Smad4 Feedback Enhances BMPR1B Transcription in Ovine Granulosa Cells

Int J Mol Sci. 2019 Jun 4;20(11):2732. doi: 10.3390/ijms20112732.

Abstract

BMPR1B is a type 1B receptor of the canonical bone morphogenetic protein (BMP)/Sma- and mad-related protein (Smad) signaling pathway and is well known as the first major gene associated with sheep prolificacy. However, little is known about the transcriptional regulation of the ovine BMPR1B gene. In this study, we identified the ovine BMPR1B gene promoter and demonstrated that its transcription was regulated by Smad4. In sheep ovarian follicles, three transcriptional variants of BMPR1B gene with distinct transcription start sites were identified using 5' RACE assay while variants II and III were more strongly expressed. Luciferase assay showed that the region -405 to -200 nt is the PII promoter region of variant II. Interestingly, two putative Smad4-binding elements (SBEs) were detected in this region. Luciferase and ChIP assay revealed that Smad4 enhances PII promoter activity of the ovine BMPR1B gene by directly interacting with SBE1 motif. Furthermore, in the ovine granulosa cells, Smad4 regulated BMPRIB expression, and BMPRIB-mediated granulosa cells apoptosis. Overall, our findings not only characterized the 5' regulatory region of the ovine BMPR1B gene, but also uncovered a feedback regulatory mechanism of the canonical BMP/Smad signaling pathway and provided an insight into the transcriptional regulation of BMPR1B gene and sheep prolificacy.

Keywords: BMPR1B; Smad4; granulosa cell apoptosis; sheep; transcription factor.

MeSH terms

  • 5' Untranslated Regions
  • Animals
  • Apoptosis / genetics
  • Base Sequence
  • Bone Morphogenetic Protein Receptors, Type I / genetics*
  • Feedback, Physiological
  • Female
  • Gene Expression Regulation
  • Granulosa Cells / metabolism*
  • Promoter Regions, Genetic
  • RNA Interference
  • RNA, Small Interfering / genetics
  • Sheep
  • Smad4 Protein / metabolism*
  • Transcription Initiation Site
  • Transcription, Genetic*
  • Transcriptional Activation

Substances

  • 5' Untranslated Regions
  • RNA, Small Interfering
  • Smad4 Protein
  • Bone Morphogenetic Protein Receptors, Type I