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

作者信息

Ruhrberg C, Williamson J A, Sheer D, Watt F M

机构信息

Keratinocyte Laboratory, Imperial Cancer Research Fund, London, United Kingdom.

出版信息

Genomics. 1996 Nov 1;37(3):381-5. doi: 10.1006/geno.1996.0573.

DOI:10.1006/geno.1996.0573
PMID:8938451
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.

摘要

相似文献

1
Chromosomal localisation of the human envoplakin gene (EVPL) to the region of the tylosis oesophageal cancer gene (TOCG) on 17q25.
Genomics. 1996 Nov 1;37(3):381-5. doi: 10.1006/geno.1996.0573.
2
Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25.内披蛋白,一种可能的局灶性先天性无汗性外胚层发育不良/食管癌(TOC)候选基因:17q25上TOC区域遗传图谱与物理图谱的整合
Genomics. 1999 Jul 15;59(2):234-42. doi: 10.1006/geno.1999.5857.
3
Infrequent mutation of the human envoplakin gene is closely linked to the tylosis oesophageal cancer locus in sporadic oesophageal squamous cell carcinomas.人类内披蛋白基因的罕见突变与散发性食管鳞状细胞癌中的掌跖角化症食管癌位点密切相关。
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The tylosis esophageal cancer (TOC) locus: more than just a familial cancer gene.掌跖角化症食管癌(TOC)基因座:不仅仅是一个家族性癌症基因。
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Tylosis esophageal cancer locus on chromosome 17q25.1 is commonly deleted in sporadic human esophageal cancer.17号染色体长臂25.1区的掌跖角化症食管癌位点在散发性人类食管癌中常发生缺失。
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Unique role for the periplakin tail in intermediate filament association: specific binding to keratin 8 and vimentin.桥粒斑蛋白尾部在中间丝结合中的独特作用:与角蛋白8和波形蛋白的特异性结合。
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J Cell Biol. 1996 Aug;134(3):715-29. doi: 10.1083/jcb.134.3.715.
8
Novel microsatellite markers and single nucleotide polymorphisms refine the tylosis with oesophageal cancer (TOC) minimal region on 17q25 to 42.5 kb: sequencing does not identify the causative gene.新型微卫星标记和单核苷酸多态性将17q25上伴有食管癌的掌跖角化症(TOC)最小区域缩小至42.5 kb:测序未鉴定出致病基因。
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Characterization of a 500 kb region on 17q25 and the exclusion of candidate genes as the familial Tylosis Oesophageal Cancer (TOC) locus.17q25上一个500 kb区域的特征分析以及作为家族性掌跖角化症食管癌(TOC)基因座的候选基因排除。
Oncogene. 2002 Sep 12;21(41):6395-402. doi: 10.1038/sj.onc.1205768.
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Tylosis A with squamous cell carcinoma of the oesophagus in a Spanish family.西班牙一家族中伴发食管鳞状细胞癌的先天性厚皮症。
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