昆虫学报 ›› 2024, Vol. 67 ›› Issue (10): 1318-1326.doi: 10.16380/j.kcxb.2024.10.003

• 研究论文 • 上一篇    下一篇

家蚕生殖调控相关miRNA(Bmo-miR-2763)的靶基因鉴定及表达分析

刘卓1, 孙妍妍1, 仝子乾1, 石慧轩1, 阚云超1,2, 乔惠丽1,*   

  1. (1. 南阳师范学院生命科学学院, 河南省伏牛山昆虫生物学重点实验室, 南阳 473061; 2. 河南科技学院资源与环境学院, 新乡 453003)
  • 出版日期:2024-10-20 发布日期:2024-11-18

Identification and expression analysis of target gene of the miRNA, Bmo-miR-2763, related to reproductive regulation in Bombyx mori

LIU Zhuo1, SUN Yan-Yan1, TONG Zi-Qian1, SHI Hui-Xuan1, KAN Yun-Chao1,2, QIAO Hui-Li1,*   

  1.  (1. Henan Provincial Key Laboratory of Insect Biology in Funiu Mountain, College of Life Science, Nanyang Normal University, Nanyang 473061, China; 2. School of Resources and Environment, Henan Institute of Science and Technology, Xinxiang 453003, China)
  • Online:2024-10-20 Published:2024-11-18

摘要: 【目的】miRNAs不仅调控昆虫的变态发育过程,在昆虫的生殖调控中也发挥重要作用。本研究旨在通过对家蚕Bombyx mori生殖调控相关miRNA(Bmo-miR-2763)的靶基因进行鉴定和表达分析,揭示miRNA在家蚕精巢和卵巢发育调控中的潜在分子机制。【方法】利用生物信息学方法预测Bmo-miR-2763的靶基因;利用qRT-PCR检测每头家蚕5龄幼虫血淋巴中注射5 μg 20-羟基蜕皮酮(20-hydroxyecdysone, 20E)后2, 6, 12和24 h时Bmo-miR-2763及其预测靶基因Bmo-GRF在脂肪体中的表达量;并利用qRT-PCR检测Bmo-miR-2763及其预测靶基因BmGRF在20E处理24 h时5龄幼虫不同组织(血淋巴、表皮、中肠、头、脂肪体、丝腺、马氏管、精巢和卵巢)以及未处理的正常家蚕4-5龄幼虫、蛹和成虫中的表达量;双荧光酶报告载体系统分析Bmo-miR-2763与其预测靶基因BmGRF的互作。【结果】与对照组相比,20E处理后家蚕5龄幼虫脂肪体中Bmo-miR-2763的表达量显著升高;Bmo-miR-2763的预测靶基因BmGRF也显著上调。Bmo-miR-2763和BmGRF在20E处理后24 h时家蚕5龄幼虫精巢和卵巢中都有较高表达量,且二者在精巢中的表达趋势一致,在卵巢中表达趋势相反;BmGRF在未处理正常家蚕不同发育阶段的表达量变化与Bmo-miR-2763的表达量呈负相关。双荧光素酶活性检测结果显示,Bmo-miR-2763模拟物和BmGRF 3′UTR过表达载体共转染时,荧光素酶活性下降56%,表明Bmo-miR-2763可与靶基因BmGRF 3′UTR区的互作抑制其在翻译水平的表达。【结论】 20E可诱导家蚕Bmo-miR-2763的表达,Bmo-miR-2763可通过调控靶基因BmGRF参与家蚕卵巢的发育调控。

关键词: 家蚕, miRNA, 精巢, 卵巢, 蜕皮激素, 发育调控

Abstract:  【Aim】 miRNAs not only regulate the metamorphosis and development of insects, but also play important roles in the reproductive regulation of insects. Throuth identifying the target gene of the miRNA, Bmo-miR-2763, related to reproductive regulation in Bombyx mori and analyzing its expression, this study aims to reveal the potential molecular mechanism of miRNAs in the regulation of the testicular and ovarian development of B. mori. 【Methods】 The target genes of Bmo-miR-2763 were predicted using bioinformatics methods. At 2, 6, 12 and 24 h after injection of 5 μg/individual of 20-hydroxyecdysone (20E) into the hemolymph of the 5th instar larvae of B. mori, the expression levels of Bmo-miR-2763 and its predicted target gene BmGRF in the fat body were detected by qRT-PCR. The expression levels of Bmo-miR-2763 and its predicted target gene BmGRF in different tissues (hemolymph, cuticle, midgut, head, fat body, silk gland, Malpighian tubules, testis and ovary) of the 5th instar larvae treated with 20E for 24 h and in the untreated normal larvae at the 4th-5th instars, pupae and adults of B. mori were also detected using qRT-PCR. The interaction between Bmo-miR-2763 and its predicted target gene BmGRF was analyzed using dual luciferase reporter assay system. 【Results】 After 20E treatment, the expression level of Bmo-miR-2763 in the fat body of the 5th instar larvae of B. mori was significantly increased, and that of the predicted target gene of Bmo-miR-2763, BmGRF, was also significantly up-regulated, as compared with those of the control group. Bmo-miR-2763 and BmGRF showed high expression levels in the testes and ovaries of the 5th instar larvae of B. mori at 24 h after 20E treatment, and their expression trends were consistent in testes, but opposite in ovaries. In the untreated normal B. mori at different developmental stages, the expression levels of BmGRF were negatively correlated with those of Bmo-miR-2763. The results of dual luciferase activity assay showed that the luciferase activity was decreased by 56% after co-transfection with Bmo-miR-2763 mimics and BmGRF 3′UTR overexpression vector, indicating that Bmo-miR-2763 could significantly inhibit the expression of luciferase reporter gene by interacting with the 3′UTR region of BmGRF. 【Conclusion】 20E can induce the expression of Bmo-miR-2763 in B. mori, and Bmo-miR-2763 mainly participates in the development regulation of B. mori ovaries by regulating the target gene BmGRF.

Key words: Bombyx mori, miRNA, testis, ovary, molting hormone, development regulation