Literature DB >> 11405340

The role of chaperone-assisted folding and quality control in inborn errors of metabolism: protein folding disorders.

N Gregersen1, P Bross, B S Andrese, C B Pedersen, T J Corydon, L Bolund.   

Abstract

Molecular chaperones are present in the various compartments of the cell and assist the folding of newly synthesized proteins. Compared to wild-type proteins, missense mutant proteins are generally synthesized in a normal fashion, but may be impaired in their folding. A broad array of diseases that are due to misfolding of mutant proteins may be labelled conformational diseases: aggregation diseases, such as Alzheimer disease; diseases caused by negative dominance from misfolded structural proteins, such as hypertrophic cardiomyopathy; and disorders where the misfolded protein is degraded by intracellular proteases. Many metabolic disorders belong to this last category, where the so-called protein quality control systems, comprising chaperones and proteases, attempt to eliminate folding intermediates or misfolded proteins. On the basis of in vitro experiments with a limited number of missense mutations identified in patients with phenylalanine hydroxylase and fatty acid oxidation deficiencies, we discuss the cellular fate of missense mutant proteins. We find that the balance between folding to functional conformers, retention (holding) and degradation of folding intermediates or misfolded proteins is dependent on the nature of the mutation and on the efficiency of the quality control. For example, low temperature may promote formation of functional conformers, while elevated temperature usually promotes retention and degradation. We conclude that disorders caused by many missense mutations are complex diseases in which the mutation itself is a necessary major primary component, but that its effect may be modified by cellular conditions and possibly by genetic variations in the quality control systems. We suggest that this new knowledge about cell handling may open new avenues of understanding of the cell pathology and treatment of patients with metabolic disorders.

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Year:  2001        PMID: 11405340     DOI: 10.1023/a:1010319001722

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  66 in total

1.  Quality control in the secretory pathway: the role of calreticulin, calnexin and BiP in the retention of glycoproteins with C-terminal truncations.

Authors:  J X Zhang; I Braakman; K E Matlack; A Helenius
Journal:  Mol Biol Cell       Date:  1997-10       Impact factor: 4.138

2.  Expression analysis of phenylketonuria mutations. Effect on folding and stability of the phenylalanine hydroxylase protein.

Authors:  A Gámez; B Pérez; M Ugarte; L R Desviat
Journal:  J Biol Chem       Date:  2000-09-22       Impact factor: 5.157

3.  Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia.

Authors:  J Hazan; N Fonknechten; D Mavel; C Paternotte; D Samson; F Artiguenave; C S Davoine; C Cruaud; A Dürr; P Wincker; P Brottier; L Cattolico; V Barbe; J M Burgunder; J F Prud'homme; A Brice; B Fontaine; B Heilig; J Weissenbach
Journal:  Nat Genet       Date:  1999-11       Impact factor: 38.330

4.  Grp78 is involved in retention of mutant low density lipoprotein receptor protein in the endoplasmic reticulum.

Authors:  M M Jørgensen; O N Jensen; H U Holst; J J Hansen; T J Corydon; P Bross; L Bolund; N Gregersen
Journal:  J Biol Chem       Date:  2000-10-27       Impact factor: 5.157

5.  Missense mutations in the phenylalanine hydroxylase gene (PAH) can cause accelerated proteolytic turnover of PAH enzyme: a mechanism underlying phenylketonuria.

Authors:  P J Waters; M A Parniak; B R Akerman; A O Jones; C R Scriver
Journal:  J Inherit Metab Dis       Date:  1999-05       Impact factor: 4.982

6.  Current clinical diagnosis in Creutzfeldt-Jakob disease: identification of uncommon variants.

Authors:  I Zerr; W J Schulz-Schaeffer; A Giese; M Bodemer; A Schröter; K Henkel; H J Tschampa; O Windl; A Pfahlberg; B J Steinhoff; O Gefeller; H A Kretzschmar; S Poser
Journal:  Ann Neurol       Date:  2000-09       Impact factor: 10.422

7.  Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlations.

