血红素加氧酶/一氧化碳信号系统介导氯化钴诱导的番茄侧根发生
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摘要
钴是植物的有益元素,作为根瘤菌中若干种酶的金属辅基,是植物固氮过程中必不可少的元素。一氧化碳(carbon monoxide, CO)由血红素加氧酶(heme oxygenase, HO, EC 1.14.99.3)催化血红素(heme)分解产生,是动物炎症反应中的重要信号分子,并介导了生长素诱导的黄瓜不定根发生过程。
     为了了解钴(Ⅱ)对番茄幼苗侧根发生的影响以及HO/CO系统在钴(Ⅱ)诱导的侧根发生过程中的作用,本文研究了氯化钴(CoCl2)、诱导型HO专一性抑制剂锌原卟啉(zinc ProtoporphyrinⅨ, ZnPPⅨ)、HO催化产物CO等处理对番茄侧根发生的影响及HO的变化。研究发现,CoCl2不仅能以浓度依赖方式促进番茄幼苗侧根发生,而且能以浓度依赖和时间进程方式促进番茄侧根发生区域LeHO-1/LeHO-2的转录水平、HO一1蛋白表达及HO活性。为了进一步验证CoCl2诱导的番茄侧根发生由HO/CO系统介导的实验假设,本文使用ZnPPⅨ以及CO水溶液处理番茄幼苗,并对侧根产生情况进行了分析。实验发现,200μM ZnPPⅨ能使明显抑制CoCl2诱导的侧根生成,而添加50%饱和度的CO水溶液则能使幼苗侧根数目达到CoCl2单独处理的水平。进一步研究表明,ZnPPⅨ能显著抑制CoCl2对HO蛋白表达和活性的诱导,50%饱和度的CO水溶液能消除ZnPPⅨ对HO活性的抑制,这与ZnPPⅨ和CO对CoCl2诱导的侧根发生的影响是一致的。上述结果说明HO可能介导了CoCl2诱导的番茄侧根发生,而且HO的功能可能是通过其催化产物C0实现的。
     进一步对CoCl2及HO/CO系统诱导番茄侧根发生的分子机理进行了研究,发现CoCl2能够不同程度上调细胞周期基因LeCYCA2;1、LeCYCA3;1、LeCYCD3;1和LeCDKA1的表达;ZnPPⅨ可以抑制CoCl2对细胞周期基因的上调,而CO则能够缓解ZnPPⅨ的抑制效果,暗示细胞周期基因与CoCl2对番茄幼苗侧根的诱导相关。
     综上所述,HO/CO信号系统可能通过影响细胞周期基因的表达参与CoCl2诱导的番茄幼苗侧根发生。
Cobalt is supposed to be a beneficial element of plant, which plays an essential role in nitrogen-fixation as the metal component of several enzymes in rhizobia. Carbon monoxide (CO), the side-production of heme degradation catalyzed by heme oxygenase (HO, EC 1.14.99.3), acts as an important signal molecular in inflammatory reactions, and was newly proved to be involved in the auxin-induced cucumber adventitious rooting process.
     In order to decode the relation among divalent cobalt ion, HO/CO system and lateral root development, morphological characters of root system and transcription and activity change of HO were investigated after various treatments. We found that CoCl2 not only induced lateral root formation in a dose-dependent manner, but also elevated the transcription of LeHO-1/LeHO-2, protein expression and activity of HO enzyme in a dose-dependent and time-course manner in lateral root initiation zoon of tomato seedlings. To testify the hypothesis that HO/CO system was involved in cobalt-induced lateral rooting process, the specific inhibitor of HO-1, zinc protoporphyrinⅨ(ZnPPⅨ) and CO aqueous solution were applied to the experimental system. We observed decreased lateral root formation in ZnPPⅨcombined CoCl2 treated seedlings; by contract, the inhibition was restored when 50% CO was added to the former mentioned system. Meanwhile, similar change was found in HO enzyme activity and protein expression. These results suggested HO's involvement in the CoCl2-induced lateral root development and the possibility that CO might be the executer of HO in this process.
