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Deep sequencing of Cotesia vestalis bracovirus reveals the complexity of a polydnavirus genome
Authors:Chen Ya-Feng  Gao Fei  Ye Xi-Qian  Wei Shu-Jun  Shi Min  Zheng Hua-Jun  Chen Xue-Xin
Affiliation:
  • a Université de Lyon, Lyon, France
  • b INRA, UMR754 Rétrovirus et Pathologie Comparée, UMS 3444/US8 Biosciences Gerland-Lyon Sud, Lyon, France
  • c Université Lyon 1, Lyon F-69007, France
  • d Ecole Nationale Vétérinaire de Lyon, Marcy L'étoile F-69000, France
  • e Ecole Pratique des Hautes Etudes, Lyon, France
  • f CNRS, Institut de Biologie et Chimie des Protéines, Lyon F-69007, France
  • Abstract:Integrase (IN) is the enzyme responsible for the integration of the retroviral genome into the host cell DNA. Herein, three mutants of conserved residues (V79, S85 and I146) of the central core domain (CCD) of an Avian Sarcoma/Leukemia Virus IN were analyzed in vitro. Our data revealed (i) the inability of S85T mutant to form dimers and tetramers in the absence of DNA and (ii) a slightly reduced ability of V79A IN in tetramers formation. Surprisingly, both mutants were still able to efficiently achieve concerted DNA integration. This could be explained by the ability of the two mutants to form complexes in the presence of DNA. These data suggest a strong structural role of the region encompassing V79 and S85 residues (β2/β3 turn-β3 strands) following binding to viral DNA and highlight the dynamic nature of IN.
    Keywords:ASLV   Retrovirus   Integrase   Concerted DNA integration   Mutants
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