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主要组织相容性复合体II类DRA启动子功能需要X和Y元件的立体特异性排列。

Stereospecific alignment of the X and Y elements is required for major histocompatibility complex class II DRA promoter function.

作者信息

Vilen B J, Cogswell J P, Ting J P

机构信息

Lineberger Cancer Research Center, Chapel Hill, North Carolina.

出版信息

Mol Cell Biol. 1991 May;11(5):2406-15. doi: 10.1128/mcb.11.5.2406-2415.1991.

Abstract

The regulatory mechanisms controlling expression of the major histocompatibility complex (MHC) class II genes involve several cis-acting DNA elements, including the X and Y boxes. These two elements are conserved within all murine and human class II genes and are required for accurate and efficient transcription from MHC class II promoters. Interestingly, the distance between the X and Y elements is also evolutionarily conserved at 18 to 20 bp. To investigate the function of the invariant spacing in the human MHC class II gene, HLA-DRA, we constructed a series of spacing mutants which alters the distance between the X and Y elements by integral and half-integral turns of the DNA helix. Transient transfection of the spacing constructs into Raji cells revealed that inserting integral turns of the DNA helix (+20 and +10 bp) did not reduce promoter activity, while inserting or deleting half-integral turns of the DNA helix (+15, +5, and -5 bp) drastically reduced promoter activity. The loss of promoter function in these half-integral turn constructs was due neither to the inability of the X and Y elements to bind proteins nor to improper binding of the X- and Y-box-binding proteins. These data indicate that the X and Y elements must be aligned on the same side of the DNA helix to ensure normal function. This requirement for stereospecific alignment strongly suggests that the X- and Y-box-binding proteins either interact directly or are components of a larger transcription complex which assembles on one face of the DNA double helix.

摘要

控制主要组织相容性复合体(MHC)II类基因表达的调控机制涉及多个顺式作用DNA元件,包括X盒和Y盒。这两个元件在所有小鼠和人类II类基因中都是保守的,并且是MHC II类启动子进行准确高效转录所必需的。有趣的是,X元件和Y元件之间的距离在进化上也保守在18至20个碱基对。为了研究人类MHC II类基因HLA - DRA中恒定间距的功能,我们构建了一系列间距突变体,这些突变体通过DNA螺旋的整数圈和半整数圈改变X元件和Y元件之间的距离。将间距构建体瞬时转染到Raji细胞中发现,插入DNA螺旋的整数圈(+20和+10个碱基对)不会降低启动子活性,而插入或删除DNA螺旋的半整数圈(+15、+5和 - 5个碱基对)则会大幅降低启动子活性。这些半整数圈构建体中启动子功能的丧失既不是由于X元件和Y元件无法结合蛋白质,也不是由于X盒和Y盒结合蛋白的结合不当。这些数据表明,X元件和Y元件必须排列在DNA螺旋的同一侧以确保正常功能。这种对立体特异性排列的要求强烈表明,X盒和Y盒结合蛋白要么直接相互作用,要么是在DNA双螺旋的一个面上组装的更大转录复合体的组成部分。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41fc/359998/59f35e18ecd9/molcellb00139-0085-a.jpg

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