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1.
J Biochem ; 175(5): 495-505, 2024 Apr 29.
Article in English | MEDLINE | ID: mdl-38378744

ABSTRACT

Mysterin is a large intracellular protein harboring a RING finger ubiquitin ligase domain and is also referred to as RING finger protein 213 (RNF213). The author performed the first molecular cloning of the mysterin gene as the final step in genetic exploration of cerebrovascular moyamoya disease (MMD) and initiated the next round of exploration to understand its molecular and cellular functions. Although much remains unknown, accumulating findings suggest that mysterin functions in cells by targeting massive intracellular structures, such as lipid droplets (LDs) and various invasive pathogens. In the latter case, mysterin appears to directly surround and ubiquitylate the surface of pathogens and stimulate cell-autonomous antimicrobial reactions, such as xenophagy and inflammatory response. To date, multiple mutations causing MMD have been identified within and near the RING finger domain of mysterin; however, their functional relevance remains largely unknown. Besides the RING finger, mysterin harbors a dynein-like ATPase core and an RZ finger, another ubiquitin ligase domain unique to mysterin, while functional exploration of these domains has also just commenced. In this review, the author attempts to summarize the core findings regarding the molecular structure and function of the mysterin protein, with an emphasis on the perspective of MMD research.


Subject(s)
Adenosine Triphosphatases , Ubiquitin-Protein Ligases , Humans , Ubiquitin-Protein Ligases/metabolism , Ubiquitin-Protein Ligases/chemistry , Animals , Moyamoya Disease/metabolism , Moyamoya Disease/genetics
2.
J Cell Biol ; 218(3): 949-960, 2019 03 04.
Article in English | MEDLINE | ID: mdl-30705059

ABSTRACT

Mysterin, also known as RNF213, is an intracellular protein that forms large toroidal oligomers. Mysterin was originally identified in genetic studies of moyamoya disease (MMD), a rare cerebrovascular disorder of unknown etiology. While mysterin is known to exert ubiquitin ligase and putative mechanical ATPase activities with a RING finger domain and two adjacent AAA+ modules, its biological role is poorly understood. Here, we report that mysterin is targeted to lipid droplets (LDs), ubiquitous organelles specialized for neutral lipid storage, and markedly increases their abundance in cells. This effect was exerted primarily through specific elimination of adipose triglyceride lipase (ATGL) from LDs. The ubiquitin ligase and ATPase activities of mysterin were both important for its proper LD targeting. Notably, MMD-related mutations in the ubiquitin ligase domain of mysterin significantly impaired its fat-stabilizing activity. Our findings identify a unique new regulator of cytoplasmic LDs and suggest a potential link between the pathogenesis of MMD and fat metabolism.


Subject(s)
Adenosine Triphosphatases/metabolism , Lipid Droplets/metabolism , Lipid Metabolism , Moyamoya Disease/metabolism , Ubiquitin-Protein Ligases/metabolism , Zebrafish Proteins/metabolism , Adenosine Triphosphatases/genetics , Animals , HEK293 Cells , HeLa Cells , Hep G2 Cells , Humans , Lipase/genetics , Lipase/metabolism , Moyamoya Disease/genetics , Moyamoya Disease/pathology , Mutation , Protein Domains , Ubiquitin-Protein Ligases/genetics , Zebrafish , Zebrafish Proteins/genetics
3.
Proc Natl Acad Sci U S A ; 115(18): E4199-E4208, 2018 05 01.
Article in English | MEDLINE | ID: mdl-29666234

ABSTRACT

Although mechanisms for protein homeostasis in the cytosol have been studied extensively, those in the nucleus remain largely unknown. Here, we identified that a protein complex mediates export of polyubiquitinated proteins from the nucleus to the cytosol. UBIN, a ubiquitin-associated (UBA) domain-containing protein, shuttled between the nucleus and the cytosol in a CRM1-dependent manner, despite the lack of intrinsic nuclear export signal (NES). Instead, the UBIN binding protein polyubiquitinated substrate transporter (POST) harboring an NES shuttled UBIN through nuclear pores. UBIN bound to polyubiquitin chain through its UBA domain, and the UBIN-POST complex exported them from the nucleus to the cytosol. Ubiquitinated proteins accumulated in the cytosol in response to proteasome inhibition, whereas cotreatment with CRM1 inhibitor led to their accumulation in the nucleus. Our results suggest that ubiquitinated proteins are exported from the nucleus to the cytosol in the UBIN-POST complex-dependent manner for the maintenance of nuclear protein homeostasis.