     Furthermore, we investigated the molecular mechanism of CoCl2-induced, HO/CO-dependent lateral root formation. We found CoCl2 differentially up-regulated cell cycle genes, such as LeCYCA2;1, LeCYCA3;1, LeCYCD3;1 and LeCDKA1; the application of ZnPPIX could inhibit CoCl2's effect and the addition of CO was able to reverse ZnPPⅨ's inhitition.
     As a conclusion, HO/CO system was involved in CoCl2-induced lateral root development process in tomato seedlings by regulating the expression of cell cycle genes.
引文
焦健,李朝周,黄高宝.钻对干旱胁迫下大豆幼苗叶片的保护作用及其机理[J].应用生态学报,2006,17(5):796-800
    李洪益.重要的微量元素钻[J].微量元素与健康研究,2004,21(1):61-62
    刘庆昌,吴国良.植物细胞组织培养[M].中国农业大学出版社,2002
    刘素萍,樊文华.钴对番茄生长发育影响的初步研究[J].土壤通报,2005,36(6):925-928
    王镜岩,朱圣庚,徐长法.生物化学上册(第三版)[M].北京:高等教育出版社,2002
    王燮.生命科学中的微量元素(下卷)[M].北京:中国计量出版社,1992.
    王智,陈楚琴,袁星星,徐晟,杨清,沈文飚.外源一氧化碳对盐胁迫下水稻悬浮细胞死亡的缓解效应[J].植物生理学通讯,2009,45(7):643-646
    武明珠,徐晟,崔为体,张博,刘雅辉,凌腾芳,沈文飚.血红素加氧酶介导GA对小麦糊粉层中α-淀粉酶的诱导表达[J].植物生理学通讯,2009,45(5):483-486
    周云龙.植物生物学(第2版)[M].北京:高等教育出版社,2004
    Ashfaq M, Ali S, Hanif MA, Bioaccumulation of cobalt in silkworm (Bombyx mori L.) in relation to mulberry, soil and wastewater metal concentrations [J]. Process Biochemistry,2009,44:1179-1184
    Bao F, Shen J, Brady SR, Muday GK, Asami T, Yang Z. Brassinosteroids interact with auxin to promote lateral root development in Arabidopsis [J]. Plant Physiology,2004,134:1-8
    Baudouin E, Frendo P, Le Gleuher M, Puppo A. A Medicago sativa haem oxygenase gene is preferentially expressed in root nodules [J]. Journal of Experimental Botany,2004,55:43-47
    Balestrasse KB, Noriega GO, Batlle AMC, Tomaro ML. Involvement of heme oxygenase as antioxidant defense in soybean nodules [J]. Free Radical Research,2005,39:145-151
    Beeckman T, Burssens S, Inze D. The peri-cell-cycle in Arabidopsis [J]. Journal of Experimental Botany,2001,52:403-411
    Benkova E, Michniewicz M, Sauer M, Teichmann T, Seifertova D, Jurgens G, Friml J. Local, efflux-dependent auxin gradients as acommon module for plant organ formation [J]. Cell,2003,115 (5):591-602
    Bhalerao RP, Eklof J, Ljung K, Marchant A, Bennett M, Sandberg G. Shoot-derived auxin is essential for early lateral root emergence in Arabidopsis seedlings [J]. The Plant Journal,2002,29: 325-332
    Blakely LM, Durham M, Evans TA, Blakely RM. Experimental studies on lateral root formation in radish seedling roots. I. General methods, developmental stages, and spontaneous formation of laterals [J]. Botanical Gazette,1982,143:341-352
    Bradford MM. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding [J]. Analytical Biochemistry,1976,72:248-254
    Casimiro I, Marchant A, Bhalerao RP, Beeckman T, Dhooge S, Swarup R, Graham N, Inze D, Sandberg G, Casero PJ, Bennett M. Auxin transport promotes Arabidopsis lateral root initiation [J]. Plant Cell,2001,13:843-852
    Cao Z, Huang B, Wang Q, Xuan W, Ling T, Zhang B, Chen X, Nie L, Shen W. Involvement of carbon monoxide produced by heme oxygenase in ABA-induced stomatal closure in Viciafaba and its proposed signal transduction pathway [J]. Chinese Science Bulletin,2007a,52:2365-2373
