Beijing Advanced Innovation Center for Genomics, Biodynamic Optical Imaging Center, School of Life Sciences and Peking-Tsinghua Center for Life Sciences, College of Engineering, Peking University, Beijing, China.
School of Life Sciences and Tsinghua-Peking Center for Life Sciences, Tsinghua University, Beijing, China.
Biophys J. 2018 Jul 17;115(2):173-180. doi: 10.1016/j.bpj.2018.06.008. Epub 2018 Jun 26.
Single-cell transcriptome analysis through next-generation sequencing (single-cell RNA-seq) has been used broadly to address important biological questions. It has proved to be very powerful, and many exciting new biological discoveries have been achieved in the last decade. Its application has greatly improved our understanding of diverse biological processes and the underlying molecular mechanisms, an understanding that would not have been achievable by conventional analysis based on bulk populations. However, so far, single-cell RNA-seq analysis has been used mostly for higher organisms. For microorganisms, single-cell RNA-seq has not been widely used, mainly because the stiff cell wall prevents effective lysis, much less starting RNA material is obtained, and the RNA lacks polyadenylated tails for universal priming of mRNA molecules. In general, the detection efficiency of current single-cell RNA-seq technologies is very low, and further development or improvement of these technologies is required for exploring the microbial world at single-cell resolution. Here, we briefly review recent developments in single-cell RNA-seq of microorganisms and discuss current challenges and future directions.
通过下一代测序进行单细胞转录组分析(单细胞 RNA-seq)已被广泛用于解决重要的生物学问题。它已被证明非常强大,在过去十年中已经取得了许多令人兴奋的新生物学发现。它的应用极大地提高了我们对各种生物过程和潜在分子机制的理解,而这种理解是基于传统的基于群体的分析所无法实现的。然而,到目前为止,单细胞 RNA-seq 分析主要用于高等生物。对于微生物来说,单细胞 RNA-seq 尚未得到广泛应用,主要是因为刚性细胞壁阻止了有效的裂解,获得的起始 RNA 材料更少,并且 RNA 缺乏多聚腺苷酸化的尾巴,无法普遍启动 mRNA 分子。通常,当前单细胞 RNA-seq 技术的检测效率非常低,因此需要进一步开发或改进这些技术,以实现单细胞分辨率的微生物世界探索。在这里,我们简要回顾了微生物单细胞 RNA-seq 的最新进展,并讨论了当前的挑战和未来的方向。