Subject(s)
Carrier Proteins/metabolism , Cell Nucleus/metabolism , Cytosol/metabolism , Human Umbilical Vein Endothelial Cells/metabolism , Membrane Proteins/metabolism , Nuclear Proteins/metabolism , Ubiquitinated Proteins/metabolism , Active Transport, Cell Nucleus/physiology , Animals , Carrier Proteins/genetics , Cell Nucleus/genetics , HEK293 Cells , HeLa Cells , Human Umbilical Vein Endothelial Cells/cytology , Humans , Membrane Proteins/genetics , Mice , NIH 3T3 Cells , Nuclear Proteins/genetics , Solute Carrier Proteins , Ubiquitinated Proteins/genetics
4.
Sci Rep ; 7: 44293, 2017 03 09.
Article in English | MEDLINE | ID: mdl-28276505

ABSTRACT

The deubiquitylating enzyme USP15 plays significant roles in multiple cellular pathways including TGF-ß signaling, RNA splicing, and innate immunity. Evolutionarily conserved skipping of exon 7 occurs during transcription of the mRNAs encoding USP15 and its paralogue USP4, yielding two major isoforms for each gene. Exon 7 of USP15 encodes a serine-rich stretch of 29 amino acid residues located in the inter-region linker that connects the N-terminal putative regulatory region and the C-terminal enzymatic region. Previous findings suggested that the variation in the linker region leads to functional differences between the isoforms of the two deubiquitylating enzymes, but to date no direct evidence regarding such functional divergence has been published. We found that the long isoform of USP15 predominantly recognizes and deubiquitylates mysterin, a large ubiquitin ligase associated with the onset of moyamoya disease. This observation represents the first experimental evidence that the conserved exon skipping alters the substrate specificity of this class of deubiquitylating enzymes. In addition, we found that the interactomes of the short and long isoforms of USP15 only partially overlapped. Thus, USP15, a key gene in multiple cellular processes, generates two functionally different isoforms via evolutionarily conserved exon skipping.


Subject(s)
Adenosine Triphosphatases/genetics , Exons/genetics , Genetic Predisposition to Disease , Moyamoya Disease/genetics , Ubiquitin-Protein Ligases/genetics , Ubiquitin-Specific Proteases/genetics , Adenosine Triphosphatases/metabolism , Alternative Splicing , HEK293 Cells , Humans , Isoenzymes/genetics , Isoenzymes/metabolism , Moyamoya Disease/metabolism , Protein Binding , Substrate Specificity , Ubiquitin-Protein Ligases/metabolism , Ubiquitin-Specific Proteases/metabolism , Ubiquitination
5.
Sci Rep ; 5: 16161, 2015 Nov 04.
Article in English | MEDLINE | ID: mdl-26530008

ABSTRACT

Mysterin (also known as RNF213) is a huge intracellular protein with two AAA+ ATPase modules and a RING finger ubiquitin ligase domain. Mysterin was originally isolated as a significant risk factor for the cryptogenic cerebrovascular disorder moyamoya disease, and was found to be involved in physiological angiogenesis in zebrafish. However, the function and the physiological significance of mysterin in other than blood vessels remain largely unknown, although mysterin is ubiquitously expressed in animal tissues. In this study, we performed antisense-mediated suppression of a mysterin orthologue in zebrafish larvae and revealed that mysterin-deficient larvae showed significant reduction in fast myofibrils and immature projection of primary motoneurons, leading to severe motor deficits. Fast muscle-specific restoration of mysterin expression cancelled these phenotypes, and interestingly both AAA+ ATPase and ubiquitin ligase activities of mysterin were indispensable for proper fast muscle formation, demonstrating an essential role of mysterin and its enzymatic activities in the neuromuscular regulation in zebrafish.


Subject(s)
Ubiquitin-Protein Ligases/metabolism , Zebrafish Proteins/metabolism , Zebrafish/metabolism , Animals , Animals, Genetically Modified/growth & development , Animals, Genetically Modified/metabolism , Humans , Immunohistochemistry , Larva/metabolism , Microscopy, Electron , Motor Activity , Motor Neurons/metabolism , Muscle Fibers, Skeletal/metabolism , Muscle Fibers, Skeletal/pathology , Neovascularization, Physiologic , Oligonucleotides, Antisense/metabolism , RING Finger Domains , Ubiquitin-Protein Ligases/antagonists & inhibitors , Ubiquitin-Protein Ligases/genetics , Zebrafish/growth & development , Zebrafish Proteins/antagonists & inhibitors , Zebrafish Proteins/genetics
6.
Mol Cell ; 59(3): 335-44, 2015 Aug 06.
Article in English | MEDLINE | ID: mdl-26253026

ABSTRACT

ER-associated degradation (ERAD) is a protein clearance mechanism by which misfolded, misassembled, or metabolically regulated proteins are specifically dislocated from the ER into the cytosol and degraded by the ubiquitin proteasome system. ERAD very likely evolved to maintain proteostasis and sterol homeostasis in the ER. However, the ironic truth is that membrane-penetrating transportation and protein degradation machineries in ERAD are preferably hijacked by exogenous pathogens such as viruses and toxins for their invasion and evasion from immunological surveillance. In this Review, we provide an overview of our current understanding of the pathogenic hijacking of the host cell ERAD, in which pathogens exploit the complex ERAD machinery in a variety of manners for their own use, suggesting flexibility and plasticity of the molecular machinery of ERAD.


Subject(s)
Endoplasmic Reticulum-Associated Degradation , Viral Proteins/metabolism , Viruses/metabolism , Animals , Cytosol/metabolism , Endoplasmic Reticulum/metabolism , Humans , Proteins/chemistry , Proteins/metabolism , Proteolysis , Virus Diseases/pathology , Virus Diseases/virology
7.
EMBO J ; 34(18): 2334-49, 2015 Sep 14.
Article in English | MEDLINE | ID: mdl-26228940

ABSTRACT

The cellular proteostasis network integrates the protein folding and clearance machineries in multiple sub-cellular compartments of the eukaryotic cell. The endoplasmic reticulum (ER) is the site of synthesis and folding of membrane and secretory proteins. A distinctive feature of the ER is its tightly controlled redox homeostasis necessary for the formation of inter- and intra-molecular disulphide bonds. Employing genetically encoded in vivo sensors reporting on the redox state in an organelle-specific manner, we show in the nematode Caenorhabditis elegans that the redox state of the ER is subject to profound changes during worm lifetime. In young animals, the ER is oxidizing and this shifts towards reducing conditions during ageing, whereas in the cytosol the redox state becomes more oxidizing with age. Likewise, the redox state in the cytosol and the ER change in an opposing manner in response to proteotoxic challenges in C. elegans and in HeLa cells revealing conservation of redox homeostasis. Moreover, we show that organelle redox homeostasis is regulated across tissues within C. elegans providing a new measure for organismal fitness.


Subject(s)
Aging/metabolism , Caenorhabditis elegans/metabolism , Endoplasmic Reticulum/metabolism , Proteostasis Deficiencies/metabolism , Aging/genetics , Animals , Caenorhabditis elegans/genetics , Endoplasmic Reticulum/genetics , Humans , Oxidation-Reduction , Proteostasis Deficiencies/genetics
8.
Sci Rep ; 4: 4442, 2014 Mar 24.
Article in English | MEDLINE | ID: mdl-24658080

ABSTRACT

Moyamoya disease is an idiopathic human cerebrovascular disorder that is characterized by progressive stenosis and abnormal collateral vessels. We recently identified mysterin/RNF213 as its first susceptibility gene, which encodes a 591-kDa protein containing enzymatically active P-loop ATPase and ubiquitin ligase domains and is involved in proper vascular development in zebrafish. Here we demonstrate that mysterin further contains two tandem AAA+ ATPase modules and forms huge ring-shaped oligomeric complex. AAA+ ATPases are known to generally mediate various biophysical and mechanical processes with the characteristic ring-shaped structure. Fluorescence correlation spectroscopy and biochemical evaluation suggested that mysterin dynamically changes its oligomeric forms through ATP/ADP binding and hydrolysis cycles. Thus, the moyamoya disease-associated gene product is a unique protein that functions as ubiquitin ligase and AAA+ ATPase, which possibly contributes to vascular development through mechanical processes in the cell.


