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MIDA1是一种具有新型DNA结合特性的序列特异性DNA结合蛋白。

MIDA1 is a sequence specific DNA binding protein with novel DNA binding properties.

作者信息

Inoue T, Shoji W, Obinata M

机构信息

Department of Cell Biology, Institute of Development, Ageing and Cancer, Tohoku University, 4-1 Seiryomachi, Aoba-ku, Sendai 980-8575, Japan.

出版信息

Genes Cells. 2000 Sep;5(9):699-709. doi: 10.1046/j.1365-2443.2000.00362.x.

DOI:10.1046/j.1365-2443.2000.00362.x
PMID:10971652
Abstract

BACKGROUND

Id proteins not only regulate cell differentiation negatively, but they also promote growth and apoptosis. To know the mechanism of how Id regulates cell fate, we previously isolated an Id-associating protein, MIDA1, which positively regulates cell growth. Its predicted amino acid sequence contains tryptophan-mediated repeats (Tryp-med repeats) similar to the DNA binding region of the c-Myb oncoprotein. We determined whether MIDA1 can bind to DNA in a sequence specific manner by PCR-assisted binding site selection.

RESULTS

We identified a 7-base sequence (GTCAAGC) surrounded by a 1-3 bp palindromic sequence as the DNA sequence recognized by the Tryp-med repeats of MIDA1. This motif is located within the 5'-flanking sequence of several growth regulating genes. Gel shift assays revealed that this sequence and a certain length of flanking DNA are necessary for MIDA1 to bind DNA in a stable manner. Methylation interference and DNase I footprint analysis suggested that the DNA binding of MIDA1 is resistant to DNA methylation and that MIDA1 does not specifically localize on this particular motif.

CONCLUSIONS

We concluded that MIDA1 is a novel sequence-specific DNA binding protein with some different properties from the usual transcription factors and that MIDA1 may act as a mediator of Id-mediated growth-promoting function through its DNA binding activity.

摘要

背景

Id蛋白不仅对细胞分化起负调控作用,还能促进细胞生长和凋亡。为了解Id蛋白调控细胞命运的机制,我们之前分离出一种与Id相关的蛋白MIDA1,它对细胞生长起正调控作用。其预测的氨基酸序列包含与c-Myb癌蛋白DNA结合区域相似的色氨酸介导重复序列(Tryp-med重复序列)。我们通过PCR辅助结合位点筛选来确定MIDA1是否能以序列特异性方式结合DNA。

结果

我们鉴定出一个7碱基序列(GTCAAGC),其两侧为1 - 3个碱基对的回文序列,作为MIDA1的Tryp-med重复序列识别的DNA序列。该基序位于几个生长调节基因的5'侧翼序列内。凝胶迁移实验表明,该序列及一定长度的侧翼DNA是MIDA1稳定结合DNA所必需的。甲基化干扰和DNase I足迹分析表明,MIDA1的DNA结合对DNA甲基化具有抗性,且MIDA1并非特异性定位于此特定基序。

结论

我们得出结论,MIDA1是一种新型的序列特异性DNA结合蛋白,具有一些与常见转录因子不同的特性,并且MIDA1可能通过其DNA结合活性作为Id介导的生长促进功能的介质。

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