cDNA isolation, expression, and chromosomal localization of the mouse Pcph proto-oncogene

被引:0
作者
Recio, JA
Zambrano, N
de la Peña, L
Powers, C
Siwarski, D
Huppi, K
Notario, V
机构
[1] Georgetown Univ, Med Ctr, Dept Radiat Med, Expt Carcinogenesis Lab, Washington, DC 20007 USA
[2] NCI, Genet Lab, NIH, Bethesda, MD 20892 USA
关键词
carcinogenesis; molecular cloning; sequencing; linkage analysis;
D O I
10.1002/(SICI)1098-2744(199910)26:2<130::AID-MC7>3.0.CO;2-N
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report here the isolation and characterization of a cDNA from mouse thymus encoding the murine homolog of the protein product of the Syrian hamster Pcph proto-oncogene. The single open reading frame identified in the cDNA sequence encoded a protein predicted to have 428 amino acids, which shared 93.7% amino acid identity with the Syrian hamster Pcph within the first 412 residues but had a shorter, highly dissimilar C-terminus. Northern and western analyses revealed that Pcph mRNA and protein were widely distributed in mouse embryo and adult tissues, with the highest expression in adults detected in kidney and liver. The mouse Pcph proto-oncogene was mapped by linkage analysis to within 3.3 +/- 2.3 cM of Pkch-rs1 I on chromosome 12. These data should prove valuable in designing studies to define the cellular function of the Pcph proto-oncogene. (C) 1999 Wiley-Liss, Inc.
引用
收藏
页码:130 / 136
页数:7
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