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1.
Genes Immun ; 17(6): 321-7, 2016 09.
Article in English | MEDLINE | ID: mdl-27307211

ABSTRACT

G Protein Signaling Modulator-3 (GPSM3) is a leukocyte-specific regulator of G protein-coupled receptors (GPCRs), which binds inactivated Gαi·GDP subunits and precludes their reassociation with Gßγ subunits. GPSM3 deficiency protects mice from inflammatory arthritis and, in humans, GPSM3 single-nucleotide polymorphisms (SNPs) are inversely associated with the risk of rheumatoid arthritis development; recently, these polymorphisms were linked to one particular SNP (rs204989) that decreases GPSM3 transcript abundance. However, the precise role of GPSM3 in leukocyte biology is unknown. Here, we show that GPSM3 is induced in the human promyelocytic leukemia NB4 cell line following retinoic acid treatment, which differentiates this cell line into a model of neutrophil physiology (NB4*). Reducing GPSM3 expression in NB4* cells, akin to the effect ascribed to the rs204989 C>T transition, disrupts cellular migration toward leukotriene B4 (LTB4) and (to a lesser extent) interleukin-8 (a.k.a. IL-8 or CXCL8), but not migration toward formylated peptides (fMLP). As the chemoattractants LTB4 and CXCL8 are involved in recruitment of neutrophils to the arthritic joint, our results suggest that the arthritis-protective GPSM3 SNP rs204989 may act to decrease neutrophil chemoattractant responsiveness.


Subject(s)
Arthritis, Rheumatoid/genetics , Chemotaxis, Leukocyte , Guanine Nucleotide Dissociation Inhibitors/physiology , Neutrophils/metabolism , Arthritis, Rheumatoid/immunology , Cell Line, Tumor , Chemotaxis, Leukocyte/genetics , Guanine Nucleotide Dissociation Inhibitors/genetics , Humans , Interleukin-8/metabolism , Leukopoiesis , Leukotriene B4/metabolism , N-Formylmethionine Leucyl-Phenylalanine/metabolism , Polymorphism, Single Nucleotide , Tretinoin/metabolism
2.
Genes Immun ; 17(2): 139-47, 2016 Mar.
Article in English | MEDLINE | ID: mdl-26821282

ABSTRACT

G protein signaling modulator 3 (GPSM3) is a regulator of G protein-coupled receptor signaling, with expression restricted to leukocytes and lymphoid organs. Previous genome-wide association studies have highlighted single-nucleotide polymorphisms (SNPs; rs204989 and rs204991) in a region upstream of the GPSM3 transcription start site as being inversely correlated to the prevalence of rheumatoid arthritis (RA)-this association is supported by the protection afforded to Gpsm3-deficient mice in models of inflammatory arthritis. Here, we assessed the functional consequences of these polymorphisms. We collected biospecimens from 50 volunteers with RA diagnoses, 50 RA-free volunteers matched to the aforementioned group and 100 unmatched healthy young volunteers. We genotyped these individuals for GPSM3 (rs204989, rs204991), CCL21 (rs2812378) and HLA gene region (rs6457620) polymorphisms, and found no significant differences in minor allele frequencies between the RA and disease-free cohorts. However, we identified that individuals homozygous for SNPs rs204989 and rs204991 had decreased GPSM3 transcript abundance relative to individuals homozygous for the major allele. In vitro promoter activity studies suggest that SNP rs204989 is the primary cause of this decrease in transcript levels. Knockdown of GPSM3 in THP-1 cells, a human monocytic cell line, was found to disrupt ex vivo migration to the chemokine MCP-1.


Subject(s)
Arthritis, Rheumatoid/genetics , Guanine Nucleotide Dissociation Inhibitors/genetics , Polymorphism, Single Nucleotide , RNA, Messenger/genetics , Adult , Aged , Alleles , Arthritis, Rheumatoid/metabolism , Arthritis, Rheumatoid/pathology , Case-Control Studies , Cell Line , Chemokine CCL2/genetics , Chemokine CCL2/metabolism , Chemotaxis , Female , Gene Expression , Gene Frequency , Genotype , Guanine Nucleotide Dissociation Inhibitors/antagonists & inhibitors , Guanine Nucleotide Dissociation Inhibitors/metabolism , Homozygote , Humans , Male , Middle Aged , Monocytes/metabolism , Monocytes/pathology , Promoter Regions, Genetic , RNA, Messenger/metabolism , RNA, Small Interfering/genetics , RNA, Small Interfering/metabolism
3.
Cell Mol Life Sci ; 62(5): 551-77, 2005 Mar.
Article in English | MEDLINE | ID: mdl-15747061

