到孵化期的所有时期,dmrt4基因在嗅基板的表达一直很强,而在端脑中的表达则存在动态变化。在胚胎发育的较早阶段,dmrt4的转录本分布于前脑中,并从神经胚期到尾芽形成期保持强表达;在早尾芽期,表达变得相对较弱,并逐渐局限于背侧端脑第一脑室周围的一小片区域。从5-6体节期到孵化期,低水平的转录本还可以在听基板中检测到。
     甲基化表观遗传修饰水平研究结果显示,牙鲆dmrt1、dmrt4和P450arom基因启动子CpG位点的甲基化水平存在两性差异: dmrt1启动子CpG位点在精巢中的甲基化水平为0,卵巢中的甲基化水平为57.69%,相应的,该基因在精巢的相对表达量约为卵巢的70倍。P450arom基因启动子CpG位点在卵巢的甲基化水平为73.33%,精巢中的甲基化水平为97.5%,该基因在卵巢的相对表达量约为精巢的40倍。dmrt4启动子CpG位点的甲基化水平在精巢中的甲基化水平(2%)较卵巢中的(7%)略低,这也与该基因在精巢中的表达强于卵巢的表达的两性差异表达模式是一致的。但是,sox9基因启动子CpG岛甲基化水平在精巢卵巢中却没有差异,都是完全去甲基化的,这与其在两性性腺中的差异表达图式不存在相关性。牙鲆从头DNA甲基化转移酶基因dnmt3存在两性差异表达,在精巢中的表达强于卵巢中的表达,在肾脏、脾脏、脑和眼睛中也有不同程度的表达。该基因在原始性腺表达较高,在性腺分化期间的表达上下浮动,在分化和发育的精巢卵巢中均具有两性表达差异。
     应用原核表达系统对Dmrt1蛋白进行体外重组表达:将牙鲆dmrt1基因序列插入到表达质粒pProEXTMHTa上,在大肠杆菌E.coli BL-21中进行体外表达与分析。该重组蛋白分子量约为32.5KDa,存在于宿主菌中,没有分泌到细胞外。诱导的菌体经超声破碎后,在沉淀和上清的样品中都有目的蛋白的条带存在,大部分的Dmrt1重组蛋白以包涵体形式出现在沉淀中,只有少量的蛋白以可溶形式存在于上清中。当诱导时间4 h、IPTG浓度0.6mmol/L时,重组蛋白表达量最大;在诱导温度为34℃时,表达的可溶蛋白的量比例最大。
In the present study, we first cloned olive flounder (Paralichthys olivaceus) dmrt1, dmrt4 and sox9 genes. Together with olive flounder P450arom gene, their expression patterns in adult tissues were analyzed using convertional RT-PCR. The result identified these four genes’sexual dimorphic expression patterns. We further studied the expression of these genes during flounder gonadal differentiation and development through real-time RT-PCR and in situ hybridization. We also expressed flounder Dmrt1 fusion protein in vitro using E.coli BL-21(DE3) expression system. Meanwhile, we studied the methylation patterns of these four genes’promoter CpG island in testis and ovary at the epigenetic level.
     Flounder dmrt1’s total cDNA sequence is 3373bp, and its binding sites of sex-related transcriptional factors Sry, Sox9 and Sox5 were identified in the promoter region. The encoded protein contains a conserved DM domain. Flounder dmrt4 gene included two exons and one intron, of which promoter region contained binding site of sex-related transcriptional factor Sox9. A conserved DM domain and a specific DMA domain were found in the encoded protein. Flounder sox9 gene included three exons and two introns, and binding sites of transcriptional factors Ftz, Foxd3 and Oct1 were identified in its promoter region. This gene encoded a protein containing a conserved HMG domain. The 5’UTR of flounder P450arom was cloned, in which a DM domain binding site, two steroidogenic factor 1 (Sf1) binding sites and a forkhead-responsive consensus site (Foxl2) binding site were identified.
     The tissue specific expression patterns of dmrt1, dmrt4, sox9 and P450arom in adult flounder indicated that these four genes were all sex-related genes with sexual dimorphic expression. In detail, flounder dmrt1’s expression was restricted to gonads, and was higher expressed in testis than that in ovary. Both dmrt4 and sox9 were stronger in testis and weaker in ovary, and were also differentially expressed in some other tissues. P450arom was higher expressed in ovary than that in testis, and was expressed in some other tissues with varied degrees too.
     Results of real-time RT-PCR indicated that flounder dmrt1 was scarcely expressed in primitive gonad and during following periods of gonadal differentiation. But its expression went up rapidly in differentiating testis, and remained very low in differentiating ovary. Flounder dmrt4 was strongly expressed in primitive gonad, and much lower expressed during following periods of gonadal differentiation. Then its expression became stronger in differentiating testis. The sox9 was also highly expressed in flounder primitive gonad, much lower expressed after that and had some fluctuated expression during gonadal differentiation period. And then, it differentially expressed in differentiating testis and ovary. However, P450arom expressed in primitive gonad at first, and its expression quantity went upward and downward during following periods of gonadal differentiation. In the early stage of differentiating ovary, its expression became stronger.
     These four genes are also differentially expressed during five developmental stages of gonad. Flounder dmrt1 was weakly expressed in the testis and ovary of stage I, and its expression quantity went up rapidly in the testis of stage II. After that, the quantity went a little down in the testis of stage IV. Then its expression quantity reached the peak in the testis of stage V. From the stage II to the stage V, the expression quantity in ovaries were all scare. The dmrt4 gene was highly expressed in the testes of stage I and II with upward trend. Then its expression quantity went down significantly in the stage III and IV, but went up a little until stage V. The expression quantities in all the five stages of ovaries were always low. Flounder sox9 had lower expression quantity in the testis of stage I than in the ovary of stage I. And then, its expression in testis began to go up. From the stage II to V, the expression quantities were higher in testes than that in ovaries. Its expression quantities in ovary reached the peak in the stage II. From the stage III to V, there was almost no expression in the ovaries. P450arom gene had higher expression quantity in the testes from stage I to V than thoes in the ovaries. The difference of quantity was bigger in the stage I and II, in which the expression quantities of ovaries were very high. And after that, the expression in ovary went down. But its expression in testis was always weak.
     Gonad tissue slice in situ hybridization results showed that transcripts of dmrt1, dmrt4 and sox9 were mainly localized in spermatocytes and Sertoli cells of flounder testis, and the signal in spermatocytes was stronger than that in Sertoli cells, but there was weak signal detected in ovary. On the contrary, flounder P450arom mRNA was located in follicular cells and oocytes of ovary, and the signal in follicular cells was stronger than that in oocytes, and there was only a little signal detected in spermatocytes of testis. Whole mount in situ hybridization analysis showed that during flounder embryogenesis, flounder dmrt4 is expressed in the ectodermally derived olfactory placodes, neuroectodermal forebrain and telencephalon and otic placodes during embryogenesis. The expression level of dmrt4 is always high in the olfactory placodes for all these stages from neurula stage to the hatching stage, but it is dynamic in the telencephalon. While transcripts are distributed throughout the forebrain at early stages, remaining strongly expressed from the neurula stage to tail-bud forming stage, the expression domain becomes more and more restricted to a small area around the first ventricle in the dorsal telencephalon and is relatively weak at the early tail-bud stage.
