Department of Medicine, Division of Translational Therapeutics, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA; Cancer Research Institute, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA; Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA.
Department of Biological Sciences, University of Pittsburgh, Pittsburgh, PA 15260, USA.
Methods. 2019 Apr 15;159-160:115-123. doi: 10.1016/j.ymeth.2019.02.017. Epub 2019 Feb 20.
Dramatic increases in the scale of programmed synthesis of nucleic acid libraries coupled with deep sequencing have powered advances in understanding nucleic acid and protein biology. Biological systems centering on nucleic acids or encoded proteins greatly benefit from such high-throughput studies, given that large DNA variant pools can be synthesized and DNA, or RNA products of transcription, can be easily analyzed by deep sequencing. Here we review the scope of various high-throughput functional assays for studies of nucleic acids and proteins in general, followed by discussion of how these types of study have yielded insights into the RNA Polymerase II (Pol II) active site as an example. We discuss methodological considerations in the design and execution of these experiments that should be valuable to studies in any system.
随着核酸文库程序化合成规模的急剧扩大和深度测序技术的发展,人们对核酸和蛋白质生物学的理解也取得了进展。以核酸或编码蛋白为中心的生物系统从这种高通量研究中受益匪浅,因为可以合成大的 DNA 变体池,并且可以通过深度测序轻松分析转录的 DNA 或 RNA 产物。在这里,我们综述了一般用于核酸和蛋白质研究的各种高通量功能测定的范围,然后讨论了这些类型的研究如何为 RNA 聚合酶 II (Pol II) 活性位点的研究提供了新的见解,以此作为示例。我们讨论了在设计和执行这些实验时需要考虑的方法学问题,这些问题对于任何系统的研究都具有重要价值。