Department of Pediatrics, University of Kentucky, Lexington, KY 40536-0509, USA.
FEBS Lett. 2010 Mar 5;584(5):903-10. doi: 10.1016/j.febslet.2009.12.058. Epub 2010 Jan 18.
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.
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。
FEBS Lett. 2010-1-18
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