TRIM28 mediates primer binding site-targeted silencing of Lys1,2 tRNA-utilizing retroviruses in embryonic cells

• DOI: 10.1073/pnas.0805540105
• Publication Date: 2008-08-20T03:52:10Z
• Authors: Daniel Wolf; Kevin Hug; Stephen P. Goff
• Keywords: 0301 basic medicine; Binding Sites; Transcription, Genetic; Nuclear Proteins; Tripartite Motif-Containing Protein 28; Virus Replication; Cell Line; Rats; 3. Good health; Leukemia Virus, Murine; Repressor Proteins; Mice; 03 medical and health sciences; Retroviridae; Cell Line, Tumor; DNA, Viral; Animals; Humans; RNA, Transfer, Lys; Gene Silencing; Embryonic Stem Cells

Murine leukemia viruses (MLVs) and related retroelements are potently restricted in embryonic cells by postintegration transcriptional silencing, likely to protect the germ line from insertional mutagenesis. This silencing is in large part attributable to the presence of a nuclear repression complex, which targets a sequence element of the proviral DNA, the repressor-binding site. The repressor-binding site closely overlaps the tRNA primer binding site, a highly conserved sequence essential for virus replication and defining the site of initiation of DNA synthesis during reverse transcription. We have recently demonstrated that the cellular corepressor TRIM28 is recruited to the proline tRNA primer-binding site used by many MLVs and is required to mediate this silencing. Here, we show that TRIM28 is also required for the restriction of retroviruses using a completely distinct tRNA for the priming of their DNA synthesis, namely Lys-1,2 tRNA. These results generalize the role of TRIM28 in retroviral restriction and suggest that this system has evolved to restrict multiple retroviruses.