Linked Life Data

15821876

Source:http://linkedlifedata.com/resource/pubmed/id/15821876

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
2
pubmed:dateCreated
2005-4-11
pubmed:abstractText
Proteins that specifically bind double-stranded RNA (dsRNA) are involved in the regulation of cellular signaling events and gene expression, and are characterized by a conserved dsRNA-binding motif (dsRBM). Here we report the biochemical properties of nine such gene products, each containing one or two dsRBMs: four Arabidopsis Dicer-like proteins (DCL1-4), Arabidopsis HYL1 and four of its homologs (DRB2, DRB4, DRB5 and OsDRB1). DCL1, DCL3, HYL1 and the four HYL1 homologs exhibit significant dsRNA-binding activity, indicating that these proteins are involved in RNA metabolism. The dsRBMs from dsRBM-containing proteins (dsRBPs) also function as a protein-protein interaction domain and homo- and heterodimerization are essential for biological functioning of these proteins. We show that DRB4 interacts specifically with DCL4, and HYL1 most strongly interacts with DCL1. These results indicate that each HYL1/DRB family protein interacts with one specific partner among the four Dicer-like proteins. Localization studies using GFP fusion proteins demonstrate that DCL1, DCL4, HYL1 and DRB4 localize in the nucleus, while DRB2 is present in the cytoplasm. Subcellular localizations of HYL1, DRB4, DCL1 and DCL4 further strengthen the notion that HYL1 and DCL1, and DRB4 and DCL4, exist as complexes. The presented data suggest that each member of the HYL1/DRB protein family may individually modulate Dicer function through heterodimerization with a Dicer-like protein in vivo.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0167-4412
pubmed:author
pubmed:issnType
Print
pubmed:volume
57
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
173-88
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:15821876-Arabidopsis, pubmed-meshheading:15821876-Arabidopsis Proteins, pubmed-meshheading:15821876-Binding, Competitive, pubmed-meshheading:15821876-Cell Cycle Proteins, pubmed-meshheading:15821876-Dimerization, pubmed-meshheading:15821876-Electrophoresis, Polyacrylamide Gel, pubmed-meshheading:15821876-Electrophoretic Mobility Shift Assay, pubmed-meshheading:15821876-Green Fluorescent Proteins, pubmed-meshheading:15821876-Microscopy, Fluorescence, pubmed-meshheading:15821876-Oryza sativa, pubmed-meshheading:15821876-Phylogeny, pubmed-meshheading:15821876-Plant Proteins, pubmed-meshheading:15821876-Protein Binding, pubmed-meshheading:15821876-RNA, Double-Stranded, pubmed-meshheading:15821876-RNA-Binding Proteins, pubmed-meshheading:15821876-Recombinant Fusion Proteins, pubmed-meshheading:15821876-Ribonuclease III, pubmed-meshheading:15821876-Tradescantia
pubmed:year
2005
pubmed:articleTitle
Specific interactions between Dicer-like proteins and HYL1/DRB-family dsRNA-binding proteins in Arabidopsis thaliana.
pubmed:affiliation
Department of Applied Biological Sciences, Tokyo University of Agriculture and Technology, Saiwaicho 3-5-8, Fuchu, Tokyo 183-8509, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't