Subject(s)
Adenosine Triphosphatases/genetics , Moyamoya Disease/genetics , Ubiquitin-Protein Ligases/genetics , Amino Acid Sequence , Genetic Predisposition to Disease , HEK293 Cells , Humans , Hydrolysis , Moyamoya Disease/metabolism , Moyamoya Disease/pathology , Protein Conformation , Ubiquitin-Protein Ligases/chemistry , Ubiquitin-Protein Ligases/metabolism
9.
Biochem Biophys Res Commun ; 439(4): 419-26, 2013 Oct 04.
Article in English | MEDLINE | ID: mdl-23994138

ABSTRACT

Moyamoya disease (MMD) is a cerebrovascular disease characterized by occlusive lesions in the Circle of Willis. The RNF213 R4810K polymorphism increases susceptibility to MMD. In the present study, we characterized phenotypes caused by overexpression of RNF213 wild type and R4810K variant in the cell cycle to investigate the mechanism of proliferation inhibition. Overexpression of RNF213 R4810K in HeLa cells inhibited cell proliferation and extended the time of mitosis 4-fold. Ablation of spindle checkpoint by depletion of mitotic arrest deficiency 2 (MAD2) did not shorten the time of mitosis. Mitotic morphology in HeLa cells revealed that MAD2 colocalized with RNF213 R4810K. Immunoprecipitation revealed an RNF213/MAD2 complex: R4810K formed a complex with MAD2 more readily than RNF213 wild-type. Desynchronized localization of MAD2 was observed more frequently during mitosis in fibroblasts from patients (n=3, 61.0 ± 8.2%) compared with wild-type subjects (n=6, 13.1 ± 7.7%; p<0.01). Aneuploidy was observed more frequently in fibroblasts (p<0.01) and induced pluripotent stem cells (iPSCs) (p<0.03) from patients than from wild-type subjects. Vascular endothelial cells differentiated from iPSCs (iPSECs) of patients and an unaffected carrier had a longer time from prometaphase to metaphase than those from controls (p<0.05). iPSECs from the patients and unaffected carrier had significantly increased mitotic failure rates compared with controls (p<0.05). Thus, RNF213 R4810K induced mitotic abnormalities and increased risk of genomic instability.


Subject(s)
Genetic Predisposition to Disease , Genetic Variation , Genomic Instability , Mitosis/genetics , Moyamoya Disease/genetics , Ubiquitin-Protein Ligases/genetics , Adenosine Triphosphatases , Genotype , HeLa Cells , Human Umbilical Vein Endothelial Cells , Humans , Mad2 Proteins/genetics , Mad2 Proteins/metabolism , Phenotype , Pluripotent Stem Cells/metabolism
10.
Biochem Biophys Res Commun ; 438(1): 13-9, 2013 Aug 16.
Article in English | MEDLINE | ID: mdl-23850618

ABSTRACT

Moyamoya disease (MMD) is a cerebrovascular disease characterized by occlusive lesions in the circle of Willis. The RNF213 R4810K polymorphism increases susceptibility to MMD. Induced pluripotent stem cells (iPSCs) were established from unaffected fibroblast donors with wild-type RNF213 alleles, and from carriers/patients with one or two RNF213 R4810K alleles. Angiogenic activities of iPSC-derived vascular endothelial cells (iPSECs) from patients and carriers were lower (49.0 ± 19.4%) than from wild-type subjects (p<0.01). Gene expression profiles in iPSECs showed that Securin was down-regulated (p<0.01) in carriers and patients. Overexpression of RNF213 R4810K downregulated Securin, inhibited angiogenic activity (36.0 ± 16.9%) and proliferation of humanumbilical vein endothelial cells (HUVECs) while overexpression of RNF213 wild type did not. Securin expression was downregulated using RNA interference techniques, which reduced the level of tube formation in iPSECs and HUVECs without inhibition of proliferation. RNF213 R4810K reduced angiogenic activities of iPSECs from patients with MMD, suggesting that it is a promising in vitro model for MMD.


