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Novel lncRNA 803 related to Marek's disease inhibits apoptosis of DF-1 cells.

Authors :
Han S
Zhao S
Ren H
Jiao Q
Wu X
Hao X
Liu M
Han L
Han L
Source :
Avian pathology : journal of the W.V.P.A [Avian Pathol] 2024 Aug; Vol. 53 (4), pp. 229-241. Date of Electronic Publication: 2024 Feb 29.
Publication Year :
2024

Abstract

Marek's disease (MD) is a neoplastic disease that significantly affects the poultry industry. Long non-coding RNAs (lncRNAs) are crucial regulatory factors in various biological processes, including tumourigenesis. However, the involvement of novel lncRNAs in the course of MD virus (MDV) infection is still underexplored. Here, we present the first comprehensive characterization of differentially expressed lncRNAs in chicken spleen at different stages of MDV infection. A series of differentially expressed lncRNAs was identified at each stage of MDV infection through screening. Notably, our investigation revealed a novel lncRNA, lncRNA 803, which exhibited significant differential expression at different stages of MDV infection and was likely to be associated with the p53 pathway. Further analyses demonstrated that the overexpression of lncRNA 803 positively regulated the expression of p53 and TP53BP1 in DF-1 cells, leading to the inhibition of apoptosis. This is the first study to focus on the lncRNA expression profiles in chicken spleens during MDV pathogenesis. Our findings highlight the potential role of the p53-related novel lncRNA 803 in MD pathogenesis and provide valuable insights for decoding the molecular mechanism of MD pathogenesis involving non-coding RNA. RESEARCH HIGHLIGHTS Differentially expressed lncRNAs in spleens of chickens infected with Marek's disease virus at different stages were identified for the first time.The effects of novel lncRNA 803 on p53 pathway and apoptosis of DF-1 cells were reported for the first time.

Details

Language :
English
ISSN :
1465-3338
Volume :
53
Issue :
4
Database :
MEDLINE
Journal :
Avian pathology : journal of the W.V.P.A
Publication Type :
Academic Journal
Accession number :
38323582
Full Text :
https://doi.org/10.1080/03079457.2024.2316817