GFI1 functions to repress neuronal gene expression in the developing inner ear hair cells

Development. 2020 Sep 11;147(17):dev186015. doi: 10.1242/dev.186015.

Abstract

Despite the known importance of the transcription factors ATOH1, POU4F3 and GFI1 in hair cell development and regeneration, their downstream transcriptional cascades in the inner ear remain largely unknown. Here, we have used Gfi1cre;RiboTag mice to evaluate changes to the hair cell translatome in the absence of GFI1. We identify a systematic downregulation of hair cell differentiation genes, concomitant with robust upregulation of neuronal genes in the GFI1-deficient hair cells. This includes increased expression of neuronal-associated transcription factors (e.g. Pou4f1) as well as transcription factors that serve dual roles in hair cell and neuronal development (e.g. Neurod1, Atoh1 and Insm1). We further show that the upregulated genes are consistent with the NEUROD1 regulon and are normally expressed in hair cells prior to GFI1 onset. Additionally, minimal overlap of differentially expressed genes in auditory and vestibular hair cells suggests that GFI1 serves different roles in these systems. From these data, we propose a dual mechanism for GFI1 in promoting hair cell development, consisting of repression of neuronal-associated genes as well as activation of hair cell-specific genes required for normal functional maturation.

Keywords: GFI1; Hair cells; Inner ear.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Basic Helix-Loop-Helix Transcription Factors / metabolism
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation*
  • Hair Cells, Auditory, Inner / cytology
  • Hair Cells, Auditory, Inner / metabolism*
  • Mice
  • Mice, Transgenic
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Transcription Factor Brn-3A / genetics
  • Transcription Factor Brn-3A / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*

Substances

  • Atoh1 protein, mouse
  • Basic Helix-Loop-Helix Transcription Factors
  • DNA-Binding Proteins
  • Gfi1 protein, mouse
  • Insm1 protein, mouse
  • Neurod1 protein, mouse
  • Pou4f1 protein, mouse
  • Repressor Proteins
  • Transcription Factor Brn-3A
  • Transcription Factors