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PNAS Plus: Tcra gene recombination is supported by a Tcra enhancer- and CTCF-dependent chromatin hub

机译:PNAS Plus:Tcra基因重组受Tcra增强子和CTCF依赖的染色质中枢支持

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摘要

Antigen receptor locus V(D)J recombination requires interactions between widely separated variable (V), diversity (D), and joining (J) gene segments, but the mechanisms that generate these interactions are not well understood. Here we assessed mechanisms that direct developmental stage-specific long-distance interactions at the Tcra/Tcrd locus. The Tcra/Tcrd locus recombines Tcrd gene segments in CD4CD8 double-negative thymocytes and Tcra gene segments in CD4+CD8+ double-positive thymocytes. Initial Vα-to-Jα recombination occurs within a chromosomal domain that displays a contracted conformation in both thymocyte subsets. We used chromosome conformation capture to demonstrate that the Tcra enhancer (Eα) interacts directly with Vα and Jα gene segments distributed across this domain, specifically in double-positive thymocytes. Moreover, Eα promotes interactions between these Vα and Jα segments that should facilitate their synapsis. We found that the CCCTC-binding factor (CTCF) binds to Eα and to many locus promoters, biases Eα to interact with these promoters, and is required for efficient Vα–Jα recombination. Our data indicate that Eα and CTCF cooperate to create a developmentally regulated chromatin hub that supports Vα–Jα synapsis and recombination.
机译:抗原受体基因座V(D)J重组需要在广泛分离的变量(V),多样性(D)和连接(J)基因片段之间进行相互作用,但产生这些相互作用的机制尚不清楚。在这里,我们评估了在Tcra / Tcrd基因座上指导特定于发育阶段的长距离相互作用的机制。 Tcra / Tcrd基因座重组CD4 - CD8 -双阴性胸腺细胞中的Tcrd基因片段和CD4 + CD8 中的Tcra基因片段+ 双阳性胸腺细胞。最初的Vα至Jα重组发生在两个胸腺细胞亚群均显示收缩构象的染色体结构域内。我们使用染色体构象捕获来证明Tcra增强子(Eα)与分布在该域中的Vα和Jα基因片段直接相互作用,特别是在双阳性胸腺细胞中。此外,Eα促进这些Vα和Jα节之间的相互作用,应促进它们的突触。我们发现CCCTC结合因子(CTCF)与Eα和许多基因座启动子结合,使Eα与这些启动子相互作用,并且是有效Vα–Jα重组所必需的。我们的数据表明,Eα和CTCF共同创建了发育受调节的染色质中心,可支持Vα–Jα突触和重组。

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