Lautner-Rieske A, Huber C, Meindl A, Pargent W, Schäble K F, Thiebe R, Zocher I, Zachau H G
Institut für Physiologische Chemie, Universität München, FRG.
Eur J Immunol. 1992 Apr;22(4):1023-9. doi: 10.1002/eji.1830220422.
The central regions of the kappa locus, the so-called A regions, have been fully characterized on cosmid and phage lambda clones. The regions, which are parts of the C kappa-proximal and -distal copies of the locus and are, therefore, called Ap and Ad regions, comprise about 140 kb each and contain together 30 V kappa genes and pseudogenes. The A regions have been linked on their 5' sides to the O regions and on their 3' sides to the L regions. Chromosomal walking has eliminated a previous gap in the Ap region. Detailed restriction maps of the Ap and Ad regions and the sequences of 9 V kappa genes are reported. Four events, which have occurred in evolution probably after the duplication of the A region, were identified: the insertion of an Alu element in Ad; the insertion of part of a LINE element in Ap; the deletion of a 17.5-kb fragment including one V kappa gene from Ap; the sequence divergence of duplicated V kappa gene regions which ranges among the five pairs studied here from 0 to 14 bp per kb and converted two genes to pseudogenes while their duplicates stayed functional. An analysis of the A regions of the lymphoid cell lines RPMI 6140 and GM607 confirmed the previous finding that the V kappa-J kappa rearrangement in these cell lines had occurred by deletion and inversion mechanisms, respectively. Thus, the structural data contribute to the understanding of the evolution and the functioning of the A regions of the kappa locus.
κ轻链基因座的中央区域,即所谓的A区域,已在黏粒和λ噬菌体克隆上得到了充分的表征。这些区域是该基因座近端和远端Cκ拷贝的一部分,因此分别称为Ap和Ad区域,每个区域约140 kb,共包含30个Vκ基因和假基因。A区域在其5'侧与O区域相连,在其3'侧与L区域相连。染色体步移消除了Ap区域先前存在的一个缺口。报告了Ap和Ad区域的详细限制性图谱以及9个Vκ基因的序列。确定了四个可能在A区域复制后发生的进化事件:一个Alu元件插入Ad区域;一部分LINE元件插入Ap区域;从Ap区域缺失一个包括一个Vκ基因的17.5 kb片段;重复的Vκ基因区域的序列分歧,在所研究的五对基因中,每千碱基的分歧范围为0至14 bp,导致两个基因转变为假基因,而它们的重复基因仍保持功能。对淋巴细胞系RPMI 6140和GM607的A区域分析证实了先前的发现,即这些细胞系中的Vκ-Jκ重排分别通过缺失和倒位机制发生。因此,这些结构数据有助于理解κ轻链基因座A区域的进化和功能。