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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
来源:
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.
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页码:1715 / 1723
页数:9
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