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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
2
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pubmed:dateCreated |
2001-1-10
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pubmed:abstractText |
RNA triphosphatase catalyzes the first step in mRNA cap formation which entails the cleavage of the beta-gamma phosphoanhydride bond of triphosphate-terminated RNA to yield a diphosphate end that is then capped with GMP by RNA guanylyltransferase. Here we characterize a 303 amino acid RNA triphosphatase (Pct1p) encoded by the fission yeast SCHIZOSACCHAROMYCES: pombe. Pct1p hydrolyzes the gamma phosphate of triphosphate-terminated poly(A) in the presence of magnesium. Pct1p also hydrolyzes ATP to ADP and P(i) in the presence of manganese or cobalt (K(m) = 19 microM ATP; k(cat) = 67 s(-1)). Hydrolysis of 1 mM ATP is inhibited with increasing potency by inorganic phosphate (I(0.5) = 1 mM), pyrophosphate (I(0.5) = 0.4 mM) and tripolyphosphate (I(0.5) = 30 microM). Velocity sedimentation indicates that Pct1p is a homodimer. Pct1p is biochemically and structurally similar to the catalytic domain of Saccharomyces cerevisiae RNA triphosphatase Cet1p. Mechanistic conservation between Pct1p and Cet1p is underscored by a mutational analysis of the putative metal-binding site of Pct1p. Pct1p is functional in vivo in S.cerevisiae in lieu of Cet1p, provided that it is coexpressed with the S.pombe guanylyltransferase. Pct1p and other yeast RNA triphosphatases are completely unrelated, mechanistically and structurally, to the metazoan RNA triphosphatases, suggesting an abrupt evolutionary divergence of the capping apparatus during the transition from fungal to metazoan species.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10198643,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10347220,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10347225,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10428848,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10506129,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10572165,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10589681,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10679253,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10756187,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10823853,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10931913,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-10954717,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-11018011,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-11018013,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-11051760,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-2005799,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-2744487,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-2744488,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-6143751,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-7991582,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-8662635,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-8662636,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-8828219,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9200605,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9371657,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9407024,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9407025,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9545288,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9696798,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9707557,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9755857,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9770468,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9811739,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9811740,
http://linkedlifedata.com/resource/pubmed/commentcorrection/11139608-9852075
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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 |
http://linkedlifedata.com/resource/pubmed/chemical/Acid Anhydride Hydrolases,
http://linkedlifedata.com/resource/pubmed/chemical/Adenosine Triphosphate,
http://linkedlifedata.com/resource/pubmed/chemical/Diphosphates,
http://linkedlifedata.com/resource/pubmed/chemical/Fungal Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Metals,
http://linkedlifedata.com/resource/pubmed/chemical/Nucleotidyltransferases,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphates,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoric Monoester Hydrolases,
http://linkedlifedata.com/resource/pubmed/chemical/Polyphosphates,
http://linkedlifedata.com/resource/pubmed/chemical/RNA Caps,
http://linkedlifedata.com/resource/pubmed/chemical/RNA triphosphatase,
http://linkedlifedata.com/resource/pubmed/chemical/guanylyltransferase,
http://linkedlifedata.com/resource/pubmed/chemical/triphosphoric acid
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1362-4962
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:day |
15
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pubmed:volume |
29
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
387-96
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:11139608-Acid Anhydride Hydrolases,
pubmed-meshheading:11139608-Adenosine Triphosphate,
pubmed-meshheading:11139608-Amino Acid Motifs,
pubmed-meshheading:11139608-Amino Acid Sequence,
pubmed-meshheading:11139608-Animals,
pubmed-meshheading:11139608-Artificial Gene Fusion,
pubmed-meshheading:11139608-Diphosphates,
pubmed-meshheading:11139608-Fungal Proteins,
pubmed-meshheading:11139608-Genetic Complementation Test,
pubmed-meshheading:11139608-Hydrolysis,
pubmed-meshheading:11139608-Kinetics,
pubmed-meshheading:11139608-Metals,
pubmed-meshheading:11139608-Mice,
pubmed-meshheading:11139608-Molecular Sequence Data,
pubmed-meshheading:11139608-Nucleotidyltransferases,
pubmed-meshheading:11139608-Phosphates,
pubmed-meshheading:11139608-Phosphoric Monoester Hydrolases,
pubmed-meshheading:11139608-Polyphosphates,
pubmed-meshheading:11139608-RNA Caps,
pubmed-meshheading:11139608-Saccharomyces cerevisiae,
pubmed-meshheading:11139608-Schizosaccharomyces,
pubmed-meshheading:11139608-Sequence Homology, Amino Acid
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pubmed:year |
2001
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pubmed:articleTitle |
Characterization of Schizosaccharomyces pombe RNA triphosphatase.
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pubmed:affiliation |
Molecular Biology Program, Sloan-Kettering Institute, New York, NY 10021, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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