Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
2002-2-13
pubmed:databankReference
pubmed:abstractText
Dlm-1 is a recently described gene which is upregulated in murine stromal cells lining tumors. The function of the 40 kDa DLM-1 protein is poorly understood. DLM-1 contains an N-terminal Z-DNA binding domain homologous to the Zalpha domain in the RNA editing enzyme ADAR1. We report the cloning of human and rat DLM-1. In addition to the Zalpha domain, three further conserved regions were identified. One of these is homologous to the second Z-DNA binding domain, Zbeta, of ADAR1. We find that human DLM-1 is predominantly expressed in lymphatic tissues. The gene spans 17 kb and consists of 10 exons. DNA transcripts are extremely heterogeneous as a result of alternative splicing and the usage of exon variants combined with at least two transcriptional start sites and 3'-terminal exons. The exon coding for the Zalpha domain was present in approximately one-third of the analyzed mRNAs. Nearly half of the transcripts contained exon variants that had premature stop codons incorporated. Based on our analysis, over 2000 different mRNAs may be produced due to alternative splicing and usage of different 5' and 3' ends. The cellular function of DLM-1 appears to call for a high degree of adaptation by this complex regulation.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-10364558, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-10383410, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-10440865, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-10564822, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-10690409, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-10892653, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-11087828, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-11134298, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-11173120, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-11237011, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-11447254, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-11509180, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-11524677, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-12086319, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-1330542, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-2006166, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-2170946, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-2921282, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-3160582, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-3658675, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-3967651, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-6304535, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-6383204, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-7499248, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-7618288, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-8622993, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-8643651, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-8662853, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-9055609, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-9199252, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-9237992, http://linkedlifedata.com/resource/pubmed/commentcorrection/11842111-9915827
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1362-4962
pubmed:author
pubmed:issnType
Electronic
pubmed:day
15
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
993-1000
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:11842111-Alleles, pubmed-meshheading:11842111-Alternative Splicing, pubmed-meshheading:11842111-Amino Acid Sequence, pubmed-meshheading:11842111-Animals, pubmed-meshheading:11842111-Base Sequence, pubmed-meshheading:11842111-Cloning, Molecular, pubmed-meshheading:11842111-DNA, pubmed-meshheading:11842111-DNA-Binding Proteins, pubmed-meshheading:11842111-Exons, pubmed-meshheading:11842111-Expressed Sequence Tags, pubmed-meshheading:11842111-Genes, pubmed-meshheading:11842111-Glycoproteins, pubmed-meshheading:11842111-Humans, pubmed-meshheading:11842111-Mice, pubmed-meshheading:11842111-Molecular Sequence Data, pubmed-meshheading:11842111-Polyadenylation, pubmed-meshheading:11842111-Protein Structure, Tertiary, pubmed-meshheading:11842111-RNA, Messenger, pubmed-meshheading:11842111-Rats, pubmed-meshheading:11842111-Sequence Homology, Amino Acid, pubmed-meshheading:11842111-Tissue Distribution
pubmed:year
2002
pubmed:articleTitle
Complex regulation of the human gene for the Z-DNA binding protein DLM-1.
pubmed:affiliation
Institute for Immunology, University Hospital Hamburg-Eppendorf, Martinistrasse 52, D-20246 Hamburg, Germany.
pubmed:publicationType
Journal Article