Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
7
pubmed:dateCreated
2009-7-29
pubmed:abstractText
Down syndrome critical region 1 (DSCR1), an oxidative stress-response gene, interacts with calcineurin and represses its phosphatase activity. Recently it was shown that hydrogen peroxide inactivates calcineurin by proteolytic cleavage. Based on these facts, we investigated whether oxidative stress affects DSCR1- mediated inactivation of calcineurin. We determined that overexpression of DSCR1 leads to increased proteolytic cleavage of calcineurin. Convertsely, knockdown of DSCR1 abolished calcineurin cleavage upon treatment with hydrogen peroxide. The PXIIXT motif in the COOH-terminus of DSCR1 is responsible for both binding and cleavage of calcineurin. The knockdown of overexpressed DSCR1 in DS fibroblast cells also abrogated calcineurin proteolysis by hydrogen peroxide. These results suggest that DSCR1 has the ability to inactivate calcineurin by inducing proteolytic cleavage of calcineurin upon oxidative stress.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-10410302, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-10722714, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-10842755, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-10861295, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-10887154, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-11096121, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-11110780, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-11483593, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-12039863, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-12063245, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-12515860, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-12526102, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-14701880, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-14738882, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-15256217, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-15263820, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-15358155, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-16131541, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-16231093, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-16406492, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-17217415, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-18187560, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-18305400, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-7725105, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-8294942, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-8901634, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-9185608, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-9482916, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-9660798, http://linkedlifedata.com/resource/pubmed/commentcorrection/19322033-9765270
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1226-3613
pubmed:author
pubmed:issnType
Print
pubmed:day
31
pubmed:volume
41
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
471-7
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:19322033-Adenoviridae, pubmed-meshheading:19322033-Adult, pubmed-meshheading:19322033-Animals, pubmed-meshheading:19322033-Calcineurin, pubmed-meshheading:19322033-Cells, Cultured, pubmed-meshheading:19322033-Chromatin Immunoprecipitation, pubmed-meshheading:19322033-Down Syndrome, pubmed-meshheading:19322033-Fibroblasts, pubmed-meshheading:19322033-Humans, pubmed-meshheading:19322033-Hydrogen Peroxide, pubmed-meshheading:19322033-Immunoglobulin G, pubmed-meshheading:19322033-Intracellular Signaling Peptides and Proteins, pubmed-meshheading:19322033-Male, pubmed-meshheading:19322033-Mice, pubmed-meshheading:19322033-Mice, Inbred ICR, pubmed-meshheading:19322033-Muscle Proteins, pubmed-meshheading:19322033-Neuroblastoma, pubmed-meshheading:19322033-Neurons, pubmed-meshheading:19322033-Oxidants, pubmed-meshheading:19322033-Oxidative Stress, pubmed-meshheading:19322033-Peptide Fragments, pubmed-meshheading:19322033-RNA, Messenger, pubmed-meshheading:19322033-RNA, Small Interfering, pubmed-meshheading:19322033-Rabbits, pubmed-meshheading:19322033-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:19322033-Skin, pubmed-meshheading:19322033-Young Adult
pubmed:year
2009
pubmed:articleTitle
Down syndrome critical region 1 enhances the proteolytic cleavage of calcineurin.
pubmed:affiliation
National Research Laboratory for Metabolic Checkpoint, Department of Biomedical Sciences and Biochemistry and Molecular Biology, Cancer Research Institute, Seoul National University College of Medicine, Seoul 110-799, Korea.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't