NEUROBLASTOMA-DIFFERENTIATION INVOLVES THE EXPRESSION OF 2 ISOFORMS OF THE ALPHA-SUBUNIT OF G0

被引:34
作者
BRABET, P [1 ]
PANTALONI, C [1 ]
RODRIGUEZ, M [1 ]
MARTINEZ, J [1 ]
BOCKAERT, J [1 ]
HOMBURGER, V [1 ]
机构
[1] CNRS, INSERM, CTR PHARMACOL & ENDOCRINOL, RUE CARDONILLE, F-34094 MONTPELLIER 2, FRANCE
关键词
ADP ribosylation; G[!sub]o[!/sub]α protein; Neuroblastoma cells;
D O I
10.1111/j.1471-4159.1990.tb01964.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
The regulation of GTP‐binding proteins (G proteins) was examined during the course of differentiation of neuroblastoma N1E‐115 cells. N1E‐115 cell membranes possess three Bordetella pertussis toxin (PTX) substrates assigned to α‐subunits (Gα) of Go (a G protein of unknown function) and “Gi (a G protein inhibitory to adenylate cyclase)‐like” proteins and one substrate of Vibrio cholerae toxin corresponding to an α‐subunit of Gs (a G protein stimulatory to adenylate cyclase). In undifferentiated cells, only one form of Goα was found, having a pI of 5.8. Goα content increased by approximately twofold from the undifferentiated state to 96 h of cell differentiation. This is mainly due to the appearance of another Goα form having a pI of 5.55. Both Goα isoforms have similar sizes on sodium dodecyl sulfate‐polyacrylamide gels, are recognized by polyclonal antibodies to bovine brain Goα, are ADP‐ribosylated by PTX, and are covalently myristylated in whole N1E‐115 cells. In addition, immunofluorescent staining of N1E‐115 cells with Goα antibodies revealed that association of Goα with the plasma membrane appears to coincide with the expression of the most acidic isoform and morphological cell differentiation. In contrast, the levels of both Giα and Gsα did not significantly change, whereas that of the common β‐subunit increased by ∼ 30% over the same period. These results demonstrate specific regulation of the expression of Goα during neuronal differentiation. Copyright © 1990, Wiley Blackwell. All rights reserved
引用
收藏
页码:1310 / 1320
页数:11
相关论文
共 44 条
[1]  
ASANO T, 1985, J BIOL CHEM, V260, P2653
[2]   GO, A GTP-BINDING PROTEIN - IMMUNOCHEMICAL AND IMMUNOHISTOCHEMICAL LOCALIZATION IN THE RAT [J].
ASANO, T ;
SEMBA, R ;
KAMIYA, N ;
OGASAWARA, N ;
KATO, K .
JOURNAL OF NEUROCHEMISTRY, 1988, 50 (04) :1164-1169
[3]   ONTOGENY OF THE GTP-BINDING PROTEIN G0 IN RAT-BRAIN AND HEART [J].
ASANO, T ;
KAMIYA, N ;
SEMBA, R ;
KATO, K .
JOURNAL OF NEUROCHEMISTRY, 1988, 51 (06) :1711-1716
[4]  
BIRNBAUMER L, 1987, KIDNEY INT, V32, pS14
[5]   DEVELOPMENT OF AN OXYNTOMODULIN GLICENTIN C-TERMINAL RADIOIMMUNOASSAY USING A THIOL-MALEOYL COUPLING METHOD FOR PREPARING THE IMMUNOGEN [J].
BLACHE, P ;
KERVRAN, A ;
MARTINEZ, J ;
BATAILLE, D .
ANALYTICAL BIOCHEMISTRY, 1988, 173 (01) :151-159
[6]  
BRABET P, 1988, J NEUROSCI, V8, P701
[7]   MULTIPLE SPECIES AND ISOFORMS OF BORDETELLA-PERTUSSIS TOXIN SUBSTRATES [J].
BRABET, P ;
PANTALONI, C ;
ROUOT, B ;
TOUTANT, M ;
GARCIASAINZ, A ;
BOCKAERT, J ;
HOMBURGER, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 152 (03) :1185-1192
[8]   LOCALIZATION OF MESSENGER-RNAS ENCODING THE ALPHA-SUBUNITS OF SIGNAL-TRANSDUCING G-PROTEINS WITHIN RAT-BRAIN AND AMONG PERIPHERAL-TISSUES [J].
BRANN, MR ;
COLLINS, RM ;
SPIEGEL, A .
FEBS LETTERS, 1987, 222 (01) :191-198
[9]   MYRISTOYLATED ALPHA-SUBUNITS OF GUANINE NUCLEOTIDE-BINDING REGULATORY PROTEINS [J].
BUSS, JE ;
MUMBY, SM ;
CASEY, PJ ;
GILMAN, AG ;
SEFTON, BM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (21) :7493-7497
[10]  
CERIONE RA, 1986, J BIOL CHEM, V261, P3901