ABSTRACT

Heterotrimeric G-proteins are intracellular partners of G-protein-coupled receptors (GPCRs). GPCRs act on inactive Galpha.GDP/Gbetagamma heterotrimers to promote GDP release and GTP binding, resulting in liberation of Galpha from Gbetagamma. Galpha.GTP and Gbetagamma target effectors including adenylyl cyclases, phospholipases and ion channels. Signaling is terminated by intrinsic GTPase activity of Galpha and heterotrimer reformation - a cycle accelerated by 'regulators of G-protein signaling' (RGS proteins). Recent studies have identified several unconventional G-protein signaling pathways that diverge from this standard model. Whereas phospholipase C (PLC) beta is activated by Galpha(q) and Gbetagamma, novel PLC isoforms are regulated by both heterotrimeric and Ras-superfamily G-proteins. An Arabidopsis protein has been discovered containing both GPCR and RGS domains within the same protein. Most surprisingly, a receptor-independent Galpha nucleotide cycle that regulates cell division has been delineated in both Caenorhabditis elegans and Drosophila melanogaster. Here, we revisit classical heterotrimeric G-protein signaling and explore these new, non-canonical G-protein signaling pathways.


Subject(s)
Cell Division/physiology , Heterotrimeric GTP-Binding Proteins/physiology , Signal Transduction/physiology , Amino Acid Sequence , Animals , Caenorhabditis elegans/physiology , Dimerization , Drosophila melanogaster/physiology , Heterotrimeric GTP-Binding Proteins/chemistry , Molecular Sequence Data , Phospholipases/chemistry , Phospholipases/metabolism , Phospholipases/physiology , Protein Structure, Secondary , Protein Subunits/chemistry , Protein Subunits/physiology , Receptors, G-Protein-Coupled/physiology
4.
J Biol Chem ; 276(51): 48257-61, 2001 Dec 21.
Article in English | MEDLINE | ID: mdl-11641393

ABSTRACT

PLC-epsilon was identified recently as a phosphoinositide-hydrolyzing phospholipase C (PLC) containing catalytic domains (X, Y, and C2) common to all PLC isozymes as well as unique CDC25- and Ras-associating domains. Novel regulation of this PLC isozyme by the Ras oncoprotein and alpha-subunits (Galpha(12)) of heterotrimeric G proteins was illustrated. Sequence analyses of PLC-epsilon revealed previously unrecognized PH and EF-hand domains in the amino terminus. The known interaction of Gbetagamma subunits with the PH domains of other proteins led us to examine the capacity of Gbetagamma to activate PLC-epsilon. Co-expression of Gbeta(1)gamma(2) with PLC-epsilon in COS-7 cells resulted in marked stimulation of phospholipase C activity. Gbeta(2) and Gbeta(4) in combination with Ggamma(1), Ggamma(2), Ggamma(3), or Ggamma(13) also activated PLC-epsilon to levels similar to those observed with Gbeta(1)-containing dimers of these Ggamma-subunits. Gbeta(3) in combination with the same Ggamma-subunits was less active, and Gbeta(5)-containing dimers were essentially inactive. Gbetagamma-promoted activation of PLC-epsilon was blocked by cotransfection with either of two Gbetagamma-interacting proteins, Galpha(i1) or the carboxyl terminus of G protein receptor kinase 2. Pharmacological inhibition of PI3-kinase-gamma had no effect on Gbeta(1)gamma(2)-promoted activation of PLC-epsilon. Similarly, activation of Ras in the action of Gbetagamma is unlikely, because a mutation in the second RA domain of PLC-epsilon that blocks Ras activation of PLC failed to alter the stimulatory activity of Gbeta(1)gamma(2). Taken together, these results reveal the presence of additional functional domains in PLC-epsilon and add a new level of complexity in the regulation of this novel enzyme by heterotrimeric G proteins.


