Genome-wide identification of altered RNA m(6)A profiles in vascular tissue of septic rats

Sepsis is the leading cause of death in hospital intensive care units. In light of recent studies showing that variations in N-6-methyladenosine (m(6)A) levels in different RNA transcripts influence inflammatory responses, we evaluated the m(6)A profiles of rat aortic mRNAs and lncRNAs after lipopolysaccharide (LPS)-induced sepsis. LC-MS-based mRNA modification analysis showed that global m(6)A levels were significantly decreased in aortic tissue of rats injected intraperitoneally with LPS. This finding was consistent with downregulated expression of METTL3 and WTAP, two members of the m(6)A writer complex, in LPS-exposed aortas. Microarray analysis of m(6)A methylation indicated that 40 transcripts (31 mRNAs and 9 lncRNAs) were hypermethylated, while 223 transcripts (156 mRNAs and 67 lncRNAs) were hypomethylated, in aortic tissue from LPS-treated rats. On GO and KEGG analyses, 'complement and coagulation cascades', 'transient receptor potential channels', and 'organic anion transmembrane transporter activity' were the major biological processes modulated by the differentially m(6)A methylated mRNAs. In turn, competing endogenous RNA network analysis suggested that decreased m(6)A levels in lncRNA-XR_343955 may affect the inflammatory response through the cell adhesion molecule pathway. Our data suggest that therapeutic modulation of the cellular m(6)A machinery may be useful to preserve vascular integrity and function during sepsis.

Automated summary

Sepsis is the leading cause of death in hospital intensive care units. Recent studies have shown that variations in N-6-methyladenosine (m(6)A) levels in RNA transcripts can influence inflammatory responses. Our evaluation of m(6)A profiles in rat aortic mRNAs and lncRNAs after LPS-induced sepsis revealed significant decreases in global m(6)A levels and downregulated expression of key m(6)A writer complex members. Further analysis suggested that differentially m(6)A methylated mRNAs may affect key biological processes and inflammatory responses during sepsis.