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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2005-2-28
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pubmed:abstractText |
The tumor suppressor protein p53 is known to undergo cytoplasmic dynein-dependent nuclear translocation in response to DNA damage. However, the molecular link between p53 and the minus end-directed microtubule motor dynein complex has not been described. We report here that the 8-kDa light chain (LC8) of dynein binds to p53-binding protein 1 (53BP1). The LC8-binding domain was mapped to a short peptide segment immediately N-terminal to the kinetochore localization region of 53BP1. The LC8-binding domain is completely separated from the p53-binding domain in 53BP1. Therefore, 53BP1 can potentially act as an adaptor to assemble p53 to the dynein complex. Unlike other known LC8-binding proteins, 53BP1 contains two distinct LC8-binding motifs that are arranged in tandem. We further showed that 53BP1 can directly associate with the dynein complex. Disruption of the interaction between LC8 and 53BP1 in vivo prevented DNA damage-induced nuclear accumulation of p53. These data illustrate that LC8 is able to function as a versatile acceptor to link a wide spectrum of molecular cargoes to the dynein motor.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cytoplasmic Dyneins,
http://linkedlifedata.com/resource/pubmed/chemical/DYNLL1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Dyneins,
http://linkedlifedata.com/resource/pubmed/chemical/Gene Products, tat,
http://linkedlifedata.com/resource/pubmed/chemical/Glutathione Transferase,
http://linkedlifedata.com/resource/pubmed/chemical/Intracellular Signaling Peptides...,
http://linkedlifedata.com/resource/pubmed/chemical/Peptides,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoproteins,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Fusion Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/TP53BP1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0021-9258
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
4
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pubmed:volume |
280
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
8172-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:15611139-Active Transport, Cell Nucleus,
pubmed-meshheading:15611139-Amino Acid Motifs,
pubmed-meshheading:15611139-Amino Acid Sequence,
pubmed-meshheading:15611139-Cell Line,
pubmed-meshheading:15611139-Cell Nucleus,
pubmed-meshheading:15611139-Chromatography, High Pressure Liquid,
pubmed-meshheading:15611139-Cytoplasmic Dyneins,
pubmed-meshheading:15611139-DNA Damage,
pubmed-meshheading:15611139-Dyneins,
pubmed-meshheading:15611139-Electrophoresis, Polyacrylamide Gel,
pubmed-meshheading:15611139-Gene Products, tat,
pubmed-meshheading:15611139-Glutathione Transferase,
pubmed-meshheading:15611139-Humans,
pubmed-meshheading:15611139-Immunoblotting,
pubmed-meshheading:15611139-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:15611139-Magnetic Resonance Spectroscopy,
pubmed-meshheading:15611139-Microscopy, Fluorescence,
pubmed-meshheading:15611139-Molecular Sequence Data,
pubmed-meshheading:15611139-Peptides,
pubmed-meshheading:15611139-Phosphoproteins,
pubmed-meshheading:15611139-Protein Binding,
pubmed-meshheading:15611139-Protein Structure, Tertiary,
pubmed-meshheading:15611139-Recombinant Fusion Proteins,
pubmed-meshheading:15611139-Tumor Suppressor Protein p53,
pubmed-meshheading:15611139-Two-Hybrid System Techniques
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pubmed:year |
2005
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pubmed:articleTitle |
The 8-kDa dynein light chain binds to p53-binding protein 1 and mediates DNA damage-induced p53 nuclear accumulation.
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pubmed:affiliation |
Department of Biochemistry, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong, People's Republic of China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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