Subject(s)
Heterotrimeric GTP-Binding Proteins/metabolism , Type C Phospholipases/metabolism , Amino Acid Sequence , Animals , Cell Line , Dimerization , Enzyme Activation , Heterotrimeric GTP-Binding Proteins/chemistry , Molecular Sequence Data , Phosphatidylinositol 3-Kinases/metabolism , Phosphoinositide Phospholipase C , Sequence Homology, Amino Acid , Signal Transduction , Type C Phospholipases/chemistry
5.
J Biol Chem ; 276(52): 49267-74, 2001 Dec 28.
Article in English | MEDLINE | ID: mdl-11675383

ABSTRACT

G gamma(13) is a divergent member of the G gamma subunit family considered to be a component of the gustducin G-protein heterotrimer involved in bitter and sweet taste reception in taste bud cells. G gamma(13) contains a C-terminal asparagine-proline-tryptophan (NPW) tripeptide, a hallmark of RGS protein G gamma-like (GGL) domains which dimerize exclusively with G beta(5) subunits. In this study, we investigated the functional range of G gamma(13) assembly with G beta subunits using multiple assays of G beta association and G beta gamma effector modulation. G gamma(13) was observed to associate with all five G beta subunits (G beta(1-5)) upon co-translation in vitro, as well as function with all five G beta subunits in the modulation of Kir3.1/3.4 (GIRK1/4) potassium and N-type (alpha(1B)) calcium channels. Multiple G beta/G gamma(13) pairings were also functional in cellular assays of phospholipase C (PLC) beta 2 activation and inhibition of G alpha(q)-stimulated PLC beta 1 activity. However, upon cellular co-expression of G gamma(13) with different G beta subunits, only G beta(1)/G gamma(13), G beta(3)/G gamma(13), and G beta(4)/G gamma(13) pairings were found to form stable dimers detectable by co-immunoprecipitation under high-detergent cell lysis conditions. Collectively, these data indicate that G gamma(13) forms functional G beta gamma dimers with a range of G beta subunits. Coupled with our detection of G gamma(13) mRNA in mouse and human brain and retina, these results imply that this divergent G gamma subunit can act in signal transduction pathways other than that dedicated to taste reception in sensory lingual tissue.


Subject(s)
Calcium Channels, N-Type/metabolism , Heterotrimeric GTP-Binding Proteins/metabolism , Potassium Channels/metabolism , Amino Acid Sequence , Animals , Cell Line , Dimerization , Enzyme Activation , Green Fluorescent Proteins , Heterotrimeric GTP-Binding Proteins/chemistry , Heterotrimeric GTP-Binding Proteins/classification , Humans , Indicators and Reagents/metabolism , Isoenzymes/metabolism , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Molecular Sequence Data , Patch-Clamp Techniques , Phospholipase C beta , Protein Isoforms , Protein Subunits , Sequence Alignment , Tissue Distribution , Type C Phospholipases/metabolism
6.
J Biol Chem ; 276(49): 45868-75, 2001 Dec 07.
Article in English | MEDLINE | ID: mdl-11577097

ABSTRACT

Normally, Rho GTPases are activated by the removal of bound GDP and the concomitant loading of GTP catalyzed by members of the Dbl family of guanine nucleotide exchange factors (GEFs). This family of GEFs invariantly contain a Dbl homology (DH) domain adjacent to a pleckstrin homology (PH) domain, and while the DH domain usually is sufficient to catalyze nucleotide exchange, possible roles for the conserved PH domain remain ambiguous. Here we demonstrate that the conserved PH domains of three distinct Dbl family proteins, intersectin, Dbs, and Tiam1, selectively bind lipid vesicles only when phosphoinositides are present. While the PH domains of intersectin and Dbs promiscuously bind several multiphosphorylated phosphoinositides, Tiam1 selectively interacts with phosphatidylinositol 3-phosphate (K(D) approximately 5-10 microm). In addition, and in contrast to recent reports, catalysis of nucleotide exchange on nonprenylated Rac1 provided by various extended portions of Tiam1 is not influenced by (a) soluble phosphoinositide head groups, (b) dibutyl versions of phosphoinositides, or (c) lipid vesicles containing phosphoinositides. Likewise, GEF activity afforded by DH/PH fragments of intersectin and Dbs are also not altered by phosphoinositide interactions. These results strongly suggest that unless all relevant components are localized to a lipid membrane surface, Dbl family GEFs generally are not intrinsically modulated by binding phosphoinositides.


