Literature DB >> 11165261

Mutation in the NDUFS4 gene of complex I abolishes cAMP-dependent activation of the complex in a child with fatal neurological syndrome.

S Papa1, S Scacco, A M Sardanelli, R Vergari, F Papa, S Budde, L van den Heuvel, J Smeitink.   

Abstract

Evidence is presented showing that in a patient with fatal neurological syndrome, the homozygous 5 bp duplication in the cDNA of the NDUFS4 18 kDa subunit of complex I abolishes cAMP-dependent phosphorylation of this protein and activation of the complex. These findings show for the first time that human complex I is regulated via phosphorylation of the subunit encoded by the NDUFS4 gene.

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Year:  2001        PMID: 11165261     DOI: 10.1016/s0014-5793(00)02334-6

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  27 in total

1.  Complex I deficiency due to loss of Ndufs4 in the brain results in progressive encephalopathy resembling Leigh syndrome.

Authors:  Albert Quintana; Shane E Kruse; Raj P Kapur; Elisenda Sanz; Richard D Palmiter
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-01       Impact factor: 11.205

2.  Human NADH:ubiquinone oxidoreductase.

Authors:  J Smeitink; R Sengers; F Trijbels; L van den Heuvel
Journal:  J Bioenerg Biomembr       Date:  2001-06       Impact factor: 2.945

Review 3.  Post-translational modifications in mitochondria: protein signaling in the powerhouse.

Authors:  Amanda R Stram; R Mark Payne
Journal:  Cell Mol Life Sci       Date:  2016-05-27       Impact factor: 9.261

4.  The transition between active and de-activated forms of NADH:ubiquinone oxidoreductase (Complex I) in the mitochondrial membrane of Neurospora crassa.

Authors:  Vera G Grivennikova; Darya V Serebryanaya; Elena P Isakova; Tatyana A Belozerskaya; Andrei D Vinogradov
Journal:  Biochem J       Date:  2003-02-01       Impact factor: 3.857

Review 5.  Mitochondrial involvement in brain function and dysfunction: relevance to aging, neurodegenerative disorders and longevity.

Authors:  V Calabrese; G Scapagnini; A M Giuffrida Stella; T E Bates; J B Clark
Journal:  Neurochem Res       Date:  2001-06       Impact factor: 3.996

Review 6.  The NADH: ubiquinone oxidoreductase (complex I) of the mammalian respiratory chain and the cAMP cascade.

Authors:  S Papa; A M Sardanelli; S Scacco; V Petruzzella; Z Technikova-Dobrova; R Vergari; A Signorile
Journal:  J Bioenerg Biomembr       Date:  2002-02       Impact factor: 2.945

7.  TNF-induced mitochondrial damage: a link between mitochondrial complex I activity and left ventricular dysfunction.

Authors:  Nithya Mariappan; Carrie M Elks; Bruno Fink; Joseph Francis
Journal:  Free Radic Biol Med       Date:  2008-11-12       Impact factor: 7.376

8.  Use of (32)P to study dynamics of the mitochondrial phosphoproteome.

Authors:  Angel M Aponte; Darci Phillips; Rachel K Hopper; D Thor Johnson; Robert A Harris; Ksenia Blinova; Emily S Boja; Stephanie French; Robert S Balaban
Journal:  J Proteome Res       Date:  2009-06       Impact factor: 4.466

Review 9.  Mitochondrial disorders: clinical presentation and diagnostic dilemmas.

Authors:  J A M Smeitink
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

10.  A novel mutation in NDUFS4 causes Leigh syndrome in an Ashkenazi Jewish family.

Authors:  S L Anderson; W K Chung; J Frezzo; J C Papp; J Ekstein; S DiMauro; B Y Rubin
Journal:  J Inherit Metab Dis       Date:  2008-12-26       Impact factor: 4.982

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