Literature DB >> 2895730

Relationship of the genes for Chediak-Higashi syndrome (beige) and the T-cell receptor gamma chain in mouse and man.

R F Holcombe1, W Strauss, F L Owen, L A Boxer, R W Warren, M E Conley, J Ferrara, R Y Leavitt, A S Fauci, B A Taylor.   

Abstract

The genetic linkage of Chediak-Higashi syndrome and its murine analog, beige (bg), to the T-cell receptor (TCR-gamma) gamma chain gene is further defined. Previous studies using recombinant inbred strains of mice demonstrated that the murine bg gene is genetically linked to a murine TCR-gamma gene. We report that in the mouse the frequency of recombination between these two markers is 0.025. Further, we tested the hypothesis that these two genes are linked in the human genome by analyzing restriction fragment length polymorphisms (RFLPs) in five families with children afflicted with Chediak-Higashi syndrome. In three families, RFLPs in TCR-gamma genes were inherited discordantly from Chediak-Higashi syndrome, demonstrating nonlinkage. We postulate that there is an evolutionary chromosomal breakpoint between the bg gene and the TCR-gamma gene.

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Year:  1987        PMID: 2895730     DOI: 10.1016/0888-7543(87)90058-9

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


  10 in total

Review 1.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M R Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Mouse chromosome 13.

Authors:  M J Justice; D A Stephenson
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 3.  Mouse chromosome 13.

Authors:  M J Justice; D A Stephenson
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

Review 4.  Mouse map of paralogous genes.

Authors:  J H Nadeau; M Kosowsky
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

Review 5.  Comparative map for mice and humans.

Authors:  J H Nadeau; M T Davisson; D P Doolittle; P Grant; A L Hillyard; M Kosowsky; T H Roderick
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

6.  Mutations in the human Ca(2+)-sensing-receptor gene that cause familial hypocalciuric hypercalcemia.

Authors:  Y H Chou; M R Pollak; M L Brandi; G Toss; H Arnqvist; A B Atkinson; S E Papapoulos; S Marx; E M Brown; J G Seidman
Journal:  Am J Hum Genet       Date:  1995-05       Impact factor: 11.025

7.  Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg).

Authors:  K Fukai; J Oh; M A Karim; K J Moore; H H Kandil; H Ito; J Bürger; R A Spritz
Journal:  Am J Hum Genet       Date:  1996-09       Impact factor: 11.025

Review 8.  Genetic defects in Chediak-Higashi syndrome and the beige mouse.

Authors:  R A Spritz
Journal:  J Clin Immunol       Date:  1998-03       Impact factor: 8.317

9.  A locus for familial hypertrophic cardiomyopathy is closely linked to the cardiac myosin heavy chain genes, CRI-L436, and CRI-L329 on chromosome 14 at q11-q12.

Authors:  S D Solomon; A A Geisterfer-Lowrance; H P Vosberg; G Hiller; J A Jarcho; C C Morton; W O McBride; A L Mitchell; A E Bale; W J McKenna
Journal:  Am J Hum Genet       Date:  1990-09       Impact factor: 11.025

10.  Familial hypertrophic cardiomyopathy is a genetically heterogeneous disease.

Authors:  S D Solomon; J A Jarcho; W McKenna; A Geisterfer-Lowrance; R Germain; R Salerni; J G Seidman; C E Seidman
Journal:  J Clin Invest       Date:  1990-09       Impact factor: 14.808

  10 in total

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