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山羊卵巢卵泡发育过程中X连锁凋亡抑制蛋白的鉴定与表达

Identification and expression of X-linked inhibitor of apoptosis protein during follicular development in goat ovary.

作者信息

Han Peng, Xin Haiyun, Peng Jiayin, Hou Jinxing, Zhang Lei, Song Yuxuan, Li Guang, Cao Binyun, An Xiaopeng

机构信息

College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, China.

College of Animal Science and Technology, Northwest A&F University, Yangling, Shaanxi, 712100, China.

出版信息

Theriogenology. 2017 Aug;98:30-35. doi: 10.1016/j.theriogenology.2017.04.048. Epub 2017 Apr 30.

DOI:10.1016/j.theriogenology.2017.04.048
PMID:28601152
Abstract

X-linked inhibitor of apoptosis protein (XIAP), an endogenous of inhibitor of caspases, plays crucial roles in regulating ovarian granulosa cell apoptosis during follicular atresia. The aim of the present study was to determine the presence and localization of XIAP in the goat ovary and its expression level during follicular development. The full length cDNA of XIAP from goat ovary cells was cloned using reverse transcription PCR. A total of 497 amino acid residues were encoded by open reading frame and had high identity with homologous sequences from other mammals. XIAP was widely expressed in adult goat tissues as determined by real-time PCR and it demonstrated higher expression in propagative organs. High level of XIAP was detected in large healthy follicles and corpus luteum in comparison with that in small antral follicles, which was in accordance with the immunohistochemistry results and atretic follicles had very low expression. XIAP was localized in both granulosa and theca cells in antral follicles but not in primordial follicles. Furthermore, luteinizing hormone stimulated the proliferation of mRNA encoding XIAP in granulosa cells in vitro. The present study demonstrated that XIAP was expressed in a follicular-stage-dependent manner in goat ovaries.

摘要

X连锁凋亡抑制蛋白(XIAP)是一种半胱天冬酶的内源性抑制剂,在卵泡闭锁过程中调节卵巢颗粒细胞凋亡方面发挥着关键作用。本研究的目的是确定XIAP在山羊卵巢中的存在、定位及其在卵泡发育过程中的表达水平。采用逆转录聚合酶链反应从山羊卵巢细胞中克隆XIAP的全长cDNA。开放阅读框编码了总共497个氨基酸残基,与其他哺乳动物的同源序列具有高度同源性。通过实时聚合酶链反应确定,XIAP在成年山羊组织中广泛表达,并且在繁殖器官中表达较高。与小腔卵泡相比,在大的健康卵泡和黄体中检测到高水平的XIAP,这与免疫组织化学结果一致,而闭锁卵泡的表达非常低。XIAP定位于腔卵泡的颗粒细胞和卵泡膜细胞中,但在原始卵泡中不表达。此外,黄体生成素在体外刺激颗粒细胞中编码XIAP的mRNA的增殖。本研究表明,XIAP在山羊卵巢中以卵泡阶段依赖性方式表达。

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