Keratinocyte growth factor (KGF/FGF-7) has a paracrine role in canine prostate: Molecular cloning of mRNA encoding canine KGF

被引:17
作者
Canatan, H
Chang, WY
Sugimoto, Y
Shidaifat, F
Kulp, SK
Brueggemeier, RW
Lin, YC
机构
[1] OHIO STATE UNIV,COLL VET MED,DEPT VET BIOSCI,LAB REPROD & MOLEC ENDOCRINOL,COLUMBUS,OH 43210
[2] OHIO STATE UNIV,COLL BIOL SCI,MOLEC CELLULAR & DEV BIOL PROGRAM,COLUMBUS,OH 43210
[3] OHIO STATE UNIV,COLL PHARM,DIV MED CHEM & PHARMACOGNOSY,COLUMBUS,OH 43210
关键词
D O I
10.1089/dna.1996.15.247
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
cDNA encoding the canine keratinocyte growth factor (KGF) was cloned from normal canine prostate tissue. The authentic canine KGF cDNA sequence, 686 bp in length, spans the protein-coding region and 88 bp of the 5' and 19 bp of the 3' untranslated regions of canine KGF. The predicted amino acid sequence of canine KGF is composed of 194 amino acid residues. Canine KGF exhibits highest homology with the human KGF cDNA and amino acid sequences (95.8% and 97.4%, respectively), while it demonstrates the Lowest homology with the rat sequences at 88.0% anti 92.3%, respectively. The degrees of homology with mouse cDNA and amino acid sequences are 91.8% and 95.9%, respectively. By using RNase protection assay, KGF was shown to be expressed in normal prostate tissues of both mature and young (5-month-old) dogs, In vitro, the recombinant canine KGF has mitogenic activity on cultured canine epithelial cells, whereas it has no effect on cultured canine prostatic stromal cells. This novel canine KGF cDNA may be a valuable tool in the study of human benign prostatic hyperplasia using the canine prostate as a model.
引用
收藏
页码:247 / 254
页数:8
相关论文
共 46 条
[1]   KERATINOCYTE GROWTH-FACTOR - A FIBROBLAST GROWTH-FACTOR FAMILY MEMBER WITH UNUSUAL TARGET-CELL SPECIFICITY [J].
AARONSON, SA ;
BOTTARO, DP ;
MIKI, T ;
RON, D ;
FINCH, PW ;
FLEMING, TP ;
AHN, J ;
TAYLOR, WG ;
RUBIN, JS .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1991, 638 :62-77
[2]   KERATINOCYTE GROWTH-FACTOR FUNCTIONS IN EPITHELIAL INDUCTION DURING SEMINAL-VESICLE DEVELOPMENT [J].
ALARID, ET ;
RUBIN, JS ;
YOUNG, P ;
CHEDID, M ;
RON, D ;
AARONSON, SA ;
CUNHA, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (03) :1074-1078
[3]  
Baird Andrew, 1994, Current Opinion in Neurobiology, V4, P78, DOI 10.1016/0959-4388(94)90035-3
[4]   EFFECT OF CYSTEINE SUBSTITUTIONS ON THE MITOGENIC ACTIVITY AND STABILITY OF RECOMBINANT HUMAN KERATINOCYTE GROWTH-FACTOR [J].
BARE, LA ;
BROWN, M ;
GOYAL, S ;
IDLER, D ;
MANSSON, PE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (01) :872-879
[5]   THE FGF FAMILY OF GROWTH-FACTORS AND ONCOGENES [J].
BASILICO, C ;
MOSCATELLI, D .
ADVANCES IN CANCER RESEARCH, 1992, 59 :115-165
[6]   DEVELOPMENT OF CANINE BENIGN PROSTATIC HYPERPLASIA WITH AGE [J].
BERRY, SJ ;
STRANDBERG, JD ;
SAUNDERS, WJ ;
COFFEY, DS .
PROSTATE, 1986, 9 (04) :363-373
[7]   THE DEVELOPMENT OF HUMAN BENIGN PROSTATIC HYPERPLASIA WITH AGE [J].
BERRY, SJ ;
COFFEY, DS ;
WALSH, PC ;
EWING, LL .
JOURNAL OF UROLOGY, 1984, 132 (03) :474-479
[8]  
BERRY SJ, 1986, AM J PHYSIOL, V250, P1039
[9]   THE HEPARIN-BINDING (FIBROBLAST) GROWTH-FACTOR FAMILY OF PROTEINS [J].
BURGESS, WH ;
MACIAG, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 :575-606
[10]  
CANATAN H, 1994, FASEB J, V8, pA930