Analysis of the transcription regulator, CNOT7, as a candidate chromosome 8 tumor suppressor gene in colorectal cancer

被引:12
作者
Flanagan, J
Healey, S
Young, J
Whitehall, V
Chenevix-Trench, G
机构
[1] Univ Queensland, Royal Brisbane Hosp, Queensland Inst Med Res, Herston, Qld 4029, Australia
[2] Univ Queensland, Royal Brisbane Hosp, Dept Pathol, Herston, Qld 4029, Australia
关键词
CNOT7; denaturing high-performance liquid chromatography; (DHPLC); 8p22; loss of heterozygosity (LOH); colorectal cancer; somatic mutation;
D O I
10.1002/ijc.11264
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Loss of heterozygosity (LOH) on the short arm of chromosome 8 occurs at high frequencies in many tumor types, including colorectal carcinoma. We have previously used microcell-mediated chromosome transfer (MMCT) to map an approximately 7.7 Mb colorectal cancer suppressor region (CRCSR) at 8p22-23. I. We have now taken a candidate gene approach to identify the putative tumor suppressor gene located within the CRCSR. CNOT7 encodes a subunit of the CCR4-Not transcription complex and is located at 8p22. We showed that CNOT7 is expressed in normal colonic mucosa and in colonic crypt cells, as well as in colorectal cell lines and primary tumors. We assembled a panel of 88 primary colorectal tumors comprising 20 MSI-high (high microsatellite instability), 19 MSI-low and 49 MSS (microsatellite stable) tumors for mutation analysis of the CNOT7 gene. Denaturing high-performance liquid chromatography (DHPLC) analysis of the entire coding region of the CNOT7 gene revealed only one somatic missense mutation in an MSS tumor. The rarity of somatic mutations in CNOT7, and its expression in primary colorectal tumors and cell lines, suggests that CNOT7 is not the target tumor suppressor gene in the 8p22-23.1 CRCSR. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:505 / 509
页数:5
相关论文
共 48 条
[1]   Isolation and characterization of human orthologs of yeast CCR4-NOT complex subunits [J].
Albert, TK ;
Lemaire, M ;
van Berkum, NL ;
Gentz, R ;
Collart, MA ;
Timmers, HTM .
NUCLEIC ACIDS RESEARCH, 2000, 28 (03) :809-817
[2]  
Badarinarayana V, 2000, GENETICS, V155, P1045
[3]   Human carbon catabolite repressor protein (CCR4)-associative factor 1: cloning, expression and characterization of its interaction with the B-cell translocation protein BTG1 [J].
Bogdan, JA ;
Adams-Burton, C ;
Pedicord, DL ;
Sukovich, DA ;
Benfield, PA ;
Corjay, MH ;
Stoltenborg, JK ;
Dicker, IB .
BIOCHEMICAL JOURNAL, 1998, 336 :471-481
[4]  
Boland CR, 1998, CANCER RES, V58, P5248
[5]   Functional identification of LZTS1 as a candidate prostate tumor suppressor gene on human chromosome 8p22 [J].
Cabeza-Arvelaiz, Y ;
Sepulveda, JL ;
Lebovitz, RM ;
Thompson, TC ;
Chinault, AC .
ONCOGENE, 2001, 20 (31) :4169-4179
[6]   Listening to silence and understanding nonsense: Exonic mutations that affect splicing [J].
Cartegni, L ;
Chew, SL ;
Krainer, AR .
NATURE REVIEWS GENETICS, 2002, 3 (04) :285-298
[7]   Predictive identification of exonic splicing enhancers in human genes [J].
Fairbrother, WG ;
Yeh, RF ;
Sharp, PA ;
Burge, CB .
SCIENCE, 2002, 297 (5583) :1007-1013
[8]  
Farrington SM, 1996, ONCOGENE, V12, P1803
[9]   The murine gene p27Kip1 is haplo-insufficient for tumour suppression [J].
Fero, ML ;
Randel, E ;
Gurley, KE ;
Roberts, JM ;
Kemp, CJ .
NATURE, 1998, 396 (6707) :177-180
[10]   The human POP2 gene:: Identification, sequencing, and mapping to the critical region of the 5q- syndrome [J].
Fidler, C ;
Wainscoat, JS ;
Boultwood, J .
GENOMICS, 1999, 56 (01) :134-136