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T细胞受体α和δ增强子对T细胞受体α/δ基因重排的时间和谱系特异性控制。

Temporal and lineage-specific control of T cell receptor alpha/delta gene rearrangement by T cell receptor alpha and delta enhancers.

作者信息

Lauzurica P, Krangel M S

机构信息

Department of Immunology, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

J Exp Med. 1994 Jun 1;179(6):1913-21. doi: 10.1084/jem.179.6.1913.

Abstract

To analyze the regulation of gene rearrangement at the T cell receptor (TCR) alpha/delta locus during T cell development, we generated transgenic mice carrying a human TCR delta gene minilocus. We previously showed that the presence of the TCR delta enhancer (E delta) within the J delta 3-C delta intron was required to activate a specific step (V-D to J) of transgene rearrangement, and that rearrangement was activated equivalently in the precursors of alpha beta and gamma delta T cells. To further explore the role of transcriptional enhancers in establishing the developmental pattern of gene rearrangement at the TCR alpha/delta locus, we substituted the TCR alpha enhancer (E alpha) in place of E delta within the transgenic minilocus. We found that V-D-J rearrangement of the E alpha+ minilocus was restricted to the alpha beta T cell subset. Further, we found that although V-D-J rearrangement of the E delta+ minilocus was initiated in the fetal thymus by day 14.5, V-D-J rearrangement of the E alpha+ minilocus did not occur until fetal day 16.5. Finally, whereas V-D-J rearrangement of the E delta+ minilocus is essentially completed within the triple negative population of postnatal thymocytes, V-D-J rearrangement of the E alpha+ minilocus is only initiated late within this population. Since the properties of minilocus rearrangement under the control of E delta and E alpha parallel the properties of V delta-D delta-J delta and V alpha-J alpha rearrangement at the endogenous TCR alpha/delta locus, we conclude that these enhancers play an important role in orchestrating the developmental program of rearrangements at this locus.

摘要

为了分析T细胞发育过程中T细胞受体(TCR)α/δ基因座处基因重排的调控机制,我们构建了携带人TCR δ基因微基因座的转基因小鼠。我们先前表明,Jδ3 - Cδ内含子中的TCR δ增强子(Eδ)的存在是激活转基因重排特定步骤(V - D至J)所必需的,并且在αβ和γδ T细胞的前体细胞中重排被同等激活。为了进一步探究转录增强子在建立TCR α/δ基因座处基因重排发育模式中的作用,我们在转基因微基因座中用TCR α增强子(Eα)替代了Eδ。我们发现Eα +微基因座的V - D - J重排仅限于αβ T细胞亚群。此外,我们发现虽然Eδ +微基因座的V - D - J重排在胚胎第14.5天的胎儿胸腺中就开始了,但Eα +微基因座的V - D - J重排直到胚胎第16.5天才发生。最后,Eδ +微基因座的V - D - J重排在出生后胸腺细胞的三阴性群体中基本完成,而Eα +微基因座的V - D - J重排在该群体中仅在后期才开始。由于在Eδ和Eα控制下的微基因座重排特性与内源性TCR α/δ基因座处的Vδ - Dδ - Jδ和Vα - Jα重排特性相似,我们得出结论,这些增强子在协调该基因座处重排的发育程序中起重要作用。

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