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
相关论文
共 35 条
  • [31] Over-expression of c-Abl in CLL cells is associated with advanced disease, and contributes to CLL-cell survival through activation of NF-kB
    Lin, K
    Harris, RJ
    Dennett, S
    Cawley, JC
    Zuzel, M
    Slupsky, JR
    BLOOD, 2005, 106 (11) : 348A - 348A
  • [32] Abnormal B-cell activation associated with TALL-1 over-expression and SOCS-1 suppression during chronic hepatitis C virus infection
    Moorman, Jonathan
    Dong, Zhi P.
    Ni, Lei
    Zhang, Chunlan
    Borthwick, Thomas
    Yao, Zhi Q.
    IMMUNOLOGY, 2009, 128 (02) : 227 - 235
  • [33] SUPPRESSION OF HEMATOPOIETIC SUPPORT FUNCTION IS ASSOCIATED WITH OVER-EXPRESSION OF IL-4 AND TGF-BETA-1 IN LP-BM5 MULV INFECTED STROMAL CELL-LINES
    GALLICCHIO, VS
    TSE, KF
    MORROW, JK
    HUGHES, NK
    EXPERIMENTAL HEMATOLOGY, 1995, 23 (08) : 770 - 770
  • [34] SUPPRESSION OF HEMATOPOIETIC SUPPORT FUNCTION IS ASSOCIATED WITH OVER-EXPRESSION OF IL-4 AND TFG-BETA-1 IN LP-BM5 MULV INFECTED STROMAL CELL-LINES
    TSE, KF
    MORROW, JK
    HUGHES, NK
    GALLICCHIO, VS
    BLOOD, 1994, 84 (10) : A702 - A702
  • [35] Methylglyoxal suppresses human colon cancer cell lines and tumor growth in a mouse model by impairing glycolytic metabolism of cancer cells associated with down-regulation of c-Myc expression
    He, Tiantian
    Zhou, Huaibin
    Li, Chunmei
    Chen, Yuan
    Chen, Xiaowan
    Li, Chenli
    Mao, Jiating
    Lyu, Jianxin
    Meng, Qing H.
    CANCER BIOLOGY & THERAPY, 2016, 17 (09) : 955 - 965