Zhu C, Roth D B
Department of Microbiology and Immunology, Baylor College of Medicine, Houston, Texas 77030, USA.
Immunity. 1995 Jan;2(1):101-12. doi: 10.1016/1074-7613(95)90082-9.
We previously identified possible intermediates in V(D)J recombination at the TCR delta locus and characterized molecules with signal ends and with covalently sealed (hairpin) coding ends in thymocytes of scid mice by Southern blotting. Here, we use a sensitive ligation-mediated PCR assay to demonstrate that all coding ends detected in scid thymocytes are covalently sealed. Neither coding nor signal ends exhibit loss or addition of nucleotides. These data imply that hairpin formation is coupled to the initial cleavage at the signal/coding border, and that the cleavage step in V(D)J recombination is conservative. In scid/+ or wild-type thymocytes, hairpin coding ends are at least 1000-fold less abundant than signal ends. These results provide insight into the mechanism of V(D)J recombination.
我们之前在TCRδ基因座的V(D)J重组中鉴定出可能的中间体,并通过Southern印迹法对严重联合免疫缺陷(scid)小鼠胸腺细胞中具有信号末端和共价封闭(发夹)编码末端的分子进行了表征。在此,我们使用一种灵敏的连接介导PCR检测方法来证明在scid胸腺细胞中检测到的所有编码末端都是共价封闭的。编码末端和信号末端均未出现核苷酸的丢失或添加。这些数据表明发夹形成与信号/编码边界处的初始切割相关联,并且V(D)J重组中的切割步骤是保守的。在scid/+或野生型胸腺细胞中,发夹编码末端的丰度比信号末端至少低1000倍。这些结果为V(D)J重组机制提供了深入了解。