Wilson P, Liu Y J, Banchereau J, Capra J D, Pascual V
Oklahoma Medical Research Foundation, Oklahoma City, USA.
Immunol Rev. 1998 Apr;162:143-51. doi: 10.1111/j.1600-065x.1998.tb01437.x.
The sequence analysis of Ig variable region genes transcribed within different B-cell subpopulations from human tonsil led us to identify a rare DNA sequence modification event consisting of bp insertions and/or deletions (I/D). Although these events were previously reported, they had never been formally associated with the somatic hypermutation process. I/D events share with more conventional somatic hypermutation events their localization within hypervariable regions and, most particularly, within DNA motifs known to be mutational hot spots. Repetitive DNA tracts or DNA elements capable of forming DNA loop intermediates seem to be the preferred substrate for I/D to occur. These characteristics suggest a model for somatic hypermutation reminiscent of the "polymerase slippage" model involved in replication and repair mutations in prokaryotes, yeast, and mammals.
对来自人扁桃体的不同B细胞亚群中转录的Ig可变区基因进行序列分析,使我们鉴定出一种罕见的DNA序列修饰事件,该事件由碱基对插入和/或缺失(I/D)组成。尽管这些事件先前已有报道,但它们从未与体细胞超突变过程正式关联。I/D事件与更常见的体细胞超突变事件一样,都定位于高变区内,尤其是定位于已知为突变热点的DNA基序内。能够形成DNA环中间体的重复DNA片段或DNA元件似乎是I/D发生的首选底物。这些特征提示了一种体细胞超突变模型,类似于原核生物、酵母和哺乳动物中参与复制和修复突变的“聚合酶滑动”模型。