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Characterization of Wolf‐Hirschhorn Syndrome Candidate 1 (Whsc1) in Pitx2‐miR‐23/24‐mediated Tooth Development
Abstract   Open access   Peer reviewed

Characterization of Wolf‐Hirschhorn Syndrome Candidate 1 (Whsc1) in Pitx2‐miR‐23/24‐mediated Tooth Development

Dan Su, Steve Eliason, Fan Shao, Huojun Cao and Brad Amendt
The FASEB journal, Vol.35(S1), p.n/a
05/2021
DOI: 10.1096/fasebj.2021.35.S1.02059
url
https://doi.org/10.1096/fasebj.2021.35.S1.02059View
Published (Version of record) Open Access

Abstract

Objective Wolf‐Hirschhorn syndrome (WHS) is a developmental disorder attributed to a partial deletion on the short arm of chromosome 4. WHS patients suffer from oral manifestations including cleft lip and palate (CLP), hypodontia and taurodontism. However, the causative factors and underlying mechanisms of these oral anomalies are relatively unknown. Wolf‐Hirschhorn syndrome candidate 1 (WHSC1) is a H3K36‐specific methyltransferase that is frequently deleted in WHS. This gene has been associated with craniofacial defects including CLP and defects in occipital ossification. In our study, we aim to understand the role of WHSC1 in tooth development. Methods To characterize the role of Whsc1 in tooth development, we profiled the Whsc1 expression pattern during mouse tooth development by immunofluorescence staining (IF). To investigate the regulatory effects between Whsc1 and Pitx2, we overexpressed either Whsc1 or Pitx2 in oral epithelial cell line LS8 and detected their expression. Then, ChIP‐PCR and luciferase assays were performed to confirm the binding on the promoter regions. To determine the negative regulation of Whsc1 by miR‐23‐3p and miR‐24‐3p, miRs were inhibited by our Plasmid‐based microRNA inhibition system in PMIS‐miR‐23‐27‐24 embryos and LS8 cells followed by detecting the mRNA and protein level of Whsc1. Luciferase assays were also conducted to confirm the direct binding between miRs and Whsc1 3’UTR. Results Whsc1 expresses from early stage of tooth development and restricts to stem cell niches in homeostatic tooth germ. Whsc1 and Pitx2 reciprocally activate each other's expression through chromosomal and transcriptional regulation. miR‐23‐3p and miR‐24‐3p, two miRs that regulated by Pitx2, directly inhibit Whsc1. Conclusion Whsc1 expresses in the developing tooth germ and participates the Whsc1‐Pitx2‐miR23/24 regulatory network in oral epithelium cells. Our observations provide new insights into the potential role of Whsc1 in regulating tooth development and a possible causer of the dental defects in WHS.

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