Peng Liu,Jinghua Jiang,Yuntong Chen ,Fei Gao,Suyan Wang,Mengmeng Yu ,Yongzhen Liu ,Ru Guo,Li Zhang,Zhuangzhuang Xu,Caiying Wang,Xiaole Qi,Yanping Zhang,Hongyu Cui,Yulu Duan,Sen Wu,Yulong Gao

J Biol Chem.2024 Sep 20:107804.doi: 10.1016/j.jbc.2024.107804. Online ahead of print.

Abstract

Avian leukosis virus subgroup J (ALV-J), a member of the genus Alpharetrovirus, possesses a small genome and exploits a vast array of host factors during its replication cycle. To identify host factors required for ALV-J replication and potentially guide the development of key therapeutic targets for ALV-J prevention, we employed a chicken genome-wide CRISPR/Cas9 knockout library to screen host factors involved in ALV-J infection within DF-1 cells. This screening revealed 42 host factors critical for ALV-J infection. Subsequent knockout assays showed that the absence of the genes encoding cycle-regulatory proteins, namely Cables1, CDK1, and DHFR, significantly inhibited ALV-J replication. Notably, Cables1 knockout cell lines displayed the most pronounced inhibitory effect. Conversely, overexpression assays confirmed that Cables1 significantly promotes ALV-J replication. Immunoprecipitation assays further indicated that Cables1 specifically interacts with the viral protein p15 (viral protease) among all ALV-J proteins, enhancing ALV-J p15 polyubiquitination. Additionally, we identified 26 lysine residues of ALV-J p15 as key sites for ubiquitination, and their replacement with arginine attenuated the replication ability of ALV-J in both in vitro and in vivo assays. This study demonstrates that Cables1 is a critical replication-dependent host factor of ALV-J by enhancing p15 ubiquitination and thereby promoting viral replication. Overall, these findings contribute to a deeper understanding of the ALJ-V replication mechanism and offer a potential target for the prevention and control of ALV-J infection.

Keywords: CRISPR screen; Cables1; Subgroup J Avian Leukosis Virus; Ubiquitination; p15.