Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
19
pubmed:dateCreated
1996-12-5
pubmed:databankReference
pubmed:abstractText
TIA-1 and TIAR are RNA binding proteins of the RNA recognition motif (RRM)/ribonucleoprotein (RNP) family that have been implicated as effectors of apoptotic cell death. We report the structures of murine TIA-1 and TIAR (mTIA-1 and mTIAR) deduced from cDNA cloning, the mRNA and protein tissue distribution of mTIA-1 and mTIAR, and the exon-intron structures of the mTIA-1 and mTIAR genes. Both mTIA-1 and mTIAR are comprised of three approximately 100 amino acid N-terminal RRM domains and a approximately 90 amino acid C-terminal auxiliary domain. This subfamily of RRM proteins is evolutionarily well conserved; mTIA-1 and mTIAR are 80% similar to each other, and 96 and 99% similar to hTIA-1 and hTIAR, respectively. The overall exon-intron structures of the mTIA-1 and mTIAR genes are also similar to each other, as well as to the human TIA-1 gene structure. While Northern blot analysis reveals that mTIA-1 and mTIAR mRNAs have a broad tissue distribution, mTIA-1 and mTIAR proteins are predominantly expressed in brain, testis and spleen. At least two isoforms of both mTIA-1 and mTIAR are generated by alternative splicing. Murine TIA-1 isoforms including or lacking the exon 5 encoded sequences are expressed at a ratio of approximately 1:1, whereas mTIAR isoforms including or lacking the 5'-end of exon 3 sequences are expressed in a approximately 1:6 ratio. Molecular characterization of murine TIA-1 and TIAR RNA binding proteins provides the basis for a genetic analysis of the functional roles of these proteins during mammalian development.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-1326761, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-1716386, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-1848010, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-1934064, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-2505080, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-2827008, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-2971730, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-3491324, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7523244, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7533298, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7543225, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7544399, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7568171, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7670487, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7673195, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7684991, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7906398, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7926753, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-7984237, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8036511, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8146191, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8176212, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8269511, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8331337, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8396236, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8500177, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-8576255, http://linkedlifedata.com/resource/pubmed/commentcorrection/8871565-942051
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0305-1048
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
24
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3829-35
pubmed:dateRevised
2010-11-18
pubmed:meshHeading
pubmed:year
1996
pubmed:articleTitle
Structure, tissue distribution and genomic organization of the murine RRM-type RNA binding proteins TIA-1 and TIAR.
pubmed:affiliation
Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't