Abstract
A gene responsible for an autosomal recessive form of hereditary spastic paraplegia (SPG7) was recently identified. This gene encodes paraplegin, a mitochondrial protein highly homologous to the yeast mitochondrial AAA proteases Afg3p, Rca1p, and Yme1p, which have both proteolytic and chaperone-like activities at the inner mitochondrial membrane. By screening the expressed sequence tag database, we identified and characterized a novel human gene, YME1L1 (YME1L1-like1, HGMW-approved symbol). This gene encodes a predicted protein of 716 amino acids highly similar to all mitochondrial AAA proteases and in particular to yeast Yme1p. Expression and immunofluorescence studies revealed that YME1L1 and paraplegin share a similar expression pattern and the same subcellular localization in the mitochondrial compartment. YME1L1 may represent a candidate gene for other forms of hereditary spastic paraplegia and possibly for other neurodegenerative disorders.
Copyright 2000 Academic Press.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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ATPases Associated with Diverse Cellular Activities
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Adult
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Amino Acid Sequence
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Animals
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Base Sequence
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Brain / metabolism
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COS Cells
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Chromosome Mapping
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DNA, Complementary / chemistry
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DNA, Complementary / isolation & purification
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Databases, Factual
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Embryo, Mammalian / metabolism
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Exons
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Expressed Sequence Tags
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Fetus / metabolism
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Fluorescent Antibody Technique
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Gene Expression Profiling
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Humans
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Infant, Newborn
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Introns
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Metalloendopeptidases / genetics*
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Mice / embryology
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Mice / genetics
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Mitochondria / genetics
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Mitochondrial Proteins
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Molecular Sequence Data
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Muscle, Skeletal / metabolism
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Myocardium / metabolism
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Pancreas / metabolism
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Paraplegia / genetics
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RNA, Messenger / metabolism
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Sequence Alignment
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Sequence Analysis, DNA
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Sequence Homology, Amino Acid
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Tissue Distribution
Substances
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DNA, Complementary
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Mitochondrial Proteins
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RNA, Messenger
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Metalloendopeptidases
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SPG7 protein, human
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Spg7 protein, mouse
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YME1L1 protein, human
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ATPases Associated with Diverse Cellular Activities