The role of CPEB family proteins in the nervous system function in the norm and pathology

被引:27
作者
Kozlov, Eugene [1 ]
Shidlovskii, Yulii V. [1 ,2 ]
Gilmutdinov, Rudolf [1 ]
Schedl, Paul [1 ,3 ]
Zhukova, Mariya [1 ]
机构
[1] Russian Acad Sci, Lab Gene Express Regulat Dev, Inst Gene Biol, Moscow 119334, Russia
[2] Sechenov Univ, Sechenov First Moscow State Med Univ, Dept Biol & Gen Genet, Moscow 119992, Russia
[3] Princeton Univ, Dept Mol Biol, Princeton, NJ 08544 USA
基金
俄罗斯科学基金会;
关键词
CPEB; Translation; Prion; Neurogenesis; Long-term memory;
D O I
10.1186/s13578-021-00577-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Posttranscriptional gene regulation includes mRNA transport, localization, translation, and regulation of mRNA stability. CPEB (cytoplasmic polyadenylation element binding) family proteins bind to specific sites within the 3 ' -untranslated region and mediate poly- and deadenylation of transcripts, activating or repressing protein synthesis. As part of ribonucleoprotein complexes, the CPEB proteins participate in mRNA transport and localization to different sub-cellular compartments. The CPEB proteins are evolutionarily conserved and have similar functions in vertebrates and invertebrates. In the nervous system, the CPEB proteins are involved in cell division, neural development, learning, and memory. Here we consider the functional features of these proteins in the nervous system of phylogenetically distant organisms: Drosophila, a well-studied model, and mammals. Disruption of the CPEB proteins functioning is associated with various pathologies, such as autism spectrum disorder and brain cancer. At the same time, CPEB gene regulation can provide for a recovery of the brain function in patients with fragile X syndrome and Huntington's disease, making the CPEB genes promising targets for gene therapy.
引用
收藏
页数:14
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