     Results of genes’promoter CpG islands methylation patterns analyses showed that there were sexual dimorphic differences in the CpG methylation level of flounder dmrt1、dmrt4和P450arom promoters. No CpG demethylation of flounder dmrt1 promoter in testis and its 57.69% CpG island (CGI) methyaltion in ovary corresponded to this gene’s about 70 times higher expression in testis than that in ovary. On the other hand, 97.5% CGI methylation of flounder P450arom promoter in testis and its 73.33% CGI methyaltion in ovary correlated to this gene’s about 40 times lower expression in testis than that in ovary. The levels of flounder dmrt4 promoter CGI methylation in gonads were also sexual dimorphic. There were 2% CGI methylation of this gene promoter in testis and 7% methylation in ovary, which was consistent with its sexual dimorphic expression with higher expression in testis than that in ovary. However, there was no difference to be detected in the levels of flounder sox9 promoter CGI methylation in both gonad, and its sox9 promoter CpGs in testis and ovary were all totally demethylated, which was inconsistent with this gene’s differential expression pattern with higher expression in testis than that in ovary. Flounder de novo DNA (cytosine-5)-methyltransferases 3 (dnmt3) had a sexual dimorphic expression pattern that was higher expressed in testis than that in ovary. And it was also differentially expressed in kidney, spleen, brain and eye. Dnmt3 was highly expressed in flounder primitive gonad, and had some fluctuated expression during gonadal differentiation period. It was sexually dimorphic expressed during differentiation and development of testis and ovary.
     Flounder dmrt1 gene (encoded 293aa protein with molecular weight of 32.5 KDa) was recombined and fused on plasmid pPROEXTMHTa, and was transferred into E.coli BL-21(DE3) for Dmrt1 expression in vitro. The result of SDS-PAGE showed that fusion protein highly expressed inside the E.coli BL-21(DE3) cell after induction. Most fusion protein expressed in the form of inclusion bodies, and only a little fusion protein expressed in the form of soluble protein. The fusion Dmrt1 protein had the highest expression quantity after 4 h induction with 0.6mmol/L IPTG. When the induction temperature was 34℃, expression quantity of the soluble protein was the maximum.
引文
常重杰,余其兴,大鳞副泥鳅ZZ/ZW型性别决定的细胞遗传学证据。遗传1997,19(3):17-19
    常重杰,周荣家,余其兴,Sox基因家族的研究现状。遗传2000,22(l):51-53
    陈玉琳,胡秀敏,朱雅珠,莫桑比克罗非鱼幼鱼的性腺发育与分化。水产学报1980,4(4):313-318
    邓思平,陈松林,田永胜等,半滑舌鳎的性腺分化和温度对性别决定的影响。中国水产科学2007,14(5):714-718
    邓思平,陈松林,半滑舌鳎Dmrt1α基因的cDNA克隆及其表达。中国水产科学2008,15(4): 577-584
    邓思平,陈松林,刘本伟等,半滑舌鳎脑芳香化酶基因cDNA克隆及表达分析。动物学研究2008,29(1):17-24
    杜启艳,常重杰,王凤羽,华慧颖,鲤鱼中Sox9b基因的克隆和表达。实验生物学报2005,38(5):397-403
    侯林,性别决定相关基因SOX9研究进展。中国优生与遗传杂志2007,15(8):1,2,9
    林浩然,鱼类生理学。广州:广东东高教出版社1999,181-196
    刘筠,中国养殖鱼类繁殖生物学。北京:农业出版社1993
    刘少军,革胡子鲶原始生殖细胞的起源、迁移及性腺分化。水生生物学报1991,15(1):1-7
    楼允东,鱼类育种学。北京:中国农业出版社1999
    马学坤,柳学周,温海深等,半滑舌鳎性腺分化的组织学观察。海洋水产研究2006,27(2):55-61
    宋卉,王树迎,鱼类原始生殖细胞的研究进展。动物医学进展2004,25(5):22-23
    宋卉,王树迎,彭克美,泰山螭霖鱼原始生殖细胞的发生及性腺分化规律的研究。动物医学进展2005,26(12):62-67
    孙朝徽,刘海金,司飞等,养殖牙鲆性腺分化的组织学观察。大连水产学院学报2008,23(6):451-454
    孙鹏,尤锋,张立敬等,牙鲆性腺分化的组织学研究。海洋科学2009,33:53-58
    唐永凯,李建林,陈文华等,奥利亚罗非鱼卵巢芳香化酶基因的克隆及其表达。中国水产科学2008,15(5):729-737
    童金苟,朱嘉濠,关海山,鱼类性别决定的遗传基础研究概况。水产学报2003,27(20):169-176
    王开顺,石鲽Kareius bicoloratus性腺发生、分化及发育的周年变化。中国海洋大学硕士学位论文2004
    王德寿,吴天利,张耀光,鱼类性别决定及其机制的研究进展。西南师范大学学报(自然科学版) 2000,25(3):296-304
    王文君,王开顺,邵明瑜等,石鲽仔、幼鱼性腺发育的组织学观察。中国水产科学2007,14(5):843-848
    温海深,宋海霞,杨立廷等,外源激素对养殖牙鲆血浆睾酮和雌二醇含量的影响研究。海洋学报2006,28(4):115-120
    吴纬,陈静娴,宋宁等,几种因素对重组大肠杆菌目标蛋白表达的影响。四川大学学报(自然科学版) 2004,39:149-151
    杨洁,吴宏达,范兆廷,鱼类性别决定机制的研究进展。渔业经济研究2007,3:14-19
    俞菊华,李建林,曹丽萍等,黄颡鱼Sox9基因的分离及分析。农业生物技术学报2005,13(5):620-623
    余先觉,周敦,李渝成等,中国淡水鱼类染色体。北京:科学出版社1989,1-9
    张修月,焦保卫,吴天利等,南方鲶性腺分化的组织学观察。动物学杂志2005,40(1):41-48
    Akiyama H, Chaboissier MC, Behringer RR, et al. Essential role of Sox9 in the pathway that controls formation of cardiac valves and septa. P Natl Acad Sci USA 2004, 101: 6502-6507
    Alam MA, Kobayashi Y, Horiguchi R. Molecular cloning and quantitative expression of sexually dimorphic markers Dmrt1 and Foxl2 during female-to-male sex change in Epinephelus merra. Gen Comp Endocr 2008, 157: 75-85
    Andreata AA, Almeida-Toledo FD, Oliverira C et al. Chromosome studies inHypoptopomatinae (Pisces, Siluriformes, Loricariidae). Cyto Cell Genet 1993, 63: 215-220
    Baroiller JF, D’Cotta H. Environment and sex determination in farmed fish. Comp Biochem Phys C 2001, 130: 399-409
    Baroiller JF, D’Cotta H, Saillant E. Environmental effects on fish sex determination and differentiation. Sex Dev 2009, 3: 118-135
    Baron D, Fostier A, Breton B, et al. Androgen and estrogen treatments alter steady state messengers RNA (mRNA) levels of testicular steroidogenic enzymes in the rainbow trout, Oncorhynchus mykiss. Mol Reprod Dev 2005, 71: 471–479
    Baron D, Houlgatte R, Fostier A, et al. Expression profiling of candidate genes during ovary-to-testis trans-differentiation in rainbow trout masculinized by androgens. Gen Comp Endocr 2008, 156: 369-378
    Barry TP. Induced fina loocyte maturation and spawning in walleye (Stizostedion vitreum). USA World Aquac Soc 1992, 3
    Bergstrom DE, Young M, Albrecht KH, et al. Related function of mouse Sox3, Sox9, and Sry HMG domains assayed by male sex determination. Genesis 2000, 28: 111-124
    Biason-Lauber A, Schoenle EJ. Apparently normal ovarian diferentiation in a prepubertal girl with transcriptionally inactive steroidogenic factor 1 (NR5A1/SF-1) and adrenocortical insufficiency. Am J Hum Genet 2000, 67: 1563-1568
    Bird A, Wolffe AP. Methylation-induced repression--belts, braces, and chromatin. Cell, 1999, 99: 451-454.
