Literature DB >> 10511540

The conversion gradient at HIS4 of Saccharomyces cerevisiae. II. A role for mismatch repair directed by biased resolution of the recombinational intermediate.

H M Foss1, K J Hillers, F W Stahl.   

Abstract

Salient features of recombination at ARG4 of Saccharomyces provoke a variation of the double-strand-break repair (DSBR) model that has the following features: (1) Holliday junction cutting is biased in favor of strands upon which DNA synthesis occurred during formation of the joint molecule (this bias ensures that cutting both junctions of the joint-molecule intermediate arising during DSBR usually leads to crossing over); (2) cutting only one junction gives noncrossovers; and (3) repair of mismatches that are semirefractory to mismatch repair and/or far from the DSB site is directed primarily by junction resolution. The bias in junction resolution favors restoration of 4:4 segregation when such mismatches and the directing junction are on the same side of the DSB site. Studies at HIS4 confirmed the predicted influence of the bias in junction resolution on the conversion gradient, type of mismatch repair, and frequency of aberrant 5:3 segregation, as well as the predicted relationship between mismatch repair and crossing over.

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Year:  1999        PMID: 10511540      PMCID: PMC1460786     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  12 in total

1.  The conversion gradient at HIS4 of Saccharomyces cerevisiae. I. Heteroduplex rejection and restoration of Mendelian segregation.

Authors:  K J Hillers; F W Stahl
Journal:  Genetics       Date:  1999-10       Impact factor: 4.562

2.  Analysis of a gene conversion gradient at the HIS4 locus in Saccharomyces cerevisiae.

Authors:  P Detloff; M A White; T D Petes
Journal:  Genetics       Date:  1992-09       Impact factor: 4.562

3.  A test of the double-strand break repair model for meiotic recombination in Saccharomyces cerevisiae.

Authors:  L A Gilbertson; F W Stahl
Journal:  Genetics       Date:  1996-09       Impact factor: 4.562

4.  DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression.

Authors:  D K Bishop; D Park; L Xu; N Kleckner
Journal:  Cell       Date:  1992-05-01       Impact factor: 41.582

5.  Meiotic gene conversion: a signal of the basic recombination event in yeast.

Authors:  S Fogel; R Mortimer; K Lusnak; F Tavares
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1979

6.  Identification of double Holliday junctions as intermediates in meiotic recombination.

Authors:  A Schwacha; N Kleckner
Journal:  Cell       Date:  1995-12-01       Impact factor: 41.582

7.  Bidirectional excision in methyl-directed mismatch repair.

Authors:  M Grilley; J Griffith; P Modrich
Journal:  J Biol Chem       Date:  1993-06-05       Impact factor: 5.157

Review 8.  The double-strand-break repair model for recombination.

Authors:  J W Szostak; T L Orr-Weaver; R J Rothstein; F W Stahl
Journal:  Cell       Date:  1983-05       Impact factor: 41.582

9.  Interaction between mismatch repair and genetic recombination in Saccharomyces cerevisiae.

Authors:  E Alani; R A Reenan; R D Kolodner
Journal:  Genetics       Date:  1994-05       Impact factor: 4.562

10.  Genetic evidence that the meiotic recombination hotspot at the HIS4 locus of Saccharomyces cerevisiae does not represent a site for a symmetrically processed double-strand break.

Authors:  S E Porter; M A White; T D Petes
Journal:  Genetics       Date:  1993-05       Impact factor: 4.562

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  22 in total

1.  Multiple functions of MutS- and MutL-related heterocomplexes.

Authors:  T Nakagawa; A Datta; R D Kolodner
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-07       Impact factor: 11.205

2.  Interchromosomal gene conversion at an endogenous human cell locus.

Authors:  P J Quintana; E A Neuwirth; A J Grosovsky
Journal:  Genetics       Date:  2001-06       Impact factor: 4.562

3.  Evidence for biased holliday junction cleavage and mismatch repair directed by junction cuts during double-strand-break repair in mammalian cells.

Authors:  M D Baker; E C Birmingham
Journal:  Mol Cell Biol       Date:  2001-05       Impact factor: 4.272

4.  Gene repeat expansion and contraction by spontaneous intrachromosomal homologous recombination in mammalian cells.

Authors:  Leah R Read; Steven J Raynard; Ania Rukść; Mark D Baker
Journal:  Nucleic Acids Res       Date:  2004-02-20       Impact factor: 16.971

5.  A two-pathway analysis of meiotic crossing over and gene conversion in Saccharomyces cerevisiae.

Authors:  Franklin W Stahl; Henriette M Foss
Journal:  Genetics       Date:  2010-08-02       Impact factor: 4.562

6.  Infrequent co-conversion of markers flanking a meiotic recombination initiation site in Saccharomyces cerevisiae.

Authors:  Lea Jessop; Thorsten Allers; Michael Lichten
Journal:  Genetics       Date:  2005-01-16       Impact factor: 4.562

7.  Analysis of one-sided marker segregation patterns resulting from mammalian gene targeting.

Authors:  Richard D McCulloch; Mark D Baker
Journal:  Genetics       Date:  2006-03       Impact factor: 4.562

8.  But see KITANI (1978).

Authors:  Franklin W Stahl; Henriette M Foss
Journal:  Genetics       Date:  2008-03       Impact factor: 4.562

9.  Testing predictions of the double-strand break repair model relating to crossing over in Mammalian cells.

Authors:  Erin C Birmingham; Shauna A Lee; Richard D McCulloch; Mark D Baker
Journal:  Genetics       Date:  2004-11       Impact factor: 4.562

10.  Reduced mismatch repair of heteroduplexes reveals "non"-interfering crossing over in wild-type Saccharomyces cerevisiae.

Authors:  Tony J Getz; Stephen A Banse; Lisa S Young; Allison V Banse; Johanna Swanson; Grace M Wang; Barclay L Browne; Henriette M Foss; Franklin W Stahl
Journal:  Genetics       Date:  2008-03       Impact factor: 4.562

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