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ALDH1A1 基因的分子特征和表达谱及其在牦牛黄体细胞中的功能。

Molecular characterization and expression profile of the ALDH1A1 gene and its functions in yak luteal cells.

机构信息

Key Laboratory for Animal Science of National Ethnic Affairs Commission, Southwest Minzu University, Chengdu, 610041, China.

Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Exploitation of Ministry of Education, Southwest Minzu University, Chengdu, 610041, China.

出版信息

Theriogenology. 2024 Jul 15;223:98-107. doi: 10.1016/j.theriogenology.2024.04.020. Epub 2024 Apr 30.

Abstract

The ALDH1A1 gene encodes a cytoplasmic member of the aldehyde dehydrogenase 1 family, which plays an important role in regulating animal reproductive performance, including estrus cycle and embryonic development. The aim of this study was to characterize ALDH1A1 activity in ovaries of 3-5 year-old yaks and to determine its effects on cell proliferation, apoptosis, and progesterone secretion in luteal cells (LCs). The coding sequence (CDS) of the ALDH1A1 gene was cloned by reverse transcription-PCR and immunohistochemical analysis was used to confirm localization of the ALDH1A1 protein in the ovary. To assess the activity of ALDH1A1 in regulating progesterone secretion, si-ALDH1A1 was transfected into LCs in vitro and progesterone levels in LC supernatants were measured by ELISA. The interference efficiency was assessed by real-time quantitative PCR (RT-qPCR) and immunofluorescence staining, and cell proliferation and apoptosis were evaluated by EdU and TUNEL staining, respectively. The cloned ALDH1A1 sequence contained 1462 bp, encoding 487 amino acids. Immunohistochemical analysis showed that ALDH1A1 protein expression, which was significantly higher in LCs, was mainly found in antral follicles and the corpus luteum (CL). The expression of ALDH1A1 mRNA in LCs was effectively inhibited by si-ALDH1A1transfection, and progesterone secretion was markedly decreased along with the significant down-regulation of progesterone pathway-related genes, STAR, CYP11A1, CYP19A1, CYP17A1, 3β-HSD, and HSD17B1. Knockdown of ALDH1A1 mRNA expression decreased cell proliferation and increased apoptosis in LCs. The mRNA expression of the proliferation-related genes, PCNA, CCND1, CCNB1 and CDC25A, was significantly down-regulated, while expression of the apoptosis-promoting CASP3 gene was significantly increased. In summary, we characterized the yak ALDH1A1 gene and revealed that ALDH1A1 knockdown promoted apoptosis, repressed cell proliferation, and decreased progesterone secretion by yak LCs, potentially by regulating the mRNA expression of genes related to proliferation, apoptosis, and progesterone synthesis and secretion.

摘要

ALDH1A1 基因编码醛脱氢酶 1 家族的细胞质成员,在调节动物生殖性能方面发挥着重要作用,包括发情周期和胚胎发育。本研究旨在研究 3-5 岁牦牛卵巢中 ALDH1A1 活性,并确定其对黄体细胞(LCs)增殖、凋亡和孕激素分泌的影响。通过逆转录-PCR 克隆 ALDH1A1 基因的编码序列(CDS),并通过免疫组织化学分析证实 ALDH1A1 蛋白在卵巢中的定位。为了评估 ALDH1A1 在调节孕激素分泌中的活性,将 si-ALDH1A1 转染到体外 LCs 中,并通过 ELISA 测量 LC 上清液中的孕激素水平。通过实时定量 PCR(RT-qPCR)和免疫荧光染色评估干扰效率,并分别通过 EdU 和 TUNEL 染色评估细胞增殖和凋亡。克隆的 ALDH1A1 序列包含 1462bp,编码 487 个氨基酸。免疫组织化学分析显示,LC 中 ALDH1A1 蛋白表达显著升高,主要存在于窦卵泡和黄体(CL)中。si-ALDH1A1 转染有效抑制了 LCs 中 ALDH1A1 mRNA 的表达,并且孕激素分泌随着孕激素途径相关基因 STAR、CYP11A1、CYP19A1、CYP17A1、3β-HSD 和 HSD17B1 的显著下调而明显降低。ALDH1A1 mRNA 表达的敲低降低了 LCs 的增殖并增加了凋亡。增殖相关基因 PCNA、CCND1、CCNB1 和 CDC25A 的 mRNA 表达显著下调,而凋亡促进基因 CASP3 的表达显著增加。总之,我们对牦牛 ALDH1A1 基因进行了特征描述,并揭示了 ALDH1A1 敲低通过牦牛 LCs 促进凋亡、抑制细胞增殖和减少孕激素分泌,可能通过调节与增殖、凋亡和孕激素合成和分泌相关的基因的 mRNA 表达。

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