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首页> 外文期刊>Neuropediatrics >Physical map of the region surrounding the ataxia-telangiectasia gene on human chromosome 11q22-23.
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Physical map of the region surrounding the ataxia-telangiectasia gene on human chromosome 11q22-23.

机译:人类染色体11q22-23上共济失调毛细血管扩张基因周围区域的物理图谱。

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摘要

Ataxia telangiectasia (A-T) is an autosomal recessive disease affecting multiple systems, including the development of the cerebellum and thymus. This results in a progressive cerebellar ataxia with onset between 1-3 years, telangiectasia occurs within the subsequent 3-5 years. We localized the A-T gene by linkage analysis to chromosome 11q22-23, between the markers D11S384, and D11S535, and constructed a series of contigs using three BACs and twelve cosmids, spanning a region of approximately 400 kb. We developed a set of sequence-tagged site (STS) markers from the ends of the BACs and cosmids. The A-T gene was isolated from within this region. It is now possible to precisely orient specific BACs, cosmids, and STSs with respect to the exons of the A-T gene (ATM). We anticipate that this information will be useful for further studies of functional domains and regulatory elements within the ATM gene, as well as for other genes in this region. In addition, these clones can be used for FISH studies of deletions, translocations and for loss of heterozygosity in various tumors.
机译:共济失调毛细血管扩张症(A-T)是一种常染色体隐性遗传疾病,影响多个系统,包括小脑和胸腺的发育。这导致进行性小脑共济失调发作在1-3年之间,毛细血管扩张发生在随后的3-5年内。我们通过连锁分析将A-T基因定位到标记D11S384和D11S535之间的染色体11q22-23,并使用三个BAC和十二个粘粒构建了一系列重叠群,覆盖大约400 kb区域。我们从BAC和粘粒的末端开发了一组序列标记位点(STS)标记。从该区域内分离出A-T基因。现在可以相对于A-T基因(ATM)的外显子精确定位特定的BAC,粘粒和STS。我们预计,该信息将有助于进一步研究ATM基因中的功能域和调控元件,以及该区域中的其他基因。另外,这些克隆可用于FISH研究各种肿瘤中的缺失,易位和杂合性丧失。

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