Literature DB >> 9247084

Sequence and structure of the human OXA1L gene and its upstream elements.

A Rötig1, B Parfait, L Heidet, G Dujardin, P Rustin, A Munnich.   

Abstract

The genes encoding proteins involved in respiratory chain assembly represent candidate genes for nuclearly-encoded multiple respiratory chain deficiency. Using the long PCR amplification procedure, we have characterized the organization and complete sequence of OXA1L, a gene involved in the assembly of several complexes of the mitochondrial respiratory chain. The OXA1L gene (5 kb) is composed of 10 exons and 9 introns and contains a 24 N-terminal amino-acid stretch is characteristic of a mitochondrial presequence. The screening of OXA1L mutation in patients with multiple respiratory chain deficiency is now feasible.

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Year:  1997        PMID: 9247084     DOI: 10.1016/s0925-4439(97)00031-8

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  4 in total

1.  Mutation detection in four candidate genes (OXA1L, MRS2L, YME1L and MIPEP) for combined deficiencies in the oxidative phosphorylation system.

Authors:  M J H Coenen; J A M Smeitink; R Smeets; F J M Trijbels; L P van den Heuvel
Journal:  J Inherit Metab Dis       Date:  2005       Impact factor: 4.982

2.  Nuclear DNA origin of mitochondrial complex I deficiency in fatal infantile lactic acidosis evidenced by transnuclear complementation of cultured fibroblasts.

Authors:  V Procaccio; B Mousson; R Beugnot; H Duborjal; F Feillet; G Putet; I Pignot-Paintrand; A Lombès; R De Coo; H Smeets; J Lunardi; J P Issartel
Journal:  J Clin Invest       Date:  1999-07       Impact factor: 14.808

3.  The role of the 3' untranslated region in mRNA sorting to the vicinity of mitochondria is conserved from yeast to human cells.

Authors:  J Sylvestre; A Margeot; C Jacq; G Dujardin; M Corral-Debrinski
Journal:  Mol Biol Cell       Date:  2003-06-13       Impact factor: 4.138

4.  OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect.

Authors:  Kyle Thompson; Nicole Mai; Monika Oláhová; Filippo Scialó; Luke E Formosa; David A Stroud; Madeleine Garrett; Nichola Z Lax; Fiona M Robertson; Cristina Jou; Andres Nascimento; Carlos Ortez; Cecilia Jimenez-Mallebrera; Steven A Hardy; Langping He; Garry K Brown; Paula Marttinen; Robert McFarland; Alberto Sanz; Brendan J Battersby; Penelope E Bonnen; Michael T Ryan; Zofia Ma Chrzanowska-Lightowlers; Robert N Lightowlers; Robert W Taylor
Journal:  EMBO Mol Med       Date:  2018-11       Impact factor: 12.137

  4 in total

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