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阿非科林诱导的FRA3B断点聚集在两个不同区域。

Aphidicolin-induced FRA3B breakpoints cluster in two distinct regions.

作者信息

Wang L, Paradee W, Mullins C, Shridhar R, Rosati R, Wilke C M, Glover T W, Smith D I

机构信息

Department of Laboratory Medicine and Pathology, Mayo Foundation, Rochester, Minnesota 55905, USA.

出版信息

Genomics. 1997 May 1;41(3):485-8. doi: 10.1006/geno.1997.4690.

Abstract

The common fragile site at chromosomal band 3p14.2 (FRA3B) is the most sensitive single site in the human genome to induced chromosomal lesions. This fragile site may predispose chromosome 3p to breakage that is commonly observed in lung, renal, and many other cancers. We previously used aphidicolin induction of FRA3B expression in a chromosome 3-only somatic cell hybrid to generate a series of hybrids with breakpoints in the 3p14.2 region. These breakpoints were localized to two distinct clusters, separated by 200 kb, that lie on either side of a region of frequent breakage within FRA3B as observed by FISH analysis. Seven proximal aphidicolin-induced breakpoints were localized at or near the end of a THE element. The THE-1 element is flanked by LINE and Alu repetitive elements. The eight distal aphidicolin-induced breakpoints clustered in a region capable of forming multiple hairpin-like structures. Thus repetitive elements and hairpin-like structures may be responsible for chromosome fragility in this region.

摘要

位于染色体3p14.2带的常见脆性位点(FRA3B)是人类基因组中对诱导染色体损伤最敏感的单一位点。该脆性位点可能使3号染色体p臂易于发生断裂,这种断裂在肺癌、肾癌和许多其他癌症中很常见。我们之前在仅含3号染色体的体细胞杂种中使用阿非科林诱导FRA3B表达,以生成一系列在3p14.2区域具有断点的杂种。通过荧光原位杂交(FISH)分析观察到,这些断点定位于两个不同的簇,相隔200 kb,位于FRA3B内频繁断裂区域的两侧。七个近端阿非科林诱导的断点位于一个THE元件末端或其附近。THE-1元件两侧是LINE和Alu重复元件。八个远端阿非科林诱导的断点聚集在一个能够形成多个发夹样结构的区域。因此,重复元件和发夹样结构可能是该区域染色体脆性的原因。

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