Literature DB >> 9647778

Alpha 4 associates with protein phosphatases 2A, 4, and 6.

J Chen1, R T Peterson, S L Schreiber.   

Abstract

Protein phosphatases participate in the regulation of a variety of cellular processes. Control of their enzymatic activity and specificity is made possible largely by an array of regulatory subunits. Novel serine/threonine phosphatases--PP4 and PP6 in human cells--have been discovered recently, for which regulatory subunits are yet to be identified. We report here the identification of a potential regulatory subunit of these phosphatases. Using the yeast two-hybrid system, we have found that alpha 4, a previously identified phosphoprotein, associates constitutively with the catalytic subunits of PP4, PP6, and both isoforms of PP2A. These interactions have been confirmed by direct binding and do not require phosphorylation of alpha 4, although it is unclear whether alpha 4 phosphorylation has any effect on its association with the phosphatases. The binding activity appears to reside in the N-terminal 50 amino acids of the phosphatases, consistent with a previous observation that the first 55 residues of PPV, a Drosophila homolog of PP6, may harbor the element for regulation. alpha 4 shares 37% sequence homology with Tap42, an S. cerevisiae protein that has been reported to associate with PP2A and Sit4 (yeast homolog of PP6) and comprises a regulatory component in the rapamycin-sensitive Tor signalling pathway. By analogy, alpha 4 and its associated phosphatases may participate in the mammalian rapamycin-sensitive pathway mediated by FRAP.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9647778     DOI: 10.1006/bbrc.1998.8792

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  59 in total

Review 1.  The target of rapamycin (TOR) proteins.

Authors:  B Raught; A C Gingras; N Sonenberg
Journal:  Proc Natl Acad Sci U S A       Date:  2001-06-19       Impact factor: 11.205

Review 2.  The role of serine/threonine protein phosphatases in exocytosis.

Authors:  Alistair T R Sim; Monique L Baldwin; John A P Rostas; Jeff Holst; Russell I Ludowyke
Journal:  Biochem J       Date:  2003-08-01       Impact factor: 3.857

3.  Specific interactions of PP2A and PP2A-like phosphatases with the yeast PTPA homologues, Ypa1 and Ypa2.

Authors:  Christine Van Hoof; Ellen Martens; Sari Longin; Jan Jordens; Ilse Stevens; Veerle Janssens; Jozef Goris
Journal:  Biochem J       Date:  2005-02-15       Impact factor: 3.857

4.  Quantitative proteomics reveals novel protein interaction partners of PP2A catalytic subunit in pancreatic β-cells.

Authors:  Xiangmin Zhang; Divyasri Damacharla; Danjun Ma; Yue Qi; Rebecca Tagett; Sorin Draghici; Anjaneyulu Kowluru; Zhengping Yi
Journal:  Mol Cell Endocrinol       Date:  2016-01-09       Impact factor: 4.102

Review 5.  Protein phosphatases in pancreatic islets.

Authors:  Henrik Ortsäter; Nina Grankvist; Richard E Honkanen; Åke Sjöholm
Journal:  J Endocrinol       Date:  2014-03-28       Impact factor: 4.286

6.  PP2A regulates the pro-apoptotic activity of FOXO1.

Authors:  Ling Yan; Viviana A Lavin; Leta R Moser; Qinghua Cui; Cindy Kanies; Elizabeth Yang
Journal:  J Biol Chem       Date:  2008-01-21       Impact factor: 5.157

7.  Quantitative proteomic analyses of mammary organoids reveals distinct signatures after exposure to environmental chemicals.

Authors:  Katherine E Williams; George A Lemieux; Maria E Hassis; Adam B Olshen; Susan J Fisher; Zena Werb
Journal:  Proc Natl Acad Sci U S A       Date:  2016-02-22       Impact factor: 11.205

8.  Functional analysis of the PP2A subfamily of protein phosphatases in regulating Drosophila S6 kinase.

Authors:  Vincent A Bielinski; Marc C Mumby
Journal:  Exp Cell Res       Date:  2007-05-16       Impact factor: 3.905

9.  Interaction with Tap42 is required for the essential function of Sit4 and type 2A phosphatases.

Authors:  Huamin Wang; Xiaodong Wang; Yu Jiang
Journal:  Mol Biol Cell       Date:  2003-07-25       Impact factor: 4.138

10.  De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism.

Authors:  Linshan Shang; Lindsay B Henderson; Megan T Cho; Donald S Petrey; Chin-To Fong; Katrina M Haude; Natasha Shur; Julie Lundberg; Natalie Hauser; Jason Carmichael; Jeffrey Innis; Jane Schuette; Yvonne W Wu; Shailesh Asaikar; Margaret Pearson; Leandra Folk; Kyle Retterer; Kristin G Monaghan; Wendy K Chung
Journal:  Neurogenetics       Date:  2015-11-17       Impact factor: 2.660

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.