    Cao Z, Xuan W, Liu Z, Li X, Zhao N, Xu P, Wang Z, Guan R, Shen W. Carbon monoxide promotes lateral root formation in rapeseed [J]. Journal of Integrative Plant Biology,2007b,49:1007-1016
    Celenza JL, Grisafi PL, Fink GR. A pathway for lateral root formation in Arabidopsis thaliana [J]. Genes & Development,1995,9:2131-2142
    Chen X, Ding X, Xu S, Wang R, Xuan W, Cao Z, Chen J, Wu H, Ye M, Shen W. Endogenous hydrogen peroxide plays a positive role in the upregulation of heme oxygenase and acclimation to oxidative stress in wheat seedling leaves [J]. Journal of Integrative Plant Biology,2009,51 (10): 951-960
    Chhun T, Uno Y, Taketa S, Azuma T, Ichii M, Okamoto T, Tsurumi S. Saturated humidity accelerates lateral root development in rice (Oryza sativa L.) seedlings by increasing phloem-based auxin transport [J]. Journal of Experimental Botany,2007,58 (7):1695-1704
    Coceani F. Carbon monoxide in vasoregulation:The promise and the challenge [J]. Circulation Research, 2000,86:1184-1186
    Correa-Aragunde N, Graziano M, Lamattina L. Nitric oxide plays a central role in determining lateral root development in tomato [J]. Planta,2004,218:900-905
    Correa-Aragunde N, Graziano M, Chevalier C, Lamattina L. Nitric oxide modulates the expression of cell cycle regulatory genes during lateral root formation in tomato [J]. Journal of Experimental Botany,2006,57 (3):581-588
    Davis SJ, Bhoo SH, Durski AM, Walker JM, Vierstra RD. The heme-oxygenase family required for phytochrome chromophore biosynthesis is necessary for proper photomorphogenesis in higher plants [J]. Plant Physiology,2001,126:656-669.
    Deak KI, Malamy J. Osmotic regulation of root system architecture [J]. The Plant Journal,2005,43: 17-28
    Delledonne M, Xia Y, Dixon RA, Lamb C. Nitric oxide functions as a signal in plant disease resistance [J]. Nature,1998,394 (6):585-588
    de Smet I, Tetsumura T, de Rybel B, Frey NF, Laplaze L, Casimiro I, Swarup R, Naudts M, Vanneste S, Audenaert D, Inze D, Bennett MJ, Beeckman T. Auxin-dependent regulation of lateral root positioning in the basal meristem of Arabidopsis [J]. Development,2007,134:681-690
    Ditengou FA, Teale WD, Kochersperger P, Flittner KA, Kneuper I, van der Graaff E, Nziengui H, Pinosa F, Li X, Nitschke R, Laux T, Palme K. Mechanical induction of lateral root initiation in Arabidopsis thaliana [J]. Proceedings of the National Academy of Sciences of the United States of America,2008,105:18818-18823
    Doncheva S, Amenos M, Poschenrieder C, Barcelo J. Root cell patterning:a primary target for aluminium toxicity in maize [J]. Journal of Experimental Botany,2005,56 (414):1213-1220
    Dubrovsky JG, Rost TL, Colon-Carmona A, Doerner P. Early primordiummorphogenesis during lateral root initiation in Arabidopsis thaliana [J]. Planta,2001,214:30-36
    Dulak J, Jozkowicz A. Carbon monoxide:A "new" gaseous modulator of gene expression [J]. Acta Biochimica Polonica,2003,50:31-47
    Davies PJ. Plant hormones [M]. Dordrecht, The Netherlands:Kluwer Academic Publishiers,2004
    Fukaki H, Okushima Y, Tasaka M. Auxin-mediated lateral root formation in higher plants [J]. International Review of Cytology,2007,256:111-137
