Abstract

Body axial patterning develops via a rostral-to-caudal sequence and relies on the temporal colinear activation of Hox genes. However, the underlying mechanism of Hox gene temporal colinear activation remains largely elusive. Here, with small-molecule inhibitors and conditional gene knockout mice, we identified Jmjd3, a subunit of TrxG, as an essential regulator of temporal colinear activation of Hox genes with its H3K27me3 demethylase activity. We demonstrated that Jmjd3 not only initiates but also maintains the temporal collinear expression of Hox genes. However, we detected no antagonistic roles between Jmjd3 and Ezh2, a core subunit of PcG repressive complex 2, during the processes of axial skeletal patterning. Our findings provide new insights into the regulation of Hox gene temporal collinear activation for body axial patterning in mice.

Highlights

  • The development of the mammalian body axis is a continuous process via a rostral-to-caudal sequence (Deschamps and Duboule, 2017; Mongera et al, 2019)

  • To test whether Jmjd3 regulates the Hox gene temporal collinear activation with its H3K27me3 demethylase activity, we firstly examined the mRNA level of Hox genes after GSK-J4 treatment at different time points

  • We demonstrated that (1) Jmjd3 regulates axial skeletal patterning and Hox gene temporal collinear activation with its H3K27me3 demethylase activity

Read more

Summary

INTRODUCTION

The development of the mammalian body axis is a continuous process via a rostral-to-caudal sequence (Deschamps and Duboule, 2017; Mongera et al, 2019). The expression of Hox genes in mammals is characterized by spatial collinearity, which means that the sequence of the Hox gene cluster from 3 to 5 on chromosomes corresponds to the expression domain of Hox genes via a rostral-to-caudal sequence on the body axis (Deschamps and van Nes, 2005; Montavon and Soshnikova, 2014; Deschamps and Duboule, 2017). We detected no dynamical interplay between Jmjd and Ezh during the process of axial skeletal patterning in mice

RESULTS
DISCUSSION
DATA AVAILABILITY STATEMENT
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call