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Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose

Magang geese exhibit a unique characteristic of follicular development, with eight largest orderly arranged pre-ovulatory follicles in the abdominal cavity. However, little is known about the mechanisms underlying this follicular development. This study aimed to compare gene expression profiles of g...

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Autores principales: LEI, Mingming, CHEN, Rong, QIN, Qingming, ZHU, Huanxi, SHI, Zhendan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Society for Reproduction and Development 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470900/
https://www.ncbi.nlm.nih.gov/pubmed/32281545
http://dx.doi.org/10.1262/jrd.2019-110
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author LEI, Mingming
CHEN, Rong
QIN, Qingming
ZHU, Huanxi
SHI, Zhendan
author_facet LEI, Mingming
CHEN, Rong
QIN, Qingming
ZHU, Huanxi
SHI, Zhendan
author_sort LEI, Mingming
collection PubMed
description Magang geese exhibit a unique characteristic of follicular development, with eight largest orderly arranged pre-ovulatory follicles in the abdominal cavity. However, little is known about the mechanisms underlying this follicular development. This study aimed to compare gene expression profiles of granulosa cells (GCs) at different stages of follicular development and provide comprehensive insights into follicle selection and the mechanisms underlying the well-defined follicle hierarchy in Magang geese. GCs of large white follicles (LWFs), small yellow follicles (SYFs), F8, F4, and F1 were used for RNA-seq analysis; 374, 1117, 791, and 593 genes were differentially expressed in stages LWFs to SYFs, SYFs to F8, F8 to F4, and F4 to F1, respectively, suggesting that these genes contribute to follicle selection and development. Reliability of sequencing data was verified through qPCR analysis of 24 genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathways revealed a complex mechanism that remodels the extracellular matrix and turnover of extracellular matrix components in follicular development and ovulation and involves multiple pathway, such as focal adhesion, adherens junction, and extracellular matrix–receptor interaction. Some unique characteristics were observed during the different follicular development stages. For instance, some differentially expressed genes were enriched in progesterone-mediated oocyte maturation and steroid biosynthesis from stage SYFs to F8, whereas others were enriched in actin cytoskeleton regulation and vascular smooth muscle contraction from stage F4 to F1. These findings enhance our current understanding of GC function and ovarian follicles during the key stages of follicular development.
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spelling pubmed-74709002020-09-09 Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose LEI, Mingming CHEN, Rong QIN, Qingming ZHU, Huanxi SHI, Zhendan J Reprod Dev Original Article Magang geese exhibit a unique characteristic of follicular development, with eight largest orderly arranged pre-ovulatory follicles in the abdominal cavity. However, little is known about the mechanisms underlying this follicular development. This study aimed to compare gene expression profiles of granulosa cells (GCs) at different stages of follicular development and provide comprehensive insights into follicle selection and the mechanisms underlying the well-defined follicle hierarchy in Magang geese. GCs of large white follicles (LWFs), small yellow follicles (SYFs), F8, F4, and F1 were used for RNA-seq analysis; 374, 1117, 791, and 593 genes were differentially expressed in stages LWFs to SYFs, SYFs to F8, F8 to F4, and F4 to F1, respectively, suggesting that these genes contribute to follicle selection and development. Reliability of sequencing data was verified through qPCR analysis of 24 genes. Gene Ontology and Kyoto Encyclopedia of Genes and Genomes pathways revealed a complex mechanism that remodels the extracellular matrix and turnover of extracellular matrix components in follicular development and ovulation and involves multiple pathway, such as focal adhesion, adherens junction, and extracellular matrix–receptor interaction. Some unique characteristics were observed during the different follicular development stages. For instance, some differentially expressed genes were enriched in progesterone-mediated oocyte maturation and steroid biosynthesis from stage SYFs to F8, whereas others were enriched in actin cytoskeleton regulation and vascular smooth muscle contraction from stage F4 to F1. These findings enhance our current understanding of GC function and ovarian follicles during the key stages of follicular development. The Society for Reproduction and Development 2020-04-11 2020-08 /pmc/articles/PMC7470900/ /pubmed/32281545 http://dx.doi.org/10.1262/jrd.2019-110 Text en ©2020 Society for Reproduction and Development This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original Article
LEI, Mingming
CHEN, Rong
QIN, Qingming
ZHU, Huanxi
SHI, Zhendan
Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose
title Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose
title_full Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose
title_fullStr Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose
title_full_unstemmed Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose
title_short Transcriptome analysis to unravel the gene expression profile of ovarian follicular development in Magang goose
title_sort transcriptome analysis to unravel the gene expression profile of ovarian follicular development in magang goose
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7470900/
https://www.ncbi.nlm.nih.gov/pubmed/32281545
http://dx.doi.org/10.1262/jrd.2019-110
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