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Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed

As a class of transcription regulators, numerous miRNAs have been verified to participate in regulating ovary follicular development in chickens (Gallus gallus). Previously we showed that gga-miR-135a-5p has significant differential expression between high and low-yield chicken ovaries, and the abun...

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Autores principales: Zhou, Yan, Liu, Jie, Lei, Qiuxia, Han, Haixia, Liu, Wei, Cunwei, Tang, Li, Fuwei, Cao, Dingguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642930/
https://www.ncbi.nlm.nih.gov/pubmed/32900904
http://dx.doi.org/10.1534/g3.120.401701
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author Zhou, Yan
Liu, Jie
Lei, Qiuxia
Han, Haixia
Liu, Wei
Cunwei, Tang
Li, Fuwei
Cao, Dingguo
author_facet Zhou, Yan
Liu, Jie
Lei, Qiuxia
Han, Haixia
Liu, Wei
Cunwei, Tang
Li, Fuwei
Cao, Dingguo
author_sort Zhou, Yan
collection PubMed
description As a class of transcription regulators, numerous miRNAs have been verified to participate in regulating ovary follicular development in chickens (Gallus gallus). Previously we showed that gga-miR-135a-5p has significant differential expression between high and low-yield chicken ovaries, and the abundance of gga-miR-135a-5p is significantly higher in follicular theca cells than in granulosa cells. However, the exact role of gga-miR-135a-5p in chicken follicular theca cells is unclear. In this study, primary chicken follicular theca cells were isolated and then transfected with gga-miR-135a-5p inhibitor. Transcriptome sequencing was performed in chicken follicular theca cells with or without transfection. Differentially expressed genes (DEGs) were analyzed using bioinformatics. A dual-luciferase reporter assay was used to verify the target relationship between gga-miR-135a-5p and predicted targets within the DEGs. Compared with the normal chicken follicle theca cells, 953 up-regulated and 1060 down-regulated genes were detected in cells with gga-miR-135a-5p inhibited. The up-regulated genes were significantly enriched in Gene Ontology terms and pathways involved in cell proliferation and differentiation. In chicken follicular theca cells, Krüppel-like factor 4 (KLF4), ATPase phospholipid transporting 8A1 (ATP8A1), and Complexin-1 (CPLX1) were significantly up-regulated when the expression of gga-miR-135a-5p was inhibited. In addition, KLF4, ATP8A1, and CPLX1 confirmed as targets of gga-miR-135a-5p by using a dual-luciferase assay in vitro. The results suggest that gga-mir-135a-5p may involve in proliferation and differentiation in chicken ovarian follicular theca cells by targeting KLF4, ATP8A1, and CPLX1.
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spelling pubmed-76429302020-11-13 Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed Zhou, Yan Liu, Jie Lei, Qiuxia Han, Haixia Liu, Wei Cunwei, Tang Li, Fuwei Cao, Dingguo G3 (Bethesda) Investigations As a class of transcription regulators, numerous miRNAs have been verified to participate in regulating ovary follicular development in chickens (Gallus gallus). Previously we showed that gga-miR-135a-5p has significant differential expression between high and low-yield chicken ovaries, and the abundance of gga-miR-135a-5p is significantly higher in follicular theca cells than in granulosa cells. However, the exact role of gga-miR-135a-5p in chicken follicular theca cells is unclear. In this study, primary chicken follicular theca cells were isolated and then transfected with gga-miR-135a-5p inhibitor. Transcriptome sequencing was performed in chicken follicular theca cells with or without transfection. Differentially expressed genes (DEGs) were analyzed using bioinformatics. A dual-luciferase reporter assay was used to verify the target relationship between gga-miR-135a-5p and predicted targets within the DEGs. Compared with the normal chicken follicle theca cells, 953 up-regulated and 1060 down-regulated genes were detected in cells with gga-miR-135a-5p inhibited. The up-regulated genes were significantly enriched in Gene Ontology terms and pathways involved in cell proliferation and differentiation. In chicken follicular theca cells, Krüppel-like factor 4 (KLF4), ATPase phospholipid transporting 8A1 (ATP8A1), and Complexin-1 (CPLX1) were significantly up-regulated when the expression of gga-miR-135a-5p was inhibited. In addition, KLF4, ATP8A1, and CPLX1 confirmed as targets of gga-miR-135a-5p by using a dual-luciferase assay in vitro. The results suggest that gga-mir-135a-5p may involve in proliferation and differentiation in chicken ovarian follicular theca cells by targeting KLF4, ATP8A1, and CPLX1. Genetics Society of America 2020-09-08 /pmc/articles/PMC7642930/ /pubmed/32900904 http://dx.doi.org/10.1534/g3.120.401701 Text en Copyright © 2020 Zhou et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Zhou, Yan
Liu, Jie
Lei, Qiuxia
Han, Haixia
Liu, Wei
Cunwei, Tang
Li, Fuwei
Cao, Dingguo
Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed
title Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed
title_full Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed
title_fullStr Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed
title_full_unstemmed Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed
title_short Transcriptome Analysis of the Chicken Follicular Theca Cells with miR-135a-5p Suppressed
title_sort transcriptome analysis of the chicken follicular theca cells with mir-135a-5p suppressed
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7642930/
https://www.ncbi.nlm.nih.gov/pubmed/32900904
http://dx.doi.org/10.1534/g3.120.401701
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