The mechanism of action of FXR1P-related miR-19b-3p in SH-SY5Y

被引:19
|
作者
Ma, Yun [1 ,2 ]
Tian, Shuai [1 ]
He, Shuya [1 ,2 ]
Chen, Qiong [3 ]
Wang, Zongbao [2 ]
Xiao, Xiao [1 ]
Fu, Liang [1 ]
Lei, Xiaoyong [2 ]
机构
[1] Univ South China, Dept Biochem & Biol, 28 Western Changsheng Rd, Hengyang City 421001, Hunan, Peoples R China
[2] Hunan Prov Cooperat Innovat Ctr Mol Target New Dr, 28 Western Changsheng Rd, Hengyang City 421001, Hunan, Peoples R China
[3] Cent S Univ, Xiangya Hosp, Dept Resp, Dept Geriatr Med, Changsha 410008, Hunan, Peoples R China
基金
中国国家自然科学基金;
关键词
miR-19b; FXR1; RAB18; USP32; Dusp6; FRAGILE-X-SYNDROME; MICRORNA TARGETS; RNA; DIFFERENTIATION; TRANSLATION; PROTEINS; FXR1P;
D O I
10.1016/j.gene.2016.04.037
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The biological effects of microRNAs (miRNAs) in the Fragile X Syndrome (FXS) have been widely studied. Dysregulation of miRNAs plays a critical role in the progression of nervous system diseases and in cell proliferation and differentiation. Our previous study validated that miR-19b-3p was associated with FXR1 (Fragile X related gene I), one of homologous genes of FMR1 (Fragile X mental retardation 1). The purpose of this study was to investigate the relationship of FXR1 and miR-19b-3p, and the crucial role of miR-19b-3p in FXS and to validate whether miR-19b-3p could regulate the growth of SH-SY5Y cells. We determined that miR-19b-3p could regulate the expression of not only USP32, RAB18 and Dttsp6 but also FXR1, and FXR1 could in turn regulate the expression of miR-19b-3p. What's more, the overexpression of miR-19b-3p significantly inhibited the proliferation, contributed the apoptosis and slowed down the cycle of SH-SY5Y cells. Taken together, our results indicate that miR-19b-3p plays a significant role in the molecular pathology of FXS by interacting with FXR1 and influencing the growth of SH-SY5Y cells. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:62 / 68
页数:7
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