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护士鲨免疫球蛋白重链基因座的体细胞高频突变和连接多样性

Somatic hypermutation and junctional diversification at Ig heavy chain loci in the nurse shark.

作者信息

Malecek Karolina, Brandman Julie, Brodsky Jennie E, Ohta Yuko, Flajnik Martin F, Hsu Ellen

机构信息

Department of Physiology and Pharmacology, State University of New York Health Science Center, Brooklyn, NY 11203, USA.

出版信息

J Immunol. 2005 Dec 15;175(12):8105-15. doi: 10.4049/jimmunol.175.12.8105.

DOI:10.4049/jimmunol.175.12.8105
PMID:16339548
Abstract

We estimate there are approximately 15 IgM H chain loci in the nurse shark genome and have characterized one locus. It consists of one V, two D, and one J germline gene segments, and the constant (C) region can be distinguished from all of the others by a unique combination of restriction endonuclease sites in Cmu2. On the basis of these Cmu2 markers, 22 cDNA clones were selected from an epigonal organ cDNA library from the same individual; their C region sequences proved to be the same up to the polyadenylation site. With the identification of the corresponding germline gene segments, CDR3 from shark H chain rearrangements could be analyzed precisely, for the first time. Considerable diversity was generated by trimming and N addition at the three junctions and by varied recombination patterns of the two D gene segments. The cDNA sequences originated from independent rearrangements events, and most carried both single and contiguous substitutions. The 53 point mutations occurred with a bias for transition changes (53%), whereas the 78 tandem substitutions, mostly 2-4 bp long, do not (36%). The nature of the substitution patterns is the same as for mutants from six loci of two nurse shark L chain isotypes, showing that somatic hypermutation events are very similar at both H and L chain genes in this early vertebrate. The cis-regulatory elements targeting somatic hypermutation must have already existed in the ancestral Ig gene, before H and L chain divergence.

摘要

我们估计护士鲨基因组中大约有15个IgM重链基因座,并对其中一个基因座进行了表征。它由一个V、两个D和一个J种系基因片段组成,恒定(C)区可通过Cmu2中独特的限制性内切酶位点组合与所有其他区区分开来。基于这些Cmu2标记,从同一个体的卵圆器官cDNA文库中选择了22个cDNA克隆;它们的C区序列在多聚腺苷酸化位点之前被证明是相同的。随着相应种系基因片段的鉴定,首次能够精确分析鲨鱼重链重排产生的CDR3。通过在三个连接点处的修剪和N添加以及两个D基因片段的不同重组模式产生了相当大的多样性。cDNA序列源自独立的重排事件,大多数携带单个和连续的替换。53个点突变以转换变化为主(53%),而78个串联替换大多为2-4个碱基对长,并非如此(36%)。替换模式的性质与来自两种护士鲨轻链同种型六个基因座的突变体相同,表明在这种早期脊椎动物中,重链和轻链基因的体细胞超突变事件非常相似。在重链和轻链分化之前,靶向体细胞超突变的顺式调控元件一定已经存在于祖先的Ig基因中。

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