Tsou Jen-Hui, Yang Ying-Chen, Pao Ping-Chieh, Lin Hui-Ching, Huang Nai-Kuei, Lin Shih-Ting, Hsu Kuei-Sen, Yeh Che-Ming, Lee Kuen-Haur, Kuo Chu-Jen, Yang De-Ming, Lin Jiann-Her, Chang Wen-Chang, Lee Yi-Chao
Graduate Institute of Medical Sciences, College of Medicine, Taipei Medical University, Taipei, Taiwan.
Department of Biotechnology and Animal Science, College of Bioresources, National Ilan University, Ilan, Taiwan.
Mol Neurobiol. 2017 Apr;54(3):2286-2300. doi: 10.1007/s12035-016-9812-7. Epub 2016 Mar 7.
Rnf112 is a member of the RING finger protein family. The expression of Rnf112 is abundant in the brain and is regulated during brain development. Our previous study has revealed that Rnf112 can promote neuronal differentiation by inhibiting the progression of the cell cycle in cell models. In this study, we further revealed the important functions of Rnf112 in embryo development and in adult brain. Our data showed that most of the Rnf112 embryos exhibited blood vascular defects and died in utero. Upon further investigation, we found that the survival rate of homozygous Rnf112 knockout mice in 129/sv and C57BL/6 mixed genetic background was increased. The survived newborns of Rnf112 mice manifested growth retardation as indicated by smaller size and a reduced weight. Although the overall organization of the brain did not appear to be severely affected in Rnf112 mice, using in vivo 3D MRI imaging, we found that when compared to wild-type littermates, brains of Rnf112 mice were smaller. In addition, Rnf112 mice displayed impairment of brain functions including motor balance, and spatial learning and memory. Our results provide important aspects for the study of Rnf112 gene functions.
Rnf112是环状结构域蛋白家族的成员之一。Rnf112在大脑中表达丰富,并在大脑发育过程中受到调控。我们之前的研究表明,在细胞模型中,Rnf112可通过抑制细胞周期进程来促进神经元分化。在本研究中,我们进一步揭示了Rnf112在胚胎发育和成年大脑中的重要功能。我们的数据显示,大多数Rnf112基因敲除胚胎表现出血管缺陷,并在子宫内死亡。进一步研究发现,在129/sv和C57BL/6混合遗传背景下,纯合Rnf112基因敲除小鼠的存活率有所提高。存活下来的Rnf112基因敲除小鼠新生幼崽表现出生长迟缓,如体型较小和体重减轻。尽管Rnf112基因敲除小鼠大脑的整体结构似乎未受到严重影响,但通过体内三维磁共振成像(3D MRI),我们发现与野生型同窝小鼠相比,Rnf112基因敲除小鼠的大脑较小。此外,Rnf112基因敲除小鼠表现出脑功能受损,包括运动平衡以及空间学习和记忆能力。我们的研究结果为Rnf112基因功能的研究提供了重要依据。