The transcriptional regulator Yin Yang 1 activates the myelin PLP gene

被引:29
作者
Berndt, JA
Kim, JG
Tosic, M
Kim, C
Hudson, LD
机构
[1] NINDS, Lab Dev Neurogenet, NIH, Bethesda, MD 20892 USA
[2] Genet Therapy Inc, Gaithersburg, MD USA
[3] CHU Vaudois, Psychiat Neurosci Ctr, CH-1011 Lausanne, Switzerland
关键词
differentiation; myelination; nuclear matrix; oligodendrocyte; proteolipid protein; target genes;
D O I
10.1046/j.1471-4159.2001.00307.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Inauguration of the myelin program in developing oligodendrocytes requires the activation of those genes that encode the myelin proteins and the enzymes responsible for the synthesis and degradation of myelin lipids. An activator of the most abundantly expressed myelin protein, proteolipid protein (PLP), has been identified in a yeast one-hybrid system. The ubiquitously expressed zinc finger protein Yin Yang 1 (YY1) recognizes the myelin PLP promoter in vitro and in vivo. When overexpressed in an oligodendrocyte cell line, YY1 enhances transcription of the PLP promoter. A truncated version of YY1 that includes only the four zinc finger domains has little effect. The binding site for YY1 in the PLP promoter (site 3) fits the YY1 consensus site and DNA-protein complexes containing site 3 can be supershifted with an antibody directed against YY1 protein. Moreover, oligonucleotides with a mutated version of the PLP promoter site 3 are unable to bind to nuclear proteins or to compete for binding in a gel shift system. Finally, mutation of this site greatly reduces the activity of a I-kb PLP promoter region in transfected glial cells. Our results suggest that PLP is a target gene for the transcriptional regulator YY1. This versatile transcription factor and nuclear matrix protein may boost transcription of the PLP gene to meet the demands of actively myelinating oligodendrocytes.
引用
收藏
页码:935 / 942
页数:8
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