Literature DB >> 8095486

Linkage localization of TGFB2 and the human homeobox gene HLX1 to chromosome 1q.

D Y Nishimura1, A F Purchio, J C Murray.   

Abstract

We have identified genetic variation within two human genes, transforming growth factor-beta 2 (TGFB2) and the homeobox gene HB24 (HLX1). Reported here are four human RFLPs and SSCPs for TGFB2 in humans and gorillas. In addition, we describe an RFLP and a SSCP for HLX1. We propose that HLX1 is the human homologue of the mouse homeobox gene Hlx based on extensive sequence homology between the genes and the close proximity of both genes to TGFB2 in their respective species. We also report the chromosomal localization of HLX1 to the long arm of human chromosome 1. Finally, utilizing the polymorphisms described for TGFB2 and HLX1, we have been able to localize these genes within a framework map of the distal long arm of chromosome 1 and to study the linkage relationship between these two genes. Pairwise linkage analysis shows that these two genes are linked, with a recombination fraction of 3.1% and a lod score of 14.49.

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Year:  1993        PMID: 8095486     DOI: 10.1006/geno.1993.1068

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


  8 in total

1.  Evidence for linkage of a candidate chromosome 1 region to human systemic lupus erythematosus.

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Journal:  J Clin Invest       Date:  1997-02-15       Impact factor: 14.808

Review 2.  Single-strand conformation polymorphism (SSCP) analysis as a tool for genetic mapping.

Authors:  D R Beier
Journal:  Mamm Genome       Date:  1993-11       Impact factor: 2.957

3.  Role of transforming growth factor-β2 in, and apossible transforming growth factor-β 2 gene polymorphism as a marker of, renal dysfunction in essential hypertension: A study in Turkish patients.

Authors:  Zerrin Bicik; Sevim Gönen; Talat Bahçebasi; Kadriye Reis; Turgay Arinsoy; Sükrü Sindel
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4.  Recurrent genetic aberrations in thymoma and thymic carcinoma.

Authors:  A Zettl; P Ströbel; K Wagner; T Katzenberger; G Ott; A Rosenwald; K Peters; A Krein; M Semik; H K Müller-Hermelink; A Marx
Journal:  Am J Pathol       Date:  2000-07       Impact factor: 4.307

5.  Gene mapping of Usher syndrome type IIa: localization of the gene to a 2.1-cM segment on chromosome 1q41.

Authors:  W J Kimberling; M D Weston; C Möller; A van Aarem; C W Cremers; J Sumegi; P S Ing; C Connolly; A Martini; M Milani
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

6.  Microsatellite-based fine mapping of the Van der Woude syndrome locus to an interval of 4.1 cM between D1S245 and D1S414.

Authors:  A Sander; J C Murray; T Scherpbier-Heddema; K H Buetow; J Weissenbach; M Zingg; K Ludwig; R Schmelzle
Journal:  Am J Hum Genet       Date:  1995-01       Impact factor: 11.025

7.  Cellular and functional characterization of immunoresistant human glioma cell clones selected with alloreactive cytotoxic T lymphocytes reveals their up-regulated synthesis of biologically active TGF-beta.

Authors:  German G Gomez; Carol A Kruse
Journal:  J Immunother       Date:  2007-04       Impact factor: 4.456

Review 8.  Transforming growth factor-β in tumour development.

Authors:  Charles B Trelford; Lina Dagnino; Gianni M Di Guglielmo
Journal:  Front Mol Biosci       Date:  2022-10-04
  8 in total

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