    Bird A. DNA methylation patterns and epigenetic memory. Gene Dev 2002, 16: 6-21
    Blazquez M, Gonzalez A, Papadaki M, et al. Sex-related changes in estrogen receptors and aromatase gene expression and enzymatic activity during early development and sex differentiation in the European sea bass (Dicentrarchus labrax). Gen Comp Endocr 2008, 158: 95-101
    Bleich S, Lenz B, Ziegenbein M, et al. Epigenetic DNA hypermethylation of the HERP gene promoter induces down-regulation of its mRNA expression in patients with alcohol dependence. Alcohol Clin Exp Res 2006, 30: 587-591.
    Brunner B, Homung U, Shan Z, et al. Genomic organization and expression of the doublesex-related gene cluster in vertebrates and detection of putative regulatory regions for DMRT1. Genomics 2001, 77: 7-8
    Bulun SE, Sebastian S, Takayama K, et al. The human CYP19 (aromatase P450) gene: update on physiologic roles and genomic organization of promoters. J Steroid Biochem Mot Biol 2003, 86: 219-224
    Burtus KC, Baker BS. Drosophila doublesex gene controls somatic sexual differentiation by producing alteratively spliced mRNAs encoding related sex-specific polypeptides. Cell 1989, 56: 997-101
    Callard GV, Petro Z, Ryan KJ. Phylogenetic distribution of aromatase and other androgen-converting enzymes in the central nervous system. Endocrinology 1978, 103: 2283-2290
    Callard GV. Autocrine and paracrine role of steroids during spermatogenesis: studies in squalus acanthias and Necturus maculosus. J Exp Zool 1992, 261: 132-140
    Callard GV, Tchoudakova AV, Kishida M, et al. Differential tissue distribution, developmental programming,estrogen regulation and promoter characteristics of cyp19 genes in teleost fish. J Steroid Biochem Mot Biol 2001, 79: 305-314
    Camern FJ, Sinclair AH. Mutations in SRY and Sox9: Testis-determining genes. Hum Mutat 1997, 9: 388-395
    Cao JL, Cao ZM, Wu TT. Generation of antibodies against DMRT1 and DMRT4 of Oreochromis aurea and analysis of their expression profile in Oreochromis aurea tissues. J Genet Genomics 2007, 34: 497-509
    Chang XT, Kobayashi D, Kobayashi, et al. Isolation and characterization of the cDNA encoding the tilapia (Oreochromis nilotius) cytochrome P-450 aromatase (P450arom): changes in P450arom mRNA protein and enzyme activity in ovarian folicles during oogenesis. J Mol Endocrinol 1997, 189: 57-66
    Chiang EFL, Pai CI, Wyatt M, et al. Two Sox9 genes on duplicated zebrafish chromosomes: expression of similar transcription activators in distinct sites. Dev Biol 2001, 231: 149-163
    Christoffels A., Koh E.G.L., Chia J.M., et al. 2004 Fugu genome analysis providesevidence for a whole-genome duplication early during the evolution of ray-finned fish. Mol Biol Evol 21: 1146-1151
    Clyne CD, Speed CJ, Zhou J, et al. Liver receptor homologue-1(LRH-1) regulates expression of aromatase in preadipocytes. J Biol Chem 2002, 277: 20591-20597
    Clyne CD, Kovacic A, Speed CJ, et al. Regulation of aromatase expression by the nuclear receptor LRH-1 in adipose tissue. Mol Cell Endocrinol 2004, 215: 39-44
    Cohen-Barak O, Hagiwara N, Arlt MF, et al. Cloning, characterization and chromosome mapping of the human Sox6 gene. Gene 2001, 265: 157-165
    Conley A, Hinshelwood M. Mammalian aromatases. Reproduction 2001, 121: 685-695
    Colburn HR, Nardi GC, Borski RJ, et al. Induced meiotic gynogenesis and sex differentiation in summer flounder (Paralichthys dentatus). Aquaculture 2009, 289: 175-180
    Connor F, Wright E, Denny P, et al. The Sry-related HMG box-containing gene Sox6 is expressed system of in the adult testis and developing nervous the mouse. Nucleic Acids Res 1995, 23: 3365-3372
    Corbin JC, Graham-Lorence S, McPhaul MJ, et al. Isolation of a full-length cDNA insert encoding human aromatase system cytochrome P-450 and its expression in non-steroidogenic cells. P Natl Acad Sci USA 1988, 85: 8948-8953
    D’Cotta H, Guiguen Y, Govoroun M, et al. Aromatase gene expression in temperature-induced gonadal sex differentiation of tilapia Oreochromis niloticus. In: Proceedings of the Sixth International Symposium on the Reproductive Physiology of Fish 2000, 197–199. Edited by B Norberg, OS Kjesbu, GL Taranger, E Andersson and SO Stefansson, Fish Symp 99, Bergen, Norway
    D’Cotta H, Fostier A, Guiguen Y, et al. Aromatase plays a key role during normal and temperature-induced sex differentiation of tilapia Oreochromis niloticus. Mol Reprod Dev 2001a, 59: 265–276
    D’Cotta H, Fostier A, Guiguen Y, et al. Search for genes involved in the temperature-induced gonadal sex differentiation in the tilapia, Oreochromis niloticus. J Exp Zool 2001b, 290: 574-585
    Davis TL, Yang GJ, McCarrey JR, et al. The H19 methylation imprint is erased and re-established differentially on the parental alleles during male germ cell development. Hum Mol Genet, 2000, 9: 2885-2894.
    Deng SP, Chen SL, Xu JY, et al. Molecular cloning, characterization and expression analysis of gonadal P450 aromatase in the half-smooth tongue-sole, Cynoglossus semilaevis. Aquaculture 2009, 287: 211-218
    Devlin RH, Nagahama Y. Sex determination and sex differentiation in fish: an overview of genetic, physiological, and environmental influences. Aquaculture 2002, 208: 191-364
    Du JL, Lin BY, Lee YH, et al. Estradiol, aromatase and steroid receptors involved in the sex change of protandrous black porgy, Acanthopagrus schlegeli. Fish Physiol Biochem 2003, 28: 131-133
    Foster JW, Dominguez-Steglich MA, Guioli S, et al.Campomelic dysplasia and autosomal sex reversed caused by mutations in an SRY-related gene. Nature 1994, 372: 525-530
    Frojdman K, Harley VR, Pelliniemi LJ. Sox9 protein in rat sertoli cells is age and stage dependent. Histochem Cell Biol 2000, 113: 31-36
    Fudu Miao, Dhinhaker S. Overexpression of Cloned genes using recombinant Escherichia coli regulated by a T7 promoter: two stage continuous cultures and model simulations. Biotechiol Bioeng 1993, 42: 74-80
    Fujita N, Watanabe S, Ichimura T, et al. Methyl-CpG binding domain 1 (MBD1) interacts with the Suv39h1-HP1 heterochromatic complex for DNA methylation-based transcriptional repression. J Biol Chem 2003, 278: 24132-24138.
