Inositides in the nucleus:: presence and characterisation of the isozymes of phospholipase β family in NIH 3T3 cells

被引:38
作者
Cocco, L [1 ]
Rubbini, S
Manzoli, L
Billi, AM
Faenza, I
Peruzzi, D
Matteucci, A
Artico, M
Gilmour, RS
Rhee, SG
机构
[1] Univ Bologna, Inst Human Anat, I-40126 Bologna, Italy
[2] Ist Ortoped Rizzoli, CNR, Cytomorphol Inst, I-40136 Bologna, Italy
[3] Ist Ortoped Rizzoli, CNR, Lab Cell Biol & Electron Microscopy, I-40136 Bologna, Italy
[4] Univ Auckland, Sch Med, Dept Mol Med, Auckland, New Zealand
[5] NHLBI, Lab Cell Signalling, NIH, Bethesda, MD 20892 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS | 1999年 / 1438卷 / 02期
关键词
inositide; nucleus; phospholipase C; isozyme; phosphatidylinositol 4,5-bisphosphate;
D O I
10.1016/S1388-1981(99)00061-X
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
Previous reports from our laboratories and others have hinted that the nucleus is a site for an autonomous signalling system acting through the activation of the inositol lipid cycle. Among phospholipases (PLC) it has been shown previously that PLC beta(1) is specifically localised in the nucleus as well as at the plasma membrane. Using NIH 3T3 cells, it has been possible to obtain, with two purification strategies, in the presence of in the absence of Nonidet P-40, both intact nuclei still maintaining the outer membrane and nuclei completely stripped of their envelope. In these nuclei, we show that not only PLC beta(1) is present, but also PLC beta(2), PLC beta(3) and PLC beta(4). The more abounding isoform is PLC beta(1) followed by PLC beta(3), PLC beta(2) and PLC beta(4), respectively. All the isoforms are enriched in nuclear preparations free from nuclear envelope and cytoplasmatic debris, indicating that the actual localisation of the PLC beta isozymes is in the inner nuclear compartment. (C) 1999 Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:295 / 299
页数:5
相关论文
共 20 条
[1]   Localization of two forms of phospholipase C-β1, a and b, in C6Bu-1 cells [J].
Bahk, YY ;
Song, H ;
Baek, SH ;
Park, BY ;
Kim, H ;
Ryu, SH ;
Suh, PG .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1998, 1389 (01) :76-80
[2]   Control of expression of PLCβ1 by LAC repressor system:: Relationship between nuclear PLCβ1 overexpression and growth factor stimulation [J].
Billi, AM ;
Matteucci, A ;
Faenza, I ;
Manzoli, L ;
Rubbini, S ;
Gilmour, RS ;
Rhee, SG ;
Cocco, L .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 241 (01) :122-126
[3]   Phosphoinositide signaling pathways in nuclei are associated with nuclear speckles containing pre-mRNA processing factors [J].
Boronenkov, IV ;
Loijens, JC ;
Umeda, M ;
Anderson, RA .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (12) :3547-3560
[4]   Inositides in the nucleus:: Taking stock of PLCβ1 [J].
Cocco, L ;
Capitani, S ;
Maraldi, NM ;
Mazzotti, G ;
Barnabei, O ;
Rizzoli, R ;
Gilmour, RS ;
Wirtz, KWA ;
Rhee, SG ;
Manzoli, FA .
ADVANCES IN ENZYME REGULATION, VOL 38, 1998, 38 :351-363
[5]   SYNTHESIS OF POLYPHOSPHOINOSITIDES IN NUCLEI OF FRIEND-CELLS - EVIDENCE FOR POLYPHOSPHOINOSITIDE METABOLISM INSIDE THE NUCLEUS WHICH CHANGES WITH CELL-DIFFERENTIATION [J].
COCCO, L ;
GILMOUR, RS ;
OGNIBENE, A ;
LETCHER, AJ ;
MANZOLI, FA ;
IRVINE, RF .
BIOCHEMICAL JOURNAL, 1987, 248 (03) :765-770
[6]   INOSITOL LIPID CYCLE IN THE NUCLEUS [J].
COCCO, L ;
MARTELLI, AM ;
GILMOUR, RS .
CELLULAR SIGNALLING, 1994, 6 (05) :481-485
[7]   THE POLYPHOSPHOINOSITIDE CYCLE EXISTS IN THE NUCLEI OF SWISS 3T3 CELLS UNDER THE CONTROL OF A RECEPTOR (FOR IGF-I) IN THE PLASMA-MEMBRANE, AND STIMULATION OF THE CYCLE INCREASES NUCLEAR DIACYLGLYCEROL AND APPARENTLY INDUCES TRANSLOCATION OF PROTEIN-KINASE-C TO THE NUCLEUS [J].
DIVECHA, N ;
BANFIC, H ;
IRVINE, RF .
EMBO JOURNAL, 1991, 10 (11) :3207-3214
[8]   The role of carboxyl-terminal basic amino acids in G(q)alpha-dependent activation, particulate association, and nuclear localization of phospholipase C-beta 1 [J].
Kim, CG ;
Park, D ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (35) :21187-21192
[9]  
LEE CW, 1993, J BIOL CHEM, V268, P21318
[10]  
MANZOLI L, 1995, CANCER RES, V55, P2978