首页> 美国卫生研究院文献>Nucleic Acids Research >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.
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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.

机译:CTCF转录因子的分子量异常:CTCF在SDS-PAGE中异常迁移表达的蛋白质大小受CTCF基因编码区内的UTR和序列影响。

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摘要

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.
机译:CTCF属于Zn指转录因子家族,并与c-myc的启动子区域结合。 CTCF在物种之间高度保守,无处不在且位于细胞核中。内源性CTCF在SDS-PAGE上以130 kDa(CTCF-130)蛋白质的形式迁移,但是CTCF cDNA的开放阅读框(ORF)仅编码82 kDa的蛋白质(CTCF-82)。在本研究中,我们调查了这种现象,并通过质谱分析表明,这种现象是由于CTCF蛋白的异常迁移而发生的。另一个矛盾是我们的原始cDNA由ORF和3'-非翻译区(3'-UTR)组成,产生的蛋白质的表观分子量为70 kDa(CTCF-70)。已经发现这种悖论是CTCF基因编码区内的UTR和序列的作用,导致CTCF-130的C端截短。电位衰减器已被识别并点突变。这将CTCF蛋白的电泳迁移率恢复到130 kDa。 CTCF-70,本身是异常迁移的CTCF N末端,在某些细胞类型中也被检测到,因此可能具有某些生物学意义。特别地,CTCF-70干扰CTCF-130的正常功能,增强了CTCF-130在COS6细胞中诱导的反式激活。讨论了CTCF-70的作用机理和CTCF-70的其他可能功能。

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