Subject(s)
Adaptor Proteins, Vesicular Transport , Carrier Proteins/metabolism , Guanine Nucleotide Exchange Factors/metabolism , Phosphatidylinositols/metabolism , Proteins/metabolism , Immunoblotting , Protein Binding , Rho Guanine Nucleotide Exchange Factors , Surface Plasmon Resonance , T-Lymphoma Invasion and Metastasis-inducing Protein 1
7.
EMBO J ; 20(16): 4414-22, 2001 Aug 15.
Article in English | MEDLINE | ID: mdl-11500369

ABSTRACT

In Drosophila, phototransduction is mediated by G(q)-activation of phospholipase C and is a well studied model system for understanding the kinetics of signal initiation, propagation and termination controlled by G proteins. The proper intracellular targeting and spatial arrangement of most proteins involved in fly phototransduction require the multi-domain scaffolding protein InaD, composed almost entirely of five PDZ domains, which independently bind various proteins including NorpA, the relevant phospho lipase C-beta isozyme. We have determined the crystal structure of the N-terminal PDZ domain of InaD bound to a peptide corresponding to the C-terminus of NorpA to 1.8 A resolution. The structure highlights an intermolecular disulfide bond necessary for high affinity interaction as determined by both in vitro and in vivo studies. Since other proteins also possess similar, cysteine-containing consensus sequences for binding PDZ domains, this disulfide-mediated 'dock-and-lock' interaction of PDZ domains with their ligands may be a relatively ubiquitous mode of coordinating signaling pathways.


Subject(s)
Disulfides/chemistry , Drosophila Proteins , Eye Proteins/chemistry , Photoreceptor Cells, Invertebrate/chemistry , Type C Phospholipases/chemistry , Amino Acid Sequence , Animals , Cell Line, Transformed , Crystallography, X-Ray , Drosophila melanogaster , Eye Proteins/physiology , Humans , Models, Molecular , Molecular Sequence Data , Peptides/chemistry , Phosphatidylinositol Diacylglycerol-Lyase , Phospholipase C beta , Photoreceptor Cells, Invertebrate/physiology , Protein Structure, Secondary , Protein Structure, Tertiary , Type C Phospholipases/physiology
8.
J Biol Chem ; 276(31): 29275-81, 2001 Aug 03.
Article in English | MEDLINE | ID: mdl-11387333

ABSTRACT

The regulators of G-protein signaling (RGS) proteins accelerate the intrinsic guanosine triphosphatase activity of heterotrimeric G-protein alpha subunits and are thus recognized as key modulators of G-protein-coupled receptor signaling. RGS12 and RGS14 contain not only the hallmark RGS box responsible for GTPase-accelerating activity but also a single G alpha(i/o)-Loco (GoLoco) motif predicted to represent a second G alpha interaction site. Here, we describe functional characterization of the GoLoco motif regions of RGS12 and RGS14. Both regions interact exclusively with G alpha(i1), G alpha(i2), and G alpha(i3) in their GDP-bound forms. In GTP gamma S binding assays, both regions exhibit guanine nucleotide dissociation inhibitor (GDI) activity, inhibiting the rate of exchange of GDP for GTP by G alpha(i1). Both regions also stabilize G alpha(i1) in its GDP-bound form, inhibiting the increase in intrinsic tryptophan fluorescence stimulated by AlF(4)(-). Our results indicate that both RGS12 and RGS14 harbor two distinctly different G alpha interaction sites: a previously recognized N-terminal RGS box possessing G alpha(i/o) GAP activity and a C-terminal GoLoco region exhibiting G alpha(i) GDI activity. The presence of two, independent G alpha interaction sites suggests that RGS12 and RGS14 participate in a complex coordination of G-protein signaling beyond simple G alpha GAP activity.


Subject(s)
Guanosine 5'-O-(3-Thiotriphosphate)/metabolism , Heterotrimeric GTP-Binding Proteins/metabolism , RGS Proteins/metabolism , Aluminum Compounds/pharmacology , Amino Acid Sequence , Amino Acid Substitution , Animals , Binding Sites , Biosensing Techniques , Cloning, Molecular , Escherichia coli , Fluorides/pharmacology , Guanosine Diphosphate/metabolism , Heterotrimeric GTP-Binding Proteins/chemistry , Kinetics , Models, Biological , Molecular Sequence Data , Mutagenesis, Site-Directed , Oligopeptides , Open Reading Frames , RGS Proteins/chemistry , RGS Proteins/genetics , Rats , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Signal Transduction , Surface Plasmon Resonance
9.
Biochem Pharmacol ; 61(11): 1329-37, 2001 Jun 01.
Article in English | MEDLINE | ID: mdl-11331068

