Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2011-2-23
pubmed:abstractText
Triplication of chromosome 21 in Down syndrome (DS) results in overexpression of the minibrain kinase/dual-specificity tyrosine phosphorylated and regulated kinase 1A gene (DYRK1A). DYRK1A phosphorylates cytoplasmic tau protein and appears in intraneuronal neurofibrillary tangles (NFTs). We have previously shown significantly more DYRK1A-positive NFTs in DS brains than in sporadic Alzheimer disease (AD) brains. This study demonstrates a gene dosage-proportional increase in the level of DYRK1A in DS in the cytoplasm and the cell nucleus, and enhanced cytoplasmic and nuclear immunoreactivity of DYRK1A in DS. The results suggest that overexpressed DYRK1A may alter both phosphorylation of tau and alternative splicing factor (ASF). Two-dimensional electrophoresis revealed modification of ASF phosphorylation in DS/AD and AD in comparison to controls. Altered phosphorylation of ASF by overexpressed nuclear DYRK1A may contribute to the alternative splicing of the tau gene and an increase by 2.68 × of the 3R/4R ratio in DS/AD, and a several-fold increase in the number of 3R tau-positive NFTs in DS/AD subjects compared with that in sporadic AD subjects. These data support the hypothesis that phosphorylation of ASF by overexpressed DYRK1A may contribute to alternative splicing of exon 10, increased expression of 3R tau, and early onset of neurofibrillary degeneration in DS.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0022-3069
pubmed:author
pubmed:issnType
Print
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
36-50
pubmed:dateRevised
2011-5-10
pubmed:meshHeading
pubmed-meshheading:21157379-Adult, pubmed-meshheading:21157379-Aged, pubmed-meshheading:21157379-Aged, 80 and over, pubmed-meshheading:21157379-Animals, pubmed-meshheading:21157379-Cattle, pubmed-meshheading:21157379-Down Syndrome, pubmed-meshheading:21157379-Female, pubmed-meshheading:21157379-Gene Dosage, pubmed-meshheading:21157379-Gene Expression Regulation, Enzymologic, pubmed-meshheading:21157379-Humans, pubmed-meshheading:21157379-Male, pubmed-meshheading:21157379-Mice, pubmed-meshheading:21157379-Middle Aged, pubmed-meshheading:21157379-Nerve Degeneration, pubmed-meshheading:21157379-Neurofibrillary Tangles, pubmed-meshheading:21157379-Phenotype, pubmed-meshheading:21157379-Protein-Serine-Threonine Kinases, pubmed-meshheading:21157379-Protein-Tyrosine Kinases, pubmed-meshheading:21157379-Rats, pubmed-meshheading:21157379-Trinucleotide Repeats, pubmed-meshheading:21157379-tau Proteins
pubmed:year
2011
pubmed:articleTitle
Link between DYRK1A overexpression and several-fold enhancement of neurofibrillary degeneration with 3-repeat tau protein in Down syndrome.
pubmed:affiliation
Department of Developmental Neurobiology, NYS Institute for Basic Research in Developmental Disabilities, Staten Island, New York 10314, USA. Jerzy.Wegiel@omr.state.ny.us
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural