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CTCF转录因子的分子量异常:CTCF在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)中迁移异常,且所表达蛋白质的大小受CTCF基因编码区内非翻译区(UTRs)和序列的影响。

Molecular weight abnormalities of the CTCF transcription factor: CTCF migrates aberrantly in SDS-PAGE and the size of the expressed protein is affected by the UTRs and sequences within the coding region of the CTCF gene.

作者信息

Klenova E M, Nicolas R H, U S, Carne A F, Lee R E, Lobanenkov V V, Goodwin G H

机构信息

Genetics Unit, Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, UK.

出版信息

Nucleic Acids Res. 1997 Feb 1;25(3):466-74. doi: 10.1093/nar/25.3.466.

Abstract

CTCF belongs to the Zn finger transcription factors family and binds to the promoter region of c-myc. CTCF is highly conserved between species, ubiquitous and localised in nuclei. The endogenous CTCF migrates as a 130 kDa (CTCF-130) protein on SDS-PAGE, however, the open reading frame (ORF) of the CTCF cDNA encodes only a 82 kDa protein (CTCF-82). In the present study we investigate this phenomenon and show with mass-spectra analysis that this occurs due to aberrant mobility of the CTCF protein. Another paradox is that our original cDNA, composed of the ORF and 3'-untranslated region (3'-UTR), produces a protein with the apparent molecular weight of 70 kDa (CTCF-70). This paradox has been found to be an effect of the UTRs and sequences within the coding region of the CTCF gene resulting in C-terminal truncation of CTCF-130. The potential attenuator has been identified and point-mutated. This restored the electrophoretic mobility of the CTCF protein to 130 kDa. CTCF-70, the aberrantly migrating CTCF N-terminus per se, is also detected in some cell types and therefore may have some biological implications. In particular, CTCF-70 interferes with CTCF-130 normal function, enhancing transactivation induced by CTCF-130 in COS6 cells. The mechanism of CTCF-70 action and other possible functions of CTCF-70 are discussed.

摘要

CTCF属于锌指转录因子家族,可与c-myc的启动子区域结合。CTCF在物种间高度保守,广泛存在且定位于细胞核中。内源性CTCF在SDS-PAGE上以130 kDa(CTCF-130)蛋白形式迁移,然而,CTCF cDNA的开放阅读框(ORF)仅编码一个82 kDa的蛋白(CTCF-82)。在本研究中,我们对这一现象进行了研究,并通过质谱分析表明,这是由于CTCF蛋白的异常迁移所致。另一个矛盾之处在于,我们最初由ORF和3'非翻译区(3'-UTR)组成的cDNA产生了一种表观分子量为70 kDa的蛋白(CTCF-70)。已发现这一矛盾是CTCF基因编码区内的UTR和序列导致CTCF-130 C末端截短的结果。已鉴定出潜在的衰减子并进行了点突变。这使CTCF蛋白的电泳迁移率恢复到130 kDa。CTCF-70,即异常迁移的CTCF N末端本身,也在某些细胞类型中被检测到,因此可能具有一些生物学意义。特别是,CTCF-70会干扰CTCF-130的正常功能,增强CTCF-130在COS6细胞中诱导的反式激活作用。本文讨论了CTCF-70的作用机制以及CTCF-70的其他可能功能。

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