Literature DB >> 1334907

The population biology and evolutionary significance of Ty elements in Saccharomyces cerevisiae.

C M Wilke1, E Maimer, J Adams.   

Abstract

The basic structure and properties of Ty elements are considered with special reference to their role as agents of evolutionary change. Ty elements may generate genetic variation for fitness by their action as mutagens, as well as by providing regions of portable homology for recombination. The mutational spectra generated by Ty1 transposition events may, due to their target specificity and gene regulatory capabilities, possess a higher frequency of adaptively favorable mutations than spectra resulting from other types of mutational processes. Laboratory strains contain between 25-35 elements, and in both these and industrial strains the insertions appear quite stable. In contrast, a wide variation in Ty number is seen in wild isolates, with a lower average number/genome. Factors which may determine Ty copy number in populations include transposition rates (dependent on Ty copy number and mating type), and stabilization of Ty elements in the genome as well as selection for and against Ty insertions in the genome. Although the average effect of Ty transpositions are deleterious, populations initiated with a single clone containing a single Ty element steadily accumulated Ty elements over 1,000 generations. Direct evidence that Ty transposition events can be selectively favored is provided by experiments in which populations containing large amounts of variability for Ty1 copy number were maintained for approximately 100 generations in a homogeneous environment. At their termination, the frequency of clones containing 0 Ty elements had decreased to approximately 0.0, and the populations had became dominated by a small number of clones containing > 0 Ty elements. No such reduction in variability was observed in populations maintained in a structured environment, though changes in Ty number were observed. The implications of genetic (mating type and ploidy) changes and environmental fluctuations for the long-term persistence of Ty elements within the S. cerevisiae species group are discussed.

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Year:  1992        PMID: 1334907     DOI: 10.1007/bf00133718

Source DB:  PubMed          Journal:  Genetica        ISSN: 0016-6707            Impact factor:   1.082


  87 in total

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Journal:  Nature       Date:  1985 Dec 12-18       Impact factor: 49.962

Review 2.  Eukaryotic transposable elements and genome evolution.

Authors:  D J Finnegan
Journal:  Trends Genet       Date:  1989-04       Impact factor: 11.639

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Journal:  Genet Res       Date:  1974-02       Impact factor: 1.588

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Journal:  Cell       Date:  1981-02       Impact factor: 41.582

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Authors:  G Cornelis
Journal:  J Gen Microbiol       Date:  1980-03

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Authors:  R Stucka; H Lochmüller; H Feldmann
Journal:  Nucleic Acids Res       Date:  1989-07-11       Impact factor: 16.971

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Journal:  Genetics       Date:  1989-12       Impact factor: 4.562

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Journal:  Cell       Date:  1979-04       Impact factor: 41.582

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Authors:  R Rothstein
Journal:  Cell       Date:  1979-05       Impact factor: 41.582

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Authors:  M J Curcio; N J Sanders; D J Garfinkel
Journal:  Mol Cell Biol       Date:  1988-09       Impact factor: 4.272

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  24 in total

1.  The Saccharomyces cerevisiae DNA recombination and repair functions of the RAD52 epistasis group inhibit Ty1 transposition.

Authors:  A J Rattray; B K Shafer; D J Garfinkel
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

2.  Evolution in Saccharomyces cerevisiae: identification of mutations increasing fitness in laboratory populations.

Authors:  Victoria M Blanc; Julian Adams
Journal:  Genetics       Date:  2003-11       Impact factor: 4.562

3.  Post-transcriptional cosuppression of Ty1 retrotransposition.

Authors:  David J Garfinkel; Katherine Nyswaner; Jun Wang; Jae-Yong Cho
Journal:  Genetics       Date:  2003-09       Impact factor: 4.562

4.  Ty1 copy number dynamics in Saccharomyces.

Authors:  David J Garfinkel; Katherine M Nyswaner; Karen M Stefanisko; Caroline Chang; Sharon P Moore
Journal:  Genetics       Date:  2005-01-31       Impact factor: 4.562

5.  Population genetics models of competition between transposable element subfamilies.

Authors:  Arnaud Le Rouzic; Pierre Capy
Journal:  Genetics       Date:  2006-08-03       Impact factor: 4.562

6.  Isw1 acts independently of the Isw1a and Isw1b complexes in regulating transcriptional silencing at the ribosomal DNA locus in Saccharomyces cerevisiae.

Authors:  John E Mueller; Mary Bryk
Journal:  J Mol Biol       Date:  2007-05-18       Impact factor: 5.469

7.  The requirements for COMPASS and Paf1 in transcriptional silencing and methylation of histone H3 in Saccharomyces cerevisiae.

Authors:  John E Mueller; Megan Canze; Mary Bryk
Journal:  Genetics       Date:  2006-04-02       Impact factor: 4.562

8.  Structure of the chromosome VII centromere region in Neurospora crassa: degenerate transposons and simple repeats.

Authors:  E B Cambareri; R Aisner; J Carbon
Journal:  Mol Cell Biol       Date:  1998-09       Impact factor: 4.272

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Authors:  M Labrador; A Fontdevila
Journal:  Mol Gen Genet       Date:  1994-12-15

10.  Identification of a mariner-like repetitive sequence in C. elegans.

Authors:  M M Sedensky; S J Hudson; B Everson; P G Morgan
Journal:  Nucleic Acids Res       Date:  1994-05-11       Impact factor: 16.971

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