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人类1型T细胞白血病病毒Tax蛋白下调人类未成熟胸腺细胞中前T细胞受体α基因的转录。

Human T-cell leukemia virus type 1 Tax protein down-regulates pre-T-cell receptor alpha gene transcription in human immature thymocytes.

作者信息

Wencker Mélanie, Sausse Céline, Derse David, Gazzolo Louis, Duc Dodon Madeleine

机构信息

Virologie Humaine U758, Ecole Normale Supérieure de Lyon, 46 allée d'Italie, 69364 Lyon Cedex 07, France.

出版信息

J Virol. 2007 Jan;81(1):301-8. doi: 10.1128/JVI.00766-06. Epub 2006 Oct 18.

Abstract

The human pre-T-cell receptor alpha (TCRalpha; pTalpha) gene encodes a polypeptide which associates with the TCRbeta chain and CD3 molecules to form the pre-TCR complex. The surface expression of the pre-TCR is pTalpha dependent, and signaling through this complex triggers an early alphabeta T-cell developmental checkpoint inside the thymus, known as beta-selection. E2A transcription factors, which are involved at multiple stages of T-cell development, regulate the transcription of the pTalpha gene. Here we show that the regulatory protein Tax of the human T-cell leukemia virus type 1 (HTLV-1) efficiently suppresses the E47-mediated activation of the pTalpha promoter. Furthermore, we report that in Tax lentivirally transduced human MOLT-4 T cells, which constitutively express the pTalpha gene, the amount of pTalpha transcripts decreases. Such a decrease is not observed in MOLT-4 cells transduced by a vector encoding the Tax mutant K88A, which is unable to interact with p300. These data underline that Tax inhibits pTalpha transcription by recruiting this coactivator. Finally, we show that the expression of Tax in human immature thymocytes results in a decrease of pTalpha gene transcription but does not modify the level of E47 transcripts. These observations indicate that Tax, by silencing E proteins, down-regulates pTalpha gene transcription during early thymocyte development. They further provide evidence that Tax can interfere with an important checkpoint during T-cell differentiation in the thymus.

摘要

人类前T细胞受体α(TCRα;pTα)基因编码一种多肽,该多肽与TCRβ链和CD3分子结合形成前TCR复合物。前TCR的表面表达依赖于pTα,通过该复合物发出的信号触发胸腺内一个早期的αβ T细胞发育检查点,即β选择。参与T细胞发育多个阶段的E2A转录因子调节pTα基因的转录。在此,我们表明人类1型T细胞白血病病毒(HTLV-1)的调节蛋白Tax能有效抑制E47介导的pTα启动子激活。此外,我们报道在慢病毒转导Tax的人类MOLT-4 T细胞中,这些细胞组成性表达pTα基因,pTα转录本的量减少。在由编码无法与p300相互作用的Tax突变体K88A的载体转导的MOLT-4细胞中未观察到这种减少。这些数据强调Tax通过招募这种共激活因子抑制pTα转录。最后,我们表明Tax在人类未成熟胸腺细胞中的表达导致pTα基因转录减少,但不改变E47转录本的水平。这些观察结果表明,Tax通过沉默E蛋白,在早期胸腺细胞发育过程中下调pTα基因转录。它们进一步证明Tax可干扰胸腺中T细胞分化过程中的一个重要检查点。

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