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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11
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pubmed:dateCreated |
1998-12-1
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pubmed:databankReference |
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF031519,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF072928,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF072929,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073482,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073879,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073880,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073881,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073882,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073883,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073996,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF073997,
http://linkedlifedata.com/resource/pubmed/xref/GENBANK/AF076432
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pubmed:abstractText |
X-linked myotubular myopathy (XLMTM) is a severe congenital muscle disorder due to mutations in the MTM1 gene. The corresponding protein, myotubularin, contains the consensus active site of tyrosine phosphatases (PTP) but otherwise shows no homology to other phosphatases. Myotubularin is able to hydrolyze a synthetic analogue of tyrosine phosphate, in a reaction inhibited by orthovanadate, and was recently shown to act on both phosphotyrosine and phosphoserine. This gene is conserved down to yeast and strong homologies were found with human ESTs, thus defining a new dual specificity phosphatase (DSP) family. We report the presence of novel members of the MTM gene family in Schizosaccharomyces pombe, Caenorhabditis elegans, zebrafish, Drosophila, mouse and man. This represents the largest family of DSPs described to date. Eight MTM-related genes were found in the human genome and we determined the chromosomal localization and expression pattern for most of them. A subclass of the myotubularin homologues lacks a functional PTP active site. Missense mutations found in XLMTM patients affect residues conserved in a Drosophila homologue. Comparison of the various genes allowed construction of a phylogenetic tree and reveals conserved residues which may be essential for function. These genes may be good candidates for other genetic diseases.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0964-6906
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
7
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1703-12
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pubmed:dateRevised |
2007-11-15
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pubmed:meshHeading |
pubmed-meshheading:9736772-Amino Acid Sequence,
pubmed-meshheading:9736772-Animals,
pubmed-meshheading:9736772-Caenorhabditis elegans,
pubmed-meshheading:9736772-Chromosome Mapping,
pubmed-meshheading:9736772-Chromosomes, Human,
pubmed-meshheading:9736772-Conserved Sequence,
pubmed-meshheading:9736772-Drosophila,
pubmed-meshheading:9736772-Expressed Sequence Tags,
pubmed-meshheading:9736772-Humans,
pubmed-meshheading:9736772-Mice,
pubmed-meshheading:9736772-Molecular Sequence Data,
pubmed-meshheading:9736772-Muscle Hypotonia,
pubmed-meshheading:9736772-Mutation, Missense,
pubmed-meshheading:9736772-Phylogeny,
pubmed-meshheading:9736772-Protein Tyrosine Phosphatases,
pubmed-meshheading:9736772-Protein Tyrosine Phosphatases, Non-Receptor,
pubmed-meshheading:9736772-Schizosaccharomyces,
pubmed-meshheading:9736772-Sequence Homology, Amino Acid,
pubmed-meshheading:9736772-Substrate Specificity,
pubmed-meshheading:9736772-Tissue Distribution,
pubmed-meshheading:9736772-Zebrafish
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pubmed:year |
1998
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pubmed:articleTitle |
Characterization of the myotubularin dual specificity phosphatase gene family from yeast to human.
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pubmed:affiliation |
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, 1 rue Laurent Fries, BP 163, 67404 Illkirch Cedex, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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