CDC23是细胞分裂周期蛋白23(Cell Division Cycle 23)的简称,属于后期促进复合物/环体(APC/C,Anaphase-Promoting Complex/Cyclosome)的核心亚基之一。APC/C是一个多亚基E3泛素连接酶,负责通过泛素-蛋白酶体系统调控细胞周期关键蛋白的降解,从而控制细胞周期的有序进行,尤其在姐妹染色单体分离和退出有丝分裂中起核心作用。CDC23作为APC/C的支架蛋白,帮助维持复合物的结构稳定性,并参与底物识别与泛素化过程。其表达产物主要定位于细胞核,在有丝分裂期富集于纺锤体和动粒(kinetochore)区域,确保染色体正确分离。若CDC23发生功能丧失性突变(如错义突变或缺失),可能导致APC/C组装或活性异常,引发染色体分离错误、非整倍体(染色体数目异常)和基因组不稳定性,进而促进癌症(如结直肠癌、乳腺癌)或发育缺陷。相反,CDC23过表达可能加速周期蛋白(如Cyclin B、Securin)的降解,导致细胞过早退出有丝分裂,同样破坏基因组完整性。CDC23属于APC/C基因家族,该家族成员(如CDC16、CDC27)均含TPR(Tetratricopeptide Repeat)蛋白互作结构域,通过形成复合物协同调控细胞周期。研究表明,CDC23在多种肿瘤中表达异常,其表达水平与化疗敏感性相关,可能成为癌症治疗的潜在靶点。专业术语解释:泛素-蛋白酶体系统(Ubiquitin-Proteasome System)是细胞内蛋白质选择性降解的主要途径;非整倍体(Aneuploidy)指细胞染色体数目偏离正常倍性;TPR结构域是一种介导蛋白质相互作用的重复序列模体。
The protein encoded by this gene shares strong similarity with Saccharomyces cerevisiae Cdc23, a protein essential for cell cycle progression through the G2/M transition. This protein is a component of anaphase-promoting complex (APC), which is composed of eight protein subunits and highly conserved in eukaryotic cells. APC catalyzes the formation of cyclin B-ubiquitin conjugate that is responsible for the ubiquitin-mediated proteolysis of B-type cyclins. This protein and 3 other members of the APC complex contain the TPR (tetratricopeptide repeat), a protein domain important for protein-protein interaction. [provided by RefSeq, Jul 2008]
由该基因股酿酒酵母Cdc23,用于通过G2 / M过渡细胞周期进程必需的蛋白很强的相似性编码的蛋白质。这种蛋白质是后期促进复合物(APC),这是由八个蛋白质亚基,并在真核细胞中的高度保守的组分。 APC的催化细胞周期蛋白B-泛素缀合物的形成,它负责B型细胞周期蛋白的遍在蛋白介导的蛋白水解。这种蛋白质和APC复合物的3其他成员包含TPR(三十四肽重复),蛋白质结构域对于蛋白质 - 蛋白质相互作用重要。 [由RefSeq的,2008年7月提供]
CDC23基因(以及对应的蛋白质)的细胞分布位置:
CDC23基因的本体(GO)信息:
名称 |
---|
4120 Ubiquitin mediated proteolysis [PATH:hsa04120] |
4110 Cell cycle [PATH:hsa04110] |
4114 Oocyte meiosis [PATH:hsa04114] |
4914 Progesterone-mediated oocyte maturation [PATH:hsa04914] |
5166 HTLV-I infection [PATH:hsa05166] |
名称 |
---|
Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins |
Adaptive Immune System |
Antigen processing: Ubiquitination & Proteasome degradation |
APC-Cdc20 mediated degradation of Nek2A |
APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint |
APC/C-mediated degradation of cell cycle proteins |
APC/C:Cdc20 mediated degradation of Cyclin B |
APC/C:Cdc20 mediated degradation of mitotic proteins |
APC/C:Cdc20 mediated degradation of Securin |
APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 |
Autodegradation of Cdh1 by Cdh1:APC/C |
Cdc20:Phospho-APC/C mediated degradation of Cyclin A |
Cell Cycle |
Cell Cycle Checkpoints |
Cell Cycle, Mitotic |
Cellular responses to stress |
Cellular Senescence |
Class I MHC mediated antigen processing & presentation |
Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase |
Immune System |
Inactivation of APC/C via direct inhibition of the APC/C complex |
Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components |
M Phase |
Mitotic Anaphase |
Mitotic Metaphase and Anaphase |
Mitotic Spindle Checkpoint |
Phosphorylation of the APC/C |
Regulation of APC/C activators between G1/S and early anaphase |
Regulation of mitotic cell cycle |
Senescence-Associated Secretory Phenotype (SASP) |
Separation of Sister Chromatids |
疾病名称 | 关系值 | NofPmids | NofSnps | 来源 |
Colonic Neoplasms | 0.00272435 | 1 | 0 | LHGDN |
Thyroid carcinoma | 0.000271442 | 1 | 0 | BeFree |
Papillary thyroid carcinoma | 0.000271442 | 1 | 0 | BeFree |
Myeloid Leukemia | 0.000271442 | 1 | 0 | BeFree |
Malignant neoplasm of thyroid | 0.000271442 | 1 | 0 | BeFree |
leukemia | 0.000271442 | 1 | 0 | BeFree |
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