Ye K, Hurt K J, Wu F Y, Fang M, Luo H R, Hong J J, Blackshaw S, Ferris C D, Snyder S H
Johns Hopkins University School of Medicine, Department of Neuroscience, North Wolfe Street 21205, Baltimore, MD, USA.
Cell. 2000 Dec 8;103(6):919-30. doi: 10.1016/s0092-8674(00)00195-1.
While cytoplasmic PI3Kinase (PI3K) is well characterized, regulation of nuclear PI3K has been obscure. A novel protein, PIKE (PI3Kinase Enhancer), interacts with nuclear PI3K to stimulate its lipid kinase activity. PIKE encodes a 753 amino acid nuclear GTPase. Dominant-negative PIKE prevents the NGF enhancement of PI3K and upregulation of cyclin D1. NGF treatment also leads to PIKE interactions with 4.1N, which has translocated to the nucleus, fitting with the initial identification of PIKE based on its binding 4.1N in a yeast two-hybrid screen. Overexpression of 4.1N abolishes PIKE effects on PI3K. Activation of nuclear PI3K by PIKE is inhibited by the NGF-stimulated 4.1N translocation to the nucleus. Thus, PIKE physiologically modulates the activation by NGF of nuclear PI3K.
虽然细胞质中的磷脂酰肌醇-3激酶(PI3K)已得到充分表征,但核PI3K的调控机制仍不清楚。一种新的蛋白质,PIKE(PI3激酶增强因子),与核PI3K相互作用以刺激其脂质激酶活性。PIKE编码一种753个氨基酸的核GTP酶。显性负性PIKE可阻止神经生长因子(NGF)对PI3K的增强作用以及细胞周期蛋白D1的上调。NGF处理还导致PIKE与已转运至细胞核的4.1N相互作用,这与基于酵母双杂交筛选中PIKE与4.1N结合而对其进行的初步鉴定相符。4.1N的过表达消除了PIKE对PI3K的影响。NGF刺激的4.1N转运至细胞核会抑制PIKE对核PI3K的激活作用。因此,PIKE在生理上调节NGF对核PI3K的激活作用。