Ryu Chun Jeih, Haines Brian B, Draganov Dobrin D, Kang Yun Hee, Whitehurst Charles E, Schmidt Tara, Hong Hyo Jeong, Chen Jianzhu
Center for Cancer Research and Department of Biology, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.
Proc Natl Acad Sci U S A. 2003 Nov 11;100(23):13465-70. doi: 10.1073/pnas.2235807100. Epub 2003 Oct 30.
The precise function of cis elements in regulating V(D)J recombination is still controversial. Here, we determined the effect of inactivation of the TCRbeta enhancer (Ebeta) on cleavage and rearrangement of Dbeta1, Dbeta2, Jbeta1, and Jbeta2 gene segments in CD4-CD8- [double-negative (DN)] and CD4+CD8+ [double-positive (DP)] thymocytes. In Ebeta-deficient mice, (i) Dbeta1 rearrangements were more severely impaired than Dbeta2 rearrangements; (ii) most of the Dbeta and Jbeta cleavages and rearrangements occurred in DP, rather than in DN, thymocytes; and (iii) most of the 3' Dbeta1 cleavages were coupled to 5' Dbeta2 cleavages instead of to Jbeta cleavages, resulting in nonstandard Dbeta1-Dbeta2-Jbeta2 joints. These findings suggest that the Ebeta regulates TCRbeta rearrangement by promoting accessibility of Dbeta and Jbeta gene segments in DN thymocytes and proper pairing between Dbeta1 and Jbeta gene segments for cleavage and joining in DP thymocytes.
顺式元件在调节V(D)J重组中的精确功能仍存在争议。在此,我们确定了TCRβ增强子(Eβ)失活对CD4-CD8-[双阴性(DN)]和CD4+CD8+[双阳性(DP)]胸腺细胞中Dβ1、Dβ2、Jβ1和Jβ2基因片段的切割和重排的影响。在Eβ缺陷小鼠中,(i)Dβ1重排比Dβ2重排受损更严重;(ii)大多数Dβ和Jβ的切割和重排发生在DP胸腺细胞而非DN胸腺细胞中;(iii)大多数3' Dβ1切割与5' Dβ2切割相连,而非与Jβ切割相连,导致非标准的Dβ1-Dβ2-Jβ2连接。这些发现表明,Eβ通过促进DN胸腺细胞中Dβ和Jβ基因片段的可及性以及DP胸腺细胞中Dβ1和Jβ基因片段的正确配对以进行切割和连接来调节TCRβ重排。