Literature DB >> 15731002

PML bodies: a meeting place for genomic loci?

Reagan W Ching1, Graham Dellaire, Christopher H Eskiw, David P Bazett-Jones.   

Abstract

Promyelocytic leukemia (PML) bodies have been implicated in a variety of cellular processes, such as cell-cycle regulation, apoptosis, proteolysis, tumor suppression, DNA repair and transcription. Despite this, the function of PML bodies is still unknown. Direct and indirect evidence supports the hypothesis that PML bodies interact with specific genes or genomic loci. This includes the finding that the stability of PML bodies is affected by cell stress and changes in chromatin structure. PML bodies also facilitate the transcription and replication of double-stranded DNA viral genomes. Moreover, PML bodies associate with specific regions of high transcriptional activity in the cellular genome. We propose that PML bodies functionally interact with chromatin and are important for the regulation of gene expression.

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Year:  2005        PMID: 15731002     DOI: 10.1242/jcs.01700

Source DB:  PubMed          Journal:  J Cell Sci        ISSN: 0021-9533            Impact factor:   5.285


  58 in total

1.  Herpes simplex virus immediate-early protein ICP0 is targeted by SIAH-1 for proteasomal degradation.

Authors:  Claus-Henning Nagel; Nina Albrecht; Kristijana Milovic-Holm; Lakshmikanth Mariyanna; Britta Keyser; Bettina Abel; Britta Weseloh; Thomas G Hofmann; Martha M Eibl; Joachim Hauber
Journal:  J Virol       Date:  2011-06-01       Impact factor: 5.103

Review 2.  PML nuclear bodies.

Authors:  Valérie Lallemand-Breitenbach; Hugues de Thé
Journal:  Cold Spring Harb Perspect Biol       Date:  2010-04-21       Impact factor: 10.005

3.  Co-expressed genes prepositioned in spatial neighborhoods stochastically associate with SC35 speckles and RNA polymerase II factories.

Authors:  Dietmar Rieder; Christian Ploner; Anne M Krogsdam; Gernot Stocker; Maria Fischer; Marcel Scheideler; Christian Dani; Ez-Zoubir Amri; Waltraud G Müller; James G McNally; Zlatko Trajanoski
Journal:  Cell Mol Life Sci       Date:  2013-09-12       Impact factor: 9.261

4.  Transcriptional regulation is affected by subnuclear targeting of reporter plasmids to PML nuclear bodies.

Authors:  Gregory J Block; Christopher H Eskiw; Graham Dellaire; David P Bazett-Jones
Journal:  Mol Cell Biol       Date:  2006-09-11       Impact factor: 4.272

5.  Nuclear retention of ICP0 in cells exposed to HDAC inhibitor or transfected with DNA before infection with herpes simplex virus 1.

Authors:  Maria Kalamvoki; Bernard Roizman
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-10       Impact factor: 11.205

6.  PML: An emerging tumor suppressor and a target with therapeutic potential.

Authors:  Erin L Reineke; Hung-Ying Kao
Journal:  Cancer Ther       Date:  2009-09-01

7.  Arsenic mediated disruption of promyelocytic leukemia protein nuclear bodies induces ganciclovir susceptibility in Epstein-Barr positive epithelial cells.

Authors:  Mark D Sides; Gregory J Block; Bin Shan; Kyle C Esteves; Zhen Lin; Erik K Flemington; Joseph A Lasky
Journal:  Virology       Date:  2011-05-24       Impact factor: 3.616

8.  Adenoviral oncoprotein E1B55K mediates colocalization of SSBP2 and PML in response to stress.

Authors:  Helen B Fleisig; Hong Liang; Lalitha Nagarajan
Journal:  J Mol Signal       Date:  2010-06-11

9.  The proteins of intra-nuclear bodies: a data-driven analysis of sequence, interaction and expression.

Authors:  Nurul Mohamad; Mikael Bodén
Journal:  BMC Syst Biol       Date:  2010-04-13

10.  Herpesvirus protein ICP27 switches PML isoform by altering mRNA splicing.

Authors:  Takayuki Nojima; Takako Oshiro-Ideue; Hiroto Nakanoya; Hidenobu Kawamura; Tomomi Morimoto; Yasushi Kawaguchi; Naoyuki Kataoka; Masatoshi Hagiwara
Journal:  Nucleic Acids Res       Date:  2009-09-03       Impact factor: 16.971

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