Gene body methylation facilitates the transcription of CTSG via antisense lncRNA AL136018.1 in dermatomyositic myoideum

Cell Biol Int. 2021 Feb;45(2):456-462. doi: 10.1002/cbin.11508. Epub 2020 Dec 8.

Abstract

Dermatomyositis (DM) is characterized as a chronic autoimmune disorder with multiple organ involvement. Our previous study has revealed that Cathepsin G (CTSG) highly expressed in dermatomyositic in vivo is regulated by DNMT3a through DNA methylation of 5'-C-phosphate-G-3' loci at exons and introns. However, the mechanism of gene body methylation on regulating CTSG transcription remains unknown. In this study, we studied quadriceps femoris tissues of six DM patients, and observed that antisense long noncoding RNA AL136018.1 contiguous to CTSG was highly expressed in skeletal muscle tissues of DM and positively correlated with the transcription level and DNA methylation level in gene body of CTSG in vivo. Moreover, we observed that the longer transcript of AL136018.1 (AL136018.1-201) could bind to third and fourth exons and third intron of CTSG via the 3'-end. Finally, AL136018.1-201 could recruit DNMT3a towards gene body via 5'-terminal for adding DNA methylation and facilitating transcription of CTSG. Taken together, our data uncovered a novel epigenetic mechanism behind the gene body methylation for transcriptional regulation of CTSG in DM.

Keywords: AL136018.1; CTSG; DNMT3a; dermatomyositic myoideum; gene body methylation.

MeSH terms

  • Cathepsin G / metabolism*
  • Cell Line
  • DNA Methylation
  • Dermatomyositis* / genetics
  • Dermatomyositis* / metabolism
  • Epigenesis, Genetic
  • Humans
  • RNA, Long Noncoding / metabolism*

Substances

  • RNA, Long Noncoding
  • CTSG protein, human
  • Cathepsin G