Arora Amit, Guduric-Fuchs Jasenka, Harwood Laura, Dellett Margaret, Cogliati Tiziana, Simpson David A
Centre for Vision and Vascular Science, Queen's University Belfast, Ophthalmic Research Centre, Institute of Clinical Science, Royal Victoria Hospital, Belfast BT12 6BA, UK.
BMC Dev Biol. 2010 Jan 6;10:1. doi: 10.1186/1471-213X-10-1.
MicroRNAs (miRNAs) are small RNA molecules (~22 nucleotides) which have been shown to play an important role both in development and in maintenance of adult tissue. Conditional inactivation of miRNAs in the eye causes loss of visual function and progressive retinal degeneration. In addition to inhibiting translation, miRNAs can mediate degradation of targeted mRNAs. We have previously shown that candidate miRNAs affecting transcript levels in a tissue can be deduced from mRNA microarray expression profiles. The purpose of this study was to predict miRNAs which affect mRNA levels in developing and adult retinal tissue and to confirm their expression.
Microarray expression data from ciliary epithelial retinal stem cells (CE-RSCs), developing and adult mouse retina were generated or downloaded from public repositories. Analysis of gene expression profiles detected the effects of multiple miRNAs in CE-RSCs and retina. The expression of 20 selected miRNAs was confirmed by RT-PCR and the cellular distribution of representative candidates analyzed by in situ hybridization. The expression levels of miRNAs correlated with the significance of their predicted effects upon mRNA expression. Highly expressed miRNAs included miR-124, miR-125a, miR-125b, miR-204 and miR-9. Over-expression of three miRNAs with significant predicted effects upon global mRNA levels resulted in a decrease in mRNA expression of five out of six individual predicted target genes assayed.
This study has detected the effect of miRNAs upon mRNA expression in immature and adult retinal tissue and cells. The validity of these observations is supported by the experimental confirmation of candidate miRNA expression and the regulation of predicted target genes following miRNA over-expression. Identified miRNAs are likely to be important in retinal development and function. Misregulation of these miRNAs might contribute to retinal degeneration and disease. Conversely, manipulation of their expression could potentially be used as a therapeutic tool in the future.
微小RNA(miRNA)是小RNA分子(约22个核苷酸),已证明其在成人组织的发育和维持中均发挥重要作用。眼睛中miRNA的条件性失活会导致视觉功能丧失和进行性视网膜变性。除了抑制翻译外,miRNA还可介导靶向mRNA的降解。我们之前已经表明,可以从mRNA微阵列表达谱中推断出影响组织中转录本水平的候选miRNA。本研究的目的是预测影响发育中和成年视网膜组织中mRNA水平的miRNA,并确认它们的表达。
生成了睫状体上皮视网膜干细胞(CE-RSC)、发育中和成年小鼠视网膜的微阵列表达数据,或从公共数据库下载了这些数据。基因表达谱分析检测到多种miRNA在CE-RSC和视网膜中的作用。通过RT-PCR确认了20种选定miRNA的表达,并通过原位杂交分析了代表性候选miRNA的细胞分布。miRNA的表达水平与其对mRNA表达的预测作用的显著性相关。高表达的miRNA包括miR-124、miR-125a、miR-125b、miR-204和miR-9。对整体mRNA水平有显著预测作用的三种miRNA的过表达导致所检测的六个单独预测靶基因中的五个的mRNA表达下降。
本研究检测到了miRNA对未成熟和成年视网膜组织及细胞中mRNA表达的影响。候选miRNA表达的实验确认以及miRNA过表达后对预测靶基因的调控支持了这些观察结果的有效性。已鉴定的miRNA可能在视网膜发育和功能中起重要作用。这些miRNA的失调可能导致视网膜变性和疾病。相反,操纵它们的表达可能在未来用作治疗工具。