Literature DB >> 17962019

The mammalian N-end rule pathway: new insights into its components and physiological roles.

Takafumi Tasaki1, Yong Tae Kwon.   

Abstract

The N-end rule pathway is a ubiquitin-dependent proteolytic system, in which destabilizing N-terminal residues of short-lived proteins function as an essential determinant of an N-terminal degradation signal (N-degron). An N-degron can be created from a pre-N-degron through specific N-terminal modifications, providing a means conditionally to destabilize otherwise stable polypeptides. The pathway has been found in all organisms examined, from prokaryotes to eukaryotes. Recent biochemical and proteomic studies identified many components of the mammalian N-end rule pathway, including a family of substrate recognition ubiquitin ligases and their substrates. The genetic dissection in animals and humans revealed its essential role in various vital physiological processes, ranging from cardiovascular development and meiosis to the pathogenesis of human genetic diseases. These discoveries have provided new insights into the components, functions and mechanics of this unique proteolytic system.

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Year:  2007        PMID: 17962019     DOI: 10.1016/j.tibs.2007.08.010

Source DB:  PubMed          Journal:  Trends Biochem Sci        ISSN: 0968-0004            Impact factor:   13.807


  86 in total

1.  A novel degradation signal derived from distal C-terminal frameshift mutations of KCNQ2 protein which cause neonatal epilepsy.

Authors:  Jun Su; Xu Cao; KeWei Wang
Journal:  J Biol Chem       Date:  2011-09-21       Impact factor: 5.157

Review 2.  The N-end rule pathway: emerging functions and molecular principles of substrate recognition.

Authors:  Shashikanth M Sriram; Bo Yeon Kim; Yong Tae Kwon
Journal:  Nat Rev Mol Cell Biol       Date:  2011-10-21       Impact factor: 94.444

3.  The N-end rule pathway counteracts cell death by destroying proapoptotic protein fragments.

Authors:  Konstantin I Piatkov; Christopher S Brower; Alexander Varshavsky
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-05       Impact factor: 11.205

4.  Working on a chain: E3s ganging up for ubiquitylation.

Authors:  Meredith B Metzger; Allan M Weissman
Journal:  Nat Cell Biol       Date:  2010-12       Impact factor: 28.824

Review 5.  E3 ubiquitin ligases in ErbB receptor quantity control.

Authors:  Kermit L Carraway
Journal:  Semin Cell Dev Biol       Date:  2010-09-22       Impact factor: 7.727

6.  The molecular principles of N-end rule recognition.

Authors:  Shashikanth M Sriram; Yong Tae Kwon
Journal:  Nat Struct Mol Biol       Date:  2010-10       Impact factor: 15.369

7.  Negative ion fragmentation of cysteic acid containing peptides: cysteic acid as a fixed negative charge.

Authors:  Brad J Williams; Christopher K Barlow; Kevin L Kmiec; William K Russell; David H Russell
Journal:  J Am Soc Mass Spectrom       Date:  2011-05-24       Impact factor: 3.109

Review 8.  Presenilin: RIP and beyond.

Authors:  Matthew R Hass; Chihiro Sato; Raphael Kopan; Guojun Zhao
Journal:  Semin Cell Dev Biol       Date:  2008-11-27       Impact factor: 7.727

9.  Substrate-binding sites of UBR1, the ubiquitin ligase of the N-end rule pathway.

Authors:  Zanxian Xia; Ailsa Webster; Fangyong Du; Konstantin Piatkov; Michel Ghislain; Alexander Varshavsky
Journal:  J Biol Chem       Date:  2008-06-19       Impact factor: 5.157

10.  Redox-sensitive sulfenic acid modification regulates surface expression of the cardiovascular voltage-gated potassium channel Kv1.5.

Authors:  Laurie K Svoboda; Khalilah G Reddie; Lian Zhang; Eileen D Vesely; Elizabeth S Williams; Sarah M Schumacher; Ryan P O'Connell; Robin Shaw; Sharlene M Day; Justus M Anumonwo; Kate S Carroll; Jeffrey R Martens
Journal:  Circ Res       Date:  2012-07-27       Impact factor: 17.367

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