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Journal ArticleDOI

RNA decay machines: the exosome.

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TLDR
This review is focused on the most comprehensively described yeast and human exosomes, and shall point out similarities or dissimilarities to prokaryotic complexes and proteins where appropriate.
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This article is published in Biochimica et Biophysica Acta.The article was published on 2013-06-01. It has received 225 citations till now. The article focuses on the topics: Exosome Multienzyme Ribonuclease Complex & Exosome complex.

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Citations
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Journal ArticleDOI

RNA exosome-regulated long non-coding RNA transcription controls super-enhancer activity.

TL;DR: It is proposed that the RNA exosome protects divergently transcribed lncRNA expressing enhancers by resolving deleterious transcription-coupled secondary DNA structures, while also regulating long-range super-enhancer chromosomal interactions important for cellular function.
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The regulation and functions of the nuclear RNA exosome complex

TL;DR: Novel, previously unappreciated functions of the nuclear exosome are introduced and discussed, including in transcription regulation and in the maintenance of genome stability.
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The DEAD-Box Protein Dhh1p Couples mRNA Decay and Translation by Monitoring Codon Optimality

TL;DR: It is established that the DEAD-box protein Dhh1p is a sensor of codon optimality that targets an mRNA for decay, and mRNAs whose translation elongation rate is slowed by inclusion of non-optimal codons are specifically degraded in a DHH1p-dependent manner.
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Stable Pausing by RNA Polymerase II Provides an Opportunity to Target and Integrate Regulatory Signals

TL;DR: It is demonstrated that paused elongation complexes can be remarkably stable, with half-lives exceeding 15 min at genes with inefficient pause release, and proposed that stable pausing of polymerase provides a temporal window of opportunity for recruitment of factors to modulate gene expression and that the nascent tssRNA represents an appealing target for these interactions.
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Distinctive Patterns of Transcription and RNA Processing for Human lincRNAs.

TL;DR: In this paper, the authors define systematic differences in transcription and RNA processing between protein-coding and lincRNA genes in human HeLa cells, based on a range of nascent transcriptomic approaches applied to different nuclear fractions, including mammalian native elongating transcript sequencing.
References
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Journal ArticleDOI

Global analysis of protein localization in budding yeast

TL;DR: The construction and analysis of a collection of yeast strains expressing full-length, chromosomally tagged green fluorescent protein fusion proteins helps reveal the logic of transcriptional co-regulation, and provides a comprehensive view of interactions within and between organelles in eukaryotic cells.
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Initial genome sequencing and analysis of multiple myeloma

TL;DR: The massively parallel sequencing of 38 tumour genomes and their comparison to matched normal DNAs indicates that cancer genome sequencing of large collections of samples will yield new insights into cancer not anticipated by existing knowledge.

Initial genome sequencing and analysis of multiple myeloma

TL;DR: In this paper, a massively parallel sequencing of 38 tumour genomes and their comparison to matched normal DNAs was reported, and several new and unexpected oncogenic mechanisms were suggested by the pattern of somatic mutation across the data set.
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The Exosome: A Conserved Eukaryotic RNA Processing Complex Containing Multiple 3′→5′ Exoribonucleases

TL;DR: The exosome constitutes a highly conserved eukaryotic RNA processing complex in S. cerevisiae that is required for 3' processing of the 5.8S rRNA.
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AU binding proteins recruit the exosome to degrade ARE-containing mRNAs.

TL;DR: Using a cell-free RNA decay system, it is demonstrated that the mammalian exosome is required for rapid degradation of ARE-containing RNAs but not for poly(A) shortening.
Related Papers (5)
Trending Questions (1)
Is dIS 3 in the RNA exosome a RNAse H?

The paper does not mention anything about a protein called "dIS 3" in the RNA exosome or its role as an RNAse H.