Literature DB >> 18948711

Variation in patterns of human meiotic recombination.

P P Khil1, R D Camerini-Otero.   

Abstract

In the last 30 years it has become evident that patterns of meiotic recombination can be highly variable among individuals. The evidence comes from both low and high resolution analyses of hotspots of recombination in human and other species. In addition, a comparison of the recombination profiles in closely related species such as human and chimpanzee reveals essentially no correlation in the position of hotspots. Although the variation in hotspots of meiotic recombination is clearly documented, the mechanisms responsible for such variation are far from being understood. Here we will review the available evidence of natural variation in meiotic recombination and will discuss potential implications of this variation on the functional mechanisms of crossover formation and control.

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Year:  2009        PMID: 18948711      PMCID: PMC3105470          DOI: 10.1159/000166623

Source DB:  PubMed          Journal:  Genome Dyn        ISSN: 1660-9263


  72 in total

1.  Patterns of meiotic recombination in human fetal oocytes.

Authors:  Charles Tease; Geraldine M Hartshorne; Maj A Hultén
Journal:  Am J Hum Genet       Date:  2002-05-01       Impact factor: 11.025

Review 2.  Initiation of meiotic recombination by formation of DNA double-strand breaks: mechanism and regulation.

Authors:  S Keeney; M J Neale
Journal:  Biochem Soc Trans       Date:  2006-08       Impact factor: 5.407

Review 3.  Meiotic recombination hotspots in plants.

Authors:  C Mézard
Journal:  Biochem Soc Trans       Date:  2006-08       Impact factor: 5.407

4.  A worldwide survey of haplotype variation and linkage disequilibrium in the human genome.

Authors:  Donald F Conrad; Mattias Jakobsson; Graham Coop; Xiaoquan Wen; Jeffrey D Wall; Noah A Rosenberg; Jonathan K Pritchard
Journal:  Nat Genet       Date:  2006-10-22       Impact factor: 38.330

5.  Variation in MLH1 distribution in recombination maps for individual chromosomes from human males.

Authors:  Fei Sun; Maria Oliver-Bonet; Thomas Liehr; Heike Starke; Paul Turek; Evelyn Ko; Alfred Rademaker; Renée H Martin
Journal:  Hum Mol Genet       Date:  2006-06-27       Impact factor: 6.150

6.  Chromosome synapsis defects and sexually dimorphic meiotic progression in mice lacking Spo11.

Authors:  F Baudat; K Manova; J P Yuen; M Jasin; S Keeney
Journal:  Mol Cell       Date:  2000-11       Impact factor: 17.970

7.  The distribution and causes of meiotic recombination in the human genome.

Authors:  S Myers; C C A Spencer; A Auton; L Bottolo; C Freeman; P Donnelly; G McVean
Journal:  Biochem Soc Trans       Date:  2006-08       Impact factor: 5.407

8.  Global analysis of the relationship between the binding of the Bas1p transcription factor and meiosis-specific double-strand DNA breaks in Saccharomyces cerevisiae.

Authors:  Piotr A Mieczkowski; Margaret Dominska; Michael J Buck; Jennifer L Gerton; Jason D Lieb; Thomas D Petes
Journal:  Mol Cell Biol       Date:  2006-02       Impact factor: 4.272

9.  High-resolution recombination patterns in a region of human chromosome 21 measured by sperm typing.

Authors:  Irene Tiemann-Boege; Peter Calabrese; David M Cochran; Rebecca Sokol; Norman Arnheim
Journal:  PLoS Genet       Date:  2006-05-05       Impact factor: 5.917

10.  Polymorphism in the activity of human crossover hotspots independent of local DNA sequence variation.

Authors:  Rita Neumann; Alec J Jeffreys
Journal:  Hum Mol Genet       Date:  2006-03-16       Impact factor: 6.150

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  3 in total

Review 1.  Genetics of mammalian meiosis: regulation, dynamics and impact on fertility.

Authors:  Mary Ann Handel; John C Schimenti
Journal:  Nat Rev Genet       Date:  2010-01-06       Impact factor: 53.242

2.  Genetic crossovers are predicted accurately by the computed human recombination map.

Authors:  Pavel P Khil; R Daniel Camerini-Otero
Journal:  PLoS Genet       Date:  2010-01-29       Impact factor: 5.917

3.  Reconstructing past changes in locus-specific recombination rates.

Authors:  Murray P Cox; Barbara R Holland; Matthew C Wilkins; Jan Schmid
Journal:  BMC Genet       Date:  2013-02-25       Impact factor: 2.797

  3 in total

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