Subject(s)
Endothelial Cells/metabolism , Moyamoya Disease/metabolism , Neoplasm Proteins/metabolism , Neovascularization, Pathologic/physiopathology , Pluripotent Stem Cells/metabolism , Ubiquitin-Protein Ligases/metabolism , Adenosine Triphosphatases , Cells, Cultured , Child , Down-Regulation , Endothelial Cells/pathology , Female , Humans , Male , Middle Aged , Moyamoya Disease/pathology , Mutation/genetics , Neovascularization, Pathologic/pathology , Pluripotent Stem Cells/pathology , Securin , Ubiquitin-Protein Ligases/genetics
11.
Front Immunol ; 3: 48, 2012.
Article in English | MEDLINE | ID: mdl-22566930

ABSTRACT

Over the past two decades, heat shock proteins (HSPs) have been implicated in inflammatory responses and autoimmunity. HSPs were originally believed to maintain protein quality control in the cytosol. However, they also exist extracellularly and appear to act as inflammatory factors. Recently, a growing body of evidence suggested that the other class of stress proteins such as, endoplasmic reticulum (ER) stress proteins, which originally act as protein quality control factors in the secretory pathway and are induced by ER stress in inflammatory lesions, also participate in inflammation and autoimmunity. The immunoglobulin heavy-chain binding protein (Bip)/glucose-regulated protein 78 (GRP78), calnexin, calreticulin, glucose-regulated protein 94 (GRP94)/gp96, oxygen regulated protein 150 (ORP150)/glucose-regulated protein 170 (GRP170), homocysteine-induced ER protein (Herp) and heat shock protein 47 (hsp47)/Serpin H1, which are expressed not only in the ER but also occasionally at the cell surface play pathophysiological roles in autoimmune and inflammatory diseases as pro- or anti-inflammatory factors. Here we describe the accumulating evidence of the participation of ER stress proteins in autoimmunity and inflammation and discuss the critical differences between the two classes of stress proteins.

12.
PLoS One ; 6(7): e22542, 2011.
Article in English | MEDLINE | ID: mdl-21799892

ABSTRACT

BACKGROUND: Moyamoya disease is an idiopathic vascular disorder of intracranial arteries. Its susceptibility locus has been mapped to 17q25.3 in Japanese families, but the susceptibility gene is unknown. METHODOLOGY/PRINCIPAL FINDINGS: Genome-wide linkage analysis in eight three-generation families with moyamoya disease revealed linkage to 17q25.3 (P<10(-4)). Fine mapping demonstrated a 1.5-Mb disease locus bounded by D17S1806 and rs2280147. We conducted exome analysis of the eight index cases in these families, with results filtered through Ng criteria. There was a variant of p.N321S in PCMTD1 and p.R4810K in RNF213 in the 1.5-Mb locus of the eight index cases. The p.N321S variant in PCMTD1 could not be confirmed by the Sanger method. Sequencing RNF213 in 42 index cases confirmed p.R4810K and revealed it to be the only unregistered variant. Genotyping 39 SNPs around RNF213 revealed a founder haplotype transmitted in 42 families. Sequencing the 260-kb region covering the founder haplotype in one index case did not show any coding variants except p.R4810K. A case-control study demonstrated strong association of p.R4810K with moyamoya disease in East Asian populations (251 cases and 707 controls) with an odds ratio of 111.8 (P = 10(-119)). Sequencing of RNF213 in East Asian cases revealed additional novel variants: p.D4863N, p.E4950D, p.A5021V, p.D5160E, and p.E5176G. Among Caucasian cases, variants p.N3962D, p.D4013N, p.R4062Q and p.P4608S were identified. RNF213 encodes a 591-kDa cytosolic protein that possesses two functional domains: a Walker motif and a RING finger domain. These exhibit ATPase and ubiquitin ligase activities. Although the mutant alleles (p.R4810K or p.D4013N in the RING domain) did not affect transcription levels or ubiquitination activity, knockdown of RNF213 in zebrafish caused irregular wall formation in trunk arteries and abnormal sprouting vessels. CONCLUSIONS/SIGNIFICANCE: We provide evidence suggesting, for the first time, the involvement of RNF213 in genetic susceptibility to moyamoya disease.


Subject(s)
Blood Vessels/physiopathology , Genetic Predisposition to Disease/genetics , Moyamoya Disease/genetics , Moyamoya Disease/physiopathology , Ubiquitin-Protein Ligases/genetics , 3' Untranslated Regions/genetics , Adenosine Triphosphatases , Adult , Alleles , Animals , Base Sequence , Blood Vessels/metabolism , Case-Control Studies , Cloning, Molecular , DNA Copy Number Variations/genetics , DNA, Complementary/genetics , Exome/genetics , Exons/genetics , Female , Gene Expression Regulation , Gene Knockdown Techniques , HEK293 Cells , HeLa Cells , Humans , Linkage Disequilibrium/genetics , Male , Molecular Sequence Data , Moyamoya Disease/ethnology , Open Reading Frames/genetics , Sequence Homology, Amino Acid , Ubiquitin-Protein Ligases/deficiency , Ubiquitin-Protein Ligases/metabolism , Zebrafish
13.
Mol Biol Cell ; 19(4): 1328-36, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18216283

