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rdf:type |
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lifeskim:mentions |
umls-concept:C0035711,
umls-concept:C0036025,
umls-concept:C0073243,
umls-concept:C0205224,
umls-concept:C0521447,
umls-concept:C0599220,
umls-concept:C1419693,
umls-concept:C1426553,
umls-concept:C1514873,
umls-concept:C1537998,
umls-concept:C1546857,
umls-concept:C1556066,
umls-concept:C1619636,
umls-concept:C1709634,
umls-concept:C1709694
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pubmed:issue |
12
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pubmed:dateCreated |
1998-7-9
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pubmed:databankReference |
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pubmed:abstractText |
RPP2, an essential gene that encodes a 15.8-kDa protein subunit of nuclear RNase P, has been identified in the genome of Saccharomyces cerevisiae. Rpp2 was detected by sequence similarity with a human protein, Rpp20, which copurifies with human RNase P. Epitope-tagged Rpp2 can be found in association with both RNase P and RNase mitochondrial RNA processing in immunoprecipitates from crude extracts of cells. Depletion of Rpp2 protein in vivo causes accumulation of precursor tRNAs with unprocessed introns and 5' and 3' termini, and leads to defects in the processing of the 35S precursor rRNA. Rpp2-depleted cells are defective in processing of the 5.8S rRNA. Rpp2 immunoprecipitates cleave both yeast precursor tRNAs and precursor rRNAs accurately at the expected sites and contain the Rpp1 protein orthologue of the human scleroderma autoimmune antigen, Rpp30. These results demonstrate that Rpp2 is a protein subunit of nuclear RNase P that is functionally conserved in eukaryotes from yeast to humans.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-1375791,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-1398074,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-1588958,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-1696176,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-1990278,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-2470644,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-2503708,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-2666172,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-2910496,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-6197186,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-7515008,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-7701567,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-7926742,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8020097,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8197106,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8247008,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8602511,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8614627,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8774895,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8787607,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-8896463,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9029160,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9037013,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9085845,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9135114,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9254694,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9308968,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9384595,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9390555,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9399804,
http://linkedlifedata.com/resource/pubmed/commentcorrection/9618478-9436903
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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/Endoribonucleases,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Catalytic,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Fungal,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Transfer,
http://linkedlifedata.com/resource/pubmed/chemical/RNA Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/RPP14 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Ribonuclease P
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0027-8424
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
9
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pubmed:volume |
95
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
6716-21
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pubmed:dateRevised |
2009-11-18
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pubmed:meshHeading |
pubmed-meshheading:9618478-Endoribonucleases,
pubmed-meshheading:9618478-Genes, Fungal,
pubmed-meshheading:9618478-Humans,
pubmed-meshheading:9618478-Molecular Sequence Data,
pubmed-meshheading:9618478-RNA, Catalytic,
pubmed-meshheading:9618478-RNA, Fungal,
pubmed-meshheading:9618478-RNA, Transfer,
pubmed-meshheading:9618478-RNA Precursors,
pubmed-meshheading:9618478-Ribonuclease P,
pubmed-meshheading:9618478-Saccharomyces cerevisiae,
pubmed-meshheading:9618478-Sequence Deletion
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pubmed:year |
1998
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pubmed:articleTitle |
Rpp2, an essential protein subunit of nuclear RNase P, is required for processing of precursor tRNAs and 35S precursor rRNA in Saccharomyces cerevisiae.
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pubmed:affiliation |
Department of Cell Biology, Yale University School of Medicine, New Haven, CT 06510, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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