ABSTRACT

The standard model of signal transduction from G-protein-coupled receptors (GPCRs) involves guanine nucleotide cycling by a heterotrimeric G-protein assembly composed of Galpha, Gbeta, and Ggamma subunits. The WD-repeat beta-propeller protein Gbeta and the alpha-helical, isoprenylated polypeptide Ggamma are considered obligate dimerization partners; moreover, conventional Gbetagamma heterodimers are considered essential to the functional coupling of Galpha subunits to receptors. However, our recent discovery of a Gbeta5 binding site (the Ggamma-like or "GGL" domain) within several regulators of G-protein signaling (RGS) proteins revealed the potential for functional GPCR/Galpha coupling in the absence of a conventional Ggamma subunit. In addition, we posit that the interaction between Gbeta5 isoforms and the GGL domains of RGS proteins represents a general mode of binding between beta-propeller proteins and their partners, extending beyond the realm of G-protein-linked signal transduction.


Subject(s)
GTP-Binding Proteins/metabolism , Signal Transduction/physiology , Amino Acid Sequence , Animals , GTP-Binding Proteins/chemistry , Humans , Models, Molecular , Molecular Sequence Data , Protein Structure, Tertiary , RGS Proteins/metabolism , Sequence Homology, Amino Acid
10.
J Biol Chem ; 276(26): 23945-53, 2001 Jun 29.
Article in English | MEDLINE | ID: mdl-11294873

ABSTRACT

Mutation of Galpha(q) or Galpha(s) N-terminal contact sites for Gbetagamma resulted in alpha subunits that failed to localize at the plasma membrane or undergo palmitoylation when expressed in HEK293 cells. We now show that overexpression of specific betagamma subunits can recover plasma membrane localization and palmitoylation of the betagamma-binding-deficient mutants of alpha(s) or alpha(q). Thus, the betagamma-binding-defective alpha is completely dependent on co-expression of exogenous betagamma for proper membrane localization. In this report, we examined the ability of beta(1-5) in combination with gamma(2) or gamma(3) to promote proper localization and palmitoylation of mutant alpha(s) or alpha(q). Immunofluorescence localization, cellular fractionation, and palmitate labeling revealed distinct subtype-specific differences in betagamma interactions with alpha subunits. These studies demonstrate that 1) alpha and betagamma reciprocally promote the plasma membrane targeting of the other subunit; 2) beta(5), when co-expressed with gamma(2) or gamma(3), fails to localize to the plasma membrane or promote plasma membrane localization of mutant alpha(s) or alpha(q); 3) beta(3) is deficient in promoting plasma membrane localization of mutant alpha(s) and alpha(q), whereas beta(4) is deficient in promoting plasma membrane localization of mutant alpha(q); 4) both palmitoylation and interactions with betagamma are required for plasma membrane localization of alpha.


Subject(s)
GTP-Binding Protein alpha Subunits, Gs/metabolism , GTP-Binding Protein beta Subunits , GTP-Binding Protein gamma Subunits , Heterotrimeric GTP-Binding Proteins/metabolism , Heterotrimeric GTP-Binding Proteins/physiology , Acylation , Cell Line , Cell Membrane/metabolism , GTP-Binding Protein alpha Subunits, Gq-G11 , GTP-Binding Protein alpha Subunits, Gs/genetics , Heterotrimeric GTP-Binding Proteins/genetics , Humans , Microscopy, Fluorescence , Mutation , Palmitates/metabolism , Protein Isoforms/physiology , Protein Transport
11.
Curr Biol ; 10(22): 1459-62, 2000 Nov 16.
Article in English | MEDLINE | ID: mdl-11102810

ABSTRACT

Mammalian telomerase is essential for the maintenance of telomere length [1-5]. Its catalytic core comprises a reverse transcriptase component (TERT) and an RNA component. While the biochemical role of mammalian TERT is well established [6-11], it is unknown whether it is sufficient for telomere-length maintenance, chromosome stability or other cellular processes. Cells from mice in which the mTert gene had been disrupted showed progressive loss of telomere DNA, a phenotype similar to cells in which the gene encoding the telomerase RNA component (mTR) has been disrupted [1,12]. On prolonged growth, mTert-deficient embryonic stem (ES) cells exhibited genomic instability, aneuploidy and telomeric fusions. ES cells heterozygous for the mTert disruption also showed telomere attrition, a phenotype that differs from heterozygous mTR cells [12]. Thus, telomere maintenance in mammals is carried out by a single, limiting TERT.


