Schroeder H W, Hillson J L, Perlmutter R M
Howard Hughes Medical Institute, University of Washington, Seattle 98195.
Int Immunol. 1990;2(1):41-50. doi: 10.1093/intimm/2.1.41.
Antibodies are encoded by a limited number of germline gene segments that undergo somatic diversification through rearrangement and mutation. Because these mutation processes are efficient, it is widely believed that there is little environmental selection pressure for the maintenance of specific antibody gene sequences. We have performed pairwise comparisons of known germline (as opposed to somatically generated) antibody VH elements with the hope of identifying conserved structural features common to sets of VH gene segments. These studies reveal that VH families arose prior to the mammalian radiation and have since been conserved, that this conservation appears to reflect selection at the level of protein sequence, and that the conserved regions are discretely localized on a solvent-exposed face of the heavy chain, at some distance from the antibody combining site. A family-specific region was also identified within the recombinase recognition sequences. Our results provide a context for theories that address the physiological significance of variations in VH family utilization during the development of the immune repertoire.
抗体由数量有限的种系基因片段编码,这些基因片段通过重排和突变进行体细胞多样化。由于这些突变过程效率很高,人们普遍认为,维持特定抗体基因序列几乎没有环境选择压力。我们对已知的种系(而非体细胞产生的)抗体VH元件进行了成对比较,希望识别出VH基因片段集合共有的保守结构特征。这些研究表明,VH家族在哺乳动物辐射之前就已出现,此后一直保守,这种保守似乎反映了蛋白质序列水平的选择,并且保守区域离散地定位在重链的溶剂暴露面上,距抗体结合位点有一定距离。在重组酶识别序列中也鉴定出一个家族特异性区域。我们的结果为探讨免疫库发育过程中VH家族利用差异的生理学意义的理论提供了背景。