Literature DB >> 8938451

Chromosomal localisation of the human envoplakin gene (EVPL) to the region of the tylosis oesophageal cancer gene (TOCG) on 17q25.

C Ruhrberg1, J A Williamson, D Sheer, F M Watt.   

Abstract

Envoplakin is a membrane-associated precursor of the epidermal cornified envelope. Envoplakin is homologous to desmoplakin I and desmoplakin II (DPI/II), bullous pemphigoid antigen 1 (BPAG1), and plectin and is proposed to link desmosomes and keratin filaments to the cornified envelope. We describe the isolation of cosmids and yeast artificial chromosomes containing the complete human envoplakin gene (EVPL) and show, by analysis of somatic cell hybrids and chromosomal in situ hybridisation, that the envoplakin gene, unlike the genes encoding BPAG1 and DPI/II, maps to 17q25 and is physically linked to D17S1603. This sequence-tagged site segregates with the autosomal dominant human disease focal nonepidermolytic palmoplantar keratosis (NEPKK; "tylosis"), which is associated with an increased risk of oesophageal cancer. The chromosomal localisation of the envoplakin gene, the homology of the encoded protein to keratin-binding proteins, and its expression in epidermal and oesophageal keratinocytes all raise the possibility that loss of envoplakin function could be responsible for this form of palmoplantar keratoderma.

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Year:  1996        PMID: 8938451     DOI: 10.1006/geno.1996.0573

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


  4 in total

1.  Localization of a novel locus for hereditary nail dysplasia to chromosome 17q25.1-17q25.3.

Authors:  M A Rafiq; M Ansar; T Pham; M Amin-ud-Din; M Anwar; S Haque; M H Chahrour; K Yan; S M Leal; W Ahmad
Journal:  Clin Genet       Date:  2004-07       Impact factor: 4.438

2.  Abnormalities of chromosome 17 in oesophageal cancer.

Authors:  Revendran Moodley; Anunathan Reddi; Runjan Chetty; Richard Naidoo
Journal:  J Clin Pathol       Date:  2006-10-17       Impact factor: 3.411

3.  Down-regulation in multiple human cancers of a novel gene, DMHC, from 17q25.1 that encodes an integral membrane protein.

Authors:  I Mikami; H Harada; H Nagai; M Tsuneizumi; Y Nobe; K Koizumi; S Sugano; S Tanaka; M Emi
Journal:  Jpn J Cancer Res       Date:  2001-04

4.  LINC00649 underexpression is an adverse prognostic marker in acute myeloid leukemia.

Authors:  Chao Guo; Ya-Yue Gao; Qian-Qian Ju; Chun-Xia Zhang; Ming Gong; Zhen-Ling Li
Journal:  BMC Cancer       Date:  2020-09-03       Impact factor: 4.430

  4 in total

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