Subject(s)
RNA , Telomerase/physiology , Telomere/physiology , Animals , Cell Line , DNA-Binding Proteins , Gene Targeting , Mice , Telomerase/genetics , Telomerase/metabolism
12.
Nature ; 408(6813): 723-7, 2000 Dec 07.
Article in English | MEDLINE | ID: mdl-11130074

ABSTRACT

Gamma-aminobutyric acid (GABA)B receptors couple to Go to inhibit N-type calcium channels in embryonic chick dorsal root ganglion neurons. The voltage-independent inhibition, mediated by means of a tyrosine-kinase pathway, is transient and lasts up to 100 seconds. Inhibition of endogenous RGS12, a member of the family of regulators of G-protein signalling, selectively alters the time course of voltage-independent inhibition. The RGS12 protein, in addition to the RGS domain, contains PDZ and PTB domains. Fusion proteins containing the PTB domain of RGS12 alter the rate of termination of the GABA(B) signal, whereas the PDZ or RGS domains of RGS 12 have no observable effects. Using primary dorsal root ganglion neurons in culture, here we show an endogenous agonist-induced tyrosine-kinase-dependent complex of RGS12 and the calcium channel. These results indicate that RGS12 is a multifunctional protein capable of direct interactions through its PTB domain with the tyrosine-phosphorylated calcium channel. Recruitment of RGS proteins to G-protein effectors may represent an additional mechanism for signal termination in G-protein-coupled pathways.


Subject(s)
Calcium Channels, N-Type/metabolism , Neurons/metabolism , Protein-Tyrosine Kinases/metabolism , RGS Proteins/metabolism , Animals , Calcium/metabolism , Cells, Cultured , Chick Embryo , Ganglia, Spinal/cytology , Ganglia, Spinal/metabolism , Humans , Molecular Sequence Data , Phosphorylation , Protein Structure, Tertiary , RGS Proteins/genetics , Rats , Receptors, GABA-B/metabolism , Recombinant Fusion Proteins , Signal Transduction
13.
Proc Natl Acad Sci U S A ; 97(26): 14364-9, 2000 Dec 19.
Article in English | MEDLINE | ID: mdl-11121039

ABSTRACT

Activator of G protein signaling 3 (AGS3) is a newly identified protein shown to act at the level of the G protein itself. AGS3 belongs to the GoLoco family of proteins, sharing the 19-aa GoLoco motif that is a Galpha(i/o) binding motif. AGS3 interacts only with members of the Galpha(i/o) subfamily. By surface plasmon resonance, we found that AGS3 binds exclusively to the GDP-bound form of Galpha(i3). In GTPgammaS binding assays, AGS3 behaves as a guanine dissociation inhibitor (GDI), inhibiting the rate of exchange of GDP for GTP by Galpha(i3). AGS3 interacts with both Galpha(i3) and Galpha(o) subunits, but has GDI activity only on Galpha(i3), not on Galpha(o). The fourth GoLoco motif of AGS3 is a major contributor to this activity. AGS3 stabilizes Galpha(i3) in its GDP-bound form, as it inhibits the increase in tryptophan fluorescence of the Galpha(i3)-GDP subunit stimulated by AlF(4)(-). AGS3 is widely expressed as it is detected by immunoblotting in brain, testis, liver, kidney, heart, pancreas, and in PC-12 cells. Several different sizes of the protein are detected. By Northern blotting, AGS3 shows 2.3-kb and 3.5-kb mRNAs in heart and brain, respectively, suggesting tissue-specific alternative splicing. Taken together, our results demonstrate that AGS3 is a GDI. To the best of our knowledge, no other GDI has been described for heterotrimeric G proteins. Inhibition of the Galpha subunit and stimulation of heterotrimeric G protein signaling, presumably by stimulating Gbetagamma, extend the possibilities for modulating signal transduction through heterotrimeric G proteins.


