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本文引用的文献

1
Cytosolic carboxypeptidase 5 removes α- and γ-linked glutamates from tubulin.胞质羧肽酶 5 从微管蛋白上切下α-和γ-连接的谷氨酸。
J Biol Chem. 2013 Oct 18;288(42):30445-30453. doi: 10.1074/jbc.M113.497917. Epub 2013 Sep 10.
2
The zebrafish orthologue of the dyslexia candidate gene DYX1C1 is essential for cilia growth and function.阅读障碍候选基因 DYX1C1 的斑马鱼同源基因对于纤毛生长和功能至关重要。
PLoS One. 2013 May 1;8(5):e63123. doi: 10.1371/journal.pone.0063123. Print 2013.
3
Identification of CRM1-dependent Nuclear Export Cargos Using Quantitative Mass Spectrometry.使用定量质谱鉴定 CRM1 依赖性核输出货物。
Mol Cell Proteomics. 2013 Mar;12(3):664-78. doi: 10.1074/mcp.M112.024877. Epub 2012 Dec 13.
4
Functional segregation and emerging role of cilia-related cytosolic carboxypeptidases (CCPs).纤毛相关胞质羧肽酶(CCPs)的功能分离和新作用。
FASEB J. 2013 Feb;27(2):424-31. doi: 10.1096/fj.12-209080. Epub 2012 Oct 19.
5
The novel structure of a cytosolic M14 metallocarboxypeptidase (CCP) from Pseudomonas aeruginosa: a model for mammalian CCPs.铜绿假单胞菌胞质 M14 金属羧肽酶(CCP)的新型结构:哺乳动物 CCP 的模型。
FASEB J. 2012 Sep;26(9):3754-64. doi: 10.1096/fj.12-209601. Epub 2012 May 29.
6
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia.轴丝动力蛋白装配因子 DNAAF3 突变导致原发性纤毛运动障碍。
Nat Genet. 2012 Mar 4;44(4):381-9, S1-2. doi: 10.1038/ng.1106.
7
Cytosolic carboxypeptidase 1 is involved in processing α- and β-tubulin.细胞质羧肽酶 1 参与α-和β-微管蛋白的加工。
J Biol Chem. 2012 Feb 24;287(9):6503-17. doi: 10.1074/jbc.M111.309138. Epub 2011 Dec 14.
8
Loss of zebrafish lgi1b leads to hydrocephalus and sensitization to pentylenetetrazol induced seizure-like behavior.斑马鱼 lgi1b 的缺失会导致脑积水,并对戊四氮诱导的类似癫痫发作的行为敏感。
PLoS One. 2011;6(9):e24596. doi: 10.1371/journal.pone.0024596. Epub 2011 Sep 16.
9
The tubulin deglutamylase CCPP-1 regulates the function and stability of sensory cilia in C. elegans.微管谷氨酰胺酶 CCPP-1 调控秀丽隐杆线虫感觉纤毛的功能和稳定性。
Curr Biol. 2011 Oct 25;21(20):1685-94. doi: 10.1016/j.cub.2011.08.049. Epub 2011 Oct 6.
10
Tumor suppressor RARRES1 interacts with cytoplasmic carboxypeptidase AGBL2 to regulate the α-tubulin tyrosination cycle.抑癌基因 RARRES1 与细胞质羧肽酶 AGBL2 相互作用,调节α-微管蛋白的酪氨酸化循环。
Cancer Res. 2011 Feb 15;71(4):1219-28. doi: 10.1158/0008-5472.CAN-10-2294. Epub 2011 Feb 8.

斑马鱼细胞质羧肽酶 1 和 5 对胚胎发育至关重要。

Zebrafish cytosolic carboxypeptidases 1 and 5 are essential for embryonic development.

机构信息

From the Departments of Molecular Pharmacology and.

Neuroscience, Albert Einstein College of Medicine, Bronx, New York 10461.

出版信息

J Biol Chem. 2013 Oct 18;288(42):30454-30462. doi: 10.1074/jbc.M113.497933. Epub 2013 Sep 10.

DOI:10.1074/jbc.M113.497933
PMID:24022483
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3798509/
Abstract

The cytosolic carboxypeptidases (CCPs) are a subfamily of metalloenzymes within the larger M14 family of carboxypeptidases that have been implicated in the post-translational modification of tubulin. It has been suggested that at least four of the six mammalian CCPs function as tubulin deglutamylases. However, it is not yet clear whether these enzymes play redundant or unique roles within the cell. To address this question, genes encoding CCPs were identified in the zebrafish genome. Analysis by quantitative polymerase chain reaction indicated that CCP1, CCP2, CCP5, and CCP6 mRNAs were detectable between 2 h and 8 days postfertilization with highest levels 5-8 days postfertilization. CCP1, CCP2, and CCP5 mRNAs were predominantly expressed in tissues such as the brain, olfactory placodes, and pronephric ducts. Morpholino oligonucleotide-mediated knockdown of CCP1 and CCP5 mRNA resulted in a common phenotype including ventral body curvature and hydrocephalus. Confocal microscopy of morphant zebrafish revealed olfactory placodes with defective morphology as well as pronephric ducts with increased polyglutamylation. These data suggest that CCP1 and CCP5 play important roles in developmental processes, particularly the development and functioning of cilia. The robust and similar defects upon knockdown suggest that each CCP may have a function in microtubule modification and ciliary function and that other CCPs are not able to compensate for the loss of one.

摘要

细胞质羧肽酶(CCPs)是 M14 家族羧肽酶中较大的金属酶亚家族的一员,与微管蛋白的翻译后修饰有关。有研究表明,哺乳动物的 CCP 中至少有四种是微管蛋白脱谷氨酰胺酶。然而,这些酶在细胞内是否发挥冗余或独特的作用还不清楚。为了解决这个问题,在斑马鱼基因组中鉴定了编码 CCP 的基因。通过定量聚合酶链反应分析表明,CCP1、CCP2、CCP5 和 CCP6 的 mRNA 可在受精后 2 小时至 8 天检测到,受精后 5-8 天达到最高水平。CCP1、CCP2 和 CCP5 的 mRNA 主要在脑组织、嗅基板和前肾管等组织中表达。CCP1 和 CCP5 mRNA 的 形态发生素寡核苷酸介导的敲低导致共同的表型,包括腹侧身体弯曲和脑积水。形态发生素斑马鱼的共聚焦显微镜显示嗅基板形态缺陷以及前肾管多聚谷氨酸化增加。这些数据表明 CCP1 和 CCP5 在发育过程中发挥重要作用,特别是纤毛的发育和功能。敲低后出现的稳健且相似的缺陷表明,每个 CCP 可能在微管蛋白修饰和纤毛功能中发挥作用,而其他 CCP 无法弥补一个 CCP 的缺失。