Effects of downregulating TEAD4 transcripts by RNA interference on early development of bovine embryos

J Reprod Dev. 2017 Apr 21;63(2):135-142. doi: 10.1262/jrd.2016-130. Epub 2016 Dec 11.

Abstract

Transcription factor TEA domain family transcription factor 4 (Tead4) is one of the key factors involved in the differentiation of the trophectoderm (TE) in murine embryos. However, knowledge on the roles of TEAD4 in preimplantation development during bovine embryos is currently limited. This study examined the transcript and protein expression patterns of TEAD4 and attempted to elucidate the functions of TEAD4 during bovine preimplantation development using RNA interference. TEAD4 mRNA was found to be upregulated between the 16-cell and morula stages, and nuclear localization of the TEAD4 protein was detected at the morula stage, as well as in subsequent developmental stages. TEAD4 downregulation did not affect embryonic development until the blastocyst stage, and TEAD4-downregulated embryos were capable of forming the TE under both 5% and 21% O2 conditions. Results of gene expression analysis showed that TEAD4 downregulation did not affect the expression levels of POU class 5 transcription factor 1 (OCT-4), NANOG, caudal-type homeobox 2 (CDX2), GATA binding protein 3 (GATA3), and interferon-tau (IFNT). In conclusion, TEAD4 might be dispensable for development until the blastocyst stage and TE differentiation in bovine embryos.

Keywords: Bovine embryo; Preimplantation development; RNA interference; TEAD4.

MeSH terms

  • Animals
  • Blastocyst / physiology*
  • CDX2 Transcription Factor / genetics
  • CDX2 Transcription Factor / metabolism
  • Cattle
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Down-Regulation*
  • Embryonic Development / physiology*
  • Female
  • GATA3 Transcription Factor / genetics
  • GATA3 Transcription Factor / metabolism
  • Gene Expression
  • Interferon Type I / genetics
  • Interferon Type I / metabolism
  • Muscle Proteins / genetics
  • Muscle Proteins / metabolism*
  • Octamer Transcription Factor-3 / genetics
  • Octamer Transcription Factor-3 / metabolism
  • Pregnancy Proteins / genetics
  • Pregnancy Proteins / metabolism
  • RNA Interference
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • CDX2 Transcription Factor
  • DNA-Binding Proteins
  • GATA3 Transcription Factor
  • Interferon Type I
  • Muscle Proteins
  • Octamer Transcription Factor-3
  • Pregnancy Proteins
  • Transcription Factors
  • interferon tau