Literature DB >> 17073750

Recent structural studies of RNA polymerases II and III.

P Cramer1.   

Abstract

Here, I review three new structural studies from our laboratory. First, the crystal structure of RNA polymerase (Pol) II in complex with an RNA inhibitor revealed that this RNA blocks transcription initiation by preventing DNA loading into the active-centre cleft. Secondly, the structure of the SRI (Set2 Rpb1-interacting) domain of the histone methyltransferase Set2 revealed a novel fold for specific interaction with the doubly phosphorylated CTD (C-terminal repeat domain) of Pol II. Finally, we obtained the first structural information on Pol III, in the form of an 11-subunit model obtained by combining a homology model of the nine-subunit core enzyme with a new X-ray structure of the subcomplex C17/25.

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Year:  2006        PMID: 17073750     DOI: 10.1042/BST0341058

Source DB:  PubMed          Journal:  Biochem Soc Trans        ISSN: 0300-5127            Impact factor:   5.407


  10 in total

1.  The RPB2 flap loop of human RNA polymerase II is dispensable for transcription initiation and elongation.

Authors:  Murali Palangat; Jeffrey A Grass; Marie-France Langelier; Benoit Coulombe; Robert Landick
Journal:  Mol Cell Biol       Date:  2011-06-13       Impact factor: 4.272

2.  Wdr82 is a C-terminal domain-binding protein that recruits the Setd1A Histone H3-Lys4 methyltransferase complex to transcription start sites of transcribed human genes.

Authors:  Jeong-Heon Lee; David G Skalnik
Journal:  Mol Cell Biol       Date:  2007-11-12       Impact factor: 4.272

3.  The Ess1 prolyl isomerase is required for transcription termination of small noncoding RNAs via the Nrd1 pathway.

Authors:  Navjot Singh; Zhuo Ma; Trent Gemmill; Xiaoyun Wu; Holland Defiglio; Anne Rossettini; Christina Rabeler; Olivia Beane; Randall H Morse; Michael J Palumbo; Steven D Hanes
Journal:  Mol Cell       Date:  2009-10-23       Impact factor: 17.970

Review 4.  Roles of RNA polymerase IV in gene silencing.

Authors:  Craig S Pikaard; Jeremy R Haag; Thomas Ream; Andrzej T Wierzbicki
Journal:  Trends Plant Sci       Date:  2008-07       Impact factor: 18.313

5.  Identification of cell-specific targets of sumoylation during mouse spermatogenesis.

Authors:  Yuxuan Xiao; Daniel Pollack; Miriam Andrusier; Avi Levy; Myrasol Callaway; Edward Nieves; Prabhakara Reddi; Margarita Vigodner
Journal:  Reproduction       Date:  2016-02       Impact factor: 3.906

6.  Point mutations in the Rpb9-homologous domain of Rpc11 that impair transcription termination by RNA polymerase III.

Authors:  James R Iben; Julie K Mazeika; Sam Hasson; Keshab Rijal; Aneeshkumar G Arimbasseri; Amy N Russo; Richard J Maraia
Journal:  Nucleic Acids Res       Date:  2011-03-30       Impact factor: 16.971

7.  Metal A and metal B sites of nuclear RNA polymerases Pol IV and Pol V are required for siRNA-dependent DNA methylation and gene silencing.

Authors:  Jeremy R Haag; Olga Pontes; Craig S Pikaard
Journal:  PLoS One       Date:  2009-01-01       Impact factor: 3.240

8.  Extragenic accumulation of RNA polymerase II enhances transcription by RNA polymerase III.

Authors:  Imke Listerman; Anita S Bledau; Inna Grishina; Karla M Neugebauer
Journal:  PLoS Genet       Date:  2007-11       Impact factor: 5.917

9.  Recruitment of RNA polymerase III in vivo.

Authors:  Niall S Kenneth; Lynne Marshall; Robert J White
Journal:  Nucleic Acids Res       Date:  2008-05-17       Impact factor: 16.971

10.  Brf1 loss and not overexpression disrupts tissues homeostasis in the intestine, liver and pancreas.

Authors:  Dritan Liko; Louise Mitchell; Kirsteen J Campbell; Rachel A Ridgway; Carolyn Jones; Kate Dudek; Ayala King; Sheila Bryson; David Stevenson; Karen Blyth; Douglas Strathdee; Jennifer P Morton; Thomas G Bird; John R P Knight; Anne E Willis; Owen J Sansom
Journal:  Cell Death Differ       Date:  2019-03-11       Impact factor: 12.067

  10 in total

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