    Fukada S, Tanaka M, Lwaya M. The Sox gene family and its expression during embryogenesis in the teleost fish, medaka (Oryzias latipes). Dev Growth Differ 1995, 37: 379-385
    Fukada S, Tanaka M, Matsuyama M, et al. Characterization and expression of cDNA encoding the medaka (Oryzias laripes) ovarian follicle cytochrome P-450 aomatase. Mol Repord Dev 1996, 45: 285-290
    Gabory A, Attig L, Junien C. Sexual dimorphism in environmental epigeneticprogramming. Mol Cell Endocrinol 2009, 304: 8-18
    Godwin J, Luckenbach JA, Borski RJ. Ecology meets endocrinology: environmental sex determination in fishes. Evol Dev 2003, 5: 40-49
    Goto T, Monk M. Regulation of X-chromosome inactivation in development in mice and humans. Microbiol Mol Biol Rev, 1998, 62: 362-378.
    Govoroun M, McMeel OM, Mecherouki H, et al. 17beta-Estradiol treatment decreases steroidogenic enzyme messenger ribonucleic acid levels in the rainbow trout testis. Endocrinology 2001, 142: 1841–1848
    Grandi AD, Calvari V, Bertini V, et al. The expression pattern of a mouse doublesex-related gene is consistent with a role in gonadal differentiation. Mech Dev 2000, 90: 323-326
    Guan G, Kobayashi T, Nagahama Y. Sexually dimorphic expression of two types of DM (Doublesex/Mab-3)-domain genes in a teleost fish, the tilapia (Oreochromis niloticus). Biochem Bioph Res Co 2000, 272: 662-666
    Guigen Y, Ricordel MJ, Foster A. Involvement of estrogens in the process of sex differentiation in rainbow trout, Oncorhynchus mykiss: in vivo treatment, aromatase activity, and aromatase gene expression. In: Proceedings l" International Symposium on the Biology of Vertebrate Sex Determination”. Honolulu, Hawaii 1997: 7-11
    Guiguen Y, Baroiller JF, Ricordel MJ, et al. Involvement of estrogens in the process of sex diferentiation in two fish species: The rainbow trout (Oncorhynchus mykiss) and a tilapia (Oreochromis niloticus). Mol Reprod 1999, 54: 154-162
    Guo YQ, Cheng HH, Huang X, et al. Gene structure, multiple alternative splicing, and expression in gonads of zebrafish dmrt1. Biochem Bioph Res Co 2005, 330: 950-957
    Guzmana JM, Norberg B, Ramos J, et al. Vitellogenin, steroid plasma levels and spawning performance of cultured female Senegalese sole (Solea senegalensis). Gen Comp Endocr 2008, 156: 285-297
    Hamaguchi S. A light- and electron-microscopic study on the migration of priordial germ cells in teleost, Oryzias latipes. Cell Tissue Res 1982, 227: 139-151
    Harley VR, Lovell-Badge R, Goodfellow PN. Definition of a consensus DNA binding site for SRY. Nucleic Acids Res 1994, 22: 1500-1501
    Hendry CI, Martin-Robichaud DJ, Benfey TJ. Gonadal sex differentiation in Atlantic halibut. J Fish Biol 2002, 60: 1431-1442
    Herman JG, Graff JR, Myohanen S, et al. Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands. P Natl Acad Sci USA 1996, 93: 9821-9826
    Hickey GJ, Krasnow JS, Beattie Wqand, et al. Hormonal regulation, tissue distribution, and content of aromatase cytochrome P450 messenger ribonucleic acid and enzyme in the rat ovarian follicles and corpora lutea: relationship to estradiol biosynthesis. Mol Endocrinol 1990, 4: 3-12
    Higashino T, Miura T, Muria C, et al. Histological studies on early oogenesis in barfin flounder (Verasper moseri). Zool Sci 2002, 19: 557-563
    Hinshelwood MM, Smith ME, Murry BA, et al. A 278 by region just upstream of the human CYP19 (aromatase) gene mediates ovary-specific expression in transgenic mice. Endocrinology 2000, 141: 2050-2053
    Hoegg S., Brinkmann H., Taylor J.S., et al. 2004 Phylogenetic timing of the fish-specific genome duplication correlates with the diversification of teleost fish. J Mol Evol 59: 190-203
    Hofsten Jv, Olsson PE. Zebrafish sex determination and differentiation: Involvement of FTZ-F1 genes. Reprod Biol Endocrin 2005, 3: 63
    Honda S, Harada N, Takagi Y. The alternative exons 1 of the mouse aromatase cytochrome P-450 gene. Biochim Biophys Acta 1996, 1305: 145-150
    Huang W, Zhou L, Li Z, et al. Expression pattern, cellular localization and promoter activity analysis of ovarian aromatase (Cyp19a1a) in protogynous hermaphrodite red-spotted grouper. Mol Cell Endocrinol 2009, 307: 224-236
    Hughes V, Benfey TJ, Martin-Robichaud DJ. Effect of rearing temperature on sex ration in juvenile Atlantic halibut, Hippoglossus hippoglossus. Environ Biol Fish 2008, 81: 415-419
    Ijiri S, Kazeto Y, Takeda N, et al. Changes in serum steroid hormones andsteroidogenic ability of ovarian follicles during artificial maturation of cultivated Japanese eel, Anguilla japonica. Aquaculture 1995, 135: 3-16
    Ijiri S, Berard C, Trant JM. Characterization of gonadal and extra-gonadal forms of the cDNA encoding the Atlantic syingray (Dasyatis Sabina) cytochromeP-450 aromatase (CYP19). Mol Cell Endocrinol 2000, 164: 169-181
    Ijiri S, Kaneko H, Kobayashi T, et al. Sexual dimorphic expression of genes in gonads during early differentiation of a teleost fish, the Nile tilapia Oreochromis niloticus. Biol Reprod 2008, 78: 333-341
    Illingworth R, Kerr A, DeSousa D, et al. A novel CpG island set identifies tissue-specific methylation at developmental gene loci. Plos Biology 2008, 6: 22 Ito M, Ishikawa M, Suzuki S. A rainbow trout SRY-type gene expressed in pituitary glands. FEBS Lett 1995, 377: 37-40
    Jaenisch R, Bird A. Epigenetic regulation of gene expression: how the genome integrates intrinsic and environmental signals. Genetic 2003, 33: 245-254
    Jaillon O, Aury JM, Brunet F, et al. Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype. Nature 431: 946-957
    Jones PL, Veenstra GJC, Wade PA, et al. Methylated DNA and MeCP2 recruit histone deacetylase to repress transcription. Nat Genet 1998, 19: 187-191.
