Characterization of a novel human cell-cycle-regulated homologue of Drosophila dlg1

被引:33
作者
Bassal, S
Nomura, N
Venter, D
Brand, K
McKay, MJ
van der Spek, PJ
机构
[1] Janssen Pharmaceut, B-2340 Beerse, Belgium
[2] Peter MacCallum Canc Inst, Div Radiat Oncol, Melbourne, Vic 8006, Australia
[3] Peter MacCallum Canc Inst, Div Res, Melbourne, Vic 8006, Australia
[4] Kazusa DNA Res Inst, Chiba 2920812, Japan
[5] Peter MacCallum Canc Inst, Trescowthick Res Labs, Victorian Breast Canc Res Consortium, Mol Pathol Lab, Melbourne, Vic 8006, Australia
[6] Peter MacCallum Canc Inst, Trescowthick Res Labs, Early Detect Lab, Melbourne, Vic 8006, Australia
关键词
D O I
10.1006/geno.2001.6570
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Cell cycle defects have been associated with the process of carcinogenesis in many studies. Here we report the cloning and analysis of the novel gene KIAA0008 (GenBank acc. no. D13633). Chromosomal localization experiments assigned the gene to chromosome 14q22-q23. The mRNA transcript was found to be cell cycle regulated, expressed at S-phase, and maintained at both G2- and M-phases. In sit-it hybridization showed expression in proliferating colon and breast (tumor) tissues. Structurally, KIAA0008 shares homology with the Drosophila melanogaster discs large-1 (dlg1) tumor suppressor gene and membrane-associated guanylate kinase protein family members. The potential involvement of KIAA0008 in cell proliferation is discussed, along with its sequence identity and tissue distribution.
引用
收藏
页码:5 / 7
页数:3
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