Literature DB >> 8709955

Gene conversion as a focusing mechanism for correlated mutations: a hypothesis.

J Ninio1.   

Abstract

Ways of producing complex mutational events without substantially raising the primary mutation rate are explored. If the small amount of DNA that is resynthesised through the action of the mismatch DNA repair system is not subject to further repair, the incidence of double mutations can increase by a factor of 100, while single mutations would increase by only 30%. Such a boost in the incidence of double mutations seems insufficient to meet the needs of higher organisms. For them, an alternative strategy would be to produce complex events by a succession of single mutations occurring in a correlated manner over several sexual generations. It is proposed that gene conversion may fulfill this role. Assuming that the resynthesis of DNA that occurs during gene conversion produces mutations in the conversion tract, one predicts a tendency for close mutations in corresponding sequences in the two homologous chromosomes, to promote, during conversion, further mutations in their vicinity. Semiquantitative calculations suggest that such a mechanism can be quite effective, provided the divergence between two paired chromosomes is around 10(-4) or less. Such a mechanism might constitute an adaptive mutation strategy acting at the population level.

Mesh:

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Year:  1996        PMID: 8709955     DOI: 10.1007/BF02173638

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  23 in total

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5.  Interspecies gene exchange in bacteria: the role of SOS and mismatch repair systems in evolution of species.

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Review 6.  Mismatch recognition in chromosomal interactions and speciation.

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7.  Mapping and sequencing of mutations in the Escherichia coli rpoB gene that lead to rifampicin resistance.

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Review 8.  Premeiotic instability of repeated sequences in Neurospora crassa.

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10.  Low nucleotide diversity in man.

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  13 in total

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Review 3.  Too many mutants with multiple mutations.

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4.  Single and coincident intragenic mutations attributable to gene conversion in a human cell line.

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7.  The evolutionary design of error-rates, and the fast fixation enigma.

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