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人类T细胞受体β链基因复合体的异常组织与重组热点相关。

Unusual organization of the human T-cell receptor beta-chain gene complex is linked to recombination hotspots.

作者信息

Seboun E, Houghton L, Hatem C J, Lincoln R, Hauser S L

机构信息

Neurogenetic Unit, Généthon, Evry, France.

出版信息

Proc Natl Acad Sci U S A. 1993 Jun 1;90(11):5026-9. doi: 10.1073/pnas.90.11.5026.

Abstract

Two rare Sfi I polymorphisms of 360 kb and 280 kb present within the human T-cell antigen receptor beta-chain gene complex were revealed by pulsed-field gel electrophoresis. They represent allelic variants of the polymorphic 330- and 300-kb Sfi I fragments previously described. The 360-kb polymorphism results from duplication of the 30-kb DNA fragment responsible for the 330/300-kb insertion/deletion-related polymorphism. The 280-kb polymorphism results from a 20-kb deletion from the 300-kb SfiI allele. The rare polymorphisms also map on either side of a Sal I site located near a recombination hotspot, suggesting that germline duplications and deletions arose from nonhomologous crossover events.

摘要

通过脉冲场凝胶电泳揭示了人类T细胞抗原受体β链基因复合体内存在的两种罕见的Sfi I多态性,大小分别为360 kb和280 kb。它们代表了先前描述的多态性330 kb和300 kb Sfi I片段的等位基因变体。360 kb的多态性是由负责330/300 kb插入/缺失相关多态性的30 kb DNA片段重复所致。280 kb的多态性是由300 kb SfiI等位基因发生20 kb缺失所致。这些罕见的多态性也定位在位于重组热点附近的Sal I位点两侧,这表明种系重复和缺失是由非同源交叉事件引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/83dc/46646/612ce65474c5/pnas01463-0273-a.jpg

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