石斑鱼性反转相关基因 ECaM的克隆及表达特征分析
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“863”国家高技术研究发展计划资助项目(2001AA620111)和国家大洋协会项目(4-2-4).


Cloning and Characterization of a Sex-Reversal-Related Gene ECaM in Epinephelus akaara Gonads
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This work was supported by grants from State 863 High Technology R&D Project of China(2001AA620111) and the National Oceanic Association Program(4-2-4).

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    摘要:

    用甲睾酮片饲喂 2 ~ 4 龄赤点石斑鱼 (Epinephelus akaara) , 6 周后 90% 以上的雌鱼性逆转为功能性雄鱼 . 运用抑制性差减杂交技术 (SSH) ,结合 SMART cDNA 合成和 RACE-PCR 方法,从性反转雄鱼性腺中克隆到钙调蛋白基因 (ECaM). 该基因 cDNA 全长为 582 bp ,开放阅读框长 450 bp ,编码的蛋白质由 149 个氨基酸组成, 5 ′端非编码区 74 bp , 3 ′端非编码区 58 bp. 虚拟 RNA 印迹表明, ECaM 在性反转雄鱼性腺中表达,而在正常雌鱼性腺中表达微弱 . 各种组织的半定量 RT-PCR 显示, ECaM 在脑、心、肝、脾、肾都有转录,在精巢和下丘脑中表达水平较高,而在肌肉中表达甚弱 . 性反转不同时期性腺的半定量 RT-PCR 及蛋白质印迹表明,性逆转过程中性腺里 ECaM 的表达量逐渐增加 . 上述结果提示钙调蛋白可能在赤点石斑鱼性逆转过程中发挥着作用, ECaM 可能是促使石斑鱼由雌向雄转变的重要功能基因之一 .

    Abstract:

    Red grouper (Epinephelus akaara) females between two and four years of age were successfully reversed to functional males by feeding 17 α -methyltestosterone (17 α -MT) over 42 days. A gene, called ECaM, was cloned from sex-reversed male gonads by using the combinative methods of suppressive subtraction hybridization (SSH), SMART cDNA synthesis and RACE-PCR. The full-length cDNA of ECaM is 582 bp, containing a 450 bp open reading frame that encodes a 149 amino acid protein. It has a 5 ′ untranslated region (UTR) of 74 nt and a 3 ′ UTR of 58 nt. Virtual Northern blotting shows that ECaM is transcribed in sex-reversed male gonads but only slightly transcribed in normal female gonads. Semi-quantitative RT-PCR analyses from various tissues indicate that mRNA of ECaM can be detected in the brain, heart, liver, spleen, and kidney but slightly in the muscle. Semi-quantitative RT-PCR and Western blotting from gonads during various stages of sex reversal reveal that expression levels of ECaM in gonads increase gradually during the transformation from female to male. Calmodulin is highly conserved across species. ECaM is one of the important genes that impels grouper sex reversal.

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李尚伟,文建军,刘世贵,龙章富.石斑鱼性反转相关基因 ECaM的克隆及表达特征分析[J].生物化学与生物物理进展,2005,32(2):147-153

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