    Gad N, Atta-Aly MA. Effect of cobalt on the formation, growth and development of adventitious roots in tomato and cucumber cuttings [J]. Journal of Applied Sciences Research,2006,2 (7):423-429
    Gault N, Sandre C, Poncy JL, Moulin C, Lefaix JL, Bresson C. Cobalt toxicity:Chemical and radiological combined effects on HaCaT keratinocyte cell line [J]. Toxicology in Vitro,2010,24 (1): 92-98
    Gohya T, Zhang X, Yoshida T, Migita CT. Spectroscopic characterization of a higher plant heme oxygenase isoform-1 from Glycine max (soybean)-coordination structure of the heme complex and catabolism of heme [J]. FEBS Journal,2006,273:5384-5399
    Guilfoyle TJ, Hagena G. Auxin response factors [J]. Current Opinion in Plant Biology,2007,10 (5): 453-460
    Han Y, Xuan W, Yu T, Fang W, Lou T, Gao Y, Chen X, Xiao X, Shen W. Exogenous hematin alleviates mercury-induced oxidative damage in the roots of Medicago sativa [J]. Journal of Integrative Plant Biology,2007,49:1703-1713
    Han Y, Zhang J, Chen X, Gao Z, Xuan W, Xu S, Ding X, She W. Carbon monoxide alleviates cadmium-induced oxidative damage by modulating glutathione metabolism in the roots of Medicago sativa [J]. New Phytologist,2008,177:155-166
    Hasnain S, Sabri AN. Growth stimulation of Triticum aestivum seedlings under Cr-stresses by non-rhizospheric pseudomonad strains [J]. Environmental Pollution,1997,97 (3):265-273
    Himanen K, Boucheron E, Vanneste S, de Almeida EJ, Inze D, Beeckman T. Auxin-mediated cell cycle activation during early lateral root initiation [J]. The Plant Cell,2002,14:2339-2351
    Himanen K, Vuylsteke M, Vanneste S, Vercruysse S, Boucheron E, Alard P, Chriqui D, Van Montagu M, Inze D, Beeckman T. Transcript profiling of early lateral root initiation [J]. Proceedings of the National Academy of Sciences of the United States of America,2004,101: 5146-5151
    Hochholdinger F, Park WJ, Sauer M, Woll K, Fromweeds to crops:genetic analysis of root development in cereals [J]. Trends in Plant Science,2004,9:42-48
    Huntley RP Murray JAH. The plant cell cycle [J]. Current Opinion in Plant Biology,1999,2:440-446
    Inze D, De Veylder L. Cell cycle regulation in plant development [J]. Annual Review of Genetics,2006, 40:77-105
    Ivanchenko MG, Muday GK, Dubrovsky JG. Ethylene-auxin interactions regulate lateral root initiation and emergence in Arabidopsis thaliana [J]. The Plant Journal,2008,55:335-341
    Iyer JK, Shi L, Shankar AH, Sullivan DJ. Zinc protoporphyrin IX binds heme crystals to inhibit the process of crystallization in Plasmodium falciparum [J]. Molecular medicine,2003,9:175-182
    Lamb C, Dixon RA. The sxidative burst in plant disease resistance [J]. Annual Review of Plant Physiology and Plant Molecular Biology,1997,48:251-275
    Lamar CA, Mahesh VB, Brann DW. Regulation of gonadotrophin-releasing hormone (GnRH) secretion by heme molecules:a regulatory role for carbon monoxide? [J]. Endocrinology,1996,137: 790-793
    Lang D, Reuter S, Buzescu T, August C, Heidenreich S. Heme-induced heme oxygenase-1 (HO-1) in human monocytes inhibits apoptosis despite caspase-3 up-regulation [J]. International Immunology, 2005,17:155-165