    Jorgensen A, Morthorst JE, Andersen O, et al. Expression profiles for six zebrafish genes during gonadal sex differentiation. Reprod Biol Endocrin 2008, 6:25
    Kallman KD. A new look at sex determination in Poeciliid fishes. In: Truner BJ Evolutionary genetics of fishes. New York: Plenum Press 1983, 95-171
    Karube M, Fernandino JI, Strobl-Mazzulla P, et al. Characterization and expression profile of the ovarian cytochrome P-450 aromatase (cyp19A1) gene during thermolabile sex determination in pejerrey, Odontesthes bonariensis. J Exp Zool Part A 2007, 307: 625-636
    Kent J, Wheatley SC, Andrews JE, et al. A male-specific role for Sox9 in verterbrate sex determination. Development 1996, 122: 2813-2822
    Kettlewell JR, Raymond CS, Zarkower D. Temperature dependent expression of turtle Dmrt1 prior to sexual differentiation. Genesis 2000, 26: 174-178
    Kim S, Kettlewell JR, Anderson RC, et al. Sexually dimorphic expression of multiple doublesex-related genes in the embryonic mouse gonad. Gene Expr Patterns 2003, 3: 77-82
    Kime DE, Hyder M. The effect of temperature and gonadaotropin on testicular steroidogenesis in Sarotherodon (Tilapia) mossambicus in vitro. Gen Comp Endocrinol 1983, 50: 105-115
    Kime DE, Manning NJ. Maturational and temperature effects on steroid hormone production by tests of the carp, Cyprinus carpio. Aquaculture 1986, 54: 44-55
    Kishida M, Callard G. Distinct cytochrome P450 aromatase isoforms in zebrafish (Denio rerio) brain and ovary are differentially programmed and estrogen regulated during early development. Endocrinology 2001, 142: 740-749
    Kitano T, Takamune K, obayashi TK, et al. Suppression of P450 aromatase gene expression in sex-reversed males produced by rearing genetically female larvae at a high water temperature during a period of sex differentiation in the Japanese flounder (Paralichthys olivaceus). J Mol Endocrinol 1999, 23: 167-176
    Kitano T, Takamune K, Nagahama Y, et al. Aromatase inhibitor and 17a-methyltestosterone cause sex-reversal from genetical femeles to phenotypic males and suppression of P450 aromatase gene expression in Japanese flounder (Paralichthys olivaceus). Mol Reprod Dev 2000, 56: 1-5
    Kobayashi T, Kajiura-Kobayashi H, Nagahama Y. Induction of XY sex reversal by estrogen involves altered gene expression in a teleost, tilapia. Cytogenet. Genome Res 2003, 101: 289-294
    Kobayashi T, Matsuda M, Kajiura-Kobayashi H, et al. Two DM domain genes, dmy and dmrt1, involved in testicular differentiation and development in the medaka, Oryzias latipes. Dev Dynam 2004, 231: 518-526
    Kobayashi T, Kajiura-Kobayashi H, Guan G, et al. Sexual dimorphic expression of dmrt1 and sox9a during gonadal differentiation and hormone-induced sex reversal in the teleost fish Nile tilapia (Oreochromis niloticus). Dev Dynam 2008, 237: 297-306
    Kobayashi T, Nagahama Y. Molecular aspects of gonadal differentiation in a teleostfish, the Nile tilapia. Sex Dev 2009, 3: 108-117
    Koopman P. The Genetics and Biology of Vertebrate Sex Determination. Cell 2001, 105: 843-847
    Koopman P, Loffler KA. Sex Determination: the Fishy Tale of Dmrt1. Curr Biol 2003, 13: 177-179
    Koya Y, Watanabe H, Soyano K, et al. Testicular development and serum steroid hormone levels in captive male spotted halibut Verasper variegates. Fisheries Sci 2003, 69: 792-798
    Kurokawa H, Saito D, Nakamura S, et al. Germ cells are essential for sexual dimorphism in the medaka gonad. P Natl Acad Sci USA 2007, 104: 16958-16963
    Kwon JY, McAndrew BJ, Penman DJ. Cloning of brain aromatase gene and expression of brain and ovarian aromatase genes during sexual differentiation in genetic male and female Nile tilapia Oreochromis nilodcus. Mot Reprod Dev 2001, 59: 359-370
    Labadie P, Budzinski H. Alteration of steroid hormone profile in juvenile turbot (Psetta maxima) as a consequence of short-term exposure to 17α-ethynylestradiol. Chemosphere 2006, 64: 1274-1286
    Lee YD, Lee TY. Sex differentiation and development of the gonad in the flounder, Paralichthys olivaceus (Temminck et Schlegel). Bulletin of the Marine Research Institute, Cheju National University 1990, 14: 61-86
    Lephart ED, Peterson KG, Noble JF, et al. The structure of cDNA clones encoding the aromatase P-450 isolated from a rat Leydig cell tumor line demonstrates differential processing of aromatase mRNA in rat ovary and a neoplastic cell line. Mol Cel Endocrinol 1990, 70: 31-40
    Lephart ED. A review of brain aromatase cytochrome P450. Brain Res 1996, 22: 1-26
    Li E, Beard C, Jaenisch R. Role for DNA methylation in genomic imprinting. Nature, 1993, 366: 362-365.
    Li L, Keverne EB, Aparicio SA, et al. Regulation of maternal behavior and offspring growth by paternally expressed Peg3. Science, 1999, 284: 330-333.
    Lister R., Pelizzola M., Dowen R.H., et al. Human DNA methylomes at baseresolution show widespread epigenomic differences. Nature, 2009, 462: 315-322.
    Lovell-Badge R, Canning C, Sekido R. Sex-determining genes in mice: building pathways. Chadwick D, Goode J. The Genetics and Biology of Sex Determination:Novartis Foundation Symposium. Chichester: Wiley 2002, 244: 4-22
    Lucifero D, Salle SL, Bourchis D, et al. Coordinate regulation of DNA methyltransferase expression during oogenesis. BMC Dev Biol 2007, 7: 36
    Luckenbach JA, Godwin J, Daniels HV, et al. Gonadal differentiation and effects of temperature on sex determination in southern flounder (Paralichthys lethostigma). Aquaculture 2003, 216: 315-327
    Luckenbach JA, Early LW, Rowe AH, et al. Aromatase cytochrome P450: cloning, intron variation, and ontogeny of gene expression in southern flounder (Paralichthys lethostigma). J Exp Zool Part A 2005, 303: 643-656.
    MacKay AB, Mhanni AA, McGowan RA, et al. Immunological detection of changes in genomic DNA methylation during early zebrafish development. Genome 2007, 50: 778-785
    Manning NJ, Kime DE. Temperature regulation of ovarian steroid production in the common carp, Cyprinus carpio, in vitro and in vivo. Gen Comp Endocrinol 1984, 56: 376-388
    Manning NJ, Kime DE. The effects of temperature on testicular steroid production in the rainbow trout, Salmo gairdneri, in vivo and in vitro. Gen Comp Endocrinol 1985, 57: 377-382
    Marchand O, Gororoun M, D'Cotta H, et al. DMRTI expression during gonadal differentiation and spermatogenesis in the rainbow trout, Oncorchynchus. Biophys Acta 2000, 1493: 180-187
    Martin CC, Laforest L, Akimenko MA, et al. A role for DNA methylation in gastrulation and somite patterning. Dev Biol 1999, 206: 189-205
    Martinowich K, Hattori D, Wu H, et al. DNA methylation-related chromatin remodeling in activity-dependent bdnf gene regulation. Science 2003, 302: 890-893
    Matouk CC, Marsden PA. Epigenetic Regulation of Vascular Endothelial Gene Expression. Circ Res 2008, 102: 873-887
    Matsuda M, Nagahama Y, Shinomiya A, et al. DMY is a Y-specific DM-domain gene required for male development in the medaka fish. Nature 2002, 417: 559-563 Matsuda M. Sex determination in the teleost medaka, Oryzias latipes. Annu Rev Genet 2005, 39: 293-307
    Matsuoka MP, van Nes S, Andersen O, et al. Real-time PCR analysis of ovary- and brain-type aromatase gene expression during Atlantic halibut (Hippoglossus hippoglossus) development. Comp Biochem Physiol B 2006, 144: 128-135
    Mhanni AA, McGowan RA. Global changes in genomic methylation levels during early development of the zebrafish embryo. Dev Genes Evol 2004, 214: 412-417
    Mahendroo MS, Means GD, Mendelson CR, et al. Tissue-specific expression of human P-450AROM. The promoter responsible for expression in adipose tissue is different from that utilized in placenta. J Biol Chem 1991, 266: 11276-11281
    McNairn AJ, David M. Epigenomic replication: linking epigene tics to DNA replication. BioEssays, 2003, 25: 647-656.
