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慢性淋巴细胞白血病中重排的Vκ基因片段分布在Vκ基因座的大部分区域,且未显示体细胞突变。

V kappa gene segments rearranged in chronic lymphocytic leukemia are distributed over a large portion of the V kappa locus and do not show somatic mutation.

作者信息

Wagner S D, Luzzatto L

机构信息

Department of Haematology, Royal Postgraduate Medical School, Hammersmith Hospital, London, GB.

出版信息

Eur J Immunol. 1993 Feb;23(2):391-7. doi: 10.1002/eji.1830230214.

Abstract

The structure of the human V kappa locus has been thoroughly investigated, but how the germ-line V kappa gene segment repertoire is actually sampled in kappa chain gene rearrangements is not known. In order to begin to answer this question we have polymerase chain reaction (PCR) amplified the rearranged V kappa genes from 26 kappa-expressing cases of chronic lymphocytic leukemia (CLL), followed by cloning and sequencing of the PCR product. All four V kappa gene families were represented amongst rearranged genes. In 25 out of 32 cases, the sequence of the rearranged gene matches perfectly that of 1 of 11 different known germ-line V kappa genes, indicating that no somatic mutation has occurred. Of the remaining 7 rearranged V kappa genes, 4 differ from known germ-line genes by only one or two amino acid residues; and 3 differ from each other and from all known sequences by 5 or more residues, suggesting that somatic mutation has occurred in these 3 cases. We conclude that: (a) in at least three-quarters of cases the rearranged genes are unmutated; (b) there is preferential usage of individual V kappa genes but not of V kappa gene families; and (c) the V kappa genes used are widely dispersed in the V kappa locus.

摘要

人类Vκ基因座的结构已得到深入研究,但在κ链基因重排过程中,生殖系Vκ基因片段库实际上是如何被取样的尚不清楚。为了开始回答这个问题,我们利用聚合酶链反应(PCR)从26例表达κ链的慢性淋巴细胞白血病(CLL)病例中扩增出重排的Vκ基因,随后对PCR产物进行克隆和测序。所有四个Vκ基因家族在重排基因中均有代表。在32例病例中的25例中,重排基因的序列与11种不同已知生殖系Vκ基因中的1种完全匹配,这表明未发生体细胞突变。在其余7个重排的Vκ基因中,4个与已知生殖系基因仅相差一两个氨基酸残基;3个彼此之间以及与所有已知序列相差5个或更多残基,这表明在这3例病例中发生了体细胞突变。我们得出以下结论:(a)至少四分之三的病例中,重排基因未发生突变;(b)存在对单个Vκ基因而非Vκ基因家族的优先使用;(c)所使用的Vκ基因在Vκ基因座中广泛分布。

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