Parng C L, Hansal S, Goldsby R A, Osborne B A
Department of Veterinary and Animal Sciences, University of Massachusetts, Amherst 01003, USA.
J Immunol. 1996 Dec 15;157(12):5478-86.
In humans and mice, extensive gene rearrangement is the major mechanism of diversification of the primary Ig repertoire. This study shows that cattle depart from this pattern because rearrangement in the light chain locus is sharply limited. Furthermore, in cattle, gene conversion contributes to the diversification of the primary light chain repertoire. Sequencing of germ-line and expressed Vlambda genes revealed three important features. First, the germ line contained a number of Vlambda pseudogenes. In fact, 14 (70%) of the 20 germ-line genes identified and sequenced were pseudogenes, because they had one or more of the following defects: lack of recombination signal sequences at the 3' end, stop codons within the reading frame or truncations, and/or insertions or deletions that resulted in loss of reading frame. Second, Vlambda cDNA from ileal Peyer's patch B cells demonstrated that the light chain repertoire arises from only a small number of V(J) rearrangements. Even though two J genes were identified in the germ line, all of the expressed Vlambda genes examined contained the same J segment, indicating that only a single J gene participates in rearrangement at the lambda locus. Third, a significant number of departures from the germ-line sequences of rearranged Vlambda can be traced to donor sequences of one or more Vlambda pseudogenes. We conclude that a limited number of rearrangements and gene conversion play a role in contributing to the diversification of the primary lambda repertoire. Furthermore, while clear indications of a role for somatic mutation in lambda diversification was seen, V gene rearrangement was not a major factor.
在人类和小鼠中,广泛的基因重排是初级免疫球蛋白库多样化的主要机制。本研究表明,牛背离了这种模式,因为轻链基因座中的重排受到严格限制。此外,在牛中,基因转换有助于初级轻链库的多样化。种系和表达的Vλ基因测序揭示了三个重要特征。首先,种系包含一些Vλ假基因。事实上,在鉴定和测序的20个种系基因中,有14个(70%)是假基因,因为它们有以下一个或多个缺陷:3'端缺乏重组信号序列、阅读框内的终止密码子或截短,和/或导致阅读框丢失的插入或缺失。其次,来自回肠派尔集合淋巴结B细胞的Vλ cDNA表明,轻链库仅源于少数V(J)重排。尽管在种系中鉴定出两个J基因,但所有检测的表达Vλ基因都包含相同的J片段,这表明只有一个J基因参与λ基因座的重排。第三,重排的Vλ与种系序列的大量差异可追溯到一个或多个Vλ假基因的供体序列。我们得出结论,有限数量的重排和基因转换在促进初级λ库的多样化中起作用。此外,虽然在λ多样化中看到了体细胞突变作用的明确迹象,但V基因重排不是主要因素。