    Laplaze L, Benkova E, Casimiro I, Maes L, Vanneste S, Swarup R, Weijers D, Calvo V, Parizot B, Herrera-Rodriguez MB, Offringa R, Graham N, Doumas P, Friml J, Bogusz D, Beeckman T, Bennette M. Cytokinins act directly on lateral root founder cells to inhibit root initiation [J]. The Plant Cell,2007,19:3889-3900
    Laskowski MJ, Williams ME, Nusbaum C, Sussex IM. Formation of lateral root meristems is a two-stage process [J]. Development,1995,121:3303-3310
    Dolan L, Janmaat K, Willemsen V, Linstead P, Poethig S, Roberts K, Scheres B. Cellular organisation of the Arabidopsis thaliana root[J]. Development,1993,119:71-84
    Li H, Gray C, Mico C, Zhao F, McGrath SP. Phytotoxicity and bioavailability of cobalt to plants in a range of soils [J]. Chemosphere,2009,75:979-986
    Ling T, Zhang B, Cui W, Wu M, Lin J, Zhou W, Huang J, Shen W. Carbon monoxide mitigates salt-induced inhibition of root growth and suppresses programmed cell death in wheat primary roots by inhibiting superoxide anion overproduction [J]. Plant Science,2009,177:331-340
    Liu K, Xu S, Xuan W, Ling T, Cao Z, Huang B, Sun Y, Fang L, Liu Z, Zhao N, Shen W. Carbon monoxide counteracts the inhibition of seed germination and alleviates oxidative damage caused by salt stress in Oryza sativa [J]. Plant Science,2007,172:544-555
    Lloret PG. Lateral root initiation. In Plant Roots:The Hidden Half, (third edition) [M], Marcel Dekker, 2002
    Lopez-Bucio J, Cruz-Ramirez A, Herrera-Estrella L. The role of nutrient availability in regulating root architecture [J]. Current Opinion in Plant Biology,2003,6:280-287
    Liittge U, Fischer K. Light-dependent net CO-evolution by C3 and C4 plants [J]. Planta,1980,149: 59-63
    Maines MD. Evidence for the catabolism of polychlorinated biphenyl-induced cytochrome P-448 by microsomal heme oxygenase, and the inhibitions of δ-aminolevulinate dehydratase by polychlorinated biphenyls [J]. The Journal of Experimental Medicine,1976,144:1509-1519
    Maines MD, Kappas A. Enzymes of heme metabolism in the kidney regulation by trace metals which do not form heme complexes [J]. The Journal of Experimental Medicine,1977,146:1286-1293
    Maines MD, Sinclair P. Cobalt Regulation of heme synthesis and degradation in avian embryo liver cell culture [J]. The Journal of Biological Chemistry,1977,252 (1):219-223
    Marilena G. New physiological importance of two classic residual products:carbon monoxide and bilirubin [J]. Biochemical and Molecular Medicine,1997,61:136-142
    Marschner H. Mineral nutrition of higher plants (second edition) [M]. Academic Press.1995
    Malamy JE, Benfey PN. Organization and cell differentiation in lateral roots of Arabidopsis thaliana [J]. Development,1997,124:33-44
    Muramoto T, Tsurui N, Terry MJ, Yokota A, Kohchi T. Expression and biochemical properties of a ferredoxin-dependent heme oxygenase required for phytochrome chromophore synthesis [J]. Plant Physiology,2002,130:1958-1966
    Negi S, Ivanchenko MG, Muday GK. Ethylene regulates lateral root formation and auxin transport in Arabidopsis thaliana [J]. The Plant Journal,2008,55:175-187