Authors:  E Kayaalp; E Treacy; P J Waters; S Byck; P Nowacki; C R Scriver
Journal:  Am J Hum Genet       Date:  1997-12       Impact factor: 11.025

8.  Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

Authors:  B S Andresen; S Olpin; B J Poorthuis; H R Scholte; C Vianey-Saban; R Wanders; L Ijlst; A Morris; M Pourfarzam; K Bartlett; E R Baumgartner; J B deKlerk; L D Schroeder; T J Corydon; H Lund; V Winter; P Bross; L Bolund; N Gregersen
Journal:  Am J Hum Genet       Date:  1999-02       Impact factor: 11.025

Review 9.  Familial hypertrophic cardiomyopathy: from mutations to functional defects.

Authors:  G Bonne; L Carrier; P Richard; B Hainque; K Schwartz
Journal:  Circ Res       Date:  1998-09-21       Impact factor: 17.367

10.  Quality control in the secretory pathway: retention of a misfolded viral membrane glycoprotein involves cycling between the ER, intermediate compartment, and Golgi apparatus.

Authors:  C Hammond; A Helenius
Journal:  J Cell Biol       Date:  1994-07       Impact factor: 10.539

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  15 in total

Review 1.  Protein misfolding, aggregation, and degradation in disease.

Authors:  Niels Gregersen; Lars Bolund; Peter Bross
Journal:  Mol Biotechnol       Date:  2005-10       Impact factor: 2.695

2.  Disease mechanisms and protein structures in fatty acid oxidation defects.

Authors:  Niels Gregersen; Rikke K J Olsen
Journal:  J Inherit Metab Dis       Date:  2010-02-12       Impact factor: 4.982

3.  Computational study of missense mutations in phenylalanine hydroxylase.

Authors:  Kamila Réblová; Petr Kulhánek; Lenka Fajkusová
Journal:  J Mol Model       Date:  2015-03-07       Impact factor: 1.810

Review 4.  Garrod's foresight; our hindsight.

Authors:  C R Scriver
Journal:  J Inherit Metab Dis       Date:  2001-04       Impact factor: 4.982

Review 5.  Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.

Authors:  Zahra Nochi; Rikke Katrine Jentoft Olsen; Niels Gregersen
Journal:  J Inherit Metab Dis       Date:  2017-05-17       Impact factor: 4.982

Review 6.  An emerging concept of prion infections as a form of transmissible cerebral amyloidosis.

Authors:  Omar Lupi; Marcius Achiame Peryassu
Journal:  Prion       Date:  2007 Oct-Dec       Impact factor: 3.931

7.  Proline residues in transmembrane segment IV are critical for activity, expression and targeting of the Na+/H+ exchanger isoform 1.

Authors:  Emily R Slepkov; Signy Chow; M Joanne Lemieux; Larry Fliegel
Journal:  Biochem J       Date:  2004-04-01       Impact factor: 3.857

8.  Cryptic exon activation by disruption of exon splice enhancer: novel mechanism causing 3-methylcrotonyl-CoA carboxylase deficiency.

Authors:  Martin Stucki; Terttu Suormala; Brian Fowler; David Valle; Matthias R Baumgartner
Journal:  J Biol Chem       Date:  2009-08-24       Impact factor: 5.157

9.  Recurrent vomiting and ethylmalonic aciduria associated with rare mutations of the short-chain acyl-CoA dehydrogenase gene.

Authors:  J Seidel; S Streck; K Bellstedt; C Vianey-Saban; C B Pedersen; J Vockley; H Korall; M Roskos; T Deufel; K F Trefz; A C Sewell; E Kauf; F Zintl; W Lehnert; N Gregersen
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

10.  Protein misfolding as an underlying molecular defect in mucopolysaccharidosis III type C.

Authors:  Matthew Feldhammer; Stéphanie Durand; Alexey V Pshezhetsky
Journal:  PLoS One       Date:  2009-10-13       Impact factor: 3.240

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