Comprehensive analysis of m6A methylomes in idiopathic pulmonary arterial hypertension

Epigenetics. 2023 Dec;18(1):2242225. doi: 10.1080/15592294.2023.2242225.

Abstract

Idiopathic pulmonary arterial hypertension (IPAH) is a serious and fatal disease. Recently, m6A has been reported to play an important role in the lungs of IPAH patients and experimental pulmonary hypertension models. However, the meaning of m6A mRNAs in the peripheral blood of IPAH patients remains largely unexplored. We aimed to construct a transcriptome-wide map of m6A mRNAs in the peripheral blood of IPAH patients. M6A RNA Methylation Quantification Kit was utilized to measure the total m6A levels in the peripheral blood of IPAH patients. A combination of MeRIP-seq, RNA-seq and bioinformatics analysis was utilized to select m6A-modified hub genes of IPAH. MeRIP-qPCR and RT-qPCR were used to measure the m6A levels and mRNA levels of TP53, RPS27A, SMAD3 and FoxO3 in IPAH patients. Western blot was performed to assess the protein levels of m6A related regulators and m6A related genes in experimental PH animal models, hypoxia-treated and PDGF-BB induced PASMCs. We found that the total m6A levels were increased in peripheral blood of IPAH patients and verified that m6A levels of RPS27A and SMAD3 were significantly elevated and m6A levels of TP53 and FoxO3 were significantly reduced. The mRNA or protein levels of RPS27A, SMAD3, TP53 and FoxO3 were changed in human blood samples, experimental PH animal models and PDGF-BB induced PASMCs. Moreover, METTL3 and YTHDF1 were increased in the hypoxia induced pulmonary hypertension rat model, hypoxia-treated and PDGF-BB induced PASMCs. These finding suggested that m6A may play an important role in IPAH.

Keywords: FoxO3; METTL3; N6-methyladenosine; RPS27A; SMAD3; TP53; YTHDF1; idiopathic pulmonary arterial hypertension.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Becaplermin / genetics
  • Becaplermin / metabolism
  • Cell Proliferation
  • DNA Methylation
  • Epigenome
  • Familial Primary Pulmonary Hypertension / genetics
  • Familial Primary Pulmonary Hypertension / metabolism
  • Humans
  • Hypertension, Pulmonary* / genetics
  • Hypertension, Pulmonary* / metabolism
  • Methyltransferases / genetics
  • Methyltransferases / metabolism
  • Myocytes, Smooth Muscle / metabolism
  • Pulmonary Artery / metabolism
  • RNA, Messenger / metabolism
  • Rats

Substances

  • Becaplermin
  • RNA, Messenger
  • METTL3 protein, human
  • Methyltransferases

Grants and funding

This study was funded by the National Natural Science Foundation of China (81500041), Hunan Provincial Health Commission Project (20200483) and Hunan Clinical Research Center for Children’s Cardiovascular Diseases (2021SK4019).