Literature DB >> 14614828

LKB1 is the upstream kinase in the AMP-activated protein kinase cascade.

Angela Woods1, Stephen R Johnstone, Kristina Dickerson, Fiona C Leiper, Lee G D Fryer, Dietbert Neumann, Uwe Schlattner, Theo Wallimann, Marian Carlson, David Carling.   

Abstract

Inactivating mutations in the protein kinase LKB1 lead to a dominantly inherited cancer in humans termed Peutz-Jeghers syndrome. The role of LKB1 is unclear, and only one target for LKB1 has been identified in vivo [3]. AMP-activated protein kinase (AMPK) is the downstream component of a protein kinase cascade that plays a pivotal role in energy homeostasis. AMPK may have a role in protecting the body from metabolic diseases including type 2 diabetes, obesity, and cardiac hypertrophy. We previously reported the identification of three protein kinases (Elm1, Pak1, and Tos3 [9]) that lie upstream of Snf1, the yeast homologue of AMPK. LKB1 shares sequence similarity with Elm1, Pak1, and Tos3, and we demonstrated that LKB1 phosphorylates AMPK on the activation loop threonine (Thr172) within the catalytic subunit and activates AMPK in vitro [9]. Here, we have investigated whether LKB1 corresponds to the major AMPKK activity present in cell extracts. AMPKK purified from rat liver corresponds to LKB1, and blocking LKB1 activity in cells abolishes AMPK activation in response to different stimuli. These results identify a link between two protein kinases, previously thought to lie in unrelated, distinct pathways, that are associated with human diseases.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 14614828     DOI: 10.1016/j.cub.2003.10.031

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  627 in total

1.  Protein kinase A contributes to the negative control of Snf1 protein kinase in Saccharomyces cerevisiae.

Authors:  LaKisha Barrett; Marianna Orlova; Marcin Maziarz; Sergei Kuchin
Journal:  Eukaryot Cell       Date:  2011-12-02

2.  The liver kinase B1 is a central regulator of T cell development, activation, and metabolism.

Authors:  Nancie J MacIver; Julianna Blagih; Donte C Saucillo; Luciana Tonelli; Takla Griss; Jeffrey C Rathmell; Russell G Jones
Journal:  J Immunol       Date:  2011-09-19       Impact factor: 5.422

Review 3.  AMP-activated protein kinase: an energy sensor that regulates all aspects of cell function.

Authors:  D Grahame Hardie
Journal:  Genes Dev       Date:  2011-09-15       Impact factor: 11.361

4.  AMP-activated protein kinase (AMPK) activating agents cause dephosphorylation of Akt and glycogen synthase kinase-3.

Authors:  Taj D King; Ling Song; Richard S Jope
Journal:  Biochem Pharmacol       Date:  2006-03-10       Impact factor: 5.858

5.  Pak1 protein kinase regulates activation and nuclear localization of Snf1-Gal83 protein kinase.

Authors:  Kristina Hedbacker; Seung-Pyo Hong; Marian Carlson
Journal:  Mol Cell Biol       Date:  2004-09       Impact factor: 4.272

6.  Genome-wide RNAi Screen for Fat Regulatory Genes in C. elegans Identifies a Proteostasis-AMPK Axis Critical for Starvation Survival.

Authors:  Christopher M Webster; Elizabeth C Pino; Christopher E Carr; Lianfeng Wu; Ben Zhou; Lucydalila Cedillo; Michael C Kacergis; Sean P Curran; Alexander A Soukas
Journal:  Cell Rep       Date:  2017-07-18       Impact factor: 9.423

7.  The AMP-activated protein kinase AAK-2 links energy levels and insulin-like signals to lifespan in C. elegans.

Authors:  Javier Apfeld; Greg O'Connor; Tom McDonagh; Peter S DiStefano; Rory Curtis
Journal:  Genes Dev       Date:  2004-12-01       Impact factor: 11.361

8.  Access denied: Snf1 activation loop phosphorylation is controlled by availability of the phosphorylated threonine 210 to the PP1 phosphatase.

Authors:  Eric M Rubenstein; Rhonda R McCartney; Chao Zhang; Kevan M Shokat; Margaret K Shirra; Karen M Arndt; Martin C Schmidt
Journal:  J Biol Chem       Date:  2007-11-08       Impact factor: 5.157

Review 9.  Metabolism of inflammation limited by AMPK and pseudo-starvation.

Authors:  Luke A J O'Neill; D Grahame Hardie
Journal:  Nature       Date:  2013-01-17       Impact factor: 49.962

10.  Ca2+-Stimulated AMPK-Dependent Phosphorylation of Exo1 Protects Stressed Replication Forks from Aberrant Resection.

Authors:  Shan Li; Zeno Lavagnino; Delphine Lemacon; Lingzhen Kong; Alessandro Ustione; Xuewen Ng; Yuanya Zhang; Yingchun Wang; Bin Zheng; Helen Piwnica-Worms; Alessandro Vindigni; David W Piston; Zhongsheng You
Journal:  Mol Cell       Date:  2019-04-30       Impact factor: 17.970

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.