Gellert M, McBlane J F
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Philos Trans R Soc Lond B Biol Sci. 1995 Jan 30;347(1319):43-7. doi: 10.1098/rstb.1995.0007.
The mechanism of lymphoid-specific gene rearrangement (V(D)J recombination) is discussed, with a focus on the existence of broken DNA intermediates. Older evidence in support of this idea includes the sequence alteration at the recombined junctions and the presence of aberrant recombinants. More recently, broken DNA molecules have been directly detected in recombinationally active cells. The signal sequence ends have normal blunt-ended DNA breaks, but the coding ends have a hairpin (self-joined) structure that provides an explanation for the self-complementary P nucleotide insertions often found after V(D)J joining in the antigen receptor genes.
本文讨论了淋巴细胞特异性基因重排(V(D)J重组)的机制,重点关注断裂DNA中间体的存在。支持这一观点的早期证据包括重组连接处的序列改变和异常重组体的存在。最近,在具有重组活性的细胞中直接检测到了断裂的DNA分子。信号序列末端具有正常的平端DNA断裂,但编码末端具有发夹(自我连接)结构,这为抗原受体基因V(D)J连接后经常发现的自我互补P核苷酸插入提供了解释。