Literature DB >> 2897163

Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.

H Y Zoghbi1, S P Daiger, A McCall, W E O'Brien, A L Beaudet.   

Abstract

A 1,161-bp EcoRI fragment from the 5' end of the cDNA coding for human factor XIIIa (gene symbol F13A) was used to identify RFLPs in human DNAs. Several different RFLPs were identified with 15 different restriction enzymes. Two RFLPs detected with the restriction enzyme BamHI and one multiallelic RFLP detected with BclI were used for further studies. Linkage relationships between these three polymorphisms and the HLA complex were studied in DNA samples from the 40 Centre d'Etude du Polymorphisme Humain families. Combining all of the data to form highly informative haplotypes, we found linkage to HLA with a maximum lod score of 11.44 at a recombination fraction of .25 for males and .35 for females. These three RFLPs at the FXIIIa locus provide a highly informative marker for the short arm of chromosome 6 with an observed heterozygosity of 91%. Using this marker and the HLA locus, one can confirm or exclude the assignment of gene loci to most of chromosome 6p.

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Year:  1988        PMID: 2897163      PMCID: PMC1715200     

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


  20 in total

1.  Analysis of the human alpha-globin gene cluster reveals a highly informative genetic locus.

Authors:  D R Higgs; J S Wainscoat; J Flint; A V Hill; S L Thein; R D Nicholls; H Teal; H Ayyub; T E Peto; A G Falusi
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

2.  Variable number of tandem repeat (VNTR) markers for human gene mapping.

Authors:  Y Nakamura; M Leppert; P O'Connell; R Wolff; T Holm; M Culver; C Martin; E Fujimoto; M Hoff; E Kumlin
Journal:  Science       Date:  1987-03-27       Impact factor: 47.728

3.  Human Factor XIII from plasma and platelets. Molecular weights, subunit structures, proteolytic activation, and cross-linking of fibrinogen and fibrin.

Authors:  M L Schwartz; S V Pizzo; R L Hill; P A McKee
Journal:  J Biol Chem       Date:  1973-02-25       Impact factor: 5.157

4.  Primary structure of blood coagulation factor XIIIa (fibrinoligase, transglutaminase) from human placenta.

Authors:  N Takahashi; Y Takahashi; F W Putnam
Journal:  Proc Natl Acad Sci U S A       Date:  1986-11       Impact factor: 11.205

5.  Genetic polymorphism of the A subunit of human coagulation factor XIII.

Authors:  P G Board
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

6.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.

Authors:  A P Feinberg; B Vogelstein
Journal:  Anal Biochem       Date:  1983-07-01       Impact factor: 3.365

7.  Genetic heterogeneity of factor XIII deficiency: first description of unstable A subunits.

Authors:  S Castle; P G Board; R A Anderson
Journal:  Br J Haematol       Date:  1981-06       Impact factor: 6.998

8.  An electrophoretic and quantitative analysis of coagulation factor XIII in normal and deficient subjects.

Authors:  P G Board; M Coggan; J W Hamer
Journal:  Br J Haematol       Date:  1980-08       Impact factor: 6.998

Review 9.  Construction of a genetic linkage map in man using restriction fragment length polymorphisms.

Authors:  D Botstein; R L White; M Skolnick; R W Davis
Journal:  Am J Hum Genet       Date:  1980-05       Impact factor: 11.025

10.  Alternative bioassays of kinship between loci.

Authors:  N E Morton; D Wu
Journal:  Am J Hum Genet       Date:  1988-01       Impact factor: 11.025

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  11 in total

1.  Molecular definition of bovine argininosuccinate synthetase deficiency.

Authors:  J A Dennis; P J Healy; A L Beaudet; W E O'Brien
Journal:  Proc Natl Acad Sci U S A       Date:  1989-10       Impact factor: 11.205

2.  Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysis.

Authors:  K A Ellison; C P Fill; J Terwilliger; L J DeGennaro; A Martin-Gallardo; M Anvret; A K Percy; J Ott; H Zoghbi
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

3.  Three F XIIIA gene loci?

Authors:  M I Kamboh; R E Ferrell
Journal:  Hum Genet       Date:  1989-12       Impact factor: 4.132

4.  Lack of close linkage between human coagulation factor F13A and HLA class I molecules.

Authors:  B Schweighofer; R Wank
Journal:  Immunogenetics       Date:  1989       Impact factor: 2.846

5.  Association of Treacher Collins syndrome and translocation 6p21.31/16p13.11: exclusion of the locus from these candidate regions.

Authors:  M J Dixon; E Haan; E Baker; D David; N McKenzie; R Williamson; J Mulley; M Farrall; D Callen
Journal:  Am J Hum Genet       Date:  1991-02       Impact factor: 11.025

6.  Hemopoietic origin of factor XIII A subunits in platelets, monocytes, and plasma. Evidence from bone marrow transplantation studies.

Authors:  M C Poon; J A Russell; S Low; G D Sinclair; A R Jones; W Blahey; B A Ruether; D I Hoar
Journal:  J Clin Invest       Date:  1989-09       Impact factor: 14.808

7.  Assignment of autosomal dominant spinocerebellar ataxia (SCA1) centromeric to the HLA region on the short arm of chromosome 6, using multilocus linkage analysis.

Authors:  H Y Zoghbi; L A Sandkuyl; J Ott; S P Daiger; M Pollack; W E O'Brien; A L Beaudet
Journal:  Am J Hum Genet       Date:  1989-02       Impact factor: 11.025

8.  Molecular heterogeneity of autosomal dominant cerebellar ataxia: analysis of flanking microsatellites of the spinocerebellar ataxia 1 locus in a northern European family unequivocally demonstrates non-linkage.

Authors:  A Lunkes; S Gispert; J Enczmann; G Auburger
Journal:  Hum Genet       Date:  1993-05       Impact factor: 4.132

9.  Linkage analysis of idiopathic generalized epilepsy (IGE) and marker loci on chromosome 6p in families of patients with juvenile myoclonic epilepsy: no evidence for an epilepsy locus in the HLA region.

Authors:  W P Whitehouse; M Rees; D Curtis; A Sundqvist; K Parker; E Chung; D Baralle; R M Gardiner
Journal:  Am J Hum Genet       Date:  1993-09       Impact factor: 11.025

10.  Autosomal dominant ataxia: genetic evidence for locus heterogeneity from a Cuban founder-effect population.

Authors:  G Auburger; G O Diaz; R F Capote; S G Sanchez; M P Perez; M E del Cueto; M G Meneses; M Farrall; R Williamson; S Chamberlain
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

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