作者: Sarah Sebastian , Jeremy Luban
DOI: 10.1007/S11908-007-0013-4
关键词:
摘要: Retroviruses are obligate intracellular parasites that have coevolved with their hosts for millions of years. It is therefore not surprising retroviruses take advantage numerous host factors during life cycle. In addition to positive cellular use the virus, cells also evolved proteins antagonize retroviral replication Such inhibitory been called restriction factors. Recently, several such cloned, including Friend virus susceptibility factor 1, apolipoprotein B mRNA-editing enzyme catalytic 3F and 3G, ZAP. Here, we review explosion publications from past 2 years concerning TRIM5, a potently inhibits HIV-1 other retroviruses.