p600/UBR4 in the central nervous system

被引:26
作者
Parsons, Kari [1 ,2 ,3 ]
Nakatani, Yoshihiro [4 ]
Minh Dang Nguyen [1 ,2 ,3 ]
机构
[1] Univ Calgary, Dept Clin Neurosci, Hotchkiss Brain Inst, Calgary, AB T2N 4N1, Canada
[2] Univ Calgary, Hotchkiss Brain Inst, Dept Cell Biol & Anat, Calgary, AB T2N 4N1, Canada
[3] Univ Calgary, Dept Biochem & Mol Biol, Hotchkiss Brain Inst, Calgary, AB T2N 4N1, Canada
[4] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02215 USA
基金
加拿大健康研究院;
关键词
p600; UBR4; CNS; Brain; Neurons; Neurological diseases; END RULE PATHWAY; E3 UBIQUITIN LIGASES; SPINDLE ORIENTATION; NEURONAL MIGRATION; E7; ONCOPROTEIN; UBR BOX; RETINOBLASTOMA PROTEIN; CLINICAL-SIGNIFICANCE; APOPTOSIS FACTOR; STRUCTURAL BASIS;
D O I
10.1007/s00018-014-1788-8
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
A decade ago, the large 600 kDa mammalian protein p600 (also known as UBR4) was discovered as a multifunctional protein with roles in anoikis, viral transformation and protein degradation. Recently, p600 has emerged as a critical protein in the mammalian brain with roles in neurogenesis, neuronal migration, neuronal signaling and survival. How p600 integrates these apparently unrelated functions to maintain tissue homeostasis and murine survival remains unclear. The common molecular basis underlying many of the actions of p600 suggests, however, certain conservation and transposition of these functions across systems. In this review, we summarize the central nervous system functions of p600 and propose new perspectives on its biological complexity in neuronal physiology and neurological diseases.
引用
收藏
页码:1149 / 1160
页数:12
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