Literature DB >> 16987664

Posttranslational modifications of NEMO and its partners in NF-kappaB signaling.

Hélène Sebban1, Shoji Yamaoka, Gilles Courtois.   

Abstract

NEMO, the regulatory subunit of the IkappaB kinase (IKK) complex that controls the activation of the transcription factor NF-kappaB, is required for IKK function in most situations, but its exact mode of action has remained elusive until recently. A series of publications now provides information about how posttranscriptional modifications of NEMO, such as ubiquitination, sumoylation or phosphorylation, regulate its function in the IKK complex. These modifications might also regulate a cytosolic pool of free NEMO that controls the activation of NF-kappaB induced by genotoxic stress. Together with a better identification of the modifications controlling partners of NEMO, a clearer picture of how IKK becomes activated upon cell stimulation is starting to emerge, providing new clues for how the NF-kappaB pathway could be modulated for therapeutic purposes.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16987664     DOI: 10.1016/j.tcb.2006.09.004

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  31 in total

1.  The LCR at the IKBKG locus is prone to recombine.

Authors:  Francesca Fusco; Michele D'Urso; Maria Giuseppina Miano; Matilde Valeria Ursini
Journal:  Am J Hum Genet       Date:  2010-04-09       Impact factor: 11.025

2.  De-ubiquitylation is the most critical step in the ubiquitin-mediated homeostatic control of the NF-kappaB/IKK basal activity.

Authors:  Linda Palma; Rita Crinelli; Marzia Bianchi; Mauro Magnani
Journal:  Mol Cell Biochem       Date:  2009-05-07       Impact factor: 3.396

3.  NF-kappaB signaling in the aging process.

Authors:  Antero Salminen; Kai Kaarniranta
Journal:  J Clin Immunol       Date:  2009-05-01       Impact factor: 8.317

Review 4.  MicroRNA: master controllers of intracellular signaling pathways.

Authors:  Pak-Yin Lui; Dong-Yan Jin; Nigel J Stevenson
Journal:  Cell Mol Life Sci       Date:  2015-06-10       Impact factor: 9.261

5.  Some findings of FADD knockdown in inhibition of HIV-1 replication in Jurkat cells and PBMCs.

Authors:  Xue Wang; Jiying Tan; Jiangqin Zhao; Viswannath Ragupathy; Mohan Haleyurgirisetty; Indira Hewlett
Journal:  Mol Cell Biochem       Date:  2014-04-22       Impact factor: 3.396

6.  A bacterial E3 ubiquitin ligase IpaH9.8 targets NEMO/IKKgamma to dampen the host NF-kappaB-mediated inflammatory response.

Authors:  Hiroshi Ashida; Minsoo Kim; Marc Schmidt-Supprian; Averil Ma; Michinaga Ogawa; Chihiro Sasakawa
Journal:  Nat Cell Biol       Date:  2009-12-13       Impact factor: 28.824

7.  TRE17/USP6 oncogene translocated in aneurysmal bone cyst induces matrix metalloproteinase production via activation of NF-kappaB.

Authors:  Y Ye; L M Pringle; A W Lau; D N Riquelme; H Wang; T Jiang; D Lev; A Welman; G A Blobel; A M Oliveira; M M Chou
Journal:  Oncogene       Date:  2010-04-26       Impact factor: 9.867

8.  Intermolecular disulfide bond formation in the NEMO dimer requires Cys54 and Cys347.

Authors:  Melanie Herscovitch; William Comb; Thomas Ennis; Kate Coleman; Sheila Yong; Brinda Armstead; Demetrios Kalaitzidis; Sushil Chandani; Thomas D Gilmore
Journal:  Biochem Biophys Res Commun       Date:  2007-12-28       Impact factor: 3.575

9.  NEMO/IKKgamma regulates an early NF-kappaB-independent cell-death checkpoint during TNF signaling.

Authors:  D Legarda-Addison; H Hase; M A O'Donnell; A T Ting
Journal:  Cell Death Differ       Date:  2009-04-17       Impact factor: 15.828

10.  Expanding the substantial interactome of NEMO using protein microarrays.

Authors:  Beau J Fenner; Michael Scannell; Jochen H M Prehn
Journal:  PLoS One       Date:  2010-01-20       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.