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核苷酸库失衡和腺苷脱氨酶缺乏会在V(D)J重组过程中诱导N区插入的改变。

Nucleotide pool imbalance and adenosine deaminase deficiency induce alterations of N-region insertions during V(D)J recombination.

作者信息

Gangi-Peterson L, Sorscher D H, Reynolds J W, Kepler T B, Mitchell B S

机构信息

Curriculum in Genetics and Molecular Biology, Department of Pharmacology, University of North Carolina-Chapel Hill, North Carolina 27599, USA.

出版信息

J Clin Invest. 1999 Mar;103(6):833-41. doi: 10.1172/JCI4320.

Abstract

Template-independent nucleotide additions (N regions) generated at sites of V(D)J recombination by terminal deoxynucleotidyl transferase (TdT) increase the diversity of antigen receptors. Two inborn errors of purine metabolism, deficiencies of adenosine deaminase (ADA) and purine nucleoside phosphorylase (PNP), result in defective lymphoid development and aberrant pools of 2'-deoxynucleotides that are substrates for TdT in lymphoid precursors. We have asked whether selective increases in dATP or dGTP pools result in altered N regions in an extrachromosomal substrate transfected into T-cell or pre-B-cell lines. Exposure of the transfected cells to 2'-deoxyadenosine and an ADA inhibitor increased the dATP pool and resulted in a marked increase in A-T insertions at recombination junctions, with an overall decreased frequency of V(D)J recombination. Sequence analysis of VH-DH-JH junctions from the IgM locus in B-cell lines from ADA-deficient patients demonstrated an increase in A-T insertions equivalent to that found in the transfected cells. In contrast, elevation of dGTP pools, as would occur in PNP deficiency, did not alter the already rich G-C content of N regions. We conclude that the frequency of V(D)J recombination and the composition of N-insertions are influenced by increases in dATP levels, potentially leading to alterations in antigen receptors and aberrant lymphoid development. Alterations in N-region insertions may contribute to the B-cell dysfunction associated with ADA deficiency.

摘要

由末端脱氧核苷酸转移酶(TdT)在V(D)J重组位点产生的不依赖模板的核苷酸添加(N区)增加了抗原受体的多样性。嘌呤代谢的两种先天性缺陷,即腺苷脱氨酶(ADA)和嘌呤核苷磷酸化酶(PNP)缺乏,导致淋巴细胞发育缺陷以及2'-脱氧核苷酸池异常,而这些2'-脱氧核苷酸是淋巴细胞前体中TdT的底物。我们研究了dATP或dGTP池的选择性增加是否会导致转染到T细胞或前B细胞系的染色体外底物中N区发生改变。将转染细胞暴露于2'-脱氧腺苷和一种ADA抑制剂会增加dATP池,并导致重组连接处A-T插入显著增加,同时V(D)J重组频率总体下降。对ADA缺陷患者B细胞系中IgM基因座的VH-DH-JH连接处进行序列分析,结果显示A-T插入增加,与在转染细胞中发现的情况相当。相比之下,PNP缺乏时会出现的dGTP池升高,并未改变N区本就丰富的G-C含量。我们得出结论,V(D)J重组频率和N插入的组成受dATP水平增加的影响,这可能导致抗原受体改变和淋巴细胞发育异常。N区插入的改变可能导致与ADA缺乏相关的B细胞功能障碍。

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