Doty R T, Xia D, Nguyen S P, Hathaway T R, Willerford D M
Departments of Medicine and Immunology, University of Washington, Puget Sound Blood Center, Seattle, WA, USA.
Blood. 1999 May 1;93(9):3017-25.
The hallmark of T- and B-lymphocyte development is the rearrangement of variable (V), diversity (D), and joining (J) segments of T-cell receptor (TCR) and immunoglobulin (Ig) genes to generate a diverse repertoire of antigen receptor specificities in the immune system. The process of V(D)J recombination is shared in the rearrangement of all seven antigen receptor genes and is controlled by changes in chromatin structure, which regulate accessibility to the recombinase apparatus in a lineage- and stage-specific manner. These chromatin changes are linked to transcription of the locus in its unrearranged (germline) configuration. To understand how germline transcription of the TCRbeta-chain gene is regulated, we determined the structure of germline transcripts initiating near the Dbeta1 segment and identified a promoter within this region. The Dbeta1 promoter is active in the presence of the TCRbeta enhancer (Ebeta), and in this context, exhibits preferential activity in pro-T versus mature T-cell lines, as well as T- versus B-lineage specificity. These studies provide insight into the developmental regulation of TCRbeta germline transcription, one of the earliest steps in T-cell differentiation.
T 淋巴细胞和 B 淋巴细胞发育的标志是 T 细胞受体(TCR)和免疫球蛋白(Ig)基因的可变(V)、多样(D)和连接(J)片段发生重排,从而在免疫系统中产生多种多样的抗原受体特异性。V(D)J 重组过程在所有七种抗原受体基因的重排中都存在,并且受染色质结构变化的控制,染色质结构变化以谱系和阶段特异性的方式调节重组酶装置的可及性。这些染色质变化与未重排(种系)构型的基因座转录相关。为了了解 TCRβ链基因的种系转录是如何被调控的,我们确定了在 Dβ1 片段附近起始的种系转录本的结构,并在该区域内鉴定出一个启动子。Dβ1 启动子在 TCRβ增强子(Eβ)存在的情况下具有活性,并在这种情况下,在原 T 细胞系与成熟 T 细胞系中以及 T 细胞系与 B 细胞系中表现出优先活性。这些研究为 TCRβ种系转录的发育调控提供了见解,TCRβ种系转录是 T 细胞分化的最早步骤之一。