Fortini Mark E
National Cancer Institute, Molecular Genetics Section, Building 560, Room 22-12, Fort Detrick, Frederick, MD 21702, USA.
Cell. 2004 Mar 5;116(5):631-2. doi: 10.1016/s0092-8674(04)00207-7.
The large number of kinases that phosphorylate the microtubule binding protein tau has posed a challenge to understanding their individual roles in turning this protein into a killer of neurons. A study in this issue of Cell (Nishimura et al., 2004) uses an elegant fusion of loss-of-function genetics and transgenic overexpression to make the case that the PAR-1 kinase stands at the head of a temporally ordered series of tau phosphorylations.
大量能够使微管结合蛋白tau发生磷酸化的激酶给理解它们在将这种蛋白转变为神经元杀手的过程中各自所起的作用带来了挑战。本期《细胞》杂志上发表的一项研究(西村等人,2004年)巧妙地融合了功能缺失遗传学和转基因过表达技术,以证明PAR-1激酶处于一系列按时间顺序发生的tau磷酸化事件之首。