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控制B29(Igbeta)启动子的沉默元件既不是启动子特异性的,也不是细胞类型特异性的。

Silencer elements controlling the B29 (Igbeta) promoter are neither promoter- nor cell-type-specific.

作者信息

Malone C S, Omori S A, Wall R

机构信息

Molecular Biology Institute and Department of Microbiology and Immunology, University of California, Los Angeles, School of Medicine, Los Angeles, CA 90095, USA.

出版信息

Proc Natl Acad Sci U S A. 1997 Nov 11;94(23):12314-9. doi: 10.1073/pnas.94.23.12314.

Abstract

The murine B29 (Igbeta) promoter is B cell specific and contains essential SP1, ETS, OCT, and Ikaros motifs. Flanking 5' DNA sequences inhibit B29 promoter activity, suggesting this region contains silencer elements. Two adjacent 5' DNA segments repress transcription by the murine B29 promoter in a position- and orientation-independent manner, analogous to known silencers. Both these 5' segments also inhibit transcription by several heterologous promoters in B cells, including mb-1, c-fos, and human B29. These 5' segments also inhibit transcription by the c-fos promoter in T cells suggesting they are not B cell-specific elements. DNase I footprint analyses show an approximately 70-bp protected region overlapping the boundary between the two negative regulatory DNA segments and corresponding to binding sites for at least two different DNA-binding proteins. Within this footprint, two unrelated 30-bp cis-acting DNA motifs (designated TOAD and FROG) function as position- and orientation-independent silencers when located directly 5' of the murine B29 promoter. These two silencer motifs act cooperatively to restrict the transcriptional activity of the B29 promoter. Neither of these motifs resembles any known silencers. Mutagenesis of the TOAD and FROG motifs in their respective 5' DNA segments eliminates the silencing activity of these upstream regions, indicating these two motifs as the principal B29 silencer elements within these regions.

摘要

小鼠B29(Igbeta)启动子具有B细胞特异性,包含必需的SP1、ETS、OCT和Ikaros基序。5'侧翼DNA序列抑制B29启动子活性,表明该区域含有沉默子元件。两个相邻的5'DNA片段以位置和方向独立的方式抑制小鼠B29启动子的转录,类似于已知的沉默子。这两个5'片段还抑制B细胞中几种异源启动子的转录,包括mb-1、c-fos和人B29。这些5'片段也抑制T细胞中c-fos启动子的转录,表明它们不是B细胞特异性元件。DNase I足迹分析显示一个约70bp的受保护区域,与两个负调控DNA片段之间的边界重叠,对应于至少两种不同DNA结合蛋白的结合位点。在这个足迹内,两个不相关的30bp顺式作用DNA基序(命名为TOAD和FROG),当直接位于小鼠B29启动子的5'端时,作为位置和方向独立的沉默子发挥作用。这两个沉默子基序协同作用以限制B29启动子的转录活性。这些基序均与任何已知的沉默子不同。对其各自5'DNA片段中的TOAD和FROG基序进行诱变消除了这些上游区域的沉默活性,表明这两个基序是这些区域内主要的B29沉默子元件。

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