Literature DB >> 11549317

Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein.

G Kremmidiotis1, A E Gardner, C Settasatian, A Savoia, G R Sutherland, D F Callen.   

Abstract

The identification of SPG7 as the gene defective in a recessive form of spastic paraplegia has drawn attention to the yeast protein family of ATP-dependent zinc metalloproteases. The protein encoded by SPG7, paraplegin, shows high homology to members of this protein family. Recently, many mammalian ATP-dependent zinc metalloproteases have been identified and considered as possible candidates for defects in other forms of hereditary spastic paraplegia and possibly other neurodegenerative disorders. So far only a partial sequence has been available for one of those genes, ATPase family gene-3, yeast-like-1 (AFG3L1). We have carried out detailed molecular analysis of this gene and identified and characterized its mouse orthologue, Afg3l1. Our data indicate that AFG3L1 is transcribed into four mRNA isoforms that are not translated in humans. Afg3l1 encodes a protein with high homology to paraplegin and the other members of the ATP-dependent zinc metalloprotease family. Like the other ATP-dependent zinc metalloproteases, Afg3l1 localizes to the mitochondria.

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Year:  2001        PMID: 11549317     DOI: 10.1006/geno.2001.6560

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  21 in total

Review 1.  Synapses and Sisyphus: life without paraplegin.

Authors:  Harris A Gelbard
Journal:  J Clin Invest       Date:  2004-01       Impact factor: 14.808

Review 2.  New roles for mitochondrial proteases in health, ageing and disease.

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Journal:  Nat Rev Mol Cell Biol       Date:  2015-05-13       Impact factor: 94.444

Review 3.  Metalloproteases of the Inner Mitochondrial Membrane.

Authors:  Roman M Levytskyy; Iryna Bohovych; Oleh Khalimonchuk
Journal:  Biochemistry       Date:  2017-08-30       Impact factor: 3.162

4.  The BTB and CNC homology 1 (BACH1) target genes are involved in the oxidative stress response and in control of the cell cycle.

Authors:  Hans-Jörg Warnatz; Dominic Schmidt; Thomas Manke; Ilaria Piccini; Marc Sultan; Tatiana Borodina; Daniela Balzereit; Wasco Wruck; Alexey Soldatov; Martin Vingron; Hans Lehrach; Marie-Laure Yaspo
Journal:  J Biol Chem       Date:  2011-05-09       Impact factor: 5.157

Review 5.  Mitochondrial protein quality control: the mechanisms guarding mitochondrial health.

Authors:  Iryna Bohovych; Sherine S L Chan; Oleh Khalimonchuk
Journal:  Antioxid Redox Signal       Date:  2015-02-11       Impact factor: 8.401

Review 6.  Mitochondrial quality control: a matter of life and death for neurons.

Authors:  Elena I Rugarli; Thomas Langer
Journal:  EMBO J       Date:  2012-02-21       Impact factor: 11.598

Review 7.  Mitochondrial AAA proteases: A stairway to degradation.

Authors:  Tyler E Steele; Steven E Glynn
Journal:  Mitochondrion       Date:  2019-08-01       Impact factor: 4.160

8.  Autocatalytic processing of m-AAA protease subunits in mitochondria.

Authors:  Mirko Koppen; Florian Bonn; Sarah Ehses; Thomas Langer
Journal:  Mol Biol Cell       Date:  2009-08-05       Impact factor: 4.138

9.  OPA1 processing reconstituted in yeast depends on the subunit composition of the m-AAA protease in mitochondria.

Authors:  Stéphane Duvezin-Caubet; Mirko Koppen; Johannes Wagener; Michael Zick; Lars Israel; Andrea Bernacchia; Ravi Jagasia; Elena I Rugarli; Axel Imhof; Walter Neupert; Thomas Langer; Andreas S Reichert
Journal:  Mol Biol Cell       Date:  2007-07-05       Impact factor: 4.138

10.  Regulation of OPA1 processing and mitochondrial fusion by m-AAA protease isoenzymes and OMA1.

Authors:  Sarah Ehses; Ines Raschke; Giuseppe Mancuso; Andrea Bernacchia; Stefan Geimer; Daniel Tondera; Jean-Claude Martinou; Benedikt Westermann; Elena I Rugarli; Thomas Langer
Journal:  J Cell Biol       Date:  2009-12-28       Impact factor: 10.539

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