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参与拟穴青蟹(Scylla paramamosain)卵黄蛋白原表达的foxl2基因的特征分析

Characterization of the foxl2 gene involved in the vtg expression in mud crab (Scylla paramamosain).

作者信息

Wan Haifu, Zhong Jinying, Zhang Ziping, Xie Yichao, Wang Yilei

机构信息

Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Fisheries College, Jimei University, Xiamen 361021, China; Fujian Engineering Research Center of Aquatic Breeding and Healthy Aquaculture, Xiamen 361021, China.

College of Animal Science, Fujian Agriculture and Forestry University, Fuzhou 350002, China; Key Laboratory of Marine Biotechnology of Fujian Province, Institute of Oceanology, Fujian Agriculture and Forestry University, Fuzhou 350002, China.

出版信息

Gene. 2021 Sep 25;798:145807. doi: 10.1016/j.gene.2021.145807. Epub 2021 Jul 2.

Abstract

Forkhead box protein L2 (Foxl2) is involved in multiple physiological processes, such as ovarian development, granulosa cell differentiation, ovarian follicle development, and oocyte growth. In this study, a Spfoxl2 gene encoded 530 amino acid protein with characteristic forkhead (FH) domain was identified from transcriptome data of mud crab Scylla paramamosain and validated the accuracy by PCR technology. Meanwhile, the orthologues of the Spfoxl2 gene in other 14 crustacean species were identified with the same method. Further multiple sequence alignment analysis revealed the Foxl2 was highly conserved, especially in the FH domain, even completely identical in several species. Besides, the semi-quantitative PCR (Sq-PCR) result showed Spfoxl2 gene was mainly expressed in the gonad (testis and ovary). Further quantitative real-time PCR (qRT-PCR) result demonstrated its expression level in the testis was significantly higher than that in the ovary (p < 0.01). In addition, the qRT-PCR result showed that in zoea V, megalopa, and larval I, the expression level of Spfoxl2 in megalopa is the highest. In addition, a putative Foxl2 binding site was identified on the promoter region of Spvtg, and knockdown of Spfoxl2 mediated by RNAi technology increased the expression of Spvtg in the ovary, suggesting Spfoxl2 might be the upstream negative regulator of Spvtg. Overall, this study provided new insights into the role of Spfoxl2 in ovary development through regulating Spvtg expression in S. paramamosain.

摘要

叉头框蛋白L2(Foxl2)参与多种生理过程,如卵巢发育、颗粒细胞分化、卵泡发育和卵母细胞生长。在本研究中,从拟穴青蟹转录组数据中鉴定出一个编码530个氨基酸且具有特征性叉头(FH)结构域的Spfoxl2基因,并通过PCR技术验证了其准确性。同时,用相同方法鉴定了其他14种甲壳类动物中Spfoxl2基因的直系同源物。进一步的多序列比对分析表明,Foxl2高度保守,尤其是在FH结构域,在几个物种中甚至完全相同。此外,半定量PCR(Sq-PCR)结果显示Spfoxl2基因主要在性腺(睾丸和卵巢)中表达。进一步的定量实时PCR(qRT-PCR)结果表明,其在睾丸中的表达水平显著高于卵巢(p < 0.01)。此外,qRT-PCR结果显示,在溞状幼体V期、大眼幼体期和仔虾I期,Spfoxl2在大眼幼体中的表达水平最高。此外,在Spvtg启动子区域鉴定出一个假定的Foxl2结合位点,RNAi技术介导的Spfoxl2敲低增加了卵巢中Spvtg的表达,表明Spfoxl2可能是Spvtg的上游负调控因子。总体而言,本研究通过调节拟穴青蟹中Spvtg的表达,为Spfoxl2在卵巢发育中的作用提供了新的见解。

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