ABSTRACT

Misfolded or improperly assembled proteins in the endoplasmic reticulum (ER) are exported into the cytosol and degraded via the ubiquitin-proteasome pathway, a process termed ER-associated degradation (ERAD). Saccharomyces cerevisiae Hrd1p/Der3p is an ER membrane-spanning ubiquitin ligase that participates in ERAD of the cystic fibrosis transmembrane conductance regulator (CFTR) when CFTR is exogenously expressed in yeast cells. Two mammalian orthologues of yeast Hrd1p/Der3p, gp78 and HRD1, have been reported. Here, we demonstrate that gp78, but not HRD1, participates in ERAD of the CFTR mutant CFTRDeltaF508, by specifically promoting ubiquitylation of CFTRDeltaF508. Domain swapping experiments and deletion analysis revealed that gp78 binds to CFTRDeltaF508 through its ubiquitin binding region, the so-called coupling of ubiquitin to ER degradation (CUE) domain. Gp78 polyubiquitylated in vitro an N-terminal ubiquitin-glutathione-S-transferase (GST)-fusion protein, but not GST alone. This suggests that gp78 recognizes the ubiquitin that is already conjugated to CFTRDeltaF508 and catalyzes further polyubiquitylation of CFTRDeltaF508 in a manner similar to that of a multiubiquitin chain assembly factor (E4). Furthermore, we revealed by small interfering RNA methods that the ubiquitin ligase RMA1 functioned as an E3 enzyme upstream of gp78. Our data demonstrates that gp78 cooperates with RMA1 with E4-like activity in the ERAD of CFTRDeltaF508.


Subject(s)
Cystic Fibrosis Transmembrane Conductance Regulator/metabolism , Endoplasmic Reticulum/metabolism , Membrane Proteins/metabolism , Receptors, Cytokine/metabolism , Ubiquitin-Protein Ligases/metabolism , Animals , Binding Sites , Cell Line , Cystic Fibrosis Transmembrane Conductance Regulator/genetics , Humans , Membrane Proteins/antagonists & inhibitors , Membrane Proteins/genetics , Mice , Models, Biological , Mutagenesis, Site-Directed , Mutation , Protein Structure, Tertiary , RNA, Small Interfering/genetics , Receptors, Autocrine Motility Factor , Receptors, Cytokine/chemistry , Receptors, Cytokine/genetics , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism , Transfection , Ubiquitin-Protein Ligases/antagonists & inhibitors , Ubiquitin-Protein Ligases/chemistry , Ubiquitin-Protein Ligases/genetics
14.
Mol Biol Cell ; 19(3): 899-911, 2008 Mar.
Article in English | MEDLINE | ID: mdl-18094050

ABSTRACT

McKusick-Kaufman syndrome (MKKS) is a recessively inherited human genetic disease characterized by several developmental anomalies. Mutations in the MKKS gene also cause Bardet-Biedl syndrome (BBS), a genetically heterogeneous disorder with pleiotropic symptoms. However, little is known about how MKKS mutations lead to disease. Here, we show that disease-causing mutants of MKKS are rapidly degraded via the ubiquitin-proteasome pathway in a manner dependent on HSC70 interacting protein (CHIP), a chaperone-dependent ubiquitin ligase. Although wild-type MKKS quickly shuttles between the centrosome and cytosol in living cells, the rapidly degraded mutants often fail to localize to the centrosome. Inhibition of proteasome functions causes MKKS mutants to form insoluble structures at the centrosome. CHIP and partner chaperones, including heat-shock protein (HSP)70/heat-shock cognate 70 and HSP90, strongly recognize MKKS mutants. Modest knockdown of CHIP by RNA interference moderately inhibited the degradation of MKKS mutants. These results indicate that the MKKS mutants have an abnormal conformation and that chaperone-dependent degradation mediated by CHIP is a key feature of MKKS/BBS diseases.


