Taxon-specific evolution of glandular kallikrein genes and identification of a progenitor of prostate-specific antigen

被引:44
作者
Olsson, AY
Lilja, H
Lundwall, Å
机构
[1] Lund Univ, Wallenberg Lab, Dept Lab Med, Div Clin Chem,Univ Hosp, S-20502 Malmo, Sweden
[2] Mem Sloan Kettering Canc Ctr, Dept Clin Labs, Dept Urol, New York, NY 10021 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Med, New York, NY 10021 USA
基金
瑞典研究理事会;
关键词
prostate-specific antigen; rat; genome; locus; duplication; paralogs;
D O I
10.1016/j.ygeno.2004.01.009
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
In a previous study we demonstrated that repeated duplications of the tissue kallikrein gene (Klk1) had resulted in 24 paralogs in mouse. Here we demonstrate a different evolution of rat glandular kallikrein genes. Repeated duplications of an approximate to 30-kb region, encompassing Klk1, Klk15, and Klk2-ps, resulted in 10 copies of each gene, but only the Klkl paralogs are functional. The number of genes varies also between nonrodent mammals, e.g., there are probably no paralogs to KLK1 in cow and pig, whereas horse could have up to 5. In the dog, the gene encoding the prostatic arginine esterase was identified as an ortholog to the progenitor of the PSA and hK2 genes, and it carries the same conserved androgen-responsive elements directing prostate transcription as these genes. This is highly interesting with respect to animal models of benign prostate hyperplasia and prostate adenocarcinoma-diseases that have been described only in humans and dogs. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:147 / 156
页数:10
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