Department of Bioengineering, University of Pennsylvania, Skirkanich Hall, Philadelphia, Pennsylvania, United States of America.
Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States of America.
PLoS Genet. 2019 Jan 9;15(1):e1007874. doi: 10.1371/journal.pgen.1007874. eCollection 2019 Jan.
Extensive cell-to-cell variation exists even among putatively identical cells, and there is great interest in understanding how the properties of transcription relate to this heterogeneity. Differential expression from the two gene copies in diploid cells could potentially contribute, yet our ability to measure from which gene copy individual RNAs originated remains limited, particularly in the context of tissues. Here, we demonstrate quantitative, single molecule allele-specific RNA FISH adapted for use on tissue sections, allowing us to determine the chromosome of origin of individual RNA molecules in formaldehyde-fixed tissues. We used this method to visualize the allele-specific expression of Xist and multiple autosomal genes in mouse kidney. By combining these data with mathematical modeling, we evaluated models for allele-specific heterogeneity, in particular demonstrating that apparent expression from only one of the alleles in single cells can arise as a consequence of low-level mRNA abundance and transcriptional bursting.
即使是在假定相同的细胞之间,也存在广泛的细胞间变异性,人们非常感兴趣的是了解转录的特性如何与这种异质性相关。二倍体细胞中两个基因拷贝的差异表达可能会有所贡献,但我们从哪个基因拷贝中测量单个 RNA 的起源的能力仍然有限,特别是在组织的背景下。在这里,我们展示了适用于组织切片的定量、单分子等位基因特异性 RNA FISH,这使我们能够确定单个 RNA 分子在甲醛固定组织中的染色体来源。我们使用这种方法可视化了 Xist 和多个常染色体基因在小鼠肾脏中的等位基因特异性表达。通过将这些数据与数学模型相结合,我们评估了等位基因特异性异质性的模型,特别是证明了单个细胞中只有一个等位基因的明显表达可能是由于低水平的 mRNA 丰度和转录爆发而产生的。