PUBLICATION

Unraveling the transcriptional regulation of TWIST1 in limb development

Authors
Hirsch, N., Eshel, R., Bar Yaacov, R., Shahar, T., Shmulevich, F., Dahan, I., Levaot, N., Kaplan, T., Lupiáñez, D.G., Birnbaum, R.Y.
ID
ZDB-PUB-181030-5
Date
2018
Source
PLoS Genetics   14: e1007738 (Journal)
Registered Authors
Keywords
none
MeSH Terms
  • Animals
  • Branchial Region/metabolism
  • Enhancer Elements, Genetic/genetics
  • Extremities/embryology
  • Gene Expression Regulation, Developmental/genetics
  • Genes, Homeobox
  • Histone Deacetylases/genetics
  • Homeodomain Proteins/genetics
  • Limb Buds/metabolism
  • Limb Deformities, Congenital/embryology
  • Limb Deformities, Congenital/genetics*
  • Mice
  • Mice, Inbred C57BL
  • Organogenesis
  • Repressor Proteins/genetics
  • Transcription Factor AP-2
  • Transcription Factors/genetics
  • Twist-Related Protein 1/genetics*
  • Twist-Related Protein 1/physiology*
  • Zebrafish/genetics
  • Zebrafish Proteins/genetics
PubMed
30372441 Full text @ PLoS Genet.
Abstract
The transcription factor TWIST1 plays a vital role in mesoderm development, particularly in limb and craniofacial formation. Accordingly, haploinsufficiency of TWIST1 can cause limb and craniofacial malformations as part of Saethre-Chotzen syndrome. However, the molecular basis of TWIST1 transcriptional regulation during development has yet to be elucidated. Here, we characterized active enhancers in the TWIST1-HDAC9 locus that drive transcription in the developing limb and branchial arches. Using available p300 and H3K27ac ChIP-seq data, we identified 12 enhancer candidates, located both within and outside the coding sequences of the neighboring gene, Histone deacetyase 9 (HDAC9). Using zebrafish and mouse enhancer assays, we showed that eight of these candidates have limb/fin and branchial arch enhancer activity that resemble Twist1 expression. Using 4C-seq, we showed that the Twist1 promoter region interacts with three enhancers (eTw-5, 6, 7) in the limb bud and branchial arch of mouse embryos at day 11.5. Furthermore, we found that two transcription factors, LMX1B and TFAP2, bind these enhancers and modulate their enhancer activity. Finally, using CRISPR/Cas9 genome editing, we showed that homozygous deletion of eTw5-7 enhancers reduced Twist1 expression in the limb bud and caused pre-axial polydactyly, a phenotype observed in Twist1+/- mice. Taken together, our findings reveal that each enhancer has a discrete activity pattern, and together comprise a spatiotemporal regulatory network of Twist1 transcription in the developing limbs/fins and branchial arches. Our study suggests that mutations in TWIST1 enhancers could lead to reduced TWIST1 expression, resulting in phenotypic outcome as seen with TWIST1 coding mutations.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping