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PMID: 10930580 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

The human homologue of the yeast mitochondrial AAA metalloprotease Yme1p complements a yeast yme1 disruptant.

FEBS letters ·Vol. 478 ·No. 3 ·2000-08-04 ·Pages 267-70

Shah ZH, Hakkaart GA, Arku B, de Jong L, van der Spek H, Grivell LA, Jacobs HT

Abstract

In yeast, three AAA superfamily metalloproteases (Yme1p, Afg3p and Rca1p) are localized to the mitochondrial inner membrane where they perform roles in the assembly and turnover of the respiratory chain complexes. We have investigated the function of the proposed human orthologue of yeast Yme1p, encoded by the YME1L gene on chromosome 10p. Transfection of both HEK-293EBNA and yeast cells with a green fluorescent protein-tagged YME1L cDNA confirmed mitochondrial targeting. When expressed in a yme1 disruptant yeast strain, YME1L restored growth on glycerol at 37 degrees C. We propose that YME1L plays a phylogenetically conserved role in mitochondrial protein metabolism and could be involved in mitochondrial pathologies.

MeSH Terms
ATP-Dependent Proteases ATPases Associated with Diverse Cellular Activities Adenosine Triphosphatases/chemistry,genetics,metabolism Cell Line Chromosomes, Human, Pair 10/genetics Cloning, Molecular Gene Deletion Genetic Complementation Test Glycerol/metabolism Humans Metalloendopeptidases/chemistry,genetics,metabolism Mitochondria/enzymology,metabolism Mitochondrial Proteins Phylogeny Recombinant Fusion Proteins/chemistry,genetics,metabolism Saccharomyces cerevisiae/enzymology,genetics,growth & development,metabolism Saccharomyces cerevisiae Proteins
Chemicals
Mitochondrial Proteins Recombinant Fusion Proteins Saccharomyces cerevisiae Proteins ATP-Dependent Proteases YME1 protein, S cerevisiae Metalloendopeptidases YME1L1 protein, human Adenosine Triphosphatases ATPases Associated with Diverse Cellular Activities Glycerol
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Shah Z H
Institute of Medical Technology and Tampere University Hospital, Finland.
Hakkaart G A
Arku B
de Jong L
van der Spek H
Grivell L A
Jacobs H T
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
2000-08-04
Pages
267-70
Language
English
Region
England
NLM ID
0155157
Subset
IM
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