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Transl Res. 2020 Oct;224:55-70. doi: 10.1016/j.trsl.2020.05.001. Epub 2020 May 17.
2
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NIK‑ and IKKβ‑binding protein contributes to gastric cancer chemoresistance by promoting epithelial‑mesenchymal transition through the NF‑κB signaling pathway.NIK 和 IKKβ 结合蛋白通过 NF-κB 信号通路促进上皮-间充质转化从而促进胃癌的化疗耐药性。
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NIBP, a novel NIK and IKK(beta)-binding protein that enhances NF-(kappa)B activation.NIBP,一种新型的与NIK和IKK(β)结合的蛋白质,可增强核因子-κB的激活。
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Defective neurite elongation and branching in Nibp/Trappc9 deficient zebrafish and mice.Nibp/Trappc9 缺陷斑马鱼和小鼠中的神经突伸长和分支缺陷。
Int J Biol Sci. 2023 Jun 19;19(10):3226-3248. doi: 10.7150/ijbs.78489. eCollection 2023.
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本文引用的文献

1
Enteric Nervous System: lessons from neurogenesis for reverse engineering and disease modelling and treatment.肠神经系统:神经发生对逆向工程和疾病建模与治疗的启示。
Curr Opin Pharmacol. 2020 Feb;50:100-106. doi: 10.1016/j.coph.2020.02.001. Epub 2020 Mar 30.
2
Profound intellectual disability caused by homozygous TRAPPC9 pathogenic variant in a man from Malta.马耳他人纯合 TRAPPC9 致病性变异导致的严重智力障碍。
Mol Genet Genomic Med. 2020 May;8(5):e1211. doi: 10.1002/mgg3.1211. Epub 2020 Mar 11.
3
Contribution of Intellectual Disability-Related Genes to ADHD Risk and to Locomotor Activity in .智力障碍相关基因对 ADHD 风险和. 运动活性的贡献
Am J Psychiatry. 2020 Jun 1;177(6):526-536. doi: 10.1176/appi.ajp.2019.18050599. Epub 2020 Feb 12.
4
Deficiencies in vesicular transport mediated by TRAPPC4 are associated with severe syndromic intellectual disability.囊泡运输中 TRAPPC4 的缺乏与严重的综合征智力残疾有关。
Brain. 2020 Jan 1;143(1):112-130. doi: 10.1093/brain/awz374.
5
[Diagnosis of a case with mental retardation due to novel compound heterozygous variants of TRAPPC9 gene].[一例因TRAPPC9基因新型复合杂合变异导致智力发育迟缓病例的诊断]
Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2019 Nov 10;36(11):1115-1119. doi: 10.3760/cma.j.issn.1003-9406.2019.11.015.
6
Prevalence and Trends of Developmental Disabilities among Children in the United States: 2009-2017.美国儿童发育障碍的患病率和趋势:2009-2017 年。
Pediatrics. 2019 Oct;144(4). doi: 10.1542/peds.2019-0811.
7
Human knockout cerebral organoids: A model system for testing AAV9-mediated gene therapy for reducing GM1 ganglioside storage in GM1 gangliosidosis.人类基因敲除脑类器官:一种用于测试AAV9介导的基因疗法以减少GM1神经节苷脂病中GM1神经节苷脂蓄积的模型系统。
Mol Genet Metab Rep. 2019 Sep 11;21:100513. doi: 10.1016/j.ymgmr.2019.100513. eCollection 2019 Dec.
8
The TRAPP complex mediates secretion arrest induced by stress granule assembly.TRAPP 复合物介导应激颗粒组装诱导的分泌阻滞。
EMBO J. 2019 Oct 1;38(19):e101704. doi: 10.15252/embj.2019101704. Epub 2019 Aug 20.
9
Ypt/Rab GTPases and their TRAPP GEFs at the Golgi.高尔基体内的 Ypt/Rab GTPases 及其 TRAPP GEFs
FEBS Lett. 2019 Sep;593(17):2488-2500. doi: 10.1002/1873-3468.13574. Epub 2019 Aug 21.
10
Plug-and-Play Protein Modification Using Homology-Independent Universal Genome Engineering.利用同源无关的通用基因组工程实现即插即用的蛋白质修饰。
Neuron. 2019 Aug 21;103(4):583-597.e8. doi: 10.1016/j.neuron.2019.05.047. Epub 2019 Jul 1.

NIK/IKK2 结合蛋白(NIBP)/运输蛋白颗粒复合物 9(TRAPPC9)在神经系统疾病中的新兴作用。

Emerging role of NIK/IKK2-binding protein (NIBP)/trafficking protein particle complex 9 (TRAPPC9) in nervous system diseases.

机构信息

Center for Metabolic Disease Research, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania; MD/PhD and Biomedical Sciences Graduate Program, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania.

Center for Metabolic Disease Research, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania; Department of Pathology and Laboratory Medicine, Temple University Lewis Katz School of Medicine, Philadelphia, Pennsylvania; Department of Molecular and Cellular Pharmacology, Peking University School of Pharmaceutical Sciences, Beijing, China.

出版信息

Transl Res. 2020 Oct;224:55-70. doi: 10.1016/j.trsl.2020.05.001. Epub 2020 May 17.

DOI:10.1016/j.trsl.2020.05.001
PMID:32434006
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7442628/
Abstract

NFκB signaling and protein trafficking network play important roles in various biological and pathological processes. NIK-and-IKK2-binding protein (NIBP), also known as trafficking protein particle complex 9 (TRAPPC9), is a prototype member of a novel protein family, and has been shown to regulate both NFκB signaling pathway and protein transport/trafficking. NIBP is extensively expressed in the nervous system and plays an important role in regulating neurogenesis and neuronal differentiation. NIBP/TRAPPC9 mutations have been linked to an autosomal recessive intellectual disability syndrome, called NIBP Syndrome, which is characterized by nonsyndromic autosomal recessive intellectual disability along with other symptoms such as obesity, microcephaly, and facial dysmorphia. As more cases of NIBP Syndrome are identified, new light is being shed on the role of NIBP/TRAPPC9 in the central nervous system developments and diseases. NIBP is also involved in the enteric nervous system. This review will highlight the importance of NIBP/TRAPPC9 in central and enteric nervous system diseases, and the established possible mechanisms for developing a potential therapeutic.

摘要

NFκB 信号转导和蛋白质运输网络在各种生物学和病理学过程中发挥着重要作用。NIK 和 IKK2 结合蛋白(NIBP),也称为运输蛋白颗粒复合物 9(TRAPPC9),是一个新型蛋白质家族的原型成员,已被证明可调节 NFκB 信号通路和蛋白质运输/运输。NIBP 在神经系统中广泛表达,在调节神经发生和神经元分化方面发挥着重要作用。NIBP/TRAPPC9 突变与常染色体隐性智力障碍综合征有关,称为 NIBP 综合征,其特征为常染色体隐性智力障碍,同时还伴有肥胖、小头畸形和面部畸形等其他症状。随着越来越多的 NIBP 综合征病例被发现,NIBP/TRAPPC9 在中枢神经系统发育和疾病中的作用也逐渐明朗。NIBP 还参与肠神经系统。本综述将重点介绍 NIBP/TRAPPC9 在中枢和肠神经系统疾病中的重要性,以及为开发潜在治疗方法而建立的可能机制。