Chromosomal localization of phospholipase A2 activating protein, an Ets2 target gene, to 9p21

被引:10
作者
Beatty, BG
Qi, S
Pienkowska, M
Herbrick, JA
Scheidl, T
Zhang, ZM
Kola, I
Scherer, SW
Seth, A
机构
[1] Ontario Canc Inst, Dept Cell & Mol Biol, Toronto, ON M5G 1L5, Canada
[2] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON M5G 1L5, Canada
[3] Womens Coll Hosp, Toronto, ON M5S 1B2, Canada
[4] Univ Toronto, MRC, Periodontal Physiol Grp, Toronto, ON M5S 1B2, Canada
[5] Hosp Sick Children, Dept Genet, Toronto, ON M5G 1X8, Canada
[6] Monash Univ, Inst Reprod & Dev, Melbourne, Vic 3004, Australia
基金
英国医学研究理事会;
关键词
D O I
10.1006/geno.1999.5999
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
A murine Ets2 target gene isolated by differential display cloning was identified as the phospholipase A2 activating protein (PLAA) gene. A 2.7-kb human cDNA demonstrating high homology to mouse and rat Plaa genes was then isolated and characterized. Human PLAA contains six WD-40 repeat motifs and three different protein kinase consensus domains. Fluorescence in situ hybridization (FISH) mapping placed PLAA on chromosome 9p21, a region frequently deleted in various cancers. A comprehensive mapping strategy was employed to define further the chromosomal localization of PLAA relative to CDKN2A within the 9p21 locus. Radiation hybrid mapping placed the gene 7.69 cR from WI-5735 (LOD >3.0), a marker in close proximity to CDKN2A and CDKN2B. Yeast artificial chromosome (YAC) mapping localized PLAA proximal to the CDKN2A/CDKN2B genes and to a region flanked by D9S171 and INFA commonly deleted in many neoplasms. Two YACs contained both PLAA. and D9S259, a marker present in a second more proximal minimal deleted region observed in cutaneous melanoma and squamous cell lung carcinoma. Double-color fiber FISH mapping confirmed the location of PLAA centromeric to D9S171 and CDKN2A/CDKN2B. The mapping data suggest a possible tumor suppressor role for this gene. (C) 1999 Academic Press.
引用
收藏
页码:529 / 532
页数:4
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