Literature DB >> 22870855

Biochemical analysis of protein SUMOylation.

Aileen Y Alontaga1, Ekaterina Bobkova, Yuan Chen.   

Abstract

SUMOylation, the covalent attachment of Small Ubiquitin-like MOdifier (SUMO) polypeptides to other proteins, is among the most important post-translational modifications that regulate the functional properties of a large number of proteins. SUMOylation is broadly involved in cellular processes such as gene transcription, hormone response, signal transduction, DNA repair, and nuclear transport. SUMO modification has also been implicated in the pathogenesis of human diseases, such as cancer, neurodegenerative disorders, and viral infection. Attachment of a SUMO protein to another protein is carried out in multiple steps catalyzed by three enzymes. This unit describes and discusses the in vitro biochemical methods used for investigating each step of the SUMOylation process. In addition, a high-throughput screening protocol is included for the identification of inhibitors of SUMOylation.

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Year:  2012        PMID: 22870855      PMCID: PMC3477621          DOI: 10.1002/0471142727.mb1029s99

Source DB:  PubMed          Journal:  Curr Protoc Mol Biol        ISSN: 1934-3647


  38 in total

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Journal:  Trends Biochem Sci       Date:  2001-05       Impact factor: 13.807

2.  RAD6-dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO.

Authors:  Carsten Hoege; Boris Pfander; George-Lucian Moldovan; George Pyrowolakis; Stefan Jentsch
Journal:  Nature       Date:  2002-09-12       Impact factor: 49.962

Review 3.  Protein modification by SUMO.

Authors:  Erica S Johnson
Journal:  Annu Rev Biochem       Date:  2004       Impact factor: 23.643

Review 4.  Huntington's disease is a disorder of the corpus striatum: focus on Rhes (Ras homologue enriched in the striatum).

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Journal:  Neuropharmacology       Date:  2010-10-31       Impact factor: 5.250

5.  Characterization of a second member of the sentrin family of ubiquitin-like proteins.

Authors:  T Kamitani; K Kito; H P Nguyen; T Fukuda-Kamitani; E T Yeh
Journal:  J Biol Chem       Date:  1998-05-01       Impact factor: 5.157

6.  The small ubiquitin-like modifier (SUMO) protein modification system in Arabidopsis. Accumulation of SUMO1 and -2 conjugates is increased by stress.

Authors:  Jasmina Kurepa; Joseph M Walker; Jan Smalle; Mark M Gosink; Seth J Davis; Tessa L Durham; Dong-Yul Sung; Richard D Vierstra
Journal:  J Biol Chem       Date:  2002-12-12       Impact factor: 5.157

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Authors:  A L Haas; I A Rose
Journal:  J Biol Chem       Date:  1982-09-10       Impact factor: 5.157

8.  Identification of a SUMO-binding motif that recognizes SUMO-modified proteins.

Authors:  Jing Song; Linda K Durrin; Thomas A Wilkinson; Theodore G Krontiris; Yuan Chen
Journal:  Proc Natl Acad Sci U S A       Date:  2004-09-23       Impact factor: 11.205

9.  UBL1, a human ubiquitin-like protein associating with human RAD51/RAD52 proteins.

Authors:  Z Shen; P E Pardington-Purtymun; J C Comeaux; R K Moyzis; D J Chen
Journal:  Genomics       Date:  1996-09-01       Impact factor: 5.736

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Journal:  Genomics       Date:  1998-01-01       Impact factor: 5.736

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  4 in total

1.  RNF4-dependent hybrid SUMO-ubiquitin chains are signals for RAP80 and thereby mediate the recruitment of BRCA1 to sites of DNA damage.

Authors:  Catherine M Guzzo; Christopher E Berndsen; Jianmei Zhu; Vibhor Gupta; Ajit Datta; Roger A Greenberg; Cynthia Wolberger; Michael J Matunis
Journal:  Sci Signal       Date:  2012-12-04       Impact factor: 8.192

2.  An electrophoretic mobility shift assay identifies a mechanistically unique inhibitor of protein sumoylation.

Authors:  Yeong Sang Kim; Katelyn Nagy; Samantha Keyser; John S Schneekloth
Journal:  Chem Biol       Date:  2013-04-18

3.  Sumoylation of histone deacetylase 1 regulates MyoD signaling during myogenesis.

Authors:  Hosouk Joung; Sehee Kwon; Kyoung-Hoon Kim; Yun-Gyeong Lee; Sera Shin; Duk-Hwa Kwon; Yeong-Un Lee; Taewon Kook; Nakwon Choe; Jeong Chul Kim; Young-Kook Kim; Gwang Hyeon Eom; Hyun Kook
Journal:  Exp Mol Med       Date:  2018-01-12       Impact factor: 8.718

4.  Sumoylation of RORγt regulates TH17 differentiation and thymocyte development.

Authors:  Zhiheng He; Jing Zhang; Zhaofeng Huang; Qian Du; Ning Li; Qiang Zhang; Yuan Chen; Zuoming Sun
Journal:  Nat Commun       Date:  2018-11-19       Impact factor: 14.919

  4 in total

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