» Articles » PMID: 12736215

Multiple Levels of Transcriptional and Post-transcriptional Regulation Are Required to Define the Domain of Hoxb4 Expression

Overview
Journal Development
Specialty Biology
Date 2003 May 9
PMID 12736215
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Hox genes are key determinants of anteroposterior patterning of animal embryos, and spatially restricted expression of these genes is crucial to this function. In this study, we demonstrate that expression of Hoxb4 in the paraxial mesoderm of the mouse embryo is transcriptionally regulated in several distinct phases, and that multiple regulatory elements interact to maintain the complete expression domain throughout embryonic development. An enhancer located within the intron of the gene (region C) is sufficient for appropriate temporal activation of expression and the establishment of the correct anterior boundary in the paraxial mesoderm (somite 6/7). However, the Hoxb4 promoter is required to maintain this expression beyond 8.5 dpc. In addition, sequences within the 3' untranslated region (region B) are necessary specifically to maintain expression in somite 7 from 9.0 dpc onwards. Neither the promoter nor region B can direct somitic expression independently, indicating that the interaction of regulatory elements is crucial for the maintenance of the paraxial mesoderm domain of Hoxb4 expression. We further report that the domain of Hoxb4 expression is restricted by regulating transcript stability in the paraxial mesoderm and by selective translation and/or degradation of protein in the neural tube. Moreover, the absence of Hoxb4 3'-untranslated sequences from transgene transcripts leads to inappropriate expression of some Hoxb4 transgenes in posterior somites, indicating that there are sequences within region B that are important for both transcriptional and post-transcriptional regulation.

Citing Articles

Shared retinoic acid responsive enhancers coordinately regulate nascent transcription of Hoxb coding and non-coding RNAs in the developing mouse neural tube.

Afzal Z, Lange J, Nolte C, McKinney S, Wood C, Paulson A Development. 2023; 150(10).

PMID: 37102683 PMC: 10233718. DOI: 10.1242/dev.201259.


Early anteroposterior regionalisation of human neural crest is shaped by a pro-mesodermal factor.

Gogolou A, Souilhol C, Granata I, Wymeersch F, Manipur I, Wind M Elife. 2022; 11.

PMID: 36154671 PMC: 9536837. DOI: 10.7554/eLife.74263.


The microRNA-23a cluster regulates the developmental HoxA cluster function during osteoblast differentiation.

Godfrey T, Wildman B, Beloti M, Kemper A, Ferraz E, Roy B J Biol Chem. 2018; 293(45):17646-17660.

PMID: 30242124 PMC: 6231122. DOI: 10.1074/jbc.RA118.003052.


MicroRNA filters Hox temporal transcription noise to confer boundary formation in the spinal cord.

Li C, Hong T, Tung Y, Yen Y, Hsu H, Lu Y Nat Commun. 2017; 8:14685.

PMID: 28337978 PMC: 5376671. DOI: 10.1038/ncomms14685.


Reorganisation of Hoxd regulatory landscapes during the evolution of a snake-like body plan.

Guerreiro I, Gitto S, Novoa A, Codourey J, Huynh T, Gonzalez F Elife. 2016; 5.

PMID: 27476854 PMC: 4969037. DOI: 10.7554/eLife.16087.