Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2003-5-30
pubmed:abstractText
Mortalin, also known as mot2/mthsp70/GRP75/PBP74, is a member of the heat-shock protein 70 family that is heat-uninducible. It is differentially distributed in cells that have normal and immortal phenotypes, has been localized to various subcellular sites, and has several binding partners and functions. Here, we describe the construction and use of mortalin-specific conventional and hybrid ribozymes to elucidate its crucial role in cell proliferation. Whereas conventional hammerhead ribozymes did not cause any repression of endogenous mortalin expression, RNA-helicase-linked hybrid ribozymes successfully suppressed the expression of mortalin, which resulted in the growth arrest of transformed human cells. We show that, first, RNA helicase-coupled hybrid ribozymes that have a linked unwinding activity can be used to target genes for which conventional hammerhead ribozymes are ineffective; second, the targeting of mortalin by RNA-helicase-coupled hybrid ribozymes causes growth suppression of transformed human cells and could be used as a treatment for cancer.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-10359720, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-10838077, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-10960319, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11096111, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11278700, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11328865, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11344300, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11420746, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11433023, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11587376, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11964387, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-11983075, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-12097172, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-12110898, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-12203005, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-12203967, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-2468181, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-3329163, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-7909191, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-7969416, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-8454632, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-8760887, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-9363898, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-9504817, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-9780007, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-9792667, http://linkedlifedata.com/resource/pubmed/commentcorrection/12776179-9971765
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
1469-221X
pubmed:author
pubmed:issnType
Print
pubmed:volume
4
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
595-601
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:12776179-Animals, pubmed-meshheading:12776179-Base Sequence, pubmed-meshheading:12776179-Blotting, Northern, pubmed-meshheading:12776179-Blotting, Western, pubmed-meshheading:12776179-COS Cells, pubmed-meshheading:12776179-Cell Division, pubmed-meshheading:12776179-Cell Line, Transformed, pubmed-meshheading:12776179-Cell Line, Tumor, pubmed-meshheading:12776179-Genes, Reporter, pubmed-meshheading:12776179-Green Fluorescent Proteins, pubmed-meshheading:12776179-HSP70 Heat-Shock Proteins, pubmed-meshheading:12776179-Humans, pubmed-meshheading:12776179-Luciferases, pubmed-meshheading:12776179-Luminescent Proteins, pubmed-meshheading:12776179-Mitochondrial Proteins, pubmed-meshheading:12776179-Molecular Sequence Data, pubmed-meshheading:12776179-Phenotype, pubmed-meshheading:12776179-Plasmids, pubmed-meshheading:12776179-Protein Binding, pubmed-meshheading:12776179-RNA, pubmed-meshheading:12776179-RNA, Catalytic, pubmed-meshheading:12776179-RNA Helicases, pubmed-meshheading:12776179-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:12776179-Transfection
pubmed:year
2003
pubmed:articleTitle
Targeting mortalin using conventional and RNA-helicase-coupled hammerhead ribozymes.
pubmed:affiliation
Gene Function Research Center, National Institute of Advanced Industrial Science and Technology, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8566, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't