Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2001-9-17
pubmed:abstractText
The presenilin (PS)-dependent site 3 (S3) cleavage of Notch liberates its intracellular domain (NICD), which is required for Notch signaling. The similar gamma-secretase cleavage of the beta-amyloid precursor protein (betaAPP) results in the secretion of amyloid beta-peptide (Abeta). However, little is known about the corresponding C-terminal cleavage product (CTFgamma). We have now identified CTFgamma in brain tissue, in living cells, as well as in an in vitro system. Generation of CTFgamma is facilitated by PSs, since a dominant-negative mutation of PS as well as a PS gene knock out prevents its production. Moreover, gamma-secretase inhibitors, including one that is known to bind to PS, also block CTFgamma generation. Sequence analysis revealed that CTFgamma is produced by a novel gamma-secretase cut, which occurs at a site corresponding to the S3 cleavage of Notch.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-10206644, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-10206645, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-10392577, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-10545183, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-10878808, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-10879540, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11024004, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11030342, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11035007, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11055423, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11056541, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11134059, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11145990, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-11252897, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-1383826, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-1465129, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-8261505, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-9195901, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-9450754, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-9620803, http://linkedlifedata.com/resource/pubmed/commentcorrection/11520861-9822712
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/1,2-dilinolenoyl-3-(4-aminobutyryl)p..., http://linkedlifedata.com/resource/pubmed/chemical/Amyloid Precursor Protein Secretases, http://linkedlifedata.com/resource/pubmed/chemical/Amyloid beta-Protein Precursor, http://linkedlifedata.com/resource/pubmed/chemical/Aspartic Acid Endopeptidases, http://linkedlifedata.com/resource/pubmed/chemical/BACE1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Bace1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/DNA, Complementary, http://linkedlifedata.com/resource/pubmed/chemical/Endopeptidases, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/PSEN1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Presenilin-1, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Notch, http://linkedlifedata.com/resource/pubmed/chemical/Triglycerides, http://linkedlifedata.com/resource/pubmed/chemical/gamma-Aminobutyric Acid
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
1469-221X
pubmed:author
pubmed:issnType
Print
pubmed:volume
2
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
835-41
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:11520861-Amino Acid Sequence, pubmed-meshheading:11520861-Amyloid Precursor Protein Secretases, pubmed-meshheading:11520861-Amyloid beta-Protein Precursor, pubmed-meshheading:11520861-Animals, pubmed-meshheading:11520861-Aspartic Acid Endopeptidases, pubmed-meshheading:11520861-Binding Sites, pubmed-meshheading:11520861-Brain, pubmed-meshheading:11520861-Cell Line, pubmed-meshheading:11520861-Cells, Cultured, pubmed-meshheading:11520861-DNA, Complementary, pubmed-meshheading:11520861-Dose-Response Relationship, Drug, pubmed-meshheading:11520861-Endopeptidases, pubmed-meshheading:11520861-Fibroblasts, pubmed-meshheading:11520861-Humans, pubmed-meshheading:11520861-Membrane Proteins, pubmed-meshheading:11520861-Mice, pubmed-meshheading:11520861-Molecular Sequence Data, pubmed-meshheading:11520861-Polymerase Chain Reaction, pubmed-meshheading:11520861-Presenilin-1, pubmed-meshheading:11520861-Protein Binding, pubmed-meshheading:11520861-Protein Structure, Tertiary, pubmed-meshheading:11520861-Receptors, Notch, pubmed-meshheading:11520861-Time Factors, pubmed-meshheading:11520861-Transfection, pubmed-meshheading:11520861-Triglycerides, pubmed-meshheading:11520861-gamma-Aminobutyric Acid
pubmed:year
2001
pubmed:articleTitle
Presenilin-dependent gamma-secretase processing of beta-amyloid precursor protein at a site corresponding to the S3 cleavage of Notch.
pubmed:affiliation
Adolf Butenandt-Institute, Department of Biochemistry, Laboratory for Alzheimer's and Parkinson's Disease Research, Ludwig-Maximilians-University, Schillerstrasse 44, 80336 Munich, Germany.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't