Subject(s)
GTP-Binding Protein alpha Subunits, Gi-Go/metabolism , GTP-Binding Proteins/metabolism , Guanine Nucleotide Dissociation Inhibitors/metabolism , Guanine/metabolism , Aluminum Compounds , Amino Acid Motifs , Amino Acid Sequence , Animals , Cell Fractionation , Fluorides , Guanosine Diphosphate/metabolism , Heterotrimeric GTP-Binding Proteins/metabolism , Molecular Sequence Data , Rats , Tissue Distribution
14.
Mol Cell Biol ; 20(21): 8178-84, 2000 Nov.
Article in English | MEDLINE | ID: mdl-11027287

ABSTRACT

TEP1 is a mammalian telomerase-associated protein with similarity to the Tetrahymena telomerase protein p80. Like p80, TEP1 is associated with telomerase activity and the telomerase reverse transcriptase, and it specifically interacts with the telomerase RNA. To determine the role of mTep1 in telomerase function in vivo, we generated mouse embryonic stem (ES) cells and mice lacking mTep1. The mTep1-deficient (mTep1(-/-)) mice were viable and were bred for seven successive generations with no obvious phenotypic abnormalities. All murine tissues from mTep1(-/-) mice possessed a level of telomerase activity comparable to that in wild-type mice. In addition, analysis of several tissues that normally lack telomerase activity revealed no reactivation of telomerase activity in mTep1(-/-) mice. Telomere length, even in later generations of mTep1(-/-) mice, was equivalent to that in wild-type animals. ES cells deficient in mTep1 also showed no detectable alteration in telomerase activity or telomere length with increased passage in culture. Thus, mTep1 appears to be completely dispensable for telomerase function in vivo. Recently, TEP1 has been identified within a second ribonucleoprotein (RNP) complex, the vault particle. TEP1 can also specifically bind to a small RNA, vRNA, which is associated with the vault particle and is unrelated in sequence to mammalian telomerase RNA. These results reveal that TEP1 is an RNA binding protein that is not restricted to the telomerase complex and that TEP1 plays a redundant role in the assembly or localization of the telomerase RNP in vivo.


Subject(s)
Carrier Proteins/physiology , Telomere/physiology , Animals , Carrier Proteins/metabolism , Catalysis , Embryo, Mammalian/metabolism , In Situ Hybridization, Fluorescence , Mice , Mice, Inbred C57BL , Mice, Inbred ICR , Mice, Transgenic , Models, Genetic , Mutagenesis, Site-Directed , Precipitin Tests , RNA/metabolism , RNA-Binding Proteins , Recombination, Genetic , Spleen/cytology , Stem Cells/metabolism , Telomerase , Telomere/ultrastructure , Thymus Gland/cytology
15.
Proc Natl Acad Sci U S A ; 97(22): 12272-7, 2000 Oct 24.
Article in English | MEDLINE | ID: mdl-11027316

ABSTRACT

Regulators of G protein signaling (RGS) proteins accelerate the GTPase activity of Galpha protein subunits in vitro, negatively regulating G protein-coupled receptor signaling. The physiological role of mammalian RGS proteins is largely unknown. The RGS family member rgs2 was cloned as an immediate early response gene up-regulated in T lymphocytes after activation. To investigate the role of RGS2 in vivo, we generated rgs2-deficient mice. We show that targeted mutation of rgs2 in mice leads to reduced T cell proliferation and IL-2 production, which translates in an impaired antiviral immunity in vivo. Interestingly, rgs2(-/-) mice also display increased anxiety responses and decreased male aggression in the absence of cognitive or motor deficits. RGS2 also controls synaptic development and basal electrical activity in hippocampal CA1 neurons. Thus, RGS2 plays an important role in T cell activation, synapse development in the hippocampus, and emotive behaviors.


Subject(s)
Aggression/physiology , Anxiety/physiopathology , Lymphocyte Activation/physiology , RGS Proteins/physiology , T-Lymphocytes/immunology , Animals , Base Sequence , Cell Division/physiology , DNA Primers , Gene Targeting , Hippocampus/cytology , Hippocampus/physiology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Neurons/physiology , Synapses/physiology
16.
J Neurosci ; 20(19): 7143-8, 2000 Oct 01.
Article in English | MEDLINE | ID: mdl-11007869

ABSTRACT

We examined the effects of G-protein beta and gamma subunit heterodimers on human alpha(1B) (N-type) Ca channels expressed in HEK293 cells. All of the known beta subunits (beta1-beta5) produced voltage-dependent inhibition of alpha(1B) Ca channels, depending on the gamma subunit found in the heterodimer. beta1-beta4 subunits inhibited Ca channels when paired with gamma1-gamma3. However, beta5 subunits only produced inhibition when paired with gamma2. In contrast, heterodimers between beta5 subunits and RGS (regulators of G-protein signaling) proteins containing GGL domains did not produce inhibition of Ca channels. However, GGL domain-containing RGS proteins (e.g., RGS6 and RGS11) did block the ability of Gbeta5/gamma2 heterodimers to inhibit Ca channels. Because all of the G-protein beta subunits are found in the nervous system, we conclude that they may all potentially participate in Ca channel inhibition. The interaction of GGL-containing RGS proteins with Gbeta5gamma2 suggests a novel way in which Ca channels can be regulated.


