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16号染色体q24.3区域的高分辨率物理图谱和转录图谱构建:散发性乳腺癌中杂合性缺失频繁的一个区域

Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.

作者信息

Whitmore S A, Crawford J, Apostolou S, Eyre H, Baker E, Lower K M, Settasatian C, Goldup S, Seshadri R, Gibson R A, Mathew C G, Cleton-Jansen A M, Savoia A, Pronk J C, Auerbach A D, Doggett N A, Sutherland G R, Callen D F

机构信息

Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital, North Adelaide, South Australia, 5006, Australia.

出版信息

Genomics. 1998 May 15;50(1):1-8. doi: 10.1006/geno.1998.5316.

Abstract

A breast cancer tumor suppressor gene has been localized to chromosome 16q24.3 by loss of heterozygosity (LOH) studies of breast tumor DNA. To identify candidate genes for this suppressor function, we have constructed a detailed physical map extending approximately 940 kb from the telomere of the long arm of chromosome 16 that encompasses the minimum LOH interval. This contig consists of a minimum overlapping set of 35 cosmids and a single PAC clone that were aligned by restriction enzyme site mapping. Cosmids were initially identified by screening filters with markers localized to the region by physical mapping using mouse/human somatic cell hybrids, and subsequently cosmid ends were used to complete the contig. A total of seven known genes, including PRSM1, PISSLRE, and the recently cloned Fanconi anemia A (FAA) gene, and potential transcripts from exon-trapping experiments have been located to this contig. A minimum of 14 new transcripts have been identified based on homology of trapped exons with database sequences. This contig and expressed sequence map will form the basis for the identification of the breast cancer tumor suppressor gene in this region.

摘要

通过对乳腺肿瘤DNA进行杂合性缺失(LOH)研究,已将一种乳腺癌肿瘤抑制基因定位于染色体16q24.3。为了鉴定具有这种抑制功能的候选基因,我们构建了一个详细的物理图谱,该图谱从16号染色体长臂的端粒延伸约940 kb,涵盖了最小的LOH区间。这个重叠群由35个黏粒和一个单一的P1人工染色体(PAC)克隆组成,它们通过限制性酶切位点图谱进行排列。黏粒最初是通过用使用小鼠/人类体细胞杂种进行物理图谱定位到该区域的标记筛选滤膜来鉴定的,随后用黏粒末端来完成重叠群的构建。共有7个已知基因,包括PRSM1、PISSLRE和最近克隆的范可尼贫血A(FAA)基因,以及外显子捕获实验中的潜在转录本已定位到这个重叠群。基于捕获的外显子与数据库序列的同源性,已鉴定出至少14个新的转录本。这个重叠群和表达序列图谱将为鉴定该区域的乳腺癌肿瘤抑制基因奠定基础。

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