Wang Clifford L, Wabl Matthias
Department of Microbiology and Immunology, University of California, San Francisco, CA 94143, USA.
J Immunol. 2005 May 1;174(9):5650-4. doi: 10.4049/jimmunol.174.9.5650.
It is generally believed that in cells undergoing Ig somatic hypermutation, more cell divisions result in more mutations. This is because DNA synthesis and replication is thought to play roles in the known mechanisms-cytidine deamination and subsequent conversion to thymidine, uracil-DNA glycosylase-mediated repair, mismatch repair, and DNA synthesis by error-prone polymerases. In this study, we manipulated the number of cell generations by varying the rate at which cultures of a mouse cell line were replenished with fresh medium. We found that the frequency of mutants does not necessarily increase with the number of cell generations. On the contrary, a greater number of divisions can lead to a lower frequency of mutants, indicating that cell division is not a rate-limiting step in the hypermutation process. Thus, when comparing mutation rates, we suggest that rates are more appropriately expressed as mutations per day than per cell generation.
一般认为,在经历免疫球蛋白体细胞超突变的细胞中,更多的细胞分裂会导致更多的突变。这是因为DNA合成和复制被认为在已知机制中发挥作用——胞嘧啶脱氨以及随后转化为胸腺嘧啶、尿嘧啶-DNA糖基化酶介导的修复、错配修复以及易错聚合酶进行的DNA合成。在本研究中,我们通过改变向小鼠细胞系培养物补充新鲜培养基的速率来操纵细胞世代数。我们发现,突变体的频率并不一定随着细胞世代数的增加而增加。相反,更多的分裂可能导致突变体频率降低,这表明细胞分裂不是超突变过程中的限速步骤。因此,在比较突变率时,我们建议将速率更恰当地表示为每天的突变数而非每细胞世代的突变数。