Zhu Baoyi, Kang Zhanfang, Zhu Sihua, Zhang Yuying, Lai Xiangmao, Zhou Lilin, Huang Hai, Gao Xiaofeng, Jiang Chonghe, Zeng Jianwen
Department of Urology, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan, China.
Department of Basic Medical Research, The Sixth Affiliated Hospital of Guangzhou Medical University, Qingyuan, China.
Front Cell Dev Biol. 2022 Jan 7;9:772534. doi: 10.3389/fcell.2021.772534. eCollection 2021.
Bladder outlet obstruction (BOO) is a common urologic disease associated with poorly understood molecular mechanisms. This study aimed to investigate the possible involvements of circRNAs (circular RNAs) and circRNA-encoded proteins in BOO development. The rat BOO model was established by the partial bladder outlet obstruction surgery. Differential expression of circRNA and protein profiles were characterized by deep RNA sequencing and iTRAQ quantitative proteomics respectively. Novel proteins encoded by circRNAs were predicted through ORF (open reading frame) selection using the GETORF software and verified by the mass spectrometry in proteomics, combined with the validation of their expressional alterations by quantitative RT-PCR. Totally 3,051 circRNAs were differentially expressed in bladder tissues of rat BOO model with widespread genomic distributions, including 1,414 up-regulated, and 1,637 down-regulated circRNAs. Our following quantitative proteomics revealed significant changes of 85 proteins in rat BOO model, which were enriched in multiple biological processes and signaling pathways such as the PPAR and Wnt pathways. Among them, 21 differentially expressed proteins were predicted to be encoded by circRNAs and showed consistent circRNA and protein levels in rat BOO model. The expression levels of five protein-encoding circRNAs were further validated by quantitative RT-PCR and mass spectrometry. The circRNA and protein profiles were substantially altered in rat BOO model, with great expressional changes of circRNA-encoded novel proteins.
膀胱出口梗阻(BOO)是一种常见的泌尿系统疾病,其分子机制尚不清楚。本研究旨在探讨环状RNA(circRNA)及其编码蛋白在BOO发生发展中的可能作用。通过部分膀胱出口梗阻手术建立大鼠BOO模型。分别采用深度RNA测序和iTRAQ定量蛋白质组学技术对circRNA和蛋白质谱的差异表达进行表征。利用GETORF软件通过开放阅读框(ORF)选择预测circRNA编码的新蛋白,并在蛋白质组学中通过质谱进行验证,同时结合定量RT-PCR对其表达变化进行验证。在大鼠BOO模型的膀胱组织中,共有3051个circRNA差异表达,其基因组分布广泛,其中1414个上调,1637个下调。随后的定量蛋白质组学研究显示,大鼠BOO模型中有85种蛋白质发生了显著变化,这些蛋白质富集于多个生物学过程和信号通路,如PPAR和Wnt通路。其中,有21种差异表达蛋白被预测为由circRNA编码,并且在大鼠BOO模型中circRNA和蛋白质水平一致。通过定量RT-PCR和质谱进一步验证了5种编码蛋白的circRNA的表达水平。大鼠BOO模型中circRNA和蛋白质谱发生了显著改变,circRNA编码的新蛋白表达变化很大。