Cis-regulatory underpinnings of human GLI3 expression in embryonic craniofacial structures and internal organs
- Authors
- Abbasi, A.A., Minhas, R., Schmidt, A., Koch, S., and Grzeschik, K.H.
- ID
- ZDB-PUB-131112-10
- Date
- 2013
- Source
- Development, growth & differentiation 55(8): 699-709 (Journal)
- Registered Authors
- Minhas, Rashid
- Keywords
- conserved non-coding elements, enhancer, GLI3 expression, transgenic mice, zebrafish
- MeSH Terms
-
- Animals
- Gene Expression Regulation, Developmental/physiology*
- Humans
- Introns/physiology*
- Kruppel-Like Transcription Factors/biosynthesis*
- Kruppel-Like Transcription Factors/genetics
- Mice
- Mice, Transgenic
- Nerve Tissue Proteins/biosynthesis*
- Nerve Tissue Proteins/genetics
- Neural Tube/embryology
- Organ Specificity/physiology
- Organogenesis/physiology*
- Skull/embryology*
- Transcription, Genetic/physiology*
- PubMed
- 24102645 Full text @ Dev. Growth Diff.
The zinc finger transcription factor Gli3 is an important mediator of Sonic hedgehog (Shh) signaling. During early embryonic development Gli3 participates in patterning and growth of the central nervous system, face, skeleton, limb, tooth and gut. Precise regulation of the temporal and spatial expression of Gli3 is crucial for the proper specification of these structures in mammals and other vertebrates. Previously we reported a set of human intronic cis-regulators controlling almost the entire known repertoire of endogenous Gli3 expression in mouse neural tube and limbs. However, the genetic underpinning of GLI3 expression in other embryonic domains such as craniofacial structures and internal organs remain elusive. Here we demonstrate in a transgenic mice assay the potential of a subset of human/fish conserved non-coding sequences (CNEs) residing within GLI3 intronic intervals to induce reporter gene expression at known regions of endogenous Gli3 transcription in embryonic domains other than central nervous system (CNS) and limbs. Highly specific reporter expression was observed in craniofacial structures, eye, gut, and genitourinary system. Moreover, the comparison of expression patterns directed by these intronic cis-acting regulatory elements in mouse and zebrafish embryos suggests that in accordance with sequence conservation, the target site specificity