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干扰素-γ对HLA II类基因的诱导作用是转录水平的,且需要一种反式作用蛋白。

Induction of HLA class II genes by IFN-gamma is transcriptional and requires a trans-acting protein.

作者信息

Amaldi I, Reith W, Berte C, Mach B

机构信息

Department of Microbiology, University of Geneva Medical School, Switzerland.

出版信息

J Immunol. 1989 Feb 1;142(3):999-1004.

PMID:2492334
Abstract

HLA class II Ag are encoded by a family of related genes clustered in the HLA-D region of the MHC. The expression of this multi-gene family is highly regulated and this regulation is essential for the control of the immune response. Class II gene expression is constitutive in a limited number of cell types and can be induced by IFN-gamma in a number of class II negative cells. In this study, we have clarified two essential aspects of the regulation of HLA class II genes by IFN-gamma. 1) The induction mechanism operates at the level of transcription and there is a long lag phase in the signal transduction process. 2) The induction of class II genes requires the de novo synthesis of a new protein(s). On this basis, we propose that IFN-gamma regulates the transcription of HLA class II genes via the de novo synthesis of a trans-acting activator protein.

摘要

HLA II类抗原由一组聚集在MHC的HLA - D区域的相关基因编码。这个多基因家族的表达受到高度调控,且这种调控对于免疫反应的控制至关重要。II类基因在有限数量的细胞类型中组成性表达,并且可在许多II类阴性细胞中被γ干扰素诱导表达。在本研究中,我们阐明了γ干扰素对HLA II类基因调控的两个重要方面。1)诱导机制在转录水平起作用,并且在信号转导过程中有一个较长的延迟期。2)II类基因的诱导需要新合成一种新的蛋白质。在此基础上,我们提出γ干扰素通过反式作用激活蛋白的从头合成来调节HLA II类基因的转录。

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