Nuclear sorting of short RNA polymerase II transcripts

William Garland, Torben Heick Jensen*

*Corresponding author af dette arbejde

Publikation: Bidrag til tidsskrift/Konferencebidrag i tidsskrift /Bidrag til avisReviewForskningpeer review

4 Citationer (Scopus)

Abstract

Mammalian genomes produce an abundance of short RNA. This is, to a large extent, due to the genome-wide and spurious activity of RNA polymerase II (RNAPII). However, it is also because the vast majority of initiating RNAPII, regardless of the transcribed DNA unit, terminates within a ∼3-kb early “pausing zone.” Given that the resultant RNAs constitute both functional and non-functional species, their proper sorting is critical. One way to think about such quality control (QC) is that transcripts, from their first emergence, are relentlessly targeted by decay factors, which may only be avoided by engaging protective processing pathways. In a molecular materialization of this concept, recent progress has found that both “destructive” and “productive” RNA effectors assemble at the 5′ end of capped RNA, orchestrated by the essential arsenite resistance protein 2 (ARS2) protein. Using this principle, we here discuss early QC mechanisms and how these might sort short RNAs to their final fates.

OriginalsprogEngelsk
TidsskriftMolecular Cell
Vol/bind84
Nummer19
Sider (fra-til)3644-3655
Antal sider12
ISSN1097-2765
DOI
StatusUdgivet - 3 okt. 2024

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