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rdf:type |
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lifeskim:mentions |
umls-concept:C0017262,
umls-concept:C0030705,
umls-concept:C0033684,
umls-concept:C0035668,
umls-concept:C0040711,
umls-concept:C0185117,
umls-concept:C0243125,
umls-concept:C0699900,
umls-concept:C1705914,
umls-concept:C2911684,
umls-concept:C2931689
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pubmed:issue |
2
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pubmed:dateCreated |
2009-7-27
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pubmed:abstractText |
Myotonic dystrophy 2 (DM2) is a multisystem skeletal muscle disease caused by an expansion of tetranucleotide CCTG repeats, the transcription of which results in the accumulation of untranslated CCUG RNA. In this study, we report that CCUG repeats both bind to and misregulate the biological functions of cytoplasmic multiprotein complexes. Two CCUG-interacting complexes were subsequently purified and analyzed. A major component of one of the complexes was found to be the 20S catalytic core complex of the proteasome. The second complex was found to contain CUG triplet repeat RNA-binding protein 1 (CUGBP1) and the translation initiation factor eIF2. Consistent with the biological functions of the 20S proteasome and the CUGBP1-eIF2 complexes, the stability of short-lived proteins and the levels of the translational targets of CUGBP1 were shown to be elevated in DM2 myoblasts. We found that the overexpression of CCUG repeats in human myoblasts from unaffected patients, in C2C12 myoblasts, and in a DM2 mouse model alters protein translation and degradation, similar to the alterations observed in DM2 patients. Taken together, these findings show that RNA CCUG repeats misregulate protein turnover on both the levels of translation and proteasome-mediated protein degradation.
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pubmed:grant |
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pubmed:commentsCorrections |
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-10921906,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-10970838,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-10976074,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-11486088,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-11564876,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-11726559,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-11884745,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-12700164,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-1346925,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-14671308,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-14685250,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-14722059,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-15065017,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-15843400,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-16480813,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-16624843,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-16717059,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-16878132,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-16931514,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-7543316,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-8789448,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-8891208,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-8948631,
http://linkedlifedata.com/resource/pubmed/commentcorrection/19590039-9563950
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1525-2191
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pubmed:author |
pubmed-author:HuichalafClaudiaC,
pubmed-author:JinBingwenB,
pubmed-author:KraheRalfR,
pubmed-author:SalisburyElizabethE,
pubmed-author:SarkarParthaP,
pubmed-author:Schneider-GoldChristianeC,
pubmed-author:SchoserBenediktB,
pubmed-author:SiritoMarioM,
pubmed-author:TimchenkoLubov TLT,
pubmed-author:TimchenkoNikolai ANA,
pubmed-author:WangGuo-LiGL
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pubmed:issnType |
Electronic
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pubmed:volume |
175
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
748-62
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pubmed:dateRevised |
2010-9-27
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pubmed:meshHeading |
pubmed-meshheading:19590039-Animals,
pubmed-meshheading:19590039-Base Sequence,
pubmed-meshheading:19590039-Cell Line,
pubmed-meshheading:19590039-Cell Nucleus,
pubmed-meshheading:19590039-Cytoplasm,
pubmed-meshheading:19590039-Eukaryotic Initiation Factor-2,
pubmed-meshheading:19590039-Humans,
pubmed-meshheading:19590039-Mice,
pubmed-meshheading:19590039-Microsatellite Repeats,
pubmed-meshheading:19590039-Myoblasts,
pubmed-meshheading:19590039-Myotonic Dystrophy,
pubmed-meshheading:19590039-Proteasome Endopeptidase Complex,
pubmed-meshheading:19590039-Protein Biosynthesis,
pubmed-meshheading:19590039-Proteins,
pubmed-meshheading:19590039-Untranslated Regions
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pubmed:year |
2009
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pubmed:articleTitle |
Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patients.
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pubmed:affiliation |
Department of Molecular Physiology and Biophysics, Baylor College of Medicine, One Baylor Plaza, Houston, Texas 77030, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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