Literature DB >> 27346717

Distinct 1-monoacylglycerol and 2-monoacylglycerol kinase activities of diacylglycerol kinase isozymes.

Yuriko Sato1, Chiaki Murakami1, Atsumi Yamaki1, Satoru Mizuno1, Hiromichi Sakai1, Fumio Sakane2.   

Abstract

Diacylglycerol kinase (DGK) consists of ten isozymes and is involved in a wide variety of patho-physiological events. However, the enzymological properties of DGKs have not been fully understood. In this study, we performed a comprehensive analysis on the 1-monoacylglycerol kinase (MGK) and 2-MGK activities of ten DGK isozymes. We revealed that type I (α, β and γ), type II (δ, η and κ) and type III (ε) DGKs have 7.9-19.2% 2-MGK activity compared to their DGK activities, whereas their 1-MGK activities were <3.0%. Both the 1-MGK and 2-MGK activities of the type IV DGKs (ζ and ι) were <1% relative to their DGK activities. Intriguingly, type V DGKθ has approximately 6% 1-MGK activity and <2% 2-MGK activity compared to its DGK activity. Purified DGKθ exhibited the same results, indicating that its 1-MGK activity is intrinsic. Therefore, DGK isozymes are categorized into three types with respect to their 1-MGK and 2-MGK activities: those having (1) 2-MGK activity relatively stronger than their 1-MGK activity (types I-III), (2) only negligible 1-MGK and 2-MGK activities (type IV), and (3) 1-MGK activity stronger than its 2-MGK activity (type V). The 1-MGK activity of DGKθ and the 2-MGK activity of DGKα were stronger than those of the acylglycerol kinase reported as 1-MGK and 2-MGK to date. The presence or absence of 1-MGK and 2-MGK activities may be essential to the patho-physiological functions of each DGK isozyme.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Diacylglycerol kinase; Lysophosphatidic acid; Monoacylglycerol kinase; Phosphatidic acid

Mesh:

Substances:

Year:  2016        PMID: 27346717     DOI: 10.1016/j.bbapap.2016.06.012

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  7 in total

1.  Diacylglycerol kinase δ and sphingomyelin synthase-related protein functionally interact via their sterile α motif domains.

Authors:  Chiaki Murakami; Fumi Hoshino; Hiromichi Sakai; Yasuhiro Hayashi; Atsushi Yamashita; Fumio Sakane
Journal:  J Biol Chem       Date:  2020-01-24       Impact factor: 5.157

Review 2.  Regulation of tumor cell - Microenvironment interaction by the autotaxin-lysophosphatidic acid receptor axis.

Authors:  Gabor J Tigyi; Junming Yue; Derek D Norman; Erzsebet Szabo; Andrea Balogh; Louisa Balazs; Guannan Zhao; Sue Chin Lee
Journal:  Adv Biol Regul       Date:  2018-09-16

3.  Membrane curvature allosterically regulates the phosphatidylinositol cycle, controlling its rate and acyl-chain composition of its lipid intermediates.

Authors:  José Carlos Bozelli; William Jennings; Stephanie Black; Yu Heng Hou; Darius Lameire; Preet Chatha; Tomohiro Kimura; Bob Berno; Adree Khondker; Maikel C Rheinstädter; Richard M Epand
Journal:  J Biol Chem       Date:  2018-09-20       Impact factor: 5.486

Review 4.  Diacylglycerol Kinase-ε: Properties and Biological Roles.

Authors:  Richard M Epand; Vincent So; William Jennings; Bijendra Khadka; Radhey S Gupta; Mathieu Lemaire
Journal:  Front Cell Dev Biol       Date:  2016-10-18

5.  Phylogenetic analysis of the diacylglycerol kinase family of proteins and identification of multiple highly-specific conserved inserts and deletions within the catalytic domain that are distinctive characteristics of different classes of DGK homologs.

Authors:  Radhey S Gupta; Richard M Epand
Journal:  PLoS One       Date:  2017-08-22       Impact factor: 3.240

Review 6.  Targeting Lysophosphatidic Acid in Cancer: The Issues in Moving from Bench to Bedside.

Authors:  Yan Xu
Journal:  Cancers (Basel)       Date:  2019-10-10       Impact factor: 6.639

7.  Expression, Purification, and Characterization of Human Diacylglycerol Kinase ζ.

Authors:  Takumi Saito; Daisuke Takahashi; Fumio Sakane
Journal:  ACS Omega       Date:  2019-03-19
  7 in total

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