Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2006-1-20
pubmed:abstractText
Here we have identified 'triple D' (3d), a recessive N-ethyl-N-nitrosourea-induced mutation and phenotype in which no signaling occurs via the intracellular Toll-like receptors 3, 7 and 9 (sensors for double-stranded RNA, single-stranded RNA and unmethylated DNA, respectively). The 3d mutation also prevented cross-presentation and diminished major histocompatibility complex class II presentation of exogenous antigen; it also caused hypersusceptibility to infection by mouse cytomegalovirus and other microbes. By positional identification, we found 3d to be a missense allele of Unc93b1, which encodes the 12-membrane-spanning protein UNC-93B, a highly conserved molecule found in the endoplasmic reticulum with multiple paralogs in mammals. Innate responses to nucleic acids and exogenous antigen presentation, which both initiate in endosomes, thus seem to depend on an endoplasmic reticulum-resident protein, which suggests communication between these organellar systems.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1529-2908
pubmed:author
pubmed:issnType
Print
pubmed:volume
7
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
156-64
pubmed:dateRevised
2007-11-8
pubmed:meshHeading
pubmed-meshheading:16415873-Animals, pubmed-meshheading:16415873-Antigen Presentation, pubmed-meshheading:16415873-Cloning, Molecular, pubmed-meshheading:16415873-Endoplasmic Reticulum, pubmed-meshheading:16415873-Endosomes, pubmed-meshheading:16415873-Histocompatibility Antigens Class II, pubmed-meshheading:16415873-Infection, pubmed-meshheading:16415873-Membrane Glycoproteins, pubmed-meshheading:16415873-Membrane Transport Proteins, pubmed-meshheading:16415873-Mice, pubmed-meshheading:16415873-Mice, Inbred C57BL, pubmed-meshheading:16415873-Mice, Mutant Strains, pubmed-meshheading:16415873-Mutation, Missense, pubmed-meshheading:16415873-Phenotype, pubmed-meshheading:16415873-Signal Transduction, pubmed-meshheading:16415873-Toll-Like Receptor 3, pubmed-meshheading:16415873-Toll-Like Receptor 7, pubmed-meshheading:16415873-Toll-Like Receptor 9
pubmed:year
2006
pubmed:articleTitle
The Unc93b1 mutation 3d disrupts exogenous antigen presentation and signaling via Toll-like receptors 3, 7 and 9.
pubmed:affiliation
Department of Immunology, The Scripps Research Institute, La Jolla, California 92037, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural