4.5 Article

Ty3 reverse transcriptase complexed with an RNA-DNA hybrid shows structural and functional asymmetry

期刊

NATURE STRUCTURAL & MOLECULAR BIOLOGY
卷 21, 期 4, 页码 389-U132

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nsmb.2785

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资金

  1. Polish National Science Center [N N301 439738]
  2. FP7 HEALTHPROT project [229676]
  3. Intramural Research Program of the National Cancer Institute
  4. US National Institutes of Health
  5. National Institutes of Health [HHSN261200800001E]
  6. Foundation for Polish Science 'Ideas for Poland' award
  7. Howard Hughes Medical Institute
  8. European Union [POIG.02.02.00-14-024/08-00]

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Retrotransposons are a class of mobile genetic elements that replicate by converting their single-stranded RNA intermediate to double-stranded DNA through the combined DNA polymerase and ribonuclease H (RNase H) activities of the element-encoded reverse transcriptase (RT). Although a wealth of structural information is available for lentiviral and gammaretroviral RTs, equivalent studies on counterpart enzymes of long terminal repeat (LTR)-containing retrotransposons, from which they are evolutionarily derived, is lacking. In this study, we report the first crystal structure of a complex of RT from the Saccharomyces cerevisiae LTR retrotransposon Ty3 in the presence of its polypurine tract-containing RNA-DNA hybrid. In contrast to its retroviral counterparts, Ty3 RT adopts an asymmetric homodimeric architecture whose assembly is substrate dependent. Moreover, our structure and biochemical data suggest that the RNase H and DNA polymerase activities are contributed by individual subunits of the homodimer.

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