Dataset Information

Accurate detection of m6A RNA modifications in native RNA sequences [Yeast]

ABSTRACT: Accurate detection of m6A RNA modifications in native RNA sequences [Yeast]

PROVIDER: PRJNA521324 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR8544281_1.fastq.gz	Fastqsanger.gz
	SRR8544282_1.fastq.gz	Fastqsanger.gz
	SRR8544283_1.fastq.gz	Fastqsanger.gz
	SRR8544284_1.fastq.gz	Fastqsanger.gz
	SRR8544285_1.fastq.gz	Fastqsanger.gz

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Project description:A broad diversity of modifications decorate RNA molecules. Originally conceived as static components, evidence is accumulating that some RNA modifications may be dynamic, contributing to cellular responses to external signals and environmental circumstances. A major difficulty in studying these modifications, however, is the need of tailored protocols to map each modification type individually. Here, we present a new approach that uses direct RNA nanopore sequencing to identify diverse RNA modification types present in native RNA molecules. First, we show that each RNA modification type results in a distinct and characteristic base-calling ‘error’ signature, which we validate using a battery of genetic strains lacking either pseudouridine (Ѱ) or 2’-O-methylation (Nm) modifications at known sites. We then demonstrate the value of these signatures for de novo transcriptome-wide prediction of Ѱ modifications, confirming known Ѱ-modified sites in rRNAs, snRNAs and mRNAs, as well as uncovering novel Ѱ sites including a previously unreported Pus4-dependent Ѱ modification in yeast mitochondrial rRNA, which we validate using orthogonal methods. To explore the dynamics of pseudouridylation across environmental stresses, we treat the cells with oxidative, cold and heat stresses, finding that yeast ribosomal rRNA modifications do not change upon environmental exposures. By contrast, our method reveals over a dozen novel heat-sensitive Ѱ-modified sites in snRNAs and snoRNAs, in addition to recovering previously reported sites. Finally, we develop a novel software, nanoRMS, which we show can estimate per-site modification stoichiometries from individual RNA molecules by identifying the reads with altered current intensity profiles, and quantify the RNA modification stoichiometry changes between two conditions. Our work demonstrates that Ѱ RNA modifications can be predicted de novo and in a quantitative manner using native RNA nanopore sequencing.

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Accurate detection of m6A RNA modifications in native RNA sequences [Yeast]

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