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22q11和11q23上的基因组不稳定区域作为复发性染色体核型t(11;22)的病因。

Regions of genomic instability on 22q11 and 11q23 as the etiology for the recurrent constitutional t(11;22).

作者信息

Kurahashi H, Shaikh T H, Hu P, Roe B A, Emanuel B S, Budarf M L

机构信息

Division of Human Genetics and Molecular Biology, The Children's Hospital of Philadelphia, PA 19104, USA.

出版信息

Hum Mol Genet. 2000 Jul 1;9(11):1665-70. doi: 10.1093/hmg/9.11.1665.

Abstract

The constitutional t(11;22)(q23;q11) is the only known recurrent, non-Robertsonian translocation. To analyze the genomic structure of the breakpoint, we have cloned the junction fragments from the der(11) and der(22) of a t(11;22) balanced carrier. On chromosome 11 the translocation occurs within a short, palindromic AT-rich region (ATRR). Likewise, the breakpoint on chromosome 22 has been localized within an ATRR that is part of a larger palindrome. Interestingly, the 22q11 breakpoint falls within one of the 'unclonable' gaps in the genomic sequence. Further, a sequenced chromosome 11 BAC clone, spanning the t(11;22) breakpoint in 11q23, is deleted within the palindromic ATRR, suggesting instability of this region in bacterial clones. Several unrelated t(11;22) families demonstrate similar breakpoints on both chromosomes, indicating that their translocations are within the same palindrome. It is likely that the palindromic ATRRs produce unstable DNA structures in 22q11 and 11q23 that are responsible for the recurrent t(11;22) translocation.

摘要

染色体结构异常t(11;22)(q23;q11)是唯一已知的常见非罗伯逊易位。为分析断点处的基因组结构,我们从一名t(11;22)平衡携带者的11号衍生染色体(der(11))和22号衍生染色体(der(22))中克隆了连接片段。在11号染色体上,易位发生在一个短的富含AT的回文区域(ATRR)内。同样,22号染色体上的断点也定位在一个更大回文结构一部分的ATRR内。有趣的是,22q11断点位于基因组序列中“不可克隆”的间隙之一内。此外,一个跨越11q23处t(11;22)断点的已测序11号染色体BAC克隆在回文ATRR内缺失,这表明该区域在细菌克隆中不稳定。几个不相关的t(11;22)家系在两条染色体上都显示出相似的断点,表明它们的易位发生在同一个回文结构内。很可能回文ATRR在22q11和11q23中产生不稳定的DNA结构,这是导致反复出现t(11;22)易位的原因。

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