Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.

Transcription of DNA is essential for cell maintenance and survival; inappropriate localization of proteins that are involved in transcription would be catastrophic. In Alzheimer's disease brains, and in vitro studies, we have found qualitative and quantitative deficits in transport into the nu...

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Main Authors: Diego Mastroeni, Leonidas Chouliaras, Andrew Grover, Winnie S Liang, Kevin Hauns, Joseph Rogers, Paul D Coleman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3540085?pdf=render
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spelling doaj-37f7bb5c09c84f67bb6ef9acc47eeb2c2020-11-25T02:46:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5334910.1371/journal.pone.0053349Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.Diego MastroeniLeonidas ChouliarasAndrew GroverWinnie S LiangKevin HaunsJoseph RogersPaul D ColemanTranscription of DNA is essential for cell maintenance and survival; inappropriate localization of proteins that are involved in transcription would be catastrophic. In Alzheimer's disease brains, and in vitro studies, we have found qualitative and quantitative deficits in transport into the nucleus of DNA methyltransferase 1 (DNMT1) and RNA polymerase II (RNA pol II), accompanied by their abnormal sequestration in the cytoplasm. RAN (RAs-related Nuclear protein) knockdown, by siRNA and oligomeric Aβ42 treatment in neurons, replicate human data which indicate that transport disruption in AD may be mechanistically linked to reduced expression of RAN, a pivotal molecule in nucleocytoplasmic transport. In vitro studies also indicate a significant role for oligomeric Aβ42 in the observed phenomena. We propose a model in which reduced transcription regulators in the nucleus and their increased presence in the cytoplasm may lead to many of the cellular manifestations of Alzheimer's disease.http://europepmc.org/articles/PMC3540085?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Diego Mastroeni
Leonidas Chouliaras
Andrew Grover
Winnie S Liang
Kevin Hauns
Joseph Rogers
Paul D Coleman
spellingShingle Diego Mastroeni
Leonidas Chouliaras
Andrew Grover
Winnie S Liang
Kevin Hauns
Joseph Rogers
Paul D Coleman
Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.
PLoS ONE
author_facet Diego Mastroeni
Leonidas Chouliaras
Andrew Grover
Winnie S Liang
Kevin Hauns
Joseph Rogers
Paul D Coleman
author_sort Diego Mastroeni
title Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.
title_short Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.
title_full Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.
title_fullStr Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.
title_full_unstemmed Reduced RAN expression and disrupted transport between cytoplasm and nucleus; a key event in Alzheimer's disease pathophysiology.
title_sort reduced ran expression and disrupted transport between cytoplasm and nucleus; a key event in alzheimer's disease pathophysiology.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Transcription of DNA is essential for cell maintenance and survival; inappropriate localization of proteins that are involved in transcription would be catastrophic. In Alzheimer's disease brains, and in vitro studies, we have found qualitative and quantitative deficits in transport into the nucleus of DNA methyltransferase 1 (DNMT1) and RNA polymerase II (RNA pol II), accompanied by their abnormal sequestration in the cytoplasm. RAN (RAs-related Nuclear protein) knockdown, by siRNA and oligomeric Aβ42 treatment in neurons, replicate human data which indicate that transport disruption in AD may be mechanistically linked to reduced expression of RAN, a pivotal molecule in nucleocytoplasmic transport. In vitro studies also indicate a significant role for oligomeric Aβ42 in the observed phenomena. We propose a model in which reduced transcription regulators in the nucleus and their increased presence in the cytoplasm may lead to many of the cellular manifestations of Alzheimer's disease.
url http://europepmc.org/articles/PMC3540085?pdf=render
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