THE STRUCTURE AND EXPRESSION OF THE FGF RECEPTOR-1 MESSENGER-RNA ISOFORMS IN RAT-TISSUES

被引:40
作者
YAZAKI, N
FUJITA, H
OHTA, M
KAWASAKI, T
ITOH, N
机构
[1] KYOTO UNIV,FAC PHARMACEUT SCI,DEPT BIOL CHEM,KYOTO 60601,JAPAN
[2] UTANO NATL HOSP,CTR CLIN RES,KYOTO,JAPAN
关键词
FGF RECEPTOR-1; GENE EXPRESSION; ISOFORM; (RAT);
D O I
10.1016/0167-4781(93)90266-G
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
In this paper, we describe the structure of rat FGF receptor-1 mRNA isoforms and their expression in a variety of rat tissues. The rat FGFR-1 has the characteristics of FGFR-1 as well as mouse, human and chicken homologs. FGFR-1 mRNA was detectable in all the tissues examined by Northern analysis or polymerase chain reaction, indicating that FGFR-1 mRNA is widely expressed in rat tissues. The rat FGFR-1 mRNA has isoforms in both the extracellular and intracellular regions. The extracellular isoforms which have two or three immunoglobulin-like domains, are expressed almost equally in the tissues except for brain. However, the large form is a major form in the brain. Furthermore, in the brain, half of FGFR-1 mRNAs have the six nucleotides, which encode a potential serine-threonine kinase phosphorylation site in the intracellular juxtamembrane region, deleted. In contrast to the brain, the deletion isoform is a minor form in the other tissues. The tissue-specific expression of the isoforms indicates that they have different physiological functions. Although other isoforms of FGFR-1 mRNA in tumor cell lines have been reported, the isoforms were undetectable in all rat tissues examined, indicating the isoforms are products of abnormal alternative splicing in tumor cell lines.
引用
收藏
页码:37 / 42
页数:6
相关论文
共 24 条
[1]  
BAIRD A, 1991, CANCER CELL-MON REV, V3, P239
[2]   EXPRESSION OF 2 DIFFERENT FORMS OF FIBROBLAST GROWTH-FACTOR RECEPTOR-1 IN DIFFERENT MOUSE-TISSUES AND CELL-LINES [J].
BERNARD, O ;
LI, M ;
REID, HH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (17) :7625-7629
[3]   THE HEPARIN-BINDING (FIBROBLAST) GROWTH-FACTOR FAMILY OF PROTEINS [J].
BURGESS, WH ;
MACIAG, T .
ANNUAL REVIEW OF BIOCHEMISTRY, 1989, 58 :575-606
[4]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[5]   CLONING AND EXPRESSION OF 2 DISTINCT HIGH-AFFINITY RECEPTORS CROSS-REACTING WITH ACIDIC AND BASIC FIBROBLAST GROWTH-FACTORS [J].
DIONNE, CA ;
CRUMLEY, G ;
BELLOT, F ;
KAPLOW, JM ;
SEARFOSS, G ;
RUTA, M ;
BURGESS, WH ;
JAYE, M ;
SCHLESSINGER, J .
EMBO JOURNAL, 1990, 9 (09) :2685-2692
[6]   THE EXPRESSION OF 2 ISOFORMS OF THE HUMAN FIBROBLAST GROWTH-FACTOR RECEPTOR (FLG) IS DIRECTED BY ALTERNATIVE SPLICING [J].
FUJITA, H ;
OHTA, M ;
KAWASAKI, T ;
ITOH, N .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 174 (02) :946-951
[7]   K-SAM, AN AMPLIFIED GENE IN STOMACH-CANCER, IS A MEMBER OF THE HEPARIN-BINDING GROWTH-FACTOR RECEPTOR GENES [J].
HATTORI, Y ;
ODAGIRI, H ;
NAKATANI, H ;
MIYAGAWA, K ;
NAITO, K ;
SAKAMOTO, H ;
KATOH, O ;
YOSHIDA, T ;
SUGIMURA, T ;
TERADA, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (15) :5983-5987
[8]   FIBROBLAST GROWTH-FACTOR RECEPTORS FROM LIVER VARY IN 3 STRUCTURAL DOMAINS [J].
HOU, JZ ;
KAN, M ;
MCKEEHAN, K ;
MCBRIDE, G ;
ADAMS, P ;
MCKEEHAN, WL .
SCIENCE, 1991, 251 (4994) :665-668
[9]   RELATED FIBROBLAST GROWTH-FACTOR RECEPTOR GENES EXIST IN THE HUMAN GENOME [J].
HOUSSAINT, E ;
BLANQUET, PR ;
CHAMPIONARNAUD, P ;
GESNEL, MC ;
TORRIGLIA, A ;
COURTOIS, Y ;
BREATHNACH, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (20) :8180-8184
[10]   COMPLETE SEQUENCE OF A HUMAN RECEPTOR FOR ACIDIC AND BASIC FIBROBLAST GROWTH-FACTORS [J].
ISACCHI, A ;
BERGONZONI, L ;
SARMIENTOS, P .
NUCLEIC ACIDS RESEARCH, 1990, 18 (07) :1906-1906