Cao Jingsong, Shan Dandan, Revett Tracy, Li Dongmei, Wu Leeying, Liu Wei, Tobin James F, Gimeno Ruth E
Department of Cardiovascular and Metabolic Diseases, Wyeth Research, Cambridge, Massachusetts 02140, USA.
J Biol Chem. 2008 Jul 4;283(27):19049-57. doi: 10.1074/jbc.M800364200. Epub 2008 May 5.
Acyl-CoA-dependent lysophospholipid acyltransferases play an important role in attaining the appropriate molecular species of phospholipids. A number of genes encoding these activities were recently identified. It has become clear that multiple genes can encode one enzymatic activity and that a given gene may encode multiple activities. Here we report the identification of a gene encoding a mammalian acyl-CoA-dependent lysophospholipid acyltransferase with prominent activity toward ethanolamine-containing lysophospholipids, which we termed acyl-CoA:lysophosphatidylethanolamine acyltransferase 2, LPEAT2 (previously annotated as AYTL3 or AGPAT7). LPEAT2 is predominantly expressed in brain, coinciding with an enrichment of phosphatidylethanolamine in this tissue. Ectopic expression of LPEAT2 in mammalian HEK293T cells led to a dramatic increase (up to 9-fold) in LPEAT activity when compared with cells transfected with empty vector or an unrelated acyltransferase. LPEAT2 also exhibited significant acyl-CoA-dependent acyltransferase activity toward 1-O-alkenyl-lysophosphatidylethanolamine, lysophosphatidylglycerol, 1-O-alkyl-lysophosphatidylcholine, lysophosphatidylserine, and lysophosphatidylcholine but lacked appreciable acylating activity toward glycerol 3-phosphate, lysophosphatidic acid, lysophosphatidylinositol, and diacylglycerol, demonstrating multiple but selective functions of LPEAT2 as an enzyme involved in phospholipid remodeling. LPEAT2 recognizes a broad range of medium and long chain fatty acyl-CoA, and its activity was not affected by Ca(2+). When overexpressed in mammalian cells, LPEAT2 is localized to the endoplasmic reticulum. siRNA-mediated knockdown of LPEAT2 in HEK293T cells significantly decreased LPEAT and 1-alkenyl-LPEAT activities but did not affect other lysophospholipid acylating activities. These findings identify LPEAT2 as an important enzyme in the biosynthesis of ethanolamine-containing phospholipids, especially in brain.
酰基辅酶A依赖性溶血磷脂酰基转移酶在获得合适的磷脂分子种类方面发挥着重要作用。最近鉴定出了许多编码这些活性的基因。已经清楚的是,多个基因可以编码一种酶活性,并且给定的基因可能编码多种活性。在此,我们报告鉴定出一个编码哺乳动物酰基辅酶A依赖性溶血磷脂酰基转移酶的基因,该酶对含乙醇胺的溶血磷脂具有显著活性,我们将其命名为酰基辅酶A:溶血磷脂酰乙醇胺酰基转移酶2,即LPEAT2(先前注释为AYTL3或AGPAT7)。LPEAT2主要在大脑中表达,这与该组织中磷脂酰乙醇胺的富集相一致。与用空载体或不相关的酰基转移酶转染的细胞相比,LPEAT2在哺乳动物HEK293T细胞中的异位表达导致LPEAT活性显著增加(高达9倍)。LPEAT2对1-O-烯基-溶血磷脂酰乙醇胺、溶血磷脂酰甘油、1-O-烷基-溶血磷脂酰胆碱、溶血磷脂酰丝氨酸和溶血磷脂酰胆碱也表现出显著的酰基辅酶A依赖性酰基转移酶活性,但对3-磷酸甘油、溶血磷脂酸、溶血磷脂酰肌醇和二酰基甘油缺乏明显的酰化活性,这表明LPEAT2作为参与磷脂重塑的酶具有多种但具有选择性的功能。LPEAT2识别广泛的中链和长链脂肪酰基辅酶A,其活性不受Ca(2+)的影响。当在哺乳动物细胞中过表达时,LPEAT2定位于内质网。在HEK293T细胞中,siRNA介导的LPEAT2敲低显著降低了LPEAT和1-烯基-LPEAT活性,但不影响其他溶血磷脂酰化活性。这些发现确定LPEAT2是含乙醇胺磷脂生物合成中的一种重要酶,尤其是在大脑中。