Suppr超能文献

多发性外生骨疣基因家族第三个成员EXTL基因的鉴定与定位。

Identification and localization of the gene for EXTL, a third member of the multiple exostoses gene family.

作者信息

Wise C A, Clines G A, Massa H, Trask B J, Lovett M

机构信息

Department of Otorhinolaryngology, Molecular Biology, and Oncology, University of Texas Southwestern Medical Center at Dallas 75235-8591, USA.

出版信息

Genome Res. 1997 Jan;7(1):10-6. doi: 10.1101/gr.7.1.10.

Abstract

Hereditary multiple exostoses (EXT) is an autosomal dominant disorder characterized by multiple bony outgrowths from the juxtaepiphyseal region of long bones. In a small proportion of cases, these exostoses progress to malignant chondrosarcomas. Genetic linkage of this disorder has been described to three independent loci on chromosomes 8q24.1 (EXT1), 11p11-13 (EXT2), and 19p (EXT-3). The EXT1 and EXT2 genes were isolated recently and show extensive sequence homology to each other. These genes are deleted in exostoses-derived tumors, supporting the hypothesis that they encode tumor suppressors. We have identified a third gene that shows striking sequence similarity to both EXT1 and EXT2 at the nucleotide and amino acid sequence levels, and have derived its entire coding sequence. Although the mRNA transcribed from this gene is similar in size to that from EXT1 and EXT2, its pattern of expression is quite different. We have localized this gene by fluorescence in situ hybridization to metaphase chromosomes and by whole genome radiation hybrid mapping to chromosome 1p36.1 between DIS458 and DIS511, region that frequently shows loss of heterozygosity in a variety of tumor types. This gene, EXTL (for EXT-like), is therefore a new member of the EXT gene family and is a potential candidate for several disease phenotypes.

摘要

遗传性多发性骨软骨瘤(EXT)是一种常染色体显性疾病,其特征是长骨的近骨骺区域出现多个骨质增生。在一小部分病例中,这些骨软骨瘤会发展为恶性软骨肉瘤。该疾病的基因连锁已被描述定位于8号染色体q24.1(EXT1)、11号染色体p11 - 13(EXT2)和19号染色体p(EXT - 3)上的三个独立位点。EXT1和EXT2基因最近已被分离出来,并且彼此显示出广泛的序列同源性。这些基因在骨软骨瘤衍生的肿瘤中缺失,支持了它们编码肿瘤抑制因子的假说。我们已经鉴定出第三个基因,该基因在核苷酸和氨基酸序列水平上与EXT1和EXT2都具有显著的序列相似性,并推导得到了其完整的编码序列。尽管从该基因转录的mRNA大小与EXT1和EXT2的相似,但其表达模式却大不相同。我们通过荧光原位杂交将该基因定位到中期染色体上,并通过全基因组辐射杂种图谱定位到1号染色体p36.1上DIS458和DIS511之间的区域,该区域在多种肿瘤类型中经常显示杂合性缺失。因此,这个基因EXTL(类EXT)是EXT基因家族的一个新成员,并且是几种疾病表型的潜在候选基因。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验