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鸽子()排卵前和排卵后卵泡潜在调控因子的转录组分析。

Transcriptome analyses of potential regulators of pre- and post-ovulatory follicles in the pigeon ().

机构信息

Institute of Animal Husbandry and Veterinary Science, Zhejiang Academy of Agricultural Science, 310021 Hangzhou, Zhejiang, China.

Institute of Ecology, Key Laboratory of Southwest China Wildlife Resources Conservation (Ministry of Education), China West Normal University, 637009 Nanchong, Sichuan, China.

出版信息

Reprod Fertil Dev. 2022 May;34(9):689-697. doi: 10.1071/RD21239.

Abstract

To identify the dominant genes controlling follicular maturation, ovulation and regression for pigeon, we used RNA-seq to explore the gene expression profiles of pre- and post-ovulatory follicles of pigeon. We obtained total of 4.73million (96% of the raw data) high-quality clean reads, which could be aligned with 20282 genes. Gene expression profile analysis identified 1461 differentially expressed genes (DEGs) between the pre- (P4) and post-ovulatory follicles (P5). Of these, 843 genes were upregulated, and 618 genes were down-regulated. Furthermore, many DEGs were significantly enriched in some pathways closely related to follicle maturation, ovulation and regression, such as ECM-receptor interaction, vascular smooth muscle contraction, progesterone-mediated oocyte maturation, phagosome. Importantly, the DGEs in ECM-receptor interaction pathway included COL1A1 , COL1A2 , COL4A1 , COL4A2 , ITGA11 , ITGB3 and SDC3 , in the progesterone-mediated oocyte maturation pathway involved CDK1 , CDC25A , CCNB3 , CDC20 and Plk1 , and in the vascular smooth muscle contraction covered CALD1 , KCNMA1 , KCNMB1 , CACNA1 , ACTA2 , MYH10 , MYL3 , MYL6 , MYL9 , closely related to promoting follicular maturation and ovulation in pre-ovulatory follicles. Moreover, it seems that the lysosomal cathepsin family has a decisive role in the regression of early stage of post-ovulatory follicle. Taken together, these data enrich the research of molecular mechanisms of pigeon follicular activities at the transcriptional level and provide novel insight of breeding-related physiology for birds.

摘要

为了鉴定控制鸽子滤泡成熟、排卵和退化的优势基因,我们使用 RNA-seq 技术研究了鸽子排卵前和排卵后滤泡的基因表达谱。我们共获得了 473 万条(原始数据的 96%)高质量的清洁读数,可以与 20282 个基因匹配。基因表达谱分析鉴定出排卵前(P4)和排卵后(P5)滤泡之间的 1461 个差异表达基因(DEG)。其中,843 个基因上调,618 个基因下调。此外,许多 DEG 显著富集在与滤泡成熟、排卵和退化密切相关的一些途径中,如 ECM-受体相互作用、血管平滑肌收缩、孕激素介导的卵母细胞成熟、吞噬体。重要的是,ECM-受体相互作用途径中的 DGE 包括 COL1A1、COL1A2、COL4A1、COL4A2、ITGA11、ITGB3 和 SDC3,孕激素介导的卵母细胞成熟途径中的 CDK1、CDC25A、CCNB3、CDC20 和 Plk1,以及血管平滑肌收缩途径中的 CALD1、KCNMA1、KCNMB1、CACNA1、ACTA2、MYH10、MYL3、MYL6、MYL9,这些基因与促进排卵前滤泡成熟和排卵密切相关。此外,溶酶体组织蛋白酶家族似乎在排卵后滤泡早期退化中起着决定性的作用。总之,这些数据丰富了鸽子滤泡活动的分子机制在转录水平上的研究,并为鸟类繁殖相关生理学提供了新的见解。

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