GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.

Non-translating RNAs that have undergone active translational repression are culled from the cytoplasm into P-bodies for decapping-dependent decay or for sequestration. Organisms that use microRNA-mediated RNA silencing have an additional pathway to remove RNAs from active translation. Consequently,...

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Main Authors: Prajal H Patel, Scott A Barbee, J Todd Blankenship
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4773245?pdf=render
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author Prajal H Patel
Scott A Barbee
J Todd Blankenship
author_facet Prajal H Patel
Scott A Barbee
J Todd Blankenship
author_sort Prajal H Patel
collection DOAJ
description Non-translating RNAs that have undergone active translational repression are culled from the cytoplasm into P-bodies for decapping-dependent decay or for sequestration. Organisms that use microRNA-mediated RNA silencing have an additional pathway to remove RNAs from active translation. Consequently, proteins that govern microRNA-mediated silencing, such as GW182/Gw and AGO1, are often associated with the P-bodies of higher eukaryotic organisms. Due to the presence of Gw, these structures have been referred to as GW-bodies. However, several reports have indicated that GW-bodies have different dynamics to P-bodies. Here, we use live imaging to examine GW-body and P-body dynamics in the early Drosophila melanogaster embryo. While P-bodies are present throughout early embryonic development, cytoplasmic GW-bodies only form in significant numbers at the midblastula transition. Unlike P-bodies, which are predominantly cytoplasmic, GW-bodies are present in both nuclei and the cytoplasm. RNA decapping factors such as DCP1, Me31B, and Hpat are not associated with GW-bodies, indicating that P-bodies and GW-bodies are distinct structures. Furthermore, known Gw interactors such as AGO1 and the CCR4-NOT deadenylation complex, which have been shown to be important for Gw function, are also not present in GW-bodies. Use of translational inhibitors puromycin and cycloheximide, which respectively increase or decrease cellular pools of non-translating RNAs, alter GW-body size, underscoring that GW-bodies are composed of non-translating RNAs. Taken together, these data indicate that active translational silencing most likely does not occur in GW-bodies. Instead GW-bodies most likely function as repositories for translationally silenced RNAs. Finally, inhibition of zygotic gene transcription is unable to block the formation of either P-bodies or GW-bodies in the early embryo, suggesting that these structures are composed of maternal RNAs.
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spelling doaj.art-22ce259860a74e37ad2b0a34ade62dae2022-12-21T19:29:21ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01113e015029110.1371/journal.pone.0150291GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.Prajal H PatelScott A BarbeeJ Todd BlankenshipNon-translating RNAs that have undergone active translational repression are culled from the cytoplasm into P-bodies for decapping-dependent decay or for sequestration. Organisms that use microRNA-mediated RNA silencing have an additional pathway to remove RNAs from active translation. Consequently, proteins that govern microRNA-mediated silencing, such as GW182/Gw and AGO1, are often associated with the P-bodies of higher eukaryotic organisms. Due to the presence of Gw, these structures have been referred to as GW-bodies. However, several reports have indicated that GW-bodies have different dynamics to P-bodies. Here, we use live imaging to examine GW-body and P-body dynamics in the early Drosophila melanogaster embryo. While P-bodies are present throughout early embryonic development, cytoplasmic GW-bodies only form in significant numbers at the midblastula transition. Unlike P-bodies, which are predominantly cytoplasmic, GW-bodies are present in both nuclei and the cytoplasm. RNA decapping factors such as DCP1, Me31B, and Hpat are not associated with GW-bodies, indicating that P-bodies and GW-bodies are distinct structures. Furthermore, known Gw interactors such as AGO1 and the CCR4-NOT deadenylation complex, which have been shown to be important for Gw function, are also not present in GW-bodies. Use of translational inhibitors puromycin and cycloheximide, which respectively increase or decrease cellular pools of non-translating RNAs, alter GW-body size, underscoring that GW-bodies are composed of non-translating RNAs. Taken together, these data indicate that active translational silencing most likely does not occur in GW-bodies. Instead GW-bodies most likely function as repositories for translationally silenced RNAs. Finally, inhibition of zygotic gene transcription is unable to block the formation of either P-bodies or GW-bodies in the early embryo, suggesting that these structures are composed of maternal RNAs.http://europepmc.org/articles/PMC4773245?pdf=render
spellingShingle Prajal H Patel
Scott A Barbee
J Todd Blankenship
GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.
PLoS ONE
title GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.
title_full GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.
title_fullStr GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.
title_full_unstemmed GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.
title_short GW-Bodies and P-Bodies Constitute Two Separate Pools of Sequestered Non-Translating RNAs.
title_sort gw bodies and p bodies constitute two separate pools of sequestered non translating rnas
url http://europepmc.org/articles/PMC4773245?pdf=render
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