| Literature DB >> 32250712 |
K Shanmugha Rajan1, Yinzhou Zhu2, Katerina Adler1, Tirza Doniger1, Smadar Cohen-Chalamish1, Ankita Srivastava2, Moran Shalev-Benami3, Donna Matzov3, Ron Unger1, Christian Tschudi4, Arthur Günzl2, Gordon G Carmichael2, Shulamit Michaeli1.
Abstract
The parasite Trypanosoma brucei cycles between insect and mammalian hosts, and is the causative agent of sleeping sickness. Here, we performed genome-wide mapping of 2'-O-methylations (Nms) on trypanosome rRNA using three high-throughput sequencing methods; RibOxi-seq, RiboMeth-seq and 2'-OMe-seq. This is the first study using three genome-wide mapping approaches on rRNA from the same species showing the discrepancy among the methods. RibOxi-seq detects all the sites, but RiboMeth-seq is the only method to evaluate the level of a single Nm site. The sequencing revealed at least ninety-nine Nms guided by eighty-five snoRNAs among these thirty-eight Nms are trypanosome specific sites. We present the sequence and target of the C/D snoRNAs guiding on rRNA. This is the highest number of Nms detected to date on rRNA of a single cell parasite. Based on RiboMeth-seq, several Nm sites were found to be differentially regulated at the two stages of the parasite life cycle, the insect procyclic form (PCF) versus the bloodstream form (BSF) in the mammalian host.Entities:
Keywords: 2ʹ-OMe-seq; RibOxi-seq; RiboMeth-seq; Trypanosomes; rRNA; snoRNA
Year: 2020 PMID: 32250712 PMCID: PMC7549662 DOI: 10.1080/15476286.2020.1750842
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652