CRY 和 PER 蛋白的降解
中文名称
通路描述
为了在早晨由 BMAL1:CLOCK 启动的新一轮转录,CRY1、CRY2 和 PER1、PER2、PER3(BMAL:CLOCK 的抑制子)在夜间被 SCF E3 连接酶复合物泛素化,随后被 26S 蛋白酶体降解。BTRC、FBXW11:CUL1:SKP1:RBX1 E3 连接酶复合物在细胞质中泛素化磷酸化的 PER1、PER2 和可能 PER3(Shirogane 等 2005,基于小鼠同源物 Reischl 等 2007、Ohsaki 等 2008 推断),FBXL3:CUL1:SKP1:RBX1 E3 连接酶复合物在细胞核中泛素化 CRY1 和 CRY2(基于小鼠同源物 Busino 等 2007、Hirano 等 2013、Yoo 等 2013 推断),而 FBXL21 通过未表征的机制抑制 FBXL3 在核内的泛素化(基于小鼠同源物 Hirano 等 2013、Yoo 等 2013 推断)。
英文描述
Phagocytosis plays an essential role in host-defense mechanisms through the uptake and destruction of infectious pathogens. Specialized cell types including macrophages, neutrophils, and monocytes take part in this process in higher organisms. After opsonization with antibodies (IgG), foreign extracellular materials are recognized by Fc gamma receptors. Cross-linking of Fc gamma receptors initiates a variety of signals mediated by tyrosine phosphorylation of multiple proteins, which lead through the actin cytoskeleton rearrangements and membrane remodeling to the formation of phagosomes. Nascent phagosomes undergo a process of maturation that involves fusion with lysosomes. The acquisition of lysosomal proteases and release of reactive oxygen species are crucial for digestion of engulfed materials in phagosomes.
所含基因
98 个基因
ACTR2
ACTR3
ACTR3B
ACTR3C
AKT1
AKT2
AKT3
AMPH
ARF6
ARPC1A
ARPC1B
ARPC2
ARPC3
ARPC4
ARPC5
ARPC5L
ASAP1
ASAP2
ASAP3
BIN1
CDC42
CFL1
CFL2
CRK
CRKL
DNM2
DOCK1
FCGR1A
FCGR2A
FCGR2B
FCGR3A
FCGR3B
GAB2
GSN
HCK
INPP5D
INPPL1
JMJD7-PLA2G4B
LAT
LIMK1
LIMK2
LOC102723407
LYN
MAP2K1
MAPK1
MAPK3
MARCKS
MARCKSL1
MYO10
NCF1
P3R3URF-PIK3R3
PAK1
PIK3CA
PIK3CB
PIK3CD
PIK3R1
PIK3R2
PIK3R3
PIP5K1A
PIP5K1B
PIP5K1C
PLA2G4A
PLA2G4B
PLA2G4C
PLA2G4D
PLA2G4E
PLA2G4F
PLA2G6
PLCG1
PLCG2
PLD1
PLD2
PLPP1
PLPP2
PLPP3
PRKCA
PRKCB
PRKCD
PRKCE
PRKCG
PTPRC
RAC1
RAC2
RAF1
RPS6KB1
RPS6KB2
SCIN
SPHK1
SPHK2
SYK
VASP
VAV1
VAV2
VAV3
WAS
WASF1
WASF2
WASF3