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Integrase C-terminal residues determine the efficiency of feline foamy viral DNA integration

Authors
Kim, JinsunLee, Ga-EunLochelt, MartinShin, Cha-Gyun
Issue Date
Jan-2018
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
Integrase; Feline foamy virus; C-terminal domain; Point mutant; Viral infectivity
Citation
VIROLOGY, v.514, pp 50 - 56
Pages
7
Journal Title
VIROLOGY
Volume
514
Start Page
50
End Page
56
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/1317
DOI
10.1016/j.virol.2017.10.022
ISSN
0042-6822
1089-862X
Abstract
Integrase (IN) is an essential enzyme in retroviral life cycle. It mediates viral cDNA integration into host cellular DNA. Feline foamy virus (FFV) is a member of the Spumavirus subfamily of Retroviridae. Recently, its life cycle has been proposed to be different from other retroviruses. Despite this important finding, FFV IN is not understood clearly. Here, we constructed point mutations in FFV IN C-terminal domain (CTD) to obtain a clear understanding of its integration mechanism. Mutation of the amino acid residues in FFV IN CTD interacting with target DNA reduced both IN enzymatic activities in vitro and viral productions in infected cells. Especially, the mutants, R307 and K340, made viral DNA integration less efficient and allowed accumulation of more unintegrated viral DNA, thereby suppressing viral replication. Therefore, we suggest that the CTD residues interacting with the target DNA play a significant role in viral DNA integration and replication.
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