Hum Mol Genet. 2013 Oct 15;22(R1):R22-6. doi: 10.1093/hmg/ddt377. Epub 2013 Aug 6.
We all start out as a single totipotent cell that is programmed to produce a multicellular organism. How do individual cells make those complex developmental switches? How do single cells within a tissue or organ differ, how do they coordinate their actions or go astray in a disease process? These are long-standing and fundamental questions in biology that are now becoming tractable because of advances in microfluidics, DNA amplification and DNA sequencing. Methods for studying single-cell transcriptomes (or at least the polyadenylated mRNA fraction of it) are by far the furthest ahead and reveal remarkable heterogeneity between morphologically identical cells. The analysis of genomic DNA variation is not far behind. The other 'omics' of single cells pose greater technological obstacles, but they are progressing and promise to yield highly integrated large data sets in the near future.
我们都从一个全能的单细胞开始,这个细胞被编程产生一个多细胞生物。单个细胞如何做出这些复杂的发育转变?组织或器官内的单个细胞如何不同,它们如何协调行动或在疾病过程中出错?这些都是生物学中长期存在的基本问题,现在由于微流控、DNA 扩增和 DNA 测序技术的进步,这些问题开始变得可行。研究单细胞转录组(或至少是其中的聚腺苷酸化 mRNA 部分)的方法目前是最先进的,它揭示了形态相同的细胞之间惊人的异质性。基因组 DNA 变异的分析也紧随其后。单细胞的其他“组学”方法则面临更大的技术障碍,但它们正在取得进展,并有望在不久的将来生成高度集成的大型数据集。