ASSIGNMENT OF THE HUMAN P27(KIP1) GENE TO 12P13 AND ITS ANALYSIS IN LEUKEMIAS

Citation
Ja. Pietenpol et al., ASSIGNMENT OF THE HUMAN P27(KIP1) GENE TO 12P13 AND ITS ANALYSIS IN LEUKEMIAS, Cancer research, 55(6), 1995, pp. 1206-1210
Citations number
36
Categorie Soggetti
Oncology
Journal title
ISSN journal
00085472
Volume
55
Issue
6
Year of publication
1995
Pages
1206 - 1210
Database
ISI
SICI code
0008-5472(1995)55:6<1206:AOTHPG>2.0.ZU;2-U
Abstract
The p27(Kip1) (p27) gene encodes an inducible inhibitor of cyclin-depe ndent kinase activity. Using a murine p27 cDNA as probe, we obtained a human cDNA clone and subsequently used it to isolate a genomic clone of this gene. The coding region of the human p27 gene was contained in two exons. Both the amino acid sequence and intron-exon organization of p27 were similar to those previously found for the related cyclin-d ependent kinase inhibitor p21(Waf1) (p21). The p27 gene was localized to chromosome band 12p13 by a combination of somatic cell hybrid and f luorescence in situ hybridization analyses. The p27 gene product is th ought to control the leukocyte cell cycle and the 12p13 chromosomal ba nd is known to be deleted in leukemias, suggesting that the p27 gene m ay act as a tumor suppressor gene in leukemias. Although p27 was found to reside in the minimal region of chromosomal loss in hematological malignancies, no mutations of p27 were observed in leukemia samples. H aploinsufficiency of p27 may confer a growth advantage to leukemia cel ls.