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L1CAM和ABCD1(肾上腺脑白质营养不良,ALD)基因中五个重排的断点序列特征分析

Characterization of breakpoint sequences of five rearrangements in L1CAM and ABCD1 (ALD) genes.

作者信息

Kutsche Kerstin, Ressler Bernadette, Katzera Heide-Gertrude, Orth Ulrike, Gillessen-Kaesbach Gabriele, Morlot Susanne, Schwinger Eberhard, Gal Andreas

机构信息

Institut für Humangenetik, Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Hum Mutat. 2002 May;19(5):526-35. doi: 10.1002/humu.10072.

Abstract

Mutations in L1CAM are responsible for X-linked hydrocephalus, whereas those in the ALD gene (ABCD1) cause adrenoleukodystrophy. In both genes, most of the mutations reported so far are short-length mutations and only a few patients with larger rearrangements have been documented. We have characterized three intragenic deletions of the ALD gene at the molecular level and describe here the first two L1CAM rearrangements resulting in deletion of several exons in one case and about 50 kb, including the entire gene, in the second case. At both breakpoints of an ALD deletion, Alu repeats have been found and, additionally, a short Alu region of approximately 130 bp was inserted, suggesting that this rearrangement is the result of a more complex non-allelic homologous recombination event. Only one Alu element was present at the breakpoint of the second ALD rearrangement, including a 26-bp Alu core sequence that was suggested to be a recombinogenic hot spot. These data suggest the involvement of an Alu core sequence-stimulated non-homologous recombination as a possible cause for this rearrangement. Short direct repeats were identified at all putative mispaired sequences in the L1CAM breakpoints and at both breakpoints of the third ALD deletion characterized, suggesting non-homologous (illegitimate) recombination as the molecular mechanism by which these latter deletions occurred. In conclusion, our results indicate that highly repetitive elements as well as short direct repeats are frequently involved in the formation of ALD and L1CAM gene rearrangements.

摘要

L1CAM基因的突变导致X连锁脑积水,而ALD基因(ABCD1)的突变则引起肾上腺脑白质营养不良。在这两个基因中,迄今为止报道的大多数突变都是短长度突变,仅有少数具有较大重排的患者被记录在案。我们在分子水平上对ALD基因的三个基因内缺失进行了特征分析,并在此描述了首例L1CAM重排,其中一例导致几个外显子缺失,另一例导致约50 kb(包括整个基因)缺失。在ALD缺失的两个断点处均发现了Alu重复序列,此外还插入了一个约130 bp的短Alu区域,这表明这种重排是更复杂的非等位基因同源重组事件的结果。在第二次ALD重排的断点处仅存在一个Alu元件,其中包括一个26 bp的Alu核心序列,该序列被认为是一个重组热点。这些数据表明,Alu核心序列刺激的非同源重组可能是这种重排的原因。在L1CAM断点处以及所分析的第三次ALD缺失的两个断点处的所有假定错配序列中均鉴定出短直接重复序列,这表明非同源(非法)重组是后一种缺失发生的分子机制。总之,我们的结果表明,高度重复元件以及短直接重复序列经常参与ALD和L1CAM基因重排的形成。

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