Literature DB >> 1737802

A multicomponent protein of a fission yeast that promotes joint molecule formation from homologous DNAs.

N Arai1, K Kawasaki, T Shibata.   

Abstract

We developed a quantitative assay ("homologous pairing gel assay") adequate for the purification of the activity promoting the formation of joint molecules, an intermediate of homologous recombination ("homologous pairing"). With this assay, one can measure the extent of homologous pairing between a single-stranded DNA and a strand of 3H-labeled double-stranded DNA by crude enzyme preparations. Since the total activity did not significantly change during the sporulation process, we tried to purify the activity from a whole cell extract of mitotic cells of a fission yeast, (Schizosaccharomyces pombe). Through quantitative assaying of a single fraction or of mixed fractions, we obtained three fractions, all of which were required for the maximum level of the ATP-independent homologous pairing: Fractions 65, 100, and 30. In Fractions 100 and 30, polypeptides of approximately 100 and approximately 30 kDa (the 100- and 30-kDa polypeptides), respectively, were the sole detectable components. Fraction 65 contained a polypeptide of approximately 65 kDa (the 65-kDa polypeptide) as the major component and also small amounts of the 30- and 100-kDa polypeptides. Fraction 65 by itself promoted homologous pairing, but the reaction was saturated at a level of approximately 20% of the maximum level achieved with the recA protein. Even when added in excess, Fraction 30 or 100 alone did not promote detectable homologous pairing. A mixture of Fractions 65 and 100 at a rather strict optimum ratio only promoted homologous pairing, the level being 50-70% that with the recA protein, suggesting a stoichiometric complex of these polypeptides as the active form. Fraction 30 alone did not enhance the reaction with Fraction 65, but stimulated homologous pairing promoted by the optimum mixture of Fractions 65 and 100 to the maximum level achieved with the recA protein. Therefore, the homologous pairing-promoting protein from the fission yeast is likely to be a multicomponent protein.

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Year:  1992        PMID: 1737802

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  7 in total

1.  Phenol-treatment and a homologous pairing-assay.

Authors:  N Arai; K Kawasaki; M Iwabuchi; T Shibata
Journal:  Nucleic Acids Res       Date:  1992-07-25       Impact factor: 16.971

2.  Characterization of two nuclear mammalian homologous DNA-pairing activities that do not require associated exonuclease activity.

Authors:  A T Akhmedov; P Bertrand; E Corteggiani; B S Lopez
Journal:  Proc Natl Acad Sci U S A       Date:  1995-02-28       Impact factor: 11.205

3.  Drosophila melanogaster RECQ5/QE DNA helicase: stimulation by GTP binding.

Authors:  Katsumi Kawasaki; Sayako Maruyama; Minoru Nakayama; Kohji Matsumoto; Takehiko Shibata
Journal:  Nucleic Acids Res       Date:  2002-09-01       Impact factor: 16.971

4.  Molecular analysis of the dhp1+ gene of Schizosaccharomyces pombe: an essential gene that has homology to the DST2 and RAT1 genes of Saccharomyces cerevisiae.

Authors:  S Sugano; T Shobuike; T Takeda; A Sugino; H Ikeda
Journal:  Mol Gen Genet       Date:  1994-04

Review 5.  The search for the right partner: homologous pairing and DNA strand exchange proteins in eukaryotes.

Authors:  W D Heyer
Journal:  Experientia       Date:  1994-03-15

6.  Saccharomyces cerevisiae cells lacking the homologous pairing protein p175SEP1 arrest at pachytene during meiotic prophase.

Authors:  J Bähler; G Hagens; G Holzinger; H Scherthan; W D Heyer
Journal:  Chromosoma       Date:  1994-04       Impact factor: 4.316

7.  DNA strand exchange catalyzed by proteins from vaccinia virus-infected cells.

Authors:  W Zhang; D H Evans
Journal:  J Virol       Date:  1993-01       Impact factor: 5.103

  7 in total

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