Subject(s)
Bardet-Biedl Syndrome/genetics , Centrosome/metabolism , Molecular Chaperones/metabolism , Mutation/genetics , Protein Processing, Post-Translational , Ubiquitin-Protein Ligases/metabolism , Ubiquitination , Animals , Cell Line , Cytosol/metabolism , Glutamic Acid/genetics , Glycine/genetics , Group II Chaperonins , Humans , Mice , Microtubules/metabolism , Mutant Proteins/metabolism , Proteasome Inhibitors , Protein Structure, Quaternary , Protein Transport , Solubility
15.
J Biol Chem ; 281(14): 9650-8, 2006 Apr 07.
Article in English | MEDLINE | ID: mdl-16431915

ABSTRACT

Quality control in the endoplasmic reticulum ensures that only properly folded proteins are retained in the cell through mechanisms that recognize and discard misfolded or unassembled proteins in a process called endoplasmic reticulum-associated degradation (ERAD). We previously cloned EDEM (ER degradation-enhancing alpha-mannosidase-like protein) and showed that it accelerates ERAD of misfolded glycoproteins. We now cloned mouse EDEM3, a soluble homolog of EDEM. EDEM3 consists of 931 amino acids and has all the signature motifs of Class I alpha-mannosidases (glycosyl hydrolase family 47) in its N-terminal domain and a protease-associated motif in its C-terminal region. EDEM3 accelerates glycoprotein ERAD in transfected HEK293 cells, as shown by increased degradation of misfolded alpha1-antitrypsin variant (null (Hong Kong)) and of TCRalpha. Overexpression of EDEM3 also greatly stimulates mannose trimming not only from misfolded alpha1-AT null (Hong Kong) but also from total glycoproteins, in contrast to EDEM, which has no apparent alpha1,2-mannosidase activity. Furthermore, overexpression of the E147Q EDEM3 mutant, which has the mutation in one of the conserved acidic residues essential for enzyme activity of alpha1,2-mannosidases, abolishes the stimulation of mannose trimming and greatly decreases the stimulation of ERAD by EDEM3. These results show that EDEM3 has alpha1,2-mannosidase activity in vivo, suggesting that the mechanism whereby EDEM3 accelerates glycoprotein ERAD is different from that of EDEM.


Subject(s)
Endoplasmic Reticulum/physiology , Glycoproteins/metabolism , Membrane Proteins/genetics , Membrane Proteins/physiology , Protein Folding , Amino Acid Sequence , Animals , Calcium-Binding Proteins , Cloning, Molecular , Expressed Sequence Tags , Mannose/metabolism , Mice , Molecular Sequence Data , Solubility , alpha-Mannosidase/metabolism
16.
Biochemistry ; 42(11): 3160-7, 2003 Mar 25.
Article in English | MEDLINE | ID: mdl-12641447

ABSTRACT

Pigment epithelium-derived factor (PEDF), a member of the serine protease inhibitor (serpin) superfamily, possesses anti-angiogenic and neurotrophic activities. PEDF has been reported to bind to extracellular matrix (ECM) components such as collagens and glycosaminoglycans (GAGs). In this study, to determine the binding sites for collagens and GAGs, we analyzed the interaction of recombinant mouse PEDF (rPEDF) with collagen I and heparin. By utilizing residue-specific chemical modification and site-directed mutagenesis techniques, we revealed that the acidic amino acid residues on PEDF (Asp(255), Asp(257), and Asp(299)) are critical to collagen binding, and three clustered basic amino acid residues (Arg(145), Lys(146), and Arg(148)) are necessary for heparin binding. Mapping of these residues on the crystal structure of human PEDF (Simonovic, M., Gettins, P. G. W., and Volz, K. (2001) Proc. Natl. Acad. Sci. U.S.A. 98, 11131-11135) demonstrated that the collagen-binding site is oriented toward the opposite side of the highly basic surface where the heparin-binding site is localized. These results indicate that PEDF possesses dual binding sites for different ECM components, and this unique localization of ECM-binding sites implies that the binding to ECM components could regulate PEDF activities.


Subject(s)
Extracellular Matrix Proteins/metabolism , Eye Proteins , Neovascularization, Physiologic/physiology , Nerve Growth Factors , Proteins/metabolism , Serpins/metabolism , Animals , Base Sequence , Binding Sites , Circular Dichroism , DNA Primers , Mice , Models, Molecular , Mutagenesis, Site-Directed , Proteins/chemistry , Proteins/physiology , Recombinant Proteins/chemistry , Recombinant Proteins/metabolism , Serpins/chemistry , Serpins/physiology
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