Literature DB >> 20399133

Proteasomal recognition of ubiquitylated substrates.

Hongyong Fu1, Ya-Ling Lin, A S Fatimababy.   

Abstract

Ubiquitin/26S proteasome-mediated proteolysis controls the half-life of numerous critical regulatory proteins and is an intimate regulatory component for nearly all aspects of cellular processes. In addition to ubiquitin conjugation, an additional level of substrate specificity is regulated at the step of proteasomal recognition of ubiquitylated substrates, which serves as an important mechanistic and regulatory component to connect the substrate from the conjugation machinery to the 26S proteasome. In this review, we discuss current knowledge and future challenges relevant to understanding the mechanism, regulation, functions and substrate specificity of proteasomal recognition mediated by a multitude of ubiquitin receptors. The mechanistic details of major recognition pathways for ubiquitylated substrates are clearly divergent within and across species, which implies functional differentiation.

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Year:  2010        PMID: 20399133     DOI: 10.1016/j.tplants.2010.03.004

Source DB:  PubMed          Journal:  Trends Plant Sci        ISSN: 1360-1385            Impact factor:   18.313


  17 in total

Review 1.  The expanding universe of ubiquitin and ubiquitin-like modifiers.

Authors:  Richard D Vierstra
Journal:  Plant Physiol       Date:  2012-06-12       Impact factor: 8.340

Review 2.  Ubiquitin on the move: the ubiquitin modification system plays diverse roles in the regulation of endoplasmic reticulum- and plasma membrane-localized proteins.

Authors:  Damian D Guerra; Judy Callis
Journal:  Plant Physiol       Date:  2012-06-22       Impact factor: 8.340

3.  Arabidopsis membrane-anchored ubiquitin-fold (MUB) proteins localize a specific subset of ubiquitin-conjugating (E2) enzymes to the plasma membrane.

Authors:  Rebecca T Dowil; Xiaolong Lu; Scott A Saracco; Richard D Vierstra; Brian P Downes
Journal:  J Biol Chem       Date:  2011-02-23       Impact factor: 5.157

4.  The ubiquitination machinery of the ubiquitin system.

Authors:  Judy Callis
Journal:  Arabidopsis Book       Date:  2014-10-06

5.  The defective proteasome but not substrate recognition function is responsible for the null phenotypes of the Arabidopsis proteasome subunit RPN10.

Authors:  Ya-Ling Lin; Shu-Chiun Sung; Hwang-Long Tsai; Ting-Ting Yu; Ramalingam Radjacommare; Raju Usharani; Antony S Fatimababy; Hsia-Yin Lin; Ya-Ying Wang; Hongyong Fu
Journal:  Plant Cell       Date:  2011-07-15       Impact factor: 11.277

6.  Ufmylation and FATylation pathways are downregulated in human alcoholic and nonalcoholic steatohepatitis, and mice fed DDC, where Mallory-Denk bodies (MDBs) form.

Authors:  H Liu; J Li; B Tillman; B A French; S W French
Journal:  Exp Mol Pathol       Date:  2014-06-02       Impact factor: 3.362

7.  In vivo relevance of substrate recognition function of major Arabidopsis ubiquitin receptors.

Authors:  Ya-Ling Lin; Hongyong Fu
Journal:  Plant Signal Behav       Date:  2012-07-01

8.  The RPT2 subunit of the 26S proteasome directs complex assembly, histone dynamics, and gametophyte and sporophyte development in Arabidopsis.

Authors:  Kwang-Hee Lee; Atsushi Minami; Richard S Marshall; Adam J Book; Lisa M Farmer; Joseph M Walker; Richard D Vierstra
Journal:  Plant Cell       Date:  2011-12-09       Impact factor: 12.085

9.  Identification of a functional docking site in the Rpn1 LRR domain for the UBA-UBL domain protein Ddi1.

Authors:  Tara A Gomez; Natalie Kolawa; Marvin Gee; Michael J Sweredoski; Raymond J Deshaies
Journal:  BMC Biol       Date:  2011-05-31       Impact factor: 7.431

10.  Coordinated degradation of replisome components ensures genome stability upon replication stress in the absence of the replication fork protection complex.

Authors:  Laura C Roseaulin; Chiaki Noguchi; Esteban Martinez; Melissa A Ziegler; Takashi Toda; Eishi Noguchi
Journal:  PLoS Genet       Date:  2013-01-17       Impact factor: 5.917

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