Back to Search Start Over

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

Authors :
Zhou Y
Liu J
Lei Q
Han H
Liu W
Cunwei T
Li F
Cao D
Source :
G3 (Bethesda, Md.) [G3 (Bethesda)] 2020 Nov 05; Vol. 10 (11), pp. 4071-4081. Date of Electronic Publication: 2020 Nov 05.
Publication Year :
2020

Abstract

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.<br /> (Copyright © 2020 Zhou et al.)

Details

Language :
English
ISSN :
2160-1836
Volume :
10
Issue :
11
Database :
MEDLINE
Journal :
G3 (Bethesda, Md.)
Publication Type :
Academic Journal
Accession number :
32900904
Full Text :
https://doi.org/10.1534/g3.120.401701