Mapping of the gene encoding the integrin-linked kinase, ILK, to human chromosome 11p15.5-p15.4

被引:39
作者
Hannigan, GE
Bayani, J
Weksberg, R
Beatty, B
Pandita, A
Dedhar, S
Squire, J
机构
[1] HOSP SICK CHILDREN,DEPT GENET,TORONTO,ON M5G 1X8,CANADA
[2] UNIV TORONTO,DEPT PATHOL,TORONTO,ON,CANADA
[3] UNIV TORONTO,DEPT MED BIOPHYS,TORONTO,ON,CANADA
[4] UNIV TORONTO,DEPT PAEDIAT,TORONTO,ON,CANADA
[5] PRINCESS MARGARET HOSP,DEPT PATHOL,TORONTO,ON M4X 1K9,CANADA
[6] ONTARIO CANC INST,TORONTO,ON M4X 1K9,CANADA
[7] SUNNYBROOK HLTH SCI CTR,DIV CANC BIOL RES,TORONTO,ON M4N 3M5,CANADA
关键词
D O I
10.1006/geno.1997.4719
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
We have recently reported the identification and cloning of the gene encoding p59(ILK), a novel protein ser/thr kinase that is found in physiologic complexes with beta integrin subunits. ILK is a potential protoonocogene that appears to function in mediating signal transduction by beta 1 family integrins. Fluorescence in situ hybridization analysis of metaphase and decondensed free chromatin fibers localized ILK to 11p15.5-p15.4. This position was also confirmed by relational mapping using well-characterized translocations with breakpoints in chromosome band 11p15. Our results indicate that ILK maps between HBBC and CALC loci, in the 11p15.5-p15.4 band interval. This location may be important in evaluating the potential role of p59(ILK) in tumorigenesis since it has been shown that this region is associated with both genomic imprinting and loss of heterozygosity in certain types of tumor. (C) 1997 Academic Press.
引用
收藏
页码:177 / 179
页数:3
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