Literature DB >> 15346807

The exosome, a molecular machine for controlled RNA degradation in both nucleus and cytoplasm.

Reinout Raijmakers1, Geurt Schilders, Ger J M Pruijn.   

Abstract

One of the most important protein complexes involved in maintaining correct RNA levels in eukaryotic cells is the exosome, a complex consisting almost exclusively of exoribonucleolytic proteins. Since the identification of the exosome complex, seven years ago, much progress has been made in the characterization of its composition, structure and function in a variety of organisms. Although the exosome seems to accumulate in the nucleolus, it has been clearly established that it is also localized in cytoplasm and nucleoplasm. In accordance with its widespread intracellular distribution, the exosome has been implicated in a variety of RNA processing and degradation processes. Nevertheless, many questions still remain unanswered. What are the factors that regulate the activity of the exosome? How and where is the complex assembled? What are the differences in the composition of the nuclear and cytoplasmic exosome? What is the detailed structure of exosome subunits? What are the mechanisms by which the exosome is recruited to substrate RNAs? Here, we summarize the current knowledge on the composition and architecture of this complex, explain its role in both the production and degradation of various types of RNA molecules and discuss the implications of recent research developments that shed some light on the questions above and the mechanisms that are controlling the exosome.

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Year:  2004        PMID: 15346807     DOI: 10.1078/0171-9335-00385

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  30 in total

1.  Nucleolar localization of the yeast RNA exosome subunit Rrp44 hints at early pre-rRNA processing as its main function.

Authors:  Ellen K Okuda; Fernando A Gonzales-Zubiate; Olivier Gadal; Carla C Oliveira
Journal:  J Biol Chem       Date:  2020-06-17       Impact factor: 5.157

2.  The Zea mays glycine-rich RNA-binding protein MA16 is bound to a ribonucleotide(s) by a stable linkage.

Authors:  Miguel Angel Freire
Journal:  J Plant Res       Date:  2012-01-21       Impact factor: 2.629

3.  A view to a kill: structure of the RNA exosome.

Authors:  Vincent Shen; Megerditch Kiledjian
Journal:  Cell       Date:  2006-12-15       Impact factor: 41.582

4.  Nuclear RNA surveillance in Saccharomyces cerevisiae: Trf4p-dependent polyadenylation of nascent hypomethylated tRNA and an aberrant form of 5S rRNA.

Authors:  Sujatha Kadaba; Xuying Wang; James T Anderson
Journal:  RNA       Date:  2006-01-23       Impact factor: 4.942

5.  Sequence-specific RNA binding mediated by the RNase PH domain of components of the exosome.

Authors:  John R Anderson; Devi Mukherjee; Karthika Muthukumaraswamy; Karen C M Moraes; Carol J Wilusz; Jeffrey Wilusz
Journal:  RNA       Date:  2006-08-15       Impact factor: 4.942

6.  The 5' external transcribed spacer in mouse ribosomal RNA contains two cleavage sites.

Authors:  Tatyana Kent; Yevgeniya R Lapik; Dimitri G Pestov
Journal:  RNA       Date:  2008-11-24       Impact factor: 4.942

Review 7.  Biomarkers in the management of scleroderma: an update.

Authors:  Giuseppina Abignano; Maya Buch; Paul Emery; Francesco Del Galdo
Journal:  Curr Rheumatol Rep       Date:  2011-02       Impact factor: 4.592

Review 8.  RNA surveillance: molecular approaches in transcript quality control and their implications in clinical diseases.

Authors:  Karen C M Moraes
Journal:  Mol Med       Date:  2009-10-07       Impact factor: 6.354

9.  Crystal structure of Escherichia coli PNPase: central channel residues are involved in processive RNA degradation.

Authors:  Zhonghao Shi; Wei-Zen Yang; Sue Lin-Chao; Kin-Fu Chak; Hanna S Yuan
Journal:  RNA       Date:  2008-09-23       Impact factor: 4.942

10.  Degradation of a polyadenylated rRNA maturation by-product involves one of the three RRP6-like proteins in Arabidopsis thaliana.

Authors:  Heike Lange; Sarah Holec; Valérie Cognat; Laurent Pieuchot; Monique Le Ret; Jean Canaday; Dominique Gagliardi
Journal:  Mol Cell Biol       Date:  2008-02-19       Impact factor: 4.272

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