An unconventional diacylglycerol kinase that regulates phospholipid synthesis and nuclear membrane growth

被引:141
作者
Han, Gil-Soo [2 ,3 ]
O'Hara, Laura [1 ]
Carman, George M. [2 ,3 ]
Siniossoglou, Symeon [1 ]
机构
[1] Univ Cambridge, Cambridge Inst Med Res, Cambridge CB2 0XY, England
[2] Rutgers State Univ, Dept Food Sci, New Brunswick, NJ 08901 USA
[3] Rutgers State Univ, Rutgers Ctr Lipid Res, New Brunswick, NJ 08901 USA
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1074/jbc.M802903200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Changes in nuclear size and shape during the cell cycle or during development require coordinated nuclear membrane remodeling, but the underlying molecular events are largely unknown. We have shown previously that the activity of the conserved phosphatidate phosphatase Pah1p/Smp2p regulates nuclear structure in yeast by controlling phospholipid synthesis and membrane biogenesis at the nuclear envelope. Two screens for novel regulators of phosphatidate led to the identification of DGK1. We show that Dgk1p is a unique diacylglycerol kinase that uses CTP, instead of ATP, to generate phosphatidate. DGK1 counteracts the activity of PAH1 at the nuclear envelope by controlling phosphatidate levels. Overexpression of DGK1 causes the appearance of phosphatidate-enriched membranes around the nucleus and leads to its expansion, without proliferating the cortical endoplasmic reticulum membrane. Mutations that decrease phosphatidate levels decrease nuclear membrane growth in pah1 Delta cells. We propose that phosphatidate metabolism is a critical factor determining nuclear structure by regulating nuclear membrane biogenesis.
引用
收藏
页码:20433 / 20442
页数:10
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