Literature DB >> 10413403

Finding new human minisatellite sequences in the vicinity of long CA-rich sequences.

F Giraudeau1, E Petit, H Avet-Loiseau, Y Hauck, G Vergnaud, V Amarger.   

Abstract

Microsatellites and minisatellites are two classes of tandem repeat sequences differing in their size, mutation processes, and chromosomal distribution. The boundary between the two classes is not defined. We have developed a convenient, hybridization-based human library screening procedure able to detect long CA-rich sequences. Analysis of cosmid clones derived from a chromosome 1 library show that cross-hybridizing sequences tested are imperfect CA-rich sequences, some of them showing a minisatellite organization. All but one of the 13 positive chromosome 1 clones studied are localized in chromosomal bands to which minisatellites have previously been assigned, such as the 1pter cluster. To test the applicability of the procedure to minisatellite detection on a larger scale, we then used a large-insert whole-genome PAC library. Altogether, 22 new minisatellites have been identified in positive PAC and cosmid clones and 20 of them are telomeric. Among the 42 positive PAC clones localized within the human genome by FISH and/or linkage analysis, 25 (60%) are assigned to a terminal band of the karyotype, 4 (9%) are juxtacentromeric, and 13 (31%) are interstitial. The localization of at least two of the interstitial PAC clones corresponds to previously characterized minisatellite-containing regions and/or ancestrally telomeric bands, in agreement with this minisatellite-like distribution. The data obtained are in close agreement with the parallel investigation of human genome sequence data and suggest that long human (CA)s are imperfect CA repeats belonging to the minisatellite class of sequences. This approach provides a new tool to efficiently target genomic clones originating from subtelomeric domains, from which minisatellite sequences can readily be obtained. [The sequence data described in this paper have been submitted to the EMBL data library under accession nos. AJ000377-AJ000383.]

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Year:  1999        PMID: 10413403      PMCID: PMC310796     

Source DB:  PubMed          Journal:  Genome Res        ISSN: 1088-9051            Impact factor:   9.043


  28 in total

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Authors:  F Giraudeau; D Aubert; I Young; S Horsley; S Knight; L Kearney; G Vergnaud; J Flint
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

2.  Analysis of distribution in the human, pig, and rat genomes points toward a general subtelomeric origin of minisatellite structures.

Authors:  V Amarger; D Gauguier; M Yerle; F Apiou; P Pinton; F Giraudeau; S Monfouilloux; M Lathrop; B Dutrillaux; J Buard; G Vergnaud
Journal:  Genomics       Date:  1998-08-15       Impact factor: 5.736

3.  Somatic mutation processes at a human minisatellite.

Authors:  A J Jeffreys; R Neumann
Journal:  Hum Mol Genet       Date:  1997-01       Impact factor: 6.150

4.  Homology-directed repair is a major double-strand break repair pathway in mammalian cells.

Authors:  F Liang; M Han; P J Romanienko; M Jasin
Journal:  Proc Natl Acad Sci U S A       Date:  1998-04-28       Impact factor: 11.205

5.  Somatic mutations in VNTR-locus D1S7 in human colorectal carcinomas are associated with microsatellite instability.

Authors:  P Hoff-Olsen; G I Meling; B Olaisen
Journal:  Hum Mutat       Date:  1995       Impact factor: 4.878

6.  Further evidence for elevated human minisatellite mutation rate in Belarus eight years after the Chernobyl accident.

Authors:  Y E Dubrova; V N Nesterov; N G Krouchinsky; V A Ostapenko; G Vergnaud; F Giraudeau; J Buard; A J Jeffreys
Journal:  Mutat Res       Date:  1997-11-28       Impact factor: 2.433

7.  Minisatellite origins in yeast and humans.

Authors:  J E Haber; E J Louis
Journal:  Genomics       Date:  1998-02-15       Impact factor: 5.736

8.  A genetic linkage map of the rat derived from recombinant inbred strains.

Authors:  M Pravenec; D Gauguier; J J Schott; J Buard; V Kren; V Bílá; C Szpirer; J Szpirer; J M Wang; H Huang; E St Lezin; M A Spence; P Flodman; M Printz; G M Lathrop; G Vergnaud; T W Kurtz
Journal:  Mamm Genome       Date:  1996-02       Impact factor: 2.957

9.  The stabilization of repetitive tracts of DNA by variant repeats requires a functional DNA mismatch repair system.

Authors:  S M Heale; T D Petes
Journal:  Cell       Date:  1995-11-17       Impact factor: 41.582

10.  Susceptibility to human type 1 diabetes at IDDM2 is determined by tandem repeat variation at the insulin gene minisatellite locus.

Authors:  S T Bennett; A M Lucassen; S C Gough; E E Powell; D E Undlien; L E Pritchard; M E Merriman; Y Kawaguchi; M J Dronsfield; F Pociot
Journal:  Nat Genet       Date:  1995-03       Impact factor: 38.330

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  1 in total

1.  Predicting human minisatellite polymorphism.

Authors:  France Denoeud; Gilles Vergnaud; Gary Benson
Journal:  Genome Res       Date:  2003-04-14       Impact factor: 9.043

  1 in total

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