Kiefer Kerstin, Oshinsky Jennifer, Kim Jiyoon, Nakajima Pamela B, Bosma Gayle C, Bosma Melvin J
Institute for Cancer Research, Fox Chase Cancer Center, 333 Cottman Avenue, Philadelphia, PA 19111, USA.
Proc Natl Acad Sci U S A. 2007 Feb 20;104(8):2843-8. doi: 10.1073/pnas.0611359104. Epub 2007 Feb 12.
The joining of DNA ends during Ig class-switch recombination (CSR) is thought to involve the same nonhomologous end-joining pathway as used in V(D)J recombination. However, we reported earlier that CSR can readily occur in Ig transgenic SCID mice lacking DNA-dependent protein kinase (DNA-PK) activity, a critical enzymatic activity for V(D)J recombination. We were thus led to question whether the catalytic subunit of DNA-PK (DNA-PKcs) is essential for CSR. To address this issue, we asked whether class switching to different Ig isotypes could occur in a line of Ig transgenic mice lacking detectable DNA-PKcs protein. The answer was affirmative. We conclude that joining of DNA ends during CSR does not require DNA-PKcs and can occur by an alternative repair pathway to that used for V(D)J recombination.
免疫球蛋白类别转换重组(CSR)过程中DNA末端的连接被认为涉及与V(D)J重组相同的非同源末端连接途径。然而,我们之前报道过,CSR能够在缺乏DNA依赖性蛋白激酶(DNA-PK)活性的免疫球蛋白转基因SCID小鼠中轻易发生,而DNA-PK活性是V(D)J重组的关键酶活性。因此,我们开始质疑DNA-PK的催化亚基(DNA-PKcs)对于CSR是否必不可少。为了解决这个问题,我们探究了在一系列缺乏可检测到的DNA-PKcs蛋白的免疫球蛋白转基因小鼠中,是否能够发生向不同免疫球蛋白同种型的类别转换。答案是肯定的。我们得出结论,CSR过程中DNA末端的连接不需要DNA-PKcs,并且可以通过一种不同于V(D)J重组所用的替代修复途径发生。