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小鼠磷脂酶D1的克隆与表达分析

Cloning and expression analysis of murine phospholipase D1.

作者信息

Colley W C, Altshuller Y M, Sue-Ling C K, Copeland N G, Gilbert D J, Jenkins N A, Branch K D, Tsirka S E, Bollag R J, Bollag W B, Frohman M A

机构信息

Department of Pharmacological Sciences, Program in Genetics, State University of New York, Stony Brook, NY 11794-8651, USA.

出版信息

Biochem J. 1997 Sep 15;326 ( Pt 3)(Pt 3):745-53. doi: 10.1042/bj3260745.

Abstract

Activation of phosphatidylcholine-specific phospholipase D(PLD) occurs as part of the complex signal-transduction cascade initiated by agonist stimulation of tyrosine kinase and G-protein-coupled receptors. A variety of mammalian PLD activities have been described, and cDNAs for two PLDs recently reported (human PLD1 and murine PLD2). We describe here the cloning and chromosomal localization of murine PLD1. Northern-blot hybridization and RNase protection analyses were used to examine the expression of murine PLD1 and PLD2 ina variety of cell lines and tissues. PLD1 and PLD2 were expressed in all RNA samples examined, although the absolute expression of each isoform varied, as well as the ratio of PLD1 to PLD2. Moreover, in situ hybridization of adult brain and murine embryo sections revealed high levels of expression of individual PLDs in some cell types and no detectable expression in others. Thus the two PLDs probably carry out distinct roles in restricted subsets of cells rather than ubiquitous roles in all cells.

摘要

磷脂酰胆碱特异性磷脂酶D(PLD)的激活是由激动剂刺激酪氨酸激酶和G蛋白偶联受体引发的复杂信号转导级联反应的一部分。已经描述了多种哺乳动物PLD活性,并且最近报道了两种PLD的cDNA(人PLD1和鼠PLD2)。我们在此描述鼠PLD1的克隆和染色体定位。采用Northern印迹杂交和核糖核酸酶保护分析来检测鼠PLD1和PLD2在多种细胞系和组织中的表达。在所检测的所有RNA样品中均表达了PLD1和PLD2,尽管每种同工型的绝对表达量有所不同,PLD1与PLD2的比例也有所不同。此外,成年脑和鼠胚胎切片的原位杂交显示,某些细胞类型中个别PLD的表达水平很高,而在其他细胞类型中则未检测到表达。因此,这两种PLD可能在有限的细胞亚群中发挥不同的作用,而不是在所有细胞中发挥普遍作用。

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Trends Cell Biol. 1996 Dec;6(12):473. doi: 10.1016/0962-8924(96)84944-0.
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