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鉴定出鼠 CGI-58 的一种新型剪接异构体。

Identification of a novel splicing isoform of murine CGI-58.

机构信息

Department of Pediatrics, University of Kentucky, Lexington, KY 40536-0509, USA.

出版信息

FEBS Lett. 2010 Mar 5;584(5):903-10. doi: 10.1016/j.febslet.2009.12.058. Epub 2010 Jan 18.


DOI:10.1016/j.febslet.2009.12.058
PMID:20083112
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2846637/
Abstract

The comparative gene identification-58 (CGI-58) gene, mutations of which are linked to Chanarin-Dorfman syndrome, encodes a protein of the alpha/beta hydrolase domain subfamily. We report here a new alternative splicing isoform of the murine CGI-58 gene, termed mCGI-58S. Sequence comparison indicates the lack of second and third exons in this cDNA variant. While the full-length protein displayed perilipin-dependent localization to lipid droplets, mCGI-58S showed a predominant cytoplasmic staining when expressed in cells. mCGI-58S was incapable of activating adipose triglyceride lipase but retained the capacity to acylate lysophosphatidic acid. Overexpression of mCGI-58S failed to promote lipid droplet turnover and loss of intracellular triacylglycerols. These results suggest that this splicing event may be involved in the regulation of lipid homeostasis.

摘要

比较基因鉴定-58(CGI-58)基因的突变与 Chanarin-Dorfman 综合征有关,该基因编码一种属于α/β水解酶结构域亚家族的蛋白质。我们在此报道了一种新的鼠 CGI-58 基因的选择性剪接异构体,称为 mCGI-58S。序列比较表明,该 cDNA 变体缺少第二和第三个外显子。全长蛋白显示出依赖于 perilipin 的脂滴定位,而 mCGI-58S 在细胞中表达时则主要呈现细胞质染色。mCGI-58S 不能激活脂肪甘油三酯脂肪酶,但保留酰化溶血磷脂酸的能力。mCGI-58S 的过表达未能促进脂滴周转和细胞内三酰基甘油的损失。这些结果表明,这种剪接事件可能参与了脂质稳态的调节。

相似文献

[1]
Identification of a novel splicing isoform of murine CGI-58.

FEBS Lett. 2010-1-18

[2]
The N-terminal region of comparative gene identification-58 (CGI-58) is important for lipid droplet binding and activation of adipose triglyceride lipase.

J Biol Chem. 2010-2-17

[3]
Adipose triglyceride lipase-mediated lipolysis of cellular fat stores is activated by CGI-58 and defective in Chanarin-Dorfman Syndrome.

Cell Metab. 2006-5

[4]
Critical roles for α/β hydrolase domain 5 (ABHD5)/comparative gene identification-58 (CGI-58) at the lipid droplet interface and beyond.

Biochim Biophys Acta Mol Cell Biol Lipids. 2017-8-4

[5]
Alternative splicing and developmental and hormonal regulation of porcine comparative gene identification-58 (CGI-58) mRNA.

J Anim Sci. 2012-7-24

[6]
Growth retardation, impaired triacylglycerol catabolism, hepatic steatosis, and lethal skin barrier defect in mice lacking comparative gene identification-58 (CGI-58).

J Biol Chem. 2009-12-18

[7]
CGI-58/ABHD5 is phosphorylated on Ser239 by protein kinase A: control of subcellular localization.

J Lipid Res. 2015-1

[8]
CGI-58 interacts with perilipin and is localized to lipid droplets. Possible involvement of CGI-58 mislocalization in Chanarin-Dorfman syndrome.

J Biol Chem. 2004-7-16

[9]
CGI-58 facilitates lipolysis on lipid droplets but is not involved in the vesiculation of lipid droplets caused by hormonal stimulation.

J Lipid Res. 2007-5

[10]
Comparative gene identification 58/α/β hydrolase domain 5 lacks lysophosphatidic acid acyltransferase activity.

J Lipid Res. 2014-8

引用本文的文献

[1]
Hints on ATGL implications in cancer: beyond bioenergetic clues.

Cell Death Dis. 2018-2-22

[2]
Adipose Triglyceride Lipase Regulation: An Overview.

Curr Protein Pept Sci. 2018

[3]
Comparative gene identification-58 (CGI-58) promotes autophagy as a putative lysophosphatidylglycerol acyltransferase.

J Biol Chem. 2014-11-21

[4]
Differential expressions of G0/G1 switch gene 2 and comparative gene identification-58 are associated with fat content in bovine muscle.

Lipids. 2014-1

[5]
Biochemistry and pathophysiology of intravascular and intracellular lipolysis.

Genes Dev. 2013-3-1

[6]
Distinct roles for alpha-beta hydrolase domain 5 (ABHD5/CGI-58) and adipose triglyceride lipase (ATGL/PNPLA2) in lipid metabolism and signaling.

Adipocyte. 2012

[7]
Recent insights into the structure and function of comparative gene identification-58.

Curr Opin Lipidol. 2011-6

[8]
Lipolysis - a highly regulated multi-enzyme complex mediates the catabolism of cellular fat stores.

Prog Lipid Res. 2010-11-16

本文引用的文献

[1]
Coatomer-dependent protein delivery to lipid droplets.

J Cell Sci. 2009-6-1

[2]
Contribution of adipose triglyceride lipase and hormone-sensitive lipase to lipolysis in hMADS adipocytes.

J Biol Chem. 2009-7-3

[3]
Neutral lipid storage disease: genetic disorders caused by mutations in adipose triglyceride lipase/PNPLA2 or CGI-58/ABHD5.

Am J Physiol Endocrinol Metab. 2009-8

[4]
Chanarin-Dorfman syndrome: deficiency in CGI-58, a lipid droplet-bound coactivator of lipase.

Biochim Biophys Acta. 2009-6

[5]
Adipose triglyceride lipase and the lipolytic catabolism of cellular fat stores.

J Lipid Res. 2009-1

[6]
CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid.

J Biol Chem. 2008-9-5

[7]
The C-terminal region of human adipose triglyceride lipase affects enzyme activity and lipid droplet binding.

J Biol Chem. 2008-6-20

[8]
YLR099C (ICT1) encodes a soluble Acyl-CoA-dependent lysophosphatidic acid acyltransferase responsible for enhanced phospholipid synthesis on organic solvent stress in Saccharomyces cerevisiae.

J Biol Chem. 2008-4-11

[9]
Adipose triglyceride lipase-mediated lipolysis of cellular fat stores is activated by CGI-58 and defective in Chanarin-Dorfman Syndrome.

Cell Metab. 2006-5

[10]
Fat mobilization in adipose tissue is promoted by adipose triglyceride lipase.

Science. 2004-11-19

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