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周焕, 陈红林, 刘峰, 欧阳苗峰, 楼宝, 顾志敏. 基于核系统酵母双杂交技术的红螯螯虾IAG互作蛋白筛选[J]. 水生生物学报. DOI: 10.7541/2024.2023.0362
引用本文: 周焕, 陈红林, 刘峰, 欧阳苗峰, 楼宝, 顾志敏. 基于核系统酵母双杂交技术的红螯螯虾IAG互作蛋白筛选[J]. 水生生物学报. DOI: 10.7541/2024.2023.0362
ZHOU Huan, CHEN Hong-Lin, LIU Feng, OUYANG Miao-Feng, LOU Bao, GU Zhi-Min. PROTEIN INTERACTION OF IAG IN CHERAX QUADRICARINATUS BASED ON NUCLEAR SYSTEM YEAST TWO-HYBRID TECHNOLOGY[J]. ACTA HYDROBIOLOGICA SINICA. DOI: 10.7541/2024.2023.0362
Citation: ZHOU Huan, CHEN Hong-Lin, LIU Feng, OUYANG Miao-Feng, LOU Bao, GU Zhi-Min. PROTEIN INTERACTION OF IAG IN CHERAX QUADRICARINATUS BASED ON NUCLEAR SYSTEM YEAST TWO-HYBRID TECHNOLOGY[J]. ACTA HYDROBIOLOGICA SINICA. DOI: 10.7541/2024.2023.0362

基于核系统酵母双杂交技术的红螯螯虾IAG互作蛋白筛选

PROTEIN INTERACTION OF IAG IN CHERAX QUADRICARINATUS BASED ON NUCLEAR SYSTEM YEAST TWO-HYBRID TECHNOLOGY

  • 摘要: 为探究胰岛素样促雄性腺激素(Insulin-like androgenic hormone, IAG)在甲壳动物性别分化过程作用的分子调控途径, 挖掘与IAG蛋白存在互作关系的候选蛋白信息, 研究使用红螯螯虾促雄性腺及输精管组织构建核体系酵母文库, 利用酵母双杂交技术筛选与IAG互作的候选蛋白, 并对关键候选蛋白的编码基因进行克隆与表达分析。获得初级文库容量为1.12×107, 次级文库容量为1.28×107; 成功筛选到25个阳性克隆, 共注释到12个蛋白编码基因; 克隆获得关键候选蛋白的编码基因muc5acl (Mucin-5AC-like)的CDS全长474 bp; 半定量与荧光定量表达结果表明, muc5acl在红螯螯虾的促雄性腺、精巢及输精管中特异表达, 且在雄性个体促雄性腺中的表达水平显著高于间性, 在输精管中的表达则相反, 推测该基因可能参与雄性激素的分泌及精子运输过程, 并与间性红螯螯虾的性腺发育有关。研究结果将为进一步解析IAG调控红螯螯虾间性性别形成的分子机制提供重要信息。

     

    Abstract: Insulin-like androgenic hormone (IAG), secreted by androgenic glands (AG), plays a crucial role in the sex differentiation of crustaceans. In the case of red claw crayfish (Cherax quadricarinatus), IAG has been confirmed to have a close association with the formation of intersex individuals. However, the molecular regulatory pathways through which IAG exerts its effects have not been fully elucidated. In order to obtain candidate protein information that interacts with the IAG protein and explore the role of interacting proteins in the regulation of sex in C. quadricarinatus, we constructed a yeast library using the testes and spermaducts of C. quadricarinatus and employed the nuclear system yeast two-hybrid technique to screen for proteins that interact with IAG. The encoding gene of the key candidate proteins was cloned, and its expression was analysed. The results revealed that the primary library had a capacity of 1.12×107, the secondary library had a capacity of 1.28×107, 25 positive clones were successfully screened and 12 protein-encoding genes were annotated. Among these genes, the coding sequence (CDS) of the key candidate protein named muc5acl (Mucin-5AC-like) was cloned, and its full length was determined to be 474 bp. Semi-quantitative and fluorescence quantitative expression analysis demonstrated that muc5acl exhibits specific expression in the androgenic glands, testes, and spermaducts of C. quadricarinatus, with significantly higher levels of expression in the spermaducts of intersex individuals were significantly higher compared to males, and the expression levels in males androgenic gland were significantly higher than that of intersex individuals. This finding suggests that the muc5acl gene is involved in gonadal development in C. quadricarinatus and may be related to the secretion of male hormones and sperm transport processes. The results of this study provide important information for further elucidating the molecular mechanisms by which IAG regulates the formation of intersex individuals in C. quadricarinatus.

     

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