    Morgan HD, Santos F, Green K, et al. Epigenetic reprogramming in mammals. Hum Mol Genet 2005, 14: 47-58
    Morohashi KI. Gonadal and extragonadal function of Ad4BP/SF-1: Development aspects. Trends Endorinol Metab 1999, 10: 169-173
    Murdock C, Wibbels T. Cloning and expression of aromstase in a turtle with temperature-dependent sex determination. Gen Comp Endocrinol 2003, 130: 109-119
    Nagahama Y. The functional morphology of teleost gonads. In: Fish Physiology, Vol, IXA, W.S. Hoar and DJ Randall (eds). Academic Press 1983: 97-135
    Nagase H., Ghosh S. Epigenetics: differential DNA methylation in mammalian somatic tissues. FEBS J 2008, 275: 1617-1623
    Nakamura M, Kobayashi T, Yashiura Y, et al. Role of endogenous steroid hormones on gonadal sex differentiation in fish. In: Proceeding of the Sixth International Symposium on the Reproductive Physiology of Fish 2000, 247-249
    Nakamoto M, Suzuki A, Matsuda M, et al. Testicular type Sox9a is not involved in sex determination but might be in the development of testicular structures in themedaka, Oryzias latipes. Biochem Bioph Res Co 2005, 333: 729-736
    Nakamoto M, Matsuda M, Wang DS, et al. Molecular cloning and analysis of gonadal expression of Foxl2 in the medaka, Oryzias latipes. Biochem Biophy Res Co 2006, 344: 353-361
    Nakamoto M, Wang DS, Suzuki A, et al. Dax1 suppresses P450arom expression in medaka ovarian follicles. Mol Reprod Dev 2007, 74: 1239-1246
    Nanda I, Shan Z, Schard M, et al. 300 million years of conserved synteny between chicken Z and human chromosome 9. Nat Genet 1999, 21: 258-259
    Nanda I, Konod M, Hornung U, et al. A duplicated copy of DMRT1 in the sex-determining region of the Y-chromosome of the madaka, Oryzias latipes. P Natl Acad Sci USA 2002, 99: 11778-11783
    Navarro-Martin L, Vinas J, Gutierrez A, et al. Sex-dependent differences in DNA-methylation levels in the promoter of the gonadal aromatase gene in a fish, the European sea bass (Dicentrarchus labrax). In: Proceedings of the 8th International Symposium on Reproductive Physiology of Fish, 2007, June 3-8, Saint-Malo
    Ooi SKT, O’Donnell AH, Bestor TH. Mammalian cytosine methylation at a glance. J Cell Science 2009, 122: 2787-2791
    Osaki E, Nishina Y, Inazawa J, et al. Identification of a novel Sry related gene and its germ cell-specific expression. Nucleic Acids Res 1999, 27: 2503
    Orban L, Sreenivasana R, Olsson P-E. Long and winding roads: Testis differentiation in zebrafish. Molecular and Cellular Endocrinology 2009, 312: 35-41
    Ospina-Alvarez N, Piferrer F. Temperature-dependent sex determination in fish revisited: prevalence, a single sex ratio response pattern, and possible effects of climate change. PLoS one 2008, 3: 1-11
    Park IS, Kim JH, Cho SH, et al. Sex differentiation and hormonal sex reversal in the bagrid catfish Pseudobagrus fulvidraco (Richardson). Aquaculture 2004, 232: 183-193
    Pasmanik M, Schlinger BA, Callard GV. In vivo steroid regulation of aromatase and 5αreductase in goldfish brain and pituitary. Gen Comp Endocrinol 1988, 71:175-182
    Pauler FM, Barlow DP. Imprinting mechanisms-it only takes two. Genes Dev, 2006, 20: 1203-1206.
    Penman DJ, Piferrer F. Fish gonadogenesis part I: Genetic and environmental mechanisms of sex determination. Fisheries Sci 2008, 16:16-34
    Piferrer F. Endocrine sex controls strategies for the feminization of teleost fish. Aquaculmre 2001, 197: 229-281
    Piferrer F., Navarro-Martin L., Ospina-Alvarez N., et al. Temperature-dependent sex determination in fish, effects of temperature on gonadal aromatase gene expression, and epigenetic regulation after early exposure to high water temperature. In: Proceedings of the 6th International Symposium on Fish Endocrinology, 2008, June 22-27, Calgary.
