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

被引:53
|
作者
Thompson, MA
Flegg, R
Westin, EH
Ramsay, RG
机构
[1] PETER MACCALLUM CANC INST,MELBOURNE,VIC 3002,AUSTRALIA
[2] ROYAL MELBOURNE HOSP,LUDWIG INST CANC RES,PARKVILLE,VIC 3050,AUSTRALIA
[3] VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT MED,RICHMOND,VA 23298
关键词
c-myb; transcriptional attenuation; colon tumour cells; NONPOLYPOSIS COLORECTAL-CANCER; MESSENGER-RNA; MULTIPLE MECHANISMS; REPLICATION ERRORS; SUPPRESSOR PROTEIN; ADENOMATOUS POLYPS; SODIUM-BUTYRATE; GENE; DIFFERENTIATION; ELONGATION;
D O I
10.1038/sj.onc.1201007
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
In the hemopoietic system c-myb expression is required for proliferation of immature cells and its downregulation 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.
引用
收藏
页码:1715 / 1723
页数:9
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