Source:http://linkedlifedata.com/resource/pubmed/id/10212139
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rdf:type | |
lifeskim:mentions | |
pubmed:dateCreated |
1999-8-13
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pubmed:abstractText |
Pre-fibronectin mRNA is subject to alternative splicing at three sites, EDA, EDB and IIICS. We analyzed the alternative splicing of fibronectin mRNA in a single cell. Reverse transcription-polymerase chain reaction analyses showed cells that produced a single form of mRNA at each one of these sites as well as cells that produced multiple forms at a given site: for example, some cells produced either the EDA(+) or EDA(-) form of the mRNA and other cells produced both forms. About 80% of the cells produced both (+) and (-) forms of the mRNA at the EDA and EDB sites, and the remaining cells contained either the (+) or (-) form. Five forms of fibronectin mRNA can result from alternative splicing at the IIICS site. Complex combinations of alternative splicing products were observed among the individual cells: there were ten different combinations of mRNA isoforms with respect to the IIICS site. Statistically significant changes in alternative splicing at the IIICS site were observed during cellular senescence.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0021-9533
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
112 ( Pt 10)
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1449-53
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:10212139-Alternative Splicing,
pubmed-meshheading:10212139-Cells, Cultured,
pubmed-meshheading:10212139-DNA Primers,
pubmed-meshheading:10212139-Fibroblasts,
pubmed-meshheading:10212139-Fibronectins,
pubmed-meshheading:10212139-Humans,
pubmed-meshheading:10212139-Models, Genetic,
pubmed-meshheading:10212139-Molecular Biology,
pubmed-meshheading:10212139-RNA, Messenger
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pubmed:year |
1999
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pubmed:articleTitle |
Detection of alternative splicing of fibronectin mRNA in a single cell.
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pubmed:affiliation |
Department of Biochemistry and Biophysics, Research Institute for Radiation Biology and Medicine, Hiroshima University, Hiroshima, Japan. kumazaki@ue.ipc.hiroshima-u.ac.jp
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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