    Raghuveer K, Senthilkumaran B. Identification of multiple dmrt1s in catfish: localization, dimorphic expression pattern, changes during testicular cycle and after methyltestosterone treatment. J Mol Endocrinol 2009, 42: 437-448
    Ramachandran B, Schlinger BA, Arnold AP, et al. Zebra finch aromatase gene expression is regulated in the brain through an alternate promoter. Gene 1999, 240: 209-216
    Raymond CS, Shamu CE, Shen MM, et al. Evidence for evolutionary conservation of sex-determining genes. Nature 1998, 391: 691-695
    Raymond CS, Parker ED, Kettlewell JR, et al. A region of human chromosome 9p required for testis development contains two genes related to known sexual regulators. Hum Mol Genet 1999, 8: 989-996
    Resko JA, Pereyra-Martinez AC, Stadelman HL, et al. Region-specific regulation of cytochrome P450 aromatase messenger ribonucleic acid by androgen in brains of male rhesus monkeys. Biol Reprod 2000, 62: 1818-1822
    Rodriguez-Mari A, Yan YL, BreMiller RA, et al. Characterization and expression pattern of zebrafish anti-Mu¨llerian hormone (amh) relative to sox9a, sox9b, and cyp19a1a, during gonad development. Gene Expr Patterns 2005, 5: 655-667
    Romer U, Beisenherz W. Environmental determination of sex in Apistogramma(Cichlidae) and two other freshwater fishes (Teleostei). J Fish Biol 1996, 48, 714-725
    Roselli CE, Resko JA. Sex differences in androgen-regulated expression of cytochrome P450 aromatase in the rat brain. J Steroid Biochem Mol Biol 1997, 61: 365-374
    Sakaia Y, Suetakeb I, Shinozaki F, et al. Co-expression of de novo DNA methyltransferases Dnmt3a2 and Dnmt3L in gonocytes of mouse embryos. Gene Expr Patterns 2004, 5: 231-237
    Salle SL, Trasler JM. Dynamic expression of DNMT3a and DNMT3b isoforms during male germ cell development in the mouse. Dev Biol 2006, 296: 71-82
    Scholz S, Gutzeit HO. 17α-ethinylestradiol affects reproduction, sexual differentiation and aromatase gene expression of the medaka (Oryzias latipes). Aquat Toxicol 2000, 50: 367–373
    Sekido R, Lovell-Badge R. Sex determination involves synergistic action of SRY and SF1 on a specific Sox9a enhancer. Nature 2008, 453: 930-934
    Seo JH, Bailey JE. Effects of recombinant plasmid content on growth properties and cloned gene product formation in Escherichia co1i. Biotechnol Bioeng 1985, 27: 1668-1674
    Shen MM, Hodgkin J. Mab-3, a gene required for sex-specific yolk protein expression and a male-specific lineage in C. elegans. Cell 1988, 54: 1019-1031
    Shen P, Campagnoni CW, Kampf K, et al. Isolation and characterization of a zebra finch aromatase cDNA: in situ hybridization reveals high aromatase expression in brain. Mol Brain Res 1994, 24: 227-237
    Shibata K, Takase M, Nakamura M. The Dmrt1 expression in sex-reversed gonads of amphibians. Gen Comp Endocrinol 2002, 127: 232-241
    Shin HS, An KW, Park MS, et al. Quantitative mRNA expression of sox3 and DMRT1 during sex reversal, and expression profiles after GnRHa administration in black porgy, Acanthopagrus schlegeli. Comp Biochem Phys B 2009, 154: 150-156
    Shinomiya A, Tanaka M, Kobayashi T, et al. The vasa-like gene, olvas, identifies the migration path of primordial germ cells during embryonic body formation stage inthe medaka Oryzias latipes. Dev Growth Differ 2000, 42: 317-326
    Siegfried Z., Cedar H. (1997) DNA methylation: a molecular lock. Curr Biol 7: 305-307.
    Simpson ER, Merrill JC, Hollub AJ, et al. Regulation of estrogen biosynthesis by human adipose cells. Endocrine Rev 1989, 10: 136-148.
    Smith CA, McClive PJ, Western PS, et al. Conservation of a sex-determining gene. Nature 1999, 402: 601-602
    Smith THL, Dueck CC, Mhanni AA, et al. Novel splice variants associated with one of the zebrafish dnmt3 genes. BMC Dev Biol 2005, 5: 23
    Specker JL, Chandlee MK. Methodology for estradiol treatment in marine larval and juvenile fish: uptake and clearance in summer flounder. Aquaculture 2003, 217: 663-672
    Strussmann CA, Patino R. Temperature manipulation of sex differentiation in fish. In: Proceedings of the Fifth International Symposium on the Reproductive Physiology of Fish 1995, 153-160. Edited by FW Goetz and P Thomas, FishSymp95, Austin, Texas
    Strussmann CA, Saito T, Takashima F. Heat-induced germ cell deficiency in the teleosts Odontesthes bonariensis and Patagonina hatcheri. Comp Biochem Phys 1998, 119: 637-644
    Strussmann CA, Patino R. Sex determination, Environmental. In: Encyclopedia of Reproduction. Academic Press 1999, 4: 402-409
    Strussmann CA, Nakamura M. Morphology, endocrinology, and environmental modulation of gonadal sex differentiation in teleost fishes. Fish Physiol Biochem 2002, 26: 13-29
    Sudhakumari C.C., Kobayashi T., Kajiura-Kobayashi H., et al. Ontogenic expression patterns of several nuclear receptors and cytochrome P450 aromatases in brain and gonads of the Nile tilapia Oreochromis niloticus suggests their involvement in sex differentiation. Fish Physiol Biochem 2005, 31: 129-135.
    Sun P, You F, Liu MX, Wu ZH, Wen AY, Li J, Xu YL, Zhang PJ. Steroid sex hormone dynamics during estradiol-17βinduced gonadal differentiation in Paralichthysolivaceus (Teleostei). Chinese Journal of Oceanology and Limnology 2010, 28: 254-259
    Tabata K. Artificial feminization of hirame Paralichthys olivaceu by administration of beta-estradiol, and estimation of stage of sexual differentiation. Bulletin of Hyogo Prefectual Fisheries Experimental Station 1989, 26:19-36
    Tabata K. Induction of gynogenetic diploid males and presumption of sex determination mechanisms in the hirame Paralichthys olivaceus. Bulletin of the Japanese Society of Scientific Fisheries 1991, 57: 845-850
    Tanaka H. Gonadal sex differentiation in flounder, Paralichthys olivaceus. Bulletin of National Research Institute of Aquaculture 1987, 11: 7-19
    Tanaka H. Effects of estradiol-17βon gonadal sex differentiation in flounder, Paralichthys olivaceus. Bulletin of National Research Institute of Aquaculture 1988, 13: 17-23
    Tanaka M, Telecky TM, Fukada S, et al. Cloning and sequence analysis of the cDNA encoding P-450 aromatase (P450arom) from a rainbow trout (Oncorhynchus mykiss) ovary, relationship between the amount of P450arom mRNA and the production of oestradiol-178 in the ovary. J Mol Endocrinol 1992, 8: 53-61
    Tanaka M, Fukada S, Matsuyama M, et al. Structure and promoter analysis of the cytochrome P-450 aromatase gene of the teleost fish, medaka (Oryzias latipes). Biochem (Tokyo) 1995, 117: 719-725
    Taylor J.S., Raes J. 2004 Duplication and divergence: the evolution of new genes and old ideas. Ann Rev Genet 38: 615-643
    Tchoudakova A, Callard GV. Identification of multiple CYP19 genes encoding different cytochrome P450 aromatase isozymes in brain and ovary. Endocrinology 1998, 139: 2179-2189
    Tchoudakova A, Kishida M, Wood E, et al. Promoter characteristics of two cyp19 genes differentially expressed in the brain and ovary of teleost fish. J Steroid Biochem Mot Biol 2001, 78: 427-39
    Tershima M, Toda K, Kawamoto T, et al. Isolation of a ful-length cDNA encoding mouse aromatase P-450. Arch Biochem Biophys 1991, 285: 231-237
    Tilmann C, Capel B. Cellular and molecular pathways regulating mammalian sex determination. Recent Prog Horm Res 2002, 57: 1-18
    Tong SK, Chung BC. Analysis of zebrafish cyp19 promoters. J Steroid Biochem Mot Biol 2003, 86: 381-386
    Trant JM. Isolation and characterization of the cDNA encoding the channel catfish (Ictalurus punctatus) farm of cytochrome P450arom. Gen Comp Endocrinol 1994, 95: 155-168
    Trant JM, Gavasso S, Ackers J, et al. Developmental expression of cytochrome P450 aromatase genes (CYP19a and CYP19b) in zebrafish fry (Danio rerio). J Exp Zool 2001, 290: 475-483
    Traut W, Winking H. Meiotic chromosomes and stages of sex b chromosome evolution in fish: Zebra fish, platy fish and guppy. Chromosome Res 2001, 9: 659-672
    Turek-plewa J, Jagodzinski PP. The role of mammalian DNA methyltransferases in the regulation of gene expression. Cell Mol Biol Lett 2005, 10: 631-647
    Uguz C. Histological evaluation of gonadal differentiation in fathead minnows (Pimephales promelas). Tissue Cell 2008, 40: 299-306
    Veith AM, Schafer M, Kluver N, et al. 2007. Characterization of early molecular sex differentiation in rainbow trout, Oncorhynchus mykiss. Dev Dyn 236: 2198-2206.
