Literature DB >> 28090582

Putting the brakes on transcription at damaged chromatin: Do Polycomb silencers do more than modify histones?

Younghoon Kee1.   

Abstract

One of the cellular responses to DNA damage is to monitor and execute temporary arrest of RNA synthesis at chromatin lesions. The Polycomb silencer BMI1 is a well-known contributor to this process. We recently described a new mode of BMI1-mediated transcription arrest at lesions that involves UBR5 E3 ligase and FACT histone chaperon.

Entities:  

Keywords:  BMI1; FACT; Polycomb

Year:  2016        PMID: 28090582      PMCID: PMC5160387          DOI: 10.1080/23723556.2016.1244513

Source DB:  PubMed          Journal:  Mol Cell Oncol        ISSN: 2372-3556


  10 in total

Review 1.  Polycomb silencers control cell fate, development and cancer.

Authors:  Anke Sparmann; Maarten van Lohuizen
Journal:  Nat Rev Cancer       Date:  2006-11       Impact factor: 60.716

Review 2.  Transcriptional regulation by Polycomb group proteins.

Authors:  Luciano Di Croce; Kristian Helin
Journal:  Nat Struct Mol Biol       Date:  2013-10       Impact factor: 15.369

Review 3.  The interface between transcription and mechanisms maintaining genome integrity.

Authors:  Jesper Q Svejstrup
Journal:  Trends Biochem Sci       Date:  2010-03-01       Impact factor: 13.807

Review 4.  The emerging role of Polycomb repressors in the response to DNA damage.

Authors:  Joseph H A Vissers; Maarten van Lohuizen; Elisabetta Citterio
Journal:  J Cell Sci       Date:  2012-09-01       Impact factor: 5.285

5.  TRIP12 and UBR5 suppress spreading of chromatin ubiquitylation at damaged chromosomes.

Authors:  Thorkell Gudjonsson; Matthias Altmeyer; Velibor Savic; Luis Toledo; Christoffel Dinant; Merete Grøfte; Jirina Bartkova; Maria Poulsen; Yasuyoshi Oka; Simon Bekker-Jensen; Niels Mailand; Beate Neumann; Jean-Karim Heriche; Robert Shearer; Darren Saunders; Jiri Bartek; Jiri Lukas; Claudia Lukas
Journal:  Cell       Date:  2012-08-09       Impact factor: 41.582

6.  BMI1-UBR5 axis regulates transcriptional repression at damaged chromatin.

Authors:  Anthony Sanchez; Angelo De Vivo; Nadima Uprety; Jonghwan Kim; Stanley M Stevens; Younghoon Kee
Journal:  Proc Natl Acad Sci U S A       Date:  2016-09-19       Impact factor: 11.205

7.  Enhanced chromatin dynamics by FACT promotes transcriptional restart after UV-induced DNA damage.

Authors:  Christoffel Dinant; Giannis Ampatziadis-Michailidis; Hannes Lans; Maria Tresini; Anna Lagarou; Malgorzata Grosbart; Arjan F Theil; Wiggert A van Cappellen; Hiroshi Kimura; Jiri Bartek; Maria Fousteri; Adriaan B Houtsmuller; Wim Vermeulen; Jurgen A Marteijn
Journal:  Mol Cell       Date:  2013-08-22       Impact factor: 17.970

8.  UBR5-mediated ubiquitination of ATMIN is required for ionizing radiation-induced ATM signaling and function.

Authors:  Tianyi Zhang; Janet Cronshaw; Nnennaya Kanu; Ambrosius P Snijders; Axel Behrens
Journal:  Proc Natl Acad Sci U S A       Date:  2014-08-04       Impact factor: 11.205

9.  Transcriptional repression by PRC1 in the absence of H2A monoubiquitylation.

Authors:  Ana Raquel Pengelly; Reinhard Kalb; Katja Finkl; Jürg Müller
Journal:  Genes Dev       Date:  2015-07-15       Impact factor: 11.361

10.  The E3 ubiquitin ligase activity of RING1B is not essential for early mouse development.

Authors:  Robert S Illingworth; Michael Moffat; Abigail R Mann; David Read; Chris J Hunter; Madapura M Pradeepa; Ian R Adams; Wendy A Bickmore
Journal:  Genes Dev       Date:  2015-09-15       Impact factor: 11.361

  10 in total

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