Bratu Diana P
Department of Molecular Genetics, Public Health Research Institute, Newark, NJ, USA.
Methods Mol Biol. 2006;319:1-14. doi: 10.1007/978-1-59259-993-6_1.
A novel approach for detecting nucleic acid in solution has been adopted for real-time imaging of native mRNAs in living cells. This method utilizes hybridization probes, called "molecular beacons", that generate fluorescent signals only when they are hybridized to a complementary target sequence. Nuclease-resistant molecular beacons are designed to efficiently hybridize to accessible regions within RNAs and then be detected via fluorescence microscopy. The target regions chosen for probe binding are selected using two computer algorithms, mfold and OligoWalk, that predict the secondary structure of RNAs and help narrow down sequence stretches to which the probes should bind with high affinity in vivo. As an example, molecular beacons were designed against regions of oskar mRNA, microinjected into living Drosophila melanogaster oocytes and imaged via confocal microscopy.
一种用于检测溶液中核酸的新方法已被用于对活细胞中的天然信使核糖核酸(mRNA)进行实时成像。该方法利用了被称为“分子信标”的杂交探针,这些探针仅在与互补靶序列杂交时才产生荧光信号。耐核酸酶的分子信标被设计用于有效地与RNA内可及区域杂交,然后通过荧光显微镜进行检测。用于探针结合的靶区域是使用两种计算机算法mfold和OligoWalk选择的,这两种算法可预测RNA的二级结构,并有助于缩小探针在体内应高亲和力结合的序列片段范围。例如,针对oskar mRNA的区域设计了分子信标,将其显微注射到活的黑腹果蝇卵母细胞中,并通过共聚焦显微镜成像。