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  The human cap-binding complex is functionally connected to the nuclear RNA exosome.

Andersen, P. R., Domanski, M., Kristiansen, M. S., Storvall, H., Ntini, E., Verheggen, C., et al. (2013). The human cap-binding complex is functionally connected to the nuclear RNA exosome. Nature Structural & Molecular Biology, 20(12), 1367-1376.

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 Creators:
Andersen, Peter Refsing, Author
Domanski, Michal, Author
Kristiansen, Maiken S, Author
Storvall, Helena, Author
Ntini, Evgenia, Author
Verheggen, Celine, Author
Schein, Aleks, Author
Bunkenborg, Jakob, Author
Poser, Ina1, Author           
Hallais, Marie, Author
Sandberg, Rickard, Author
Hyman, Anthony1, Author           
Lacava, John, Author
Rout, Michael P, Author
Andersen, Jens S, Author
Bertrand, Edouard, Author
Jensen, Torben Heick, Author
Affiliations:
1Max Planck Institute of Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Abstract: Nuclear processing and quality control of eukaryotic RNA is mediated by the RNA exosome, which is regulated by accessory factors. However, the mechanism of exosome recruitment to its ribonucleoprotein (RNP) targets remains poorly understood. Here we report a physical link between the human exosome and the cap-binding complex (CBC). The CBC associates with the ARS2 protein to form CBC-ARS2 (CBCA) and then further connects, together with the ZC3H18 protein, to the nuclear exosome targeting (NEXT) complex, thus forming CBC-NEXT (CBCN). RNA immunoprecipitation using CBCN factors as well as the analysis of combinatorial depletion of CBCN and exosome components underscore the functional relevance of CBC-exosome bridging at the level of target RNA. Specifically, CBCA suppresses read-through products of several RNA families by promoting their transcriptional termination. We suggest that the RNP 5' cap links transcription termination to exosomal RNA degradation through CBCN.

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 Dates: 2013
 Publication Status: Issued
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 Rev. Type: -
 Identifiers: eDoc: 688605
Other: 5558
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Title: Nature Structural & Molecular Biology
Source Genre: Journal
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Pages: - Volume / Issue: 20 (12) Sequence Number: - Start / End Page: 1367 - 1376 Identifier: -