Expression analysis and subcellular distribution of the two G-protein regulators AGS3 and LGN indicate distinct functionality - Localization of LGN to the midbody during cytokinesis

被引:95
作者
Blumer, JB
Chandler, LJ
Lanier, SM
机构
[1] Louisiana State Univ, Hlth Sci Ctr, Dept Pharmacol & Expt Therapeut, New Orleans, LA 70112 USA
[2] Med Univ S Carolina, Dept Physiol & Neurosci, Charleston, SC 29425 USA
关键词
D O I
10.1074/jbc.M112185200
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
Activator of G-protein signaling 3 (AGS3) and LGN have a similar domain structure and contain four G-protein regulatory motifs that serve as anchors for the binding of the GDP-bound conformation of specific G-protein a subunits. As an initial approach to define further the different functional roles of AGS3 and LGN, we determined their expression profile and subcellular distribution. AGS3- and LGN-specific antisera indicated a widespread tissue distribution of LGN, whereas AGS3 is primarily enriched in brain. Brain punch biopsies of 13 discrete brain regions indicated that both AGS3 and LGN are expressed in all areas tested but are differentially regulated during development. LGN is expressed in neuronal, astroglial, and microglial cultures, whereas AGS3 expression is restricted to neurons. In primary neuronal cultures as well as in dividing cultures of PC12 cells, immunocytochemistry indicated distinct subcellular locations of AGS3 and LGN. The subcellular locations of the two proteins were differentially regulated by external stimuli and the cell cycle. In PC12 and COS7 cells, LGN moves from the nucleus to the midbody structure separating daughter cells during the later stages of mitosis, suggesting a role for G-proteins in cytokinesis. Thus, although AGS3 and LGN share a similar overall motif structure and both bind G-proteins, nature has endowed these proteins with different regulatory elements that allow functional diversity by virtue of tissue-specific expression and subcellular positioning.
引用
收藏
页码:15897 / 15903
页数:7
相关论文
共 45 条
[1]   INCENP binds the Aurora-related kinase AIRK2 and is required to target it to chromosomes, the central spindle and cleavage furrow [J].
Adams, RR ;
Wheatley, SP ;
Gouldsworthy, AM ;
Kandels-Lewis, SE ;
Carmena, M ;
Smythe, C ;
Gerloff, DL ;
Earnshaw, WD .
CURRENT BIOLOGY, 2000, 10 (17) :1075-1078
[2]   The partner of inscuteable/discs-large complex is required to establish planar polarity during asymmetric cell division in Drosophila [J].
Bellaïche, Y ;
Radovic, A ;
Woods, DF ;
Hough, CD ;
Parmentier, ML ;
O'Kane, CJ ;
Bryant, PJ ;
Schweisguth, F .
CELL, 2001, 106 (03) :355-366
[3]   Selective interaction of AGS3 with G-proteins and the influence of AGS3 on the activation state of G-proteins [J].
Bernard, ML ;
Peterson, YK ;
Chung, P ;
Jourdan, J ;
Lanier, SM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :1585-1593
[4]   Chronic ethanol increases N-methyl-D-aspartate-stimulated nitric oxide formation but not receptor density in cultured cortical neurons [J].
Chandler, LJ ;
Sutton, G ;
Norwood, D ;
Sumners, C ;
Crews, FT .
MOLECULAR PHARMACOLOGY, 1997, 51 (05) :733-740
[5]   Novel alternative splicing and nuclear localization of human RGS12 gene products [J].
Chatterjee, TK ;
Fisher, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (38) :29660-29671
[6]   Cytoplasmic, nuclear, and Golgi localization of RGS proteins - Evidence for N-terminal and RGS domain sequences as intracellular targeting motifs [J].
Chatterjee, TK ;
Fisher, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) :24013-24021
[7]   Down-regulation of survivin by antisense oligonucleotides increases apoptosis, inhibits cytokinesis and anchorage-independent growth [J].
Chen, J ;
Wu, W ;
Tahir, SK ;
Kroeger, PE ;
Rosenberg, SH ;
Cowsert, LM ;
Bennett, F ;
Krajewski, S ;
Krajewska, M ;
Welsh, K ;
Reed, JC ;
Ng, SC .
NEOPLASIA, 2000, 2 (03) :235-241
[8]   Activation of heterotrimeric G-protein signaling by a Ras-related protein - Implications for signal integration [J].
Cismowski, MJ ;
Ma, CL ;
Ribas, C ;
Xie, XB ;
Spruyt, M ;
Lizano, JS ;
Lanier, SM ;
Duzic, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (31) :23421-23424
[9]   Genetic screens in yeast to identify mammalian nonreceptor modulators of G-protein signaling [J].
Cismowski, MJ ;
Takesono, A ;
Ma, CL ;
Lizano, JS ;
Xie, XB ;
Fuernkranz, H ;
Lanier, SM ;
Duzic, E .
NATURE BIOTECHNOLOGY, 1999, 17 (09) :878-883
[10]   Activator of G protein signaling 3 is a guanine dissociation inhibitor for Gαi subunits [J].
De Vries, L ;
Fischer, T ;
Tronchère, H ;
Brothers, GM ;
Strockbine, B ;
Siderovski, DP ;
Farquhar, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (26) :14364-14369