Hall Neil
School of Biological Sciences, Biosciences Building, Crown Street, University of Liverpool, Liverpool L69 7ZB, UK.
J Exp Biol. 2007 May;210(Pt 9):1518-25. doi: 10.1242/jeb.001370.
In the past 10 years, microbiology has undergone a revolution that has been driven by access to cheap high-throughput DNA sequencing. It was not long ago that the cloning and sequencing of a target gene could take months or years, whereas now this entire process has been replaced by a 10 min Internet search of a public genome database. There has been no single innovation that has initiated this rapid technological change; in fact, the core chemistry of DNA sequencing is the same as it was 30 years ago. Instead, progress has been driven by large sequencing centers that have incrementally industrialized the Sanger sequencing method. A side effect of this industrialization is that large-scale sequencing has moved out of small research labs, and the vast majority of sequence data is now generated by large genome centers. Recently, there have been advances in technology that will enable high-throughput genome sequencing to be established in research labs using bench-top instrumentation. These new technologies are already being used to explore the vast microbial diversity in the natural environment and the untapped genetic variation that can occur in bacterial species. It is expected that these powerful new methods will open up new questions to genomic investigation and will also allow high-throughput sequencing to be more than just a discovery exercise but also a routine assay for hypothesis testing. While this review will concentrate on microorganisms, many of the important arguments about the need to measure and understand variation at the species, population and ecosystem level will hold true for many other biological systems.
在过去十年中,微生物学经历了一场革命,这场革命是由廉价的高通量DNA测序技术推动的。不久之前,克隆和测序一个目标基因可能需要数月或数年时间,而现在整个过程已被在公共基因组数据库中进行10分钟的网络搜索所取代。引发这一快速技术变革的并非某一项创新;事实上,DNA测序的核心化学原理与30年前相同。相反,进步是由大型测序中心推动的,这些中心逐步将桑格测序方法工业化。这种工业化的一个副作用是大规模测序已从小型研究实验室转移出来,现在绝大多数序列数据是由大型基因组中心产生的。最近,技术取得了进展,这将使研究实验室能够使用台式仪器开展高通量基因组测序。这些新技术已被用于探索自然环境中丰富的微生物多样性以及细菌物种中未开发的遗传变异。预计这些强大的新方法将为基因组研究带来新问题,也将使高通量测序不仅仅是一项发现工作,还能成为用于假设检验的常规分析方法。虽然本综述将集中讨论微生物,但许多关于在物种、种群和生态系统层面测量和理解变异的必要性的重要观点,对许多其他生物系统同样适用。