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14-3-3蛋白:通过分子干扰调控亚细胞定位

14-3-3 proteins: regulation of subcellular localization by molecular interference.

作者信息

Muslin A J, Xing H

机构信息

Center for Cardiovascular Research, Department of Medicine, School of Medicine, Washington University, Box 8086 - Cardiology, 660 South Euclid Avenue, 63110, St. Louis, MO, USA.

出版信息

Cell Signal. 2000 Dec;12(11-12):703-9. doi: 10.1016/s0898-6568(00)00131-5.

Abstract

14-3-3 family of proteins plays a key regulatory role in signal transduction, checkpoint control, apoptotic, and nutrient-sensing pathways. 14-3-3 proteins act by binding to partner proteins, and this binding often leads to the altered subcellular localization of the partner. 14-3-3 proteins promote the cytoplasmic localization of many binding partners, including the pro-apoptotic protein BAD and the cell cycle regulatory phosphatase Cdc25C, but they can also promote the nuclear localization of other partners, such as the catalytic subunit of telomerase (TERT). In some cases, 14-3-3 binding has no effect on the subcellular localization of a partner. 14-3-3 may affect the localization of a protein by interfering with the function of a nearby targeting sequence, such as a nuclear localization sequence (NLS) or a nuclear export sequence (NES), on the binding partner.

摘要

14-3-3蛋白家族在信号转导、关卡控制、细胞凋亡和营养感知途径中发挥关键的调节作用。14-3-3蛋白通过与伙伴蛋白结合来发挥作用,这种结合常常导致伙伴蛋白亚细胞定位的改变。14-3-3蛋白促进许多结合伙伴的细胞质定位,包括促凋亡蛋白BAD和细胞周期调节磷酸酶Cdc25C,但它们也能促进其他伙伴的核定位,如端粒酶催化亚基(TERT)。在某些情况下,14-3-3结合对伙伴蛋白的亚细胞定位没有影响。14-3-3可能通过干扰结合伙伴上附近靶向序列(如核定位序列(NLS)或核输出序列(NES))的功能来影响蛋白质的定位。

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