    Velagaleti GV, Bien-Willner GA, Northup JK, et al. Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia. Am J Hum Genet 2005, 76: 652-662
    Volff JN. Tissue-specific expression of dmrt genes in embryos and adults of the platyfish Xiphophorus maculates. Zebrafish 2006, 3: 325-337
    Wagner T, Wirth J, Meyer J, et al. Autosomal sex reversal and campomelic dysplasia are caused by mutations in and around the SRY-related gene Sox9. Cell 1994, 79: 1111-1120
    Walter RB, Li HY, Intano GW, et al. Absence of global genomic cytosine methylation pattern erasure during medaka (Oryzias latipes) early embryo development. CompBiochem Phys B 2002, 133: 597-607
    Wang DS, Kobayashi T, Zhou LY, et al. Foxl2 up-regulates aromatase gene transcription in a female-specific manner by binding to the promoter as well as interacting with ad4 binding protein/steroidogenic factor 1. Mol Endocrinol 2007, 21: 712-725
    Wang DS, Zhou LY, Kobayashi T, et al. Doublesex- and mab-3-related transcription factor-1 repression of aromatase transcription, a possible mechanism favoring the male pathway in tilapia. Endocrinology 2010, Epub ahead of print Wats M, Pankhurst NW, King HR. Maintenance of Atlantic salmon (Salmo salar) at elevated temperature inhibits cytochrome P450 aromatase activity in isolated ovarian follicles. Gen Comp Endocrinol 2004, 135: 381-390
    Wegner M. From head to toes: the multiple facets of Sox proteins. Nucleic Acids Res 1999, 27: 1409-1420
    Winkler C, Hornung U, Kondo M, et al. Developmentally regulated and non-sex-specific expression of autosomal dmrt genes in embryos of the Medaka fish (Oryzias latipes). Mech Develop 2004, 121: 997-1005
    Wolffe AP, Matzke MA. Epigenetics: regulation through repression. Science, 1999, 286: 481-486.
    Wrigbt EM, et al. Seven new members of the Sox gene family expressed during development. Nucleic Acids Res 1993, 21: 744
    Wu GC, Tomy S, Nakamura M, et al. Dual Roles of cyp19a1a in Gonadal Sex Differentiation and Development in the Protandrous Black Porgy, Acanthopagrus schlegeli. Biol Reprod 2008, 79: 1111-1120
    Xia W, Zhou L, Yao B, et al. Differential and spermatogenic cell-specific expression of DMRT1 during sex reversal in protogynous hermaphroditic groupers. Mol Cell Endocrinol 2007, 263: 156-172
    Yamaguchi A, Lee KH, Fujimoto H, et al. Expression of the dmrt gene and its roles in early gonadal development of the Japanese puffer fish Takifugu rubripes. Comp Biochem Phys D 2006, 1: 59-68
    Yamaguchi T, Yamaguchi S, Hirai T, et al. Follicle-stimulating hormone signaling andfoxl2 are involved in transcriptional regulation of aromatase gene during gonadal sex differentiation in Japanese flounder, Paralichthys olivaceus. Biochem Bioph Res Co 2007, 359: 935-940
    Yamamoto E. Studies on sex-manipulation and production of cloned populations in hirame, Paralichthys olivaceus (Temminck et Sehlege1). Bulletin of the Tottori Prefectual Fisheries Experimental Station 1995, 34: 1-145
    Yamamoto E. Studies on sex-manipulation and production of cloned populations in hirame, Paralichthys olivaceus (Temminck et Schlegel). Aquaculture 1999, 173: 235-246
    Yamamoto T. Sex differentiation. In: Hoar WS, Randall DJ. (Eds.), Fish Physiology, 3. Academic Press, New York 1969: 117-175
    Yamane K, Toumazou C, Tsukada YI, et al. JHDM2A, a JmjC-containing H3K9 demethylase, facilitates transcription activation by androgen receptor. Cell 2006, 125: 483-495
    Yokomori N, Kobayashi R, Moore R, et al. A DNA methylation site in the male-specific P450 (Cyp 2d-9) promoter and binding of the heteromeric transcription factor GABP. Mol Cell Biol 1995a, 15: 5355-5362
    Yokomori N, Moore R, Negishi M, et al. Sexually dimorphic DNA demethylation in the promoter of the Slp (sex-limited protein) gene in mouse liver. P Natl Acad Sci USA 1995b, 92: 1302-1306
    Yong EL, Hillier SG, Turner M, et al. Differential regulation of cholesterol side-chain cleavage (P450scc)and aromatase (P450arom) enzyme mRNA expression by gonadotrophins and cyclic AMP in human granulosa cells. J Mol Endocrinol 1994, 12: 239-249
    Yong G, Kagawa H, Nagahama Y. Evidence for a decrease in aromatase activity in the ovarian granulose cell of amago salmon (Oncorhynchus rhadurus) associated with final oocyte maturation. Biol Repord 1983, 29: 310-315
    Yoon C, Kawakami K, Hopkins N. Zebrafish vasa homologue RNA is localized to the cleavage planes of 2-and 4-cell-stage embryos and is expressed in the primordial germ cells. Development 1997, 124: 3157-3166
    Yoshinaga N, Shiraishi E, Yamamoto T, et al. Sexually dimorphic expression of a teleost homologue of Mullerian inhibiting substance during gonadal sex differentiation in Japanese flounder, Paralichthys olivaceus. Biochem Bioph Res Co 2004, 322: 508-513
    Yoshizaki G, Sakatani S, Tominaga H, et al. Cloning and characterization of vasa-like gene in rainbow trout and its expression in the germ cell lineage. Mol Reprod Dev 2000, 55: 364-371
    Zhang Y, Dufau ML. Dual mechanisms of regulation of transcription of luteinizing hormone receptor gene by nuclear orphan receptors and histone deacetylase complexes. J Steroid Biochem Mol Biol 2003, 85: 401-414.
    Zhang Y, Zhang WM, Zhang LH, et al. Two distinct cytochrome P450 aromatases in the orange-spotted grouper (Epinephelus coioides): cDNA cloning and differential mRNA expression. J Steroid Biochem Mol Biol 2004, 92: 39-50
    Zhou R, Cheng H, Zhang Q, et al. SRY-related genes in the genome of the rice field eel (Monopterus albus). Genet Sel Evol 2002, 34: 129-137
    Zhou R, Liu L, Guo Y, et al. Similar gene structure of two Sox9 genes and their expression patterns during gonad differentiation in a teleost fish, rice field eel (Monopterus albus). Mol Reprod 2003, 66: 211-217
    Zhou LY, Wang DS, Shibata Y, et al. Characterization, expression and transcriptional regulation of P450c17-I and -II in the medaka, Oryzias latipes. Biochem Bioph Res Co 2007, 362: 619-625
    Zhuang ZM, Wu D, Zhang SC, et al. G-banding patterns of the chromosomes of tonguefish Cynoglossus semilaevis Günther, 1873, J Appl Ichthyol 2006, 22: 437-440

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700