Roberto V P, Tiago D M, Gautvik K, Cancela M L
Centre of Marine Sciences, University of Algarve, Faro, Portugal; PhD Program in Biomedical Sciences, University of Algarve, Faro, Portugal.
Centre of Marine Sciences, University of Algarve, Faro, Portugal.
Gene. 2015 Jul 15;566(1):54-62. doi: 10.1016/j.gene.2015.04.022. Epub 2015 Apr 11.
MicroRNAs (miRNAs) are an abundant and conserved class of small RNAs, which play important regulatory functions by interacting with the 3' untranslated region (UTR) of target mRNAs. Through this mechanism, miR-223 was shown to regulate genes involved in mammalian haematopoiesis, both in physiological and pathological contexts. MiR-223 is essential for normal myelopoiesis in mammals, promoting granulocyte, osteoclast and megakaryocyte differentiation and suppressing erythropoiesis. However, there is a general lack of knowledge regarding miR-223 function in other vertebrates, which could help to clarify its role in other processes, such as development. In this work, we explored the functional conservation of miR-223 using zebrafish as a model. We show that miR-223 gene structure and genomic context have been maintained between human and zebrafish. In addition, we identified 22 novel sequences of miR-223 precursor and demonstrate that it contains domains highly conserved among vertebrates, suggesting function preservation throughout evolution. Furthermore, collected evidences show that miR-223 expression is highly correlated with haematopoietic events and osteoclastogenesis throughout zebrafish development. In adults, expression of miR-223 in zebrafish tissues mimics the distribution in mice, with high levels found in the major fish haematopoietic organ, the head kidney. These results suggest a conservation of miR-223 role in haematopoiesis, and osteoclastogenesis between zebrafish and human. Accordingly, validated targets of miR-223 in mammalian models were investigated and defined as putative targets in zebrafish, by in silico and gene expression analysis. Our data compiles critical evidence showing that miR-223, a highly conserved miRNA, appears to have kept similar regulatory functions throughout evolution.
微小RNA(miRNA)是一类丰富且保守的小RNA,通过与靶mRNA的3'非翻译区(UTR)相互作用发挥重要的调控功能。通过这种机制,已证明miR - 223在生理和病理情况下均能调节参与哺乳动物造血的基因。miR - 223对哺乳动物正常的骨髓生成至关重要,可促进粒细胞、破骨细胞和巨核细胞的分化,并抑制红细胞生成。然而,对于miR - 223在其他脊椎动物中的功能普遍缺乏了解,而这有助于阐明其在其他过程(如发育)中的作用。在这项研究中,我们以斑马鱼为模型探索了miR - 223的功能保守性。我们发现miR - 223的基因结构和基因组背景在人类和斑马鱼之间得以保留。此外,我们鉴定出了22个miR - 223前体的新序列,并证明它包含在脊椎动物中高度保守的结构域,这表明其功能在整个进化过程中得以保留。此外,收集到的证据表明,在斑马鱼的整个发育过程中,miR - 223的表达与造血事件和破骨细胞生成高度相关。在成年斑马鱼中,miR - 223在组织中的表达模式与小鼠相似,在主要的鱼类造血器官——头肾中含量很高。这些结果表明,miR - 223在斑马鱼和人类的造血及破骨细胞生成中的作用具有保守性。因此,通过计算机模拟和基因表达分析,我们研究了miR - 223在哺乳动物模型中的已验证靶标,并将其定义为斑马鱼中的假定靶标。我们的数据汇集了关键证据,表明miR - 223这种高度保守的miRNA在整个进化过程中似乎保持了相似的调控功能。