4.4 Article

An inhibitory function of WW domain-containing host proteins in RNA virus replication

期刊

VIROLOGY
卷 426, 期 2, 页码 106-119

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2012.01.020

关键词

WW domain; Host-virus interaction; Antiviral factor; Tomato bushy stunt virus; FHV; NoV; Replication; Viral replicase; Yeast; Rsp5; E3 ubiquitin ligase

类别

资金

  1. National Science Foundation [IOB-0517218]
  2. NIH-NIAID [5R21AI079457-02]
  3. Kentucky Tobacco Research and Development Center
  4. Direct For Biological Sciences [0817790] Funding Source: National Science Foundation
  5. Division Of Integrative Organismal Systems [0817790] Funding Source: National Science Foundation

向作者/读者索取更多资源

To identify new genes affecting Tomato bushy stunt virus (TBSV) replication in yeast model host, we are studying protein families, whose members have been identified during previous high throughput screening. In this paper, we have characterized the WW domain-containing protein family from yeast and plants. We find that, in addition to Rsp5 E3 ubiquitin ligase, yeast Wwm1 and Prp40 and three Arabidopsis WW domain-containing proteins are strong inhibitors of TBSV replication. The tombusvirus replicase complex isolated from yeast with down-regulated Wwm1 protein level was more active. Accumulation of viral p92(pol) was reduced when Wwm1 was over-expressed, suggesting that the stability of p921(pol) might be reduced, as observed with Rsp5. Moreover, replication of two insect RNA viruses is also inhibited by Wwm1 and Rsp5, suggesting that WW domain-containing proteins might have broad regulatory effects on RNA viruses. Thus, artificial antiviral proteins with WW domains could be useful antiviral strategy. (C) 2012 Published by Elsevier Inc.

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