Brasch Michael A, Hartley James L, Vidal Marc
Atto Bioscience, Rockville, Maryland 20850, USA.
Genome Res. 2004 Oct;14(10B):2001-9. doi: 10.1101/gr.2769804.
Together with metabolites, proteins and RNAs form complex biological systems through highly intricate networks of physical and functional interactions. Large-scale studies aimed at a molecular understanding of the structure, function, and dynamics of proteins and RNAs in the context of cellular networks require novel approaches and technologies. This Special Issue of Genome Research features strategies for the high-throughput construction and manipulation of complete sets of protein-encoding open reading frames (ORFeome), gene promoters (promoterome), and noncoding RNAs, as predicted from genome and transcriptome sequences. Here we discuss the use of a recombinational cloning system that allows efficiency, adaptability, and compatibility in the generation of ORFeome, promoterome, and other resources.
蛋白质和RNA与代谢物一起,通过高度复杂的物理和功能相互作用网络形成复杂的生物系统。旨在从分子层面理解细胞网络中蛋白质和RNA的结构、功能及动态变化的大规模研究需要新颖的方法和技术。本期《基因组研究》特刊重点介绍了从基因组和转录组序列预测的蛋白质编码开放阅读框(ORFeome)、基因启动子(启动子组)和非编码RNA完整集合的高通量构建及操作策略。在此,我们讨论一种重组克隆系统的应用,该系统在ORFeome、启动子组及其他资源的生成过程中具备高效性、适应性和兼容性。