Whitehead Institute, Cambridge, USA.
Methods. 2010 May;51(1):87-91. doi: 10.1016/j.ymeth.2009.12.011. Epub 2010 Jan 4.
qPCR tomography was developed to study mRNA localization in complex biological samples that are embedded and cryo-sectioned. After total RNA extraction and reverse transcription, the spatial profiles of mRNAs and other functional RNAs were determined by qPCR. The Xenopus laevis oocyte was selected as model, because of its large size (more than 1mm) and large amount of total RNA (approximately 5microg). Fifteen sections along the animal-vegetal axis were cut and prepared for quantification of 31 RNA targets using the high-throughput real-time RT-PCR (qPCR) BioMark platform. mRNAs were found to have two localization patterns, animal/central or vegetal. Because of the high resolution in sectioning, it was possible to distinguish two subgroups of the vegetal gene patterns: germ plasm determinant pattern and profile of other vegetal genes.
qPCR 断层扫描技术被开发出来,用于研究嵌入和冷冻切片的复杂生物样本中的 mRNA 定位。在提取总 RNA 并进行反转录后,通过 qPCR 确定了 mRNAs 和其他功能 RNA 的空间分布。选择非洲爪蟾卵母细胞作为模型,因为它的体积较大(超过 1 毫米),总 RNA 含量丰富(约 5 微克)。沿着动物-植物轴切取 15 个切片,并使用高通量实时 RT-PCR(qPCR)BioMark 平台对 31 个 RNA 靶标进行定量。发现 mRNAs 具有两种定位模式,即动物/中央或植物。由于切片的高分辨率,有可能区分植物基因模式的两个亚群:生殖质决定子模式和其他植物基因的分布模式。