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Expression of macro non-coding RNAs Meg8 and Irm in mouse embryonic development

  • Tiantian Gu
  • , Hongjuan He
  • , Zhengbin Han
  • , Tiebo Zeng
  • , Zhijun Huang
  • , Qi Liu
  • , Ning Gu
  • , Yan Chen
  • , Kenkichi Sugimoto
  • , Huijie Jiang
  • , Qiong Wu*
  • *Corresponding author for this work
  • Harbin Institute of Technology
  • Niigata University
  • University Health Network
  • Ludong University

Research output: Contribution to journalArticlepeer-review

Abstract

Non-coding RNAs (ncRNAs) . Meg8 and . Irm were previously identified as alternatively splicing isoforms of . Rian gene. Ascertaining ncRNAs spatiotemporal expression patterns is crucial for understanding the physiological roles of ncRNAs during tissue and organ development. In this study in mouse embryos, we focused on the developmental regulation expression of imprinted macro ncRNAs, . Meg8 and . Irm by using . in situ hybridization and quantitative real-time RT-PCR (QRT-PCR). The . in situ hybridization results showed that . Meg8 and . Irm were expressed in the developing brain at embryonic day 10.5 (E10.5) and E11.5, while . Irm expression signals were strikingly detected in the somite, where . Meg8 expression signals were undetectable. By E15.5, they were expressed in brain, tongue, liver, lung and neuroendocrine tissues, while . Irm displayed more restricted expression in tongue and skeletal muscle than . Meg8. Furthermore, quantitative analysis confirmed that they were highly expressed in tongue and brain at E12.5, E15.5 and E18.5. These results indicated that . Meg8 and . Irm might be coordinately expressed and functionally correlated in diverse of organs. Notably, . Irm was more closely associated with morphogenesis of skeletal muscle in contrast to . Meg8 during embryonic development.

Original languageEnglish
Pages (from-to)392-399
Number of pages8
JournalActa Histochemica
Volume114
Issue number4
DOIs
StatePublished - Jul 2012

Keywords

  • In situ hybridization
  • Irm
  • Macro ncRNA
  • Meg8
  • Mouse embryo
  • QRT-PCR

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