Linked Life Data

20852131

Source:http://linkedlifedata.com/resource/pubmed/id/20852131

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
25
pubmed:dateCreated
2010-12-17
pubmed:abstractText
Point mutations that trigger ligand-independent proteolysis of the Notch1 ectodomain occur frequently in human T-cell acute lymphoblastic leukemia (T-ALL) but are rare in murine T-ALL, suggesting that other mechanisms account for Notch1 activation in murine tumors. Here we show that most murine T-ALLs harbor Notch1 deletions that fall into 2 types, both leading to ligand-independent Notch1 activation. Type 1 deletions remove exon 1 and the proximal promoter, appear to be RAG-mediated, and are associated with mRNA transcripts that initiate from 3' regions of Notch1. In line with the RAG dependency of these rearrangements, RAG2 binds to the 5' end of Notch1 in normal thymocytes near the deletion breakpoints. Type 2 deletions remove sequences between exon 1 and exons 26 to 28 of Notch1, appear to be RAG-independent, and are associated with transcripts in which exon 1 is spliced out of frame to 3' Notch1 exons. Translation of both types of transcripts initiates at a conserved methionine residue, M1727, which lies within the Notch1 transmembrane domain. Polypeptides initiating at M1727 insert into membranes and are subject to constitutive cleavage by ?-secretase. Thus, like human T-ALL, murine T-ALL is often associated with acquired mutations that cause ligand-independent Notch1 activation.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1528-0020
pubmed:author
pubmed:issnType
Electronic
pubmed:day
16
pubmed:volume
116
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5455-64
pubmed:dateRevised
2011-3-4
pubmed:meshHeading
pubmed-meshheading:20852131-Amino Acid Sequence, pubmed-meshheading:20852131-Animals, pubmed-meshheading:20852131-Base Sequence, pubmed-meshheading:20852131-Blotting, Northern, pubmed-meshheading:20852131-Blotting, Southern, pubmed-meshheading:20852131-Blotting, Western, pubmed-meshheading:20852131-Bone Neoplasms, pubmed-meshheading:20852131-Gene Expression Regulation, Neoplastic, pubmed-meshheading:20852131-Homeodomain Proteins, pubmed-meshheading:20852131-Humans, pubmed-meshheading:20852131-Ikaros Transcription Factor, pubmed-meshheading:20852131-Mice, pubmed-meshheading:20852131-Mice, Knockout, pubmed-meshheading:20852131-Molecular Sequence Data, pubmed-meshheading:20852131-Mutation, pubmed-meshheading:20852131-Osteosarcoma, pubmed-meshheading:20852131-Peptide Chain Initiation, Translational, pubmed-meshheading:20852131-Precursor T-Cell Lymphoblastic Leukemia-Lymphoma, pubmed-meshheading:20852131-Promoter Regions, Genetic, pubmed-meshheading:20852131-RNA, Messenger, pubmed-meshheading:20852131-Receptor, Notch1, pubmed-meshheading:20852131-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:20852131-Sequence Deletion, pubmed-meshheading:20852131-Sequence Homology, Nucleic Acid, pubmed-meshheading:20852131-Transcriptional Activation, pubmed-meshheading:20852131-Tumor Cells, Cultured
pubmed:year
2010
pubmed:articleTitle
Deletion-based mechanisms of Notch1 activation in T-ALL: key roles for RAG recombinase and a conserved internal translational start site in Notch1.
pubmed:affiliation
Department of Pathology, Harvard Medical School, Boston, MA, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural