TISSUE-SPECIFIC AND CELL-SPECIFIC EXPRESSION OF INS(1,4,5)P-3 3-KINASE ISOENZYMES

被引:51
作者
VANWEYENBERG, V
COMMUNI, D
DSANTOS, CS
ERNEUX, C
机构
[1] Interdisciplinary Research Institute, Campus Erasme, Bldg C, 1070 Brussels
关键词
D O I
10.1042/bj3060429
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
The phosphorylation of Ins(1,4,5)P-3 (InsP(3)) to Ins(1,3,4,5)P-4 (InsP(4)) is catalysed by InsP(3) 3-kinase. Molecular-biological data have shown the presence of two human isoenzymes of InsP(3) 3-kinase, namely InsP(3) 3-kinases A and B. We have isolated from a rat thymus cDNA library a 2235 bp cDNA (clone B15) encoding rat InsP(3) 3-kinase B. Northern-blot analysis of mRNA isolated from rat tissues (thymus, testis, brain, spleen, liver, kidney, heart, lung and intestine) revealed that a rat InsP(3) 3-kinase B probe hybridized to a 6 kb mRNA in lung, thymus, testis, brain and heart. In contrast, Northern-blot analysis of the same tissues probed under stringent conditions with a rat InsP(3) 3-kinase A probe hybridized to a 2 kb mRNA only in brain and a 1.8-2.0 kb mRNA species in testis. Northern-blot analysis of three human cell lines (HL-60, SH-SY5Y and HTB-138) probed with a human InsP(3) 3-kinase B probe showed the presence of a 6 kb mRNA in all cell lines, except in the human neuroblastoma cell line (SH-SY5Y), where two mRNA species of 5.7 and 6 kb were detected. Using the same blot, no hybridization signal could be seen with a human InsP(3) 3-kinase A probe. Altogether, our data are consistent with the notion that the two InsP(3) 3-kinase isoenzymes, A and B, are specifically expressed in different tissues and cells.
引用
收藏
页码:429 / 435
页数:7
相关论文
共 38 条
[1]   INOSITOL PHOSPHATES AND CELL SIGNALING [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1989, 341 (6239) :197-205
[2]  
BRADFORD PG, 1992, J BIOL CHEM, V267, P20959
[3]  
CHADWICK CC, 1992, J BIOL CHEM, V267, P3473
[4]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[5]   PURIFICATION AND BIOCHEMICAL-PROPERTIES OF A HIGH-MOLECULAR-MASS INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE ISOENZYME IN HUMAN PLATELETS [J].
COMMUNI, D ;
VANWEYENBERG, V ;
ERNEUX, C .
BIOCHEMICAL JOURNAL, 1994, 298 :669-673
[6]   LYS-197 AND ASP-414 ARE CRITICAL RESIDUES FOR BINDING OF ATP/MG2+ BY RAT-BRAIN INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE [J].
COMMUNI, D ;
TAKAZAWA, K ;
ERNEUX, C .
BIOCHEMICAL JOURNAL, 1993, 291 :811-816
[7]   A PURIFICATION STRATEGY FOR INOSITOL 1,4,5-TRISPHOSPHATE 3-KINASE FROM RAT-LIVER BASED UPON HEPARIN INTERACTION CHROMATOGRAPHY [J].
CONIGRAVE, A ;
PATWARDHAN, A ;
BROOMHEAD, L ;
ROUFOGALIS, B .
CELLULAR SIGNALLING, 1992, 4 (03) :303-&
[8]   SPECIFIC BINDING-SITES FOR INOSITOL 1,3,4,5-TETRAKISPHOSPHATE ARE LOCATED PREDOMINANTLY IN THE PLASMA-MEMBRANES OF HUMAN PLATELETS [J].
CULLEN, PJ ;
PATEL, Y ;
KAKKAR, VV ;
IRVINE, RF ;
AUTHI, KS .
BIOCHEMICAL JOURNAL, 1994, 298 :739-742
[9]   INOSITOL 1,3,4,5-TETRAKISPHOSPHATE BINDING-SITES IN NEURONAL AND NONNEURONAL TISSUES - PROPERTIES, COMPARISONS AND POTENTIAL PHYSIOLOGICAL SIGNIFICANCE [J].
CULLEN, PJ ;
IRVINE, RF .
BIOCHEMICAL JOURNAL, 1992, 288 :149-154
[10]   INOSITOL 1,4,5-TRISPHOSPHATE RECEPTORS - DISTINCT NEURONAL AND NONNEURONAL FORMS DERIVED BY ALTERNATIVE SPLICING DIFFER IN PHOSPHORYLATION [J].
DANOFF, SK ;
FERRIS, CD ;
DONATH, C ;
FISCHER, GA ;
MUNEMITSU, S ;
ULLRICH, A ;
SNYDER, SH ;
ROSS, CA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (07) :2951-2955