| Literature DB >> 33384993 |
Heling Yu1, Hengyong Xu1, Chaoyang Yan1, Shiliang Zhu1, Xi Lan2, Yuxiang Lu1, Qijian He1, Huadong Yin1, Qing Zhu1, Xiaoling Zhao1, Diyan Li1, Yiping Liu1, Yan Wang1.
Abstract
Avian leukosis virus subgroup J disease (ALV-J) is a contagious and immunosuppressive avian disease caused by ALV-J virus. Although miRNA participate in various biological processes of tumors, little is known about the potential role of miRNA in ALV-J. Our previous miRNA and RNA sequencing data showed that the expression of gga-miR-148a-5p was significantly different in ALV-J-infected chicken spleens compared with non-infected chickens. The aim of this study was to investigate the functional roles of gga-miR-148a-5p and identify downstream targets regulated by gga-miR-148a-5p in ALV-J-infected chickens. We found that the expression of gga-miR-148a-5p was significantly downregulated during ALV-J infection of chicken embryo fibroblasts (CEF). Dual luciferase reporter assays demonstrated that PDPK1 is a direct target gene of gga-miR-148a-5p. In vitro, overexpression of gga-miR-148a-5p significantly promoted ALV-J-infected CEF cell proliferation, included cell cycle, whereas inhibition of gga-miR-148a-5p had an opposite effect. Inhibition of PDPK1 promoted the proliferation of ALV-J-infected cells but had no effect on the activity of NF-κB. Together, these results suggested that gga-miR-148a-5p targets PDPK1 to inhibit the proliferation and cell cycle of ALV-J-infected CEF cells. Our study provides a new understanding for the tumor mechanism of ALV-J infection.Entities:
Keywords: ALV-J infection; PDPK1; cell cycle; chicken; gga-miR-148a-5p; proliferation
Year: 2020 PMID: 33384993 PMCID: PMC7769946 DOI: 10.3389/fcell.2020.587889
Source DB: PubMed Journal: Front Cell Dev Biol ISSN: 2296-634X