Literature DB >> 1740328

A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers.

J Hazan1, C Dubay, M P Pankowiak, N Becuwe, J Weissenbach.   

Abstract

Twenty-six (CA)n polymorphic microsatellites were isolated from a flow-sorted chromosome 20 library. To reduce the number of sequencing gels, these microsatellites were genotyped on 15 CEPH families using a procedure derived from the multiplex sequencing technique of G. M. Church and S. Kieffer-Higgins (1988, Science 240:185-188). A primary map with a strongly supported order was constructed with 15 (CA)n markers. Regional localizations for the 11 other microsatellites were obtained with regard to the primary map. The 26 loci span approximately 160 cM. Regional localizations for a set of index markers (D20S4, D20S6, D20S16, and D20S19) and for other markers from the CEPH Public Database (D20S5, D20S15, D20S17, and D20S18) have also been determined. The total map spans a genetic distance of approximately 195 cM extending from the (CA)n marker IP20M7 on 20p to D20S19 on 20q. The density of microsatellite markers is markedly higher in the pericentromeric region, with an average distance of 3 to 4 cM between adjacent markers over a distance of 43 cM. Two-thirds of these randomly isolated microsatellites are clustered in that region between D20S5 and D20S16 representing approximately one-fourth of the linkage map. This might suggest a nonrandom distribution of (CA)n simple sequence repeats on this chromosome.

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Year:  1992        PMID: 1740328     DOI: 10.1016/0888-7543(92)90364-x

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  33 in total

1.  Perils of gene mapping with microsatellite markers.

Authors:  J A Knowles; V J Vieland; T C Gilliam
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

2.  Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.

Authors:  A Lezin; G Cancel; G Stevanin; D Smadja; J C Vernant; A Dürr; J Martial; G G Buisson; R Bellance; H Chneiweiss; Y Agid; A Brice
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

3.  Single locus microsatellites isolated using 5' anchored PCR.

Authors:  P J Fisher; R C Gardner; T E Richardson
Journal:  Nucleic Acids Res       Date:  1996-11-01       Impact factor: 16.971

4.  The incidence of mini- and micro-satellite repetitive DNA in the canine genome.

Authors:  J Rothuizen; J Wolfswinkel; J A Lenstra; R R Frants
Journal:  Theor Appl Genet       Date:  1994-10       Impact factor: 5.699

5.  High-precision genotyping by denaturing capillary electrophoresis.

Authors:  H Wenz; J M Robertson; S Menchen; F Oaks; D M Demorest; D Scheibler; B B Rosenblum; C Wike; D A Gilbert; J W Efcavitch
Journal:  Genome Res       Date:  1998-01       Impact factor: 9.043

6.  Improved single-strand DNA sizing accuracy in capillary electrophoresis.

Authors:  B B Rosenblum; F Oaks; S Menchen; B Johnson
Journal:  Nucleic Acids Res       Date:  1997-10-01       Impact factor: 16.971

7.  Targeted development of microsatellite markers from the defined region of bovine chromosome 6q21-31.

Authors:  R Weikard; T Goldammer; C Kühn; W Barendse; M Schwerin
Journal:  Mamm Genome       Date:  1997       Impact factor: 2.957

8.  Deleted chromosome 20 from a patient with Alagille syndrome isolated in a cell hybrid through leucine transport selection: study of three candidate genes.

Authors:  J F Deleuze; S Dhorne; J Hazan; E Borghi; N Raynaud; N Pollet; M Meunier-Rotival; J Deschatrette; D Alagille; M Hadchouel
Journal:  Mamm Genome       Date:  1994-11       Impact factor: 2.957

9.  Cytologically balanced t(2;20) in a two-generation family with alagille syndrome: cytogenetic and molecular studies.

Authors:  N B Spinner; E B Rand; P Fortina; A Genin; R Taub; A Semeraro; D A Piccoli
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

10.  Towards fully automated genotyping: use of an X linked recessive spastic paraplegia family to test alternative analysis methods.

Authors:  H Kobayashi; T C Matise; M W Perlin; H G Marks; E P Hoffman
Journal:  Hum Genet       Date:  1995-05       Impact factor: 4.132

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