Literature DB >> 32434006

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

Brittany Bodnar1, Arianna DeGruttola1, Yuanjun Zhu2, Yuan Lin3, Yonggang Zhang4, Xianming Mo5, Wenhui Hu6.   

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.
Copyright © 2020 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Intellectual disability; NFκB; NIBP; NIBP syndrome; Neurogenesis; TRAPPC9

Mesh:

Substances:

Year:  2020        PMID: 32434006      PMCID: PMC7442628          DOI: 10.1016/j.trsl.2020.05.001

Source DB:  PubMed          Journal:  Transl Res        ISSN: 1878-1810            Impact factor:   7.012


  133 in total

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