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与结肠肿瘤细胞系中过表达相关的c-myb转录衰减子区域的微卫星缺失。

Microsatellite deletions in the c-myb transcriptional attenuator region associated with over-expression in colon tumour cell lines.

作者信息

Thompson M A, Flegg R, Westin E H, Ramsay R G

机构信息

Ludwig Institute for Cancer Research, PO Royal Melbourne Hospital, Australia.

出版信息

Oncogene. 1997 Apr 10;14(14):1715-23. doi: 10.1038/sj.onc.1201007.

Abstract

In the hemopoietic system c-myb expression is required for proliferation of immature cells and its down-regulation is required for differentiation. In colonic mucosa c-myb expression occurs at levels comparable to immature hemopoietic cells. Inhibition of c-myb expression in colon cell lines, using anti-sense oligonucleotides, indicates that c-myb expression is required for proliferation. However, the mechanism of c-myb regulation during colon cell differentiation has not been explored. Using the LIM1215 and CaCo-2 colon carcinoma cell lines induced to differentiate with sodium butyrate, we demonstrate that c-myb mRNA is down-regulated as an early event in differentiation by a mechanism involving transcriptional attenuation in intron 1. By analogy with procaryotic and eucaryotic genes, transcriptional attenuation probably occurs in a region containing nineteen consecutive thymidine residues. Computer prediction of the secondary structure of the nascent mRNA chain encoded by this region suggests a strong potential for stem-loop formation. Sequence analysis of several colon tumour cell lines reveals mutations in this region that may disrupt transcriptional attenuation and result in the increased c-myb expression observed in colon tumours and tumour cell lines.

摘要

在造血系统中,未成熟细胞的增殖需要c-myb表达,而细胞分化则需要其表达下调。在结肠黏膜中,c-myb的表达水平与未成熟造血细胞相当。使用反义寡核苷酸抑制结肠癌细胞系中的c-myb表达,表明细胞增殖需要c-myb表达。然而,尚未探索结肠细胞分化过程中c-myb的调控机制。利用丁酸钠诱导分化的LIM1215和CaCo-2结肠癌细胞系,我们证明c-myb mRNA作为分化的早期事件被下调,其机制涉及内含子1中的转录衰减。与原核和真核基因类似,转录衰减可能发生在一个含有19个连续胸腺嘧啶残基的区域。对该区域编码的新生mRNA链二级结构的计算机预测表明,其具有很强的形成茎环结构的潜力。对几种结肠肿瘤细胞系的序列分析揭示了该区域的突变,这些突变可能破坏转录衰减,并导致在结肠肿瘤和肿瘤细胞系中观察到的c-myb表达增加。

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