    Noriega GO, Balestrasse KB, Batlle A, Tomaro ML. Heme oxygenase exerts a protective role against oxidative stress in soybean leaves [J]. Biochemical and Biophysical Research Communications,2004, 323:1003-1008
    Noriega GO, Yannarelli GG, Balestrasse KB, Batlle A, Tomaro ML. The effect of nitric oxide on heme oxygenase gene expression in soybean leaves [J]. Planta,2007,226:1155-1163
    Osmont KS, Sibout R, Hardtke CS. Hidden branches:developments in root system architecture [J]. Annual Review of Plant Biology,2007,58:93-113
    Pasternaka T, Rudasa V, Potters G, Jansen MAK. Morphogenic effects of abiotic stress:reorientation of growth in Arabidopsis thaliana seedlings [J]. Environmental and Experimental Botany,2005,53: 299-314
    Peret B, de Rybel B, Casimiro I, Benkova E, Swarup R, Laplaze L, Beeckman T, Bennett MJ. Arabidopsis lateral root development:An emerging story [J]. Trends in Plant Science,2009,14 (7): 1360-1385
    Pilon-Smits EAH, Quinn CF, Tapken W, Malagoli M, Schiavon M. Physiological functions of beneficial elements [J]. Current Opinion in Plant Biology,2009,12:1-8.
    Potters G, Pasternak TP, Guisez Y, Palme KJ, Jansen MAK. Stress-induced morphogenic responses: growing out of trouble? [J]. Trends in Plant Science,2007,12 (3):98-105
    Potuschak T, Doerner P. Cell cycle controls:genome-wide analysis in Arabidopsis [J]. Current Opinion in Plant Biology,2001,4:501-506
    Reichheld JP, Chaubet N, Shen WH, Renaudin JP, Gigot C. Multiple A-type cyclins express sequentially during the cell cycle in Nicotiana tabacum BY-2 cells [J]. Proceedings of the National Academy of Sciences of the United States of America,1996,93:13819-13824
    Sagi M, Davydov O, Orazova S, Yesbergenova Z, Ophir R, Stratmann JW, Fluhr R. Plant respiratory burst oxidase homologs impinge on wound responsiveness and development in Lycopersicon esculentum [J]. Plant Cell,2004,16:616-628
    Sandermann H Jr, Ernst D, Heller W, Langegartels C. Ozone:an abiotic elictor of plant defence reactions [J]. Trends in Plant Science,1998,3 (2):47-50
    Siegel SM, Renwick G, Rosen LA. Formation of carbon monoxide during seed germination and seedling growth [J]. Science,1962,137:683-684
    Silverstone AL, Chang CW, Krol E, Sun TP. Developmental regulation of gibberellin biosynthetic gene GA1 in Arabidopsis thaliana [J]. The Plant Journal,1997,12:9-19
    Song X, She X, Zhang B. Carbon monoxide-induced stomatal closure in Vicia faba is dependent on nitric oxide synthesis [J]. Plant Physiology,2008,132:514-525
    Srisook K, Cha Y. Biphasic induction of heme oxygenase-1 expression in macrophages stimulated with lipopolysaccharide [J]. Biochemical Pharmacology,2004,68:1709-1720
    Steinmann T, Geldner N, Grebe M, Mangold S, Jackson CL, Paris S, Galweiler L, Palme K, Jiirgens G. Coordinated polar localization of auxin efflux carrier PIN1 by GNOM ARF GEF [J]. Science,1999,286:316-318
    Su G, Zhang W, Liu Y. Involvement of hydrogen peroxide generated by polyamine oxidative degradation in the development of lateral roots in soybean [J]. Journal of Integrative Plant Biology, 2006,48 (4):426-432
