Developmental expression of three prmt genes in Xenopus

Zool Res. 2019 Mar 18;40(2):102-107. doi: 10.24272/j.issn.2095-8137.2018.064. Epub 2018 Aug 20.

Abstract

Protein arginine methyltransferases (PRMTs) are involved in many cellular processes via the arginine methylation of histone or non-histone proteins. We examined the expression patterns of prmt4, prmt7, and prmt9 during embryogenesis in Xenopus using whole-mount in situ hybridization and quantitative reverse transcription polymerase chain reaction (RT-PCR). Xenopus prmt4 and prmt7 were expressed in the neural crest, brain, and spinal cord, and also detected in the eye, branchial arches, and heart at the tailbud stage. Specific prmt9 signals were not detected in Xenopus embryos until the late tailbud stage when weak expression was observed in the branchial arches. Quantitative RT-PCR indicated that the expressions of prmt4 and prmt7 were up-regulated during the neurula stage, whereas prmt9 maintained its low expression until the late tailbud stage, consistent with the whole-mount in situ hybridization results. Thus, the developmental expression patterns of these three prmt genes in Xenopus embryos provide a basis for further functional study of such genes.

Keywords: Arginine methylation; Gene expression pattern; Xenopus; prmt.

Publication types

  • Letter

MeSH terms

  • Animals
  • Embryo, Nonmammalian / metabolism*
  • Gene Expression Regulation, Developmental / physiology*
  • Gene Expression Regulation, Enzymologic / physiology
  • Protein-Arginine N-Methyltransferases / genetics
  • Protein-Arginine N-Methyltransferases / metabolism*
  • Xenopus / embryology*
  • Xenopus / metabolism*

Substances

  • Protein-Arginine N-Methyltransferases

Grants and funding

This work was supported by grants from the Research Grants Council of Hong Kong CUHK14167017, CUHK24100414 to H.Z., and the Shenzhen Innovation Committee of Science and Technology grants (JCYJ20150331101823691) and Guangdong Provincial Key Laboratory of Cell Microenvironment and Disease Research (2017B030301018) to Y.D.