Coskun Fatma S, Srivastava Shashikant, Raj Prithvi, Dozmorov Igor, Belkaya Serkan, Mehra Smriti, Golden Nadia A, Bucsan Allison N, Chapagain Moti L, Wakeland Edward K, Kaushal Deepak, Gumbo Tawanda, van Oers Nicolai S C
Department of Immunology, University of Texas Southwestern Medical Center, Dallas, TX, United States.
Center for Infectious Diseases Research and Experimental Therapeutics, Baylor Research Institute, Baylor University Medical Center, Dallas, TX, United States.
Front Microbiol. 2020 Jul 28;11:1631. doi: 10.3389/fmicb.2020.01631. eCollection 2020.
Nearly one third of the world's population is infected with (). While much work has focused on the role of different encoded proteins in pathogenesis, recent studies have revealed that also transcribes many noncoding RNAs whose functions remain poorly characterized. We performed RNA sequencing and identified a subset of H37Rv-encoded small RNAs (<30 nts in length) that were produced in infected macrophages. Designated as smaller noncoding RNAs (sncRNAs), three of these predominated the read counts. Each of the three, sncRNA-1, sncRNA-6, and sncRNA-8 had surrounding sequences with predicted stable secondary RNA stem loops. Site-directed mutagenesis of the precursor sequences suggest the existence of a hairpin loop dependent RNA processing mechanism. A functional assessment of sncRNA-1 suggested that it positively regulated two mycobacterial transcripts involved in oleic acid biosynthesis. Complementary loss- and gain- of-function approaches revealed that sncRNA-1 positively supports growth and survival in nutrient-depleted cultures as well as in infected macrophages. Overall, the findings reveal that produces sncRNAs in infected cells, with sncRNA-1 modulating mycobacterial gene expression including genes coupled to oleic acid biogenesis.
世界上近三分之一的人口感染了()。虽然许多研究工作集中在不同编码蛋白在发病机制中的作用,但最近的研究表明,()还转录了许多功能仍未明确的非编码RNA。我们进行了RNA测序,并鉴定出一组由H37Rv编码的小RNA(长度小于30个核苷酸),它们在受感染的巨噬细胞中产生。这些被指定为较小的非编码RNA(sncRNAs),其中三种在读取计数中占主导地位。sncRNA-1、sncRNA-6和sncRNA-8这三种中的每一种都有周围序列,具有预测的稳定二级RNA茎环。前体序列的定点诱变表明存在一种依赖发夹环的RNA加工机制。对sncRNA-1的功能评估表明,它正向调节参与油酸生物合成的两种分枝杆菌转录本。互补的功能丧失和功能获得方法表明,sncRNA-1在营养耗尽的培养物以及受感染的巨噬细胞中正向支持()的生长和存活。总体而言,这些发现揭示了()在受感染细胞中产生sncRNAs,其中sncRNA-1调节分枝杆菌基因表达,包括与油酸生物合成相关的基因。