    Swarup K, Benkova E, Swarup R, Casimiro I, Peret B, Yang Y, Parry G, Nielsen E, de Smet I, Vanneste S, Levesque MP, Carrier D, James N, Calvo V, Ljung K, Kramer E, Roberts R, Graham N, Marillonnet S, Patel K, Jones JDG, Taylor CG, Schachtman DP, May S, Sandberg G, Benfey P, Friml J, Kerr I, Beeckman T, Laplaze L, Bennett MJ. The auxin influx carrier LAX3 promotes lateral root emergence [J]. Nature Cell Biology,2008,10:946-954
    Tarr MA, Miller WL, Zepp RG. Direct carbon monoxide photoproduction from plant matter [J]. Journal of Geophysical Research,1995,100:11403-11413
    Terry MJ, Linley PJ, Kohchi T. Making light of it. The role of plant haem oxygenases in phytochrome chromophore synthesis [J]. Biochemical Society Transactions,2002,30 (4):604-609
    Vile GF, Basu-Modak S, Waltner C, Tyrrell RM. Heme oxygenase 1 mediates an adaptive response to oxidative stress in human skin fibroblasts [J]. Proceedings of the National Academy of Sciences of the United States of America,1994,91 (7):2607-2610
    Visser EJW, Cohen JD, Barendse CWM, Blom CWPM, Voesenek LACJ. An ethylene-mediated increase in sensitivity to auxin induces adventitious root formation in flooded Rumex palustris Sm [J]. Plant Physiology,1996,112:1687-1692
    Weis N, Weigert A, von Knethen A, Briine B. Heme oxygenase-1 contributes to an alternative macrophage activation profle induced by apoptotic cell supernatants [J]. Molecular Biology of the Cell,2009,20:1280-1288
    Xie Y, Ling T, Han Y, Liu K, Zheng Q, Huang L, Yuan X, He Z, Hu B, Fang L, Shen Z, Yang Q, Shen W. Carbon monoxide enhances salt tolerance by nitric oxide-mediated maintenance of ion homeostasis and up-regulation of antioxidant defense in wheat seedling roots [J]. Plant, Cell and Environment,2008,31:1864-1881
    Xu J, Xuan W, Huang B, Zhou Y, Ling T, Xu S, Shen W. Carbon monoxide-induced adventitious rooting of hypocotyl cutting from mung bean seedling [J]. Chinese Science Bulletin,2006,51: 668-674
    Xuan W, Huang L, Li M, Huang B, Xu S, Liu H, Gao Y, Shen W. Induction of growth elongation in wheat root segments by heme molecules:a regulatory role of carbon monoxide in plants? [J]. Plant Growth Regulation,2007,52:41-51
    Xuan W, Zhu F, Xu S, Huang B, Ling T, Qi J, Ye M, Shen W. The Heme oxygenase/carbon monoxide system is involved in auxin-induced cucumber adventitious rooting process [J]. Plant Physiology, 2008,148:881-893
    Yang Z, Chen F, Yuan J, Zeng Z, Wong M. Responses of Sesbania rostrata and S. cannabina to Pb, Zn, Cu and Cd toxicities [J]. Journal of Environmental Sciences (China),2004,16:670-673
    Yannarelli GG, Noriega GO, Batlle A, Tomaro ML. Heme oxygenase up-regulation in ultraviolet-B irradiated soybean plants involves reactive oxygen species [J]. Planta,2006,224:1154-1162
    Zimmermann R, Sakai H, Hochholdinger F. The gibberellic acid stimulated-like gene family in maize and its role in lateral root development [J]. Plant Physiology,2010,152:356-365
    Zuckerbraun BS, Billiar TR, Otterbein SL, Kim PKM, Liu F, Choi AMK, Fritz HB, Otterbein LE. Carbon monoxide protects against liver failure through nitric oxide-induced heme oxygenase [J]. The Journal of Experimental Medicine,2003,198:1707-1716.