Varade W S, Marin E, Kittelberger A M, Insel R A
Department of Pediatrics and Microbiology, University of Rochester School of Medicine and Dentistry, NY 14642.
J Immunol. 1993 Jun 1;150(11):4985-95.
VH6, the most 3' human H chain V region gene, is preferentially expressed in the preimmune repertoire of the developing human fetus. To determine whether VH6 contributes to the immune repertoire, we amplified and sequenced from human spleen RNA VH6 rearrangements that were isotype-switched to IgG. Eighteen distinct in-frame VH6 clones were sequenced. Definitive assignment to C gamma 1 could be made in the majority of clones, and all had undergone extensive somatic hypermutation in the V region with an average of 14 (range, 2 to 25) mutations/281 bp in the VH6 segment. The overall frequency of somatic mutation was 5.2% of the total nucleotides sequenced. Replacement somatic mutations were targeted to the complementarity determining region, and the complementarity determining region had higher replacement to silent mutation ratios, consistent with antigenic selection. Silent somatic mutations were also significantly more frequent in the complementarity determining region compared to the framework region. Five clones were derived from the same VH6Dxp'1JH6 rearrangement, each containing unique and shared mutations. All DH segments used by independently arising clones were unique, and all DH reading frames were seen. N segments were lacking at either the 5'DH-JH junction or the 3'DH-JH junction in 7 of 13 independent rearrangements. DH-DH recombinations were frequently observed, and there was biased usage of JH3b and JH4b in the clones. The data imply that a high degree of diversity arises from use of this 3'-VH gene in the immune repertoire.
VH6是人类重链V区基因中最靠3'端的基因,在发育中的人类胎儿的免疫前库中优先表达。为了确定VH6是否对免疫库有贡献,我们从人脾脏RNA中扩增并测序了已同种型转换为IgG的VH6重排。对18个不同的读框内VH6克隆进行了测序。大多数克隆可明确指定为Cγ1,并且所有克隆在V区都经历了广泛的体细胞超突变,VH6片段中平均每281 bp有14个(范围为2至25个)突变。体细胞突变的总体频率为测序总核苷酸的5.2%。置换性体细胞突变靶向互补决定区,互补决定区的置换与沉默突变比率更高,这与抗原选择一致。与框架区相比,互补决定区的沉默体细胞突变也明显更频繁。5个克隆源自相同的VH6Dxp'1JH6重排,每个克隆都包含独特和共享的突变。独立出现的克隆所使用的所有DH片段都是独特的,并且观察到了所有DH读框。在13个独立重排中的7个中,5'DH-JH或3'DH-JH连接处缺少N片段。经常观察到DH-DH重组,并且在克隆中JH3b和JH4b存在偏向性使用。这些数据表明,在免疫库中使用这个3'-VH基因会产生高度的多样性。