Subject(s)
Calcium Channels, N-Type/metabolism , Heterotrimeric GTP-Binding Proteins/metabolism , RGS Proteins/metabolism , Analysis of Variance , Animals , Barium/pharmacology , Calcium Channels, N-Type/drug effects , Cells, Cultured , Cloning, Molecular , Cytomegalovirus/genetics , Dimerization , Gene Expression , Heterotrimeric GTP-Binding Proteins/genetics , Humans , Kidney/cytology , Kidney/metabolism , Membrane Potentials/drug effects , Mice , RNA, Messenger/biosynthesis , Transfection
18.
Crit Rev Biochem Mol Biol ; 34(4): 215-51, 1999.
Article in English | MEDLINE | ID: mdl-10517644

ABSTRACT

Studies of the desensitization of G protein-coupled signal transduction have led to the discovery of a family of guanosine triphosphatase-activating proteins (GAPs) for heterotrimeric G protein alpha subunits - the "regulator of G protein signaling" or RGS proteins. In considering both documented and potential functions of several RGS protein family members with demonstrable multidomain compositions (p115RhoGEF, PDZRhoGEF, Axin, Axil/Conductin, D-AKAP2, the G protein-coupled receptor kinases [GRKs], the DEP/GGL/RGS subfamily [RGS6, RGS7, RGS9, RGS11], and RGS12), this review explores the shift in our appreciation of the RGS proteins from unidimensional desensitizing agents to multifocal signal transduction regulators.


Subject(s)
Adaptor Proteins, Signal Transducing , RGS Proteins/metabolism , RGS Proteins/physiology , Repressor Proteins , Signal Transduction , A Kinase Anchor Proteins , Amino Acid Sequence , Animals , Axin Protein , Carrier Proteins/physiology , Cell Cycle/physiology , Cyclic AMP-Dependent Protein Kinases/physiology , Cytoskeletal Proteins/physiology , Fungal Proteins/physiology , GTP-Binding Proteins/physiology , Humans , Models, Biological , Molecular Sequence Data , Protein-Tyrosine Kinases/physiology , Proteins/physiology , Sequence Homology, Amino Acid , rho GTP-Binding Proteins/physiology
20.
Proc Natl Acad Sci U S A ; 96(11): 6489-94, 1999 May 25.
Article in English | MEDLINE | ID: mdl-10339615

ABSTRACT

Several regulators of G protein signaling (RGS) proteins contain a G protein gamma-subunit-like (GGL) domain, which, as we have shown, binds to Gbeta5 subunits. Here, we extend our original findings by describing another GGL-domain-containing RGS, human RGS6. When RGS6 is coexpressed with different Gbeta subunits, only RGS6 and Gbeta5 interact. The expression of mRNA for RGS6 and Gbeta5 in human tissues overlaps. Predictions of alpha-helical and coiled-coil character within GGL domains, coupled with measurements of Gbeta binding by GGL domain mutants, support the contention that Ggamma-like regions within RGS proteins interact with Gbeta5 subunits in a fashion comparable to conventional Gbeta/Ggamma pairings. Mutation of the highly conserved Phe-61 residue of Ggamma2 to tryptophan, the residue present in all GGL domains, increases the stability of the Gbeta5/Ggamma2 heterodimer, highlighting the importance of this residue to GGL/Gbeta5 association.


Subject(s)
GTP-Binding Proteins/metabolism , Proteins/metabolism , RGS Proteins , Amino Acid Sequence , Animals , Binding Sites , COS Cells , DNA, Complementary , GTP-Binding Proteins/chemistry , GTP-Binding Proteins/genetics , Humans , Macromolecular Substances , Models, Molecular , Molecular Sequence Data , Protein Biosynthesis , Protein Conformation , Proteins/chemistry , Proteins/genetics , RNA, Messenger/genetics , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Sequence Alignment , Sequence Homology, Amino Acid , Transcription, Genetic , Transfection
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