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一种抑制小鼠髓鞘碱性蛋白基因转录的序列特异性单链DNA结合蛋白的鉴定。

Identification of a sequence-specific single-stranded DNA binding protein that suppresses transcription of the mouse myelin basic protein gene.

作者信息

Haas S, Steplewski A, Siracusa L D, Amini S, Khalili K

机构信息

Jefferson Institute of Molecular Medicine, Department of Biochemistry and Molecular Biology, Thomas-Jefferson University, Philadelphia, Pennsylvania 19107, USA.

出版信息

J Biol Chem. 1995 May 26;270(21):12503-10. doi: 10.1074/jbc.270.21.12503.

Abstract

The myelin basic protein (MBP) gene is expressed only in oligodendrocytes and Schwann cells, and expression follows a tightly regulated developmental time course. Cell type- and developmental stage-specific expression of the MBP gene appears to be regulated by a series of cis-acting elements located upstream of the transcription start site. The proximal element of the MBP regulatory region (MB1), located between nucleotides -14 and -50, is one of several elements participating in the programmed expression of MBP. In this report, we describe the molecular cloning and characterization of myelin gene expression factor-2 (Myef-2), a protein isolated from mouse brain that binds specifically to single-stranded DNA derived from the MB1 element and represses transcription of the MBP gene in transient transfection assay. Myef-2 mRNA is developmentally regulated in mouse brain; its peak expression occurs at postnatal day 7, prior to the onset of MBP expression. The developmental pattern of Myef-2 mRNA expression coincides with that previously described for SCIP, a POU domain transcription factor that also represses myelin basic protein expression. The myef-2 gene maps to mouse chromosome 2. The relevance of these findings for regulation of MBP gene expression and oligodendrocyte differentiation is discussed.

摘要

髓鞘碱性蛋白(MBP)基因仅在少突胶质细胞和施万细胞中表达,且其表达遵循严格调控的发育时间进程。MBP基因的细胞类型和发育阶段特异性表达似乎受位于转录起始位点上游的一系列顺式作用元件调控。MBP调控区的近端元件(MB1)位于核苷酸-14至-50之间,是参与MBP程序性表达的几个元件之一。在本报告中,我们描述了髓鞘基因表达因子2(Myef-2)的分子克隆和特性,Myef-2是一种从小鼠脑部分离的蛋白质,它能特异性结合源自MB1元件的单链DNA,并在瞬时转染实验中抑制MBP基因的转录。Myef-2 mRNA在小鼠脑中受发育调控;其表达峰值出现在出生后第7天,早于MBP表达开始的时间。Myef-2 mRNA表达的发育模式与先前描述的SCIP一致,SCIP是一种POU结构域转录因子,也能抑制髓鞘碱性蛋白的表达。myef-2基因定位于小鼠2号染色体。文中讨论了这些发现与MBP基因表达调控和少突胶质细胞分化的相关性。

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