Literature DB >> 11859482

Evolutionary fate of an unstable human minisatellite deduced from sperm-mutation spectra of individual alleles.

Jérôme Buard1, Charles Brenner, Alec J Jeffreys.   

Abstract

Although mutation processes at some human minisatellites have been extensively characterized, the evolutionary fate of these unstable loci is unknown. Minisatellite instability is largely germline specific, with mutation rates up to several percent and with expansion events predominating over contractions. Using allele-specific small-pool polymerase chain reaction, we have determined sperm-mutation spectra of individual alleles of the highly unstable human minisatellite CEB1 (i.e., D2S90). We show that, as allele size increases, the proportion of contractions rises from <5% to 50%, with the average size of deletion increasing and eventually exceeding the average size of expansion. The expected net effect of these trends after many generations is an equilibrium distribution of allele sizes, and allele-frequency data suggest that this equilibrium state has been reached in some contemporary human populations.

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Year:  2002        PMID: 11859482      PMCID: PMC379099          DOI: 10.1086/339608

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN: 0002-9297            Impact factor:   11.025


  27 in total

1.  The direction of microsatellite mutations is dependent upon allele length.

Authors:  X Xu; M Peng; Z Fang
Journal:  Nat Genet       Date:  2000-04       Impact factor: 38.330

2.  Meiotic recombination and flanking marker exchange at the highly unstable human minisatellite CEB1 (D2S90).

Authors:  J Buard; A C Shone; A J Jeffreys
Journal:  Am J Hum Genet       Date:  2000-06-26       Impact factor: 11.025

3.  Unequal crossingover between homologous chromosomes is not the major mechanism involved in the generation of new alleles at VNTR loci.

Authors:  R K Wolff; R Plaetke; A J Jeffreys; R White
Journal:  Genomics       Date:  1989-08       Impact factor: 5.736

4.  Spontaneous mutation rates to new length alleles at tandem-repetitive hypervariable loci in human DNA.

Authors:  A J Jeffreys; N J Royle; V Wilson; Z Wong
Journal:  Nature       Date:  1988-03-17       Impact factor: 49.962

5.  Molecular characterization of a spontaneously generated new allele at a VNTR locus: no exchange of flanking DNA sequence.

Authors:  R K Wolff; Y Nakamura; R White
Journal:  Genomics       Date:  1988-11       Impact factor: 5.736

6.  GT repeats are associated with recombination on human chromosome 22.

Authors:  J Majewski; J Ott
Journal:  Genome Res       Date:  2000-08       Impact factor: 9.043

7.  Extremely complex repeat shuffling during germline mutation at human minisatellite B6.7.

Authors:  K Tamaki; C A May; Y E Dubrova; A J Jeffreys
Journal:  Hum Mol Genet       Date:  1999-05       Impact factor: 6.150

8.  Somatic versus germline mutation processes at minisatellite CEB1 (D2S90) in humans and transgenic mice.

Authors:  J Buard; A Collick; J Brown; A J Jeffreys
Journal:  Genomics       Date:  2000-04-15       Impact factor: 5.736

Review 9.  Evolutionary dynamics of microsatellite DNA.

Authors:  C Schlötterer
Journal:  Chromosoma       Date:  2000-09       Impact factor: 4.316

10.  High frequencies of short frameshifts in poly-CA/TG tandem repeats borne by bacteriophage M13 in Escherichia coli K-12.

Authors:  G Levinson; G A Gutman
Journal:  Nucleic Acids Res       Date:  1987-07-10       Impact factor: 16.971

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  2 in total

1.  Response to: DNA identification by pedigree likelihood ratio accommodating population substructure and mutations.

Authors:  Thore Egeland; A Philip Dawid; Julia Mortera; Petter Mostad; Andreas Tillmar
Journal:  Investig Genet       Date:  2011-03-25

2.  Response to: DNA identification by pedigree likelihood ratio accommodating population substructure and mutations- authors' reply.

Authors:  Ranajit Chakraborty; Jianye Ge; Bruce Budowle
Journal:  Investig Genet       Date:  2011-03-25
  2 in total

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