Literature DB >> 19853618

Factors that determine the efficiency of HIV-1 strand transfer initiated at a specific site.

Sean T Rigby1, Keith P Van Nostrand, April E Rose, Robert J Gorelick, David H Mathews, Robert A Bambara.   

Abstract

Human immunodeficiency virus-1 employs strand transfer for recombination between two viral genomes. We have previously provided evidence that strand transfer proceeds by an invasion-mediated mechanism in which a DNA segment on the original RNA template is invaded by a second RNA template at a gap site. The initial RNA-DNA hybrid then expands until the DNA is fully transferred. Ribonuclease H (RNase H) cleavages and nucleocapsid protein (NC) were required for long-distance propagation of the hybrid. Evaluation was performed on a unique substrate, with a short gap serving as a precreated invasion site. In our current work, this substrate provided an opportunity for us to test what factors influence a specific invasion site to support transfer, and to distinguish factors that influence invasion site creation from those that impact later steps. RNase H can act in a polymerization-dependent or polymerization-independent mode. Polymerization-dependent and polymerization-independent RNase H were found to be important in creating efficiently used invasion sites in the primer-donor complex, with or without NC. Propagation and terminus transfer steps, emanating from a precreated invasion site in the presence of NC, were stimulated by polymerization-dependent, but not polymerization-independent, RNase H. RNase H can carry out primary and secondary cleavages during synthesis. While both modes of cleavage promoted invasion, only primary cleavage promoted propagation in the presence of NC in our system. These observations suggest that once invasion is initiated at a short gap, it can propagate through an adjacent region interrupted only by nicks, with help by NC. We considered the possibility that propagation solely by strand exchange was a significant contributor to transfers. However, it did not promote transfer even if synthetic progress of reverse transcriptase was intentionally slowed, consistent with strand exchange by random walk in which rate declines precipitously with distance.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19853618      PMCID: PMC2860860          DOI: 10.1016/j.jmb.2009.10.036

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  46 in total

1.  Dynamic copy choice: steady state between murine leukemia virus polymerase and polymerase-dependent RNase H activity determines frequency of in vivo template switching.

Authors:  C K Hwang; E S Svarovskaia; V K Pathak
Journal:  Proc Natl Acad Sci U S A       Date:  2001-10-02       Impact factor: 11.205

2.  Strand transfer occurs in retroviruses by a pause-initiated two-step mechanism.

Authors:  Ricardo H Roda; Mini Balakrishnan; Jin K Kim; Bernard P Roques; Philip J Fay; Robert A Bambara
Journal:  J Biol Chem       Date:  2002-10-04       Impact factor: 5.157

3.  Human immunodeficiency virus reverse transcriptase displays a partially processive 3' to 5' endonuclease activity.

Authors:  J J DeStefano; R G Buiser; L M Mallaber; R A Bambara; P J Fay
Journal:  J Biol Chem       Date:  1991-12-25       Impact factor: 5.157

4.  Point mutations in conserved amino acid residues within the C-terminal domain of HIV-1 reverse transcriptase specifically repress RNase H function.

Authors:  O Schatz; F V Cromme; F Grüninger-Leitch; S F Le Grice
Journal:  FEBS Lett       Date:  1989-11-06       Impact factor: 4.124

5.  The sequential mechanism of HIV reverse transcriptase RNase H.

Authors:  M Wisniewski; M Balakrishnan; C Palaniappan; P J Fay; R A Bambara
Journal:  J Biol Chem       Date:  2000-12-01       Impact factor: 5.157

6.  Mutations of a conserved residue within HIV-1 ribonuclease H affect its exo- and endonuclease activities.

Authors:  B M Wöhrl; S Volkmann; K Moelling
Journal:  J Mol Biol       Date:  1991-08-05       Impact factor: 5.469

7.  Reverse transcriptase.RNase H from the human immunodeficiency virus. Relationship of the DNA polymerase and RNA hydrolysis activities.

Authors:  E S Furfine; J E Reardon
Journal:  J Biol Chem       Date:  1991-01-05       Impact factor: 5.157

8.  Polymerization and RNase H activities of the reverse transcriptases from avian myeloblastosis, human immunodeficiency, and Moloney murine leukemia viruses are functionally uncoupled.

Authors:  J J DeStefano; R G Buiser; L M Mallaber; T W Myers; R A Bambara; P J Fay
Journal:  J Biol Chem       Date:  1991-04-25       Impact factor: 5.157

9.  Incomplete removal of the RNA primer for minus-strand DNA synthesis by human immunodeficiency virus type 1 reverse transcriptase.

Authors:  K A Pullen; L K Ishimoto; J J Champoux
Journal:  J Virol       Date:  1992-01       Impact factor: 5.103

10.  Role of the Reverse Transcriptase, Nucleocapsid Protein, and Template Structure in the Two-step Transfer Mechanism in Retroviral Recombination.

Authors:  Ricardo H Roda; Mini Balakrishnan; Mark N Hanson; Birgitta M Wohrl; Stuart F J Le Grice; Bernard P Roques; Robert J Gorelick; Robert A Bambara
Journal:  J Biol Chem       Date:  2003-06-11       Impact factor: 5.157

View more
  3 in total

1.  Host SAMHD1 protein promotes HIV-1 recombination in macrophages.

Authors:  Laura A Nguyen; Dong-Hyun Kim; Michele B Daly; Kevin C Allan; Baek Kim
Journal:  J Biol Chem       Date:  2013-12-18       Impact factor: 5.157

2.  Altered strand transfer activity of a multiple-drug-resistant human immunodeficiency virus type 1 reverse transcriptase mutant with a dipeptide fingers domain insertion.

Authors:  Laura A Nguyen; Waaqo Daddacha; Sean Rigby; Robert A Bambara; Baek Kim
Journal:  J Mol Biol       Date:  2011-11-12       Impact factor: 5.469

3.  HIV-1 reverse transcriptase dissociates during strand transfer.

Authors:  John M Muchiri; Sean T Rigby; Laura A Nguyen; Baek Kim; Robert A Bambara
Journal:  J Mol Biol       Date:  2011-07-29       Impact factor: 5.469

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.