Lange Miles D, Waldbieser Geoffrey C, Lobb Craig J
Department of Microbiology, University of Mississippi Medical Center, Jackson, MS 39216, USA.
J Immunol. 2009 May 1;182(9):5605-22. doi: 10.4049/jimmunol.0801013.
H chain cDNA libraries were constructed from the RNA derived from seven different organs and tissues from the same individual catfish. Sequence analysis of >300 randomly selected clones identified clonal set members within the same or different tissues, and some of these represented mosaic or hybrid sequences. These hybrids expressed V(H) members of the same or different V(H) families within different regions of the same clone. Within some clonal sets multiple hybrids were identified, and some of these represented the products of sequential V(H) replacement events. Different experimental methods confirmed that hybrid clones identified in the cDNA library from one tissue could be reisolated in the cDNA pool or from the total RNA derived from the same or a different tissue, indicating that these hybrids likely represented the products of in vivo receptor revision events. Murine statistical recombination models were used to evaluate cryptic recombination signal sequences (cRSS), and significant cRSS pairs in the predicted V(H) donor and recipient were identified. These models supported the hypothesis that seamless revisions may have occurred via hybrid joint formation. The heptamers of the cRSS pairs were located at different locations within the coding region, and different events resulted in the replacement of one or both CDR as well as events that replaced the upstream untranslated region and the leader region. These studies provide phylogenetic evidence that receptor revision may occur in clonally expanded B cell lineages, which supports the hypothesis that additional levels of somatic H chain diversification may exist.
从同一条鲶鱼的七种不同器官和组织提取的RNA构建了重链cDNA文库。对300多个随机挑选的克隆进行序列分析,确定了同一组织或不同组织内的克隆集成员,其中一些代表嵌合或杂交序列。这些杂交体在同一克隆的不同区域表达相同或不同V(H)家族的V(H)成员。在一些克隆集中鉴定出多个杂交体,其中一些代表连续V(H)替换事件的产物。不同的实验方法证实,在一个组织的cDNA文库中鉴定出的杂交克隆可以在cDNA文库或来自相同或不同组织的总RNA中重新分离出来,这表明这些杂交体可能代表体内受体编辑事件的产物。使用小鼠统计重组模型评估隐蔽重组信号序列(cRSS),并在预测的V(H)供体和受体中鉴定出显著的cRSS对。这些模型支持无缝编辑可能通过杂交接头形成发生的假设。cRSS对的七聚体位于编码区内的不同位置,不同的事件导致一个或两个互补决定区(CDR)的替换,以及替换上游非翻译区和前导区的事件。这些研究提供了系统发育证据,表明受体编辑可能发生在克隆扩增的B细胞谱系中,这支持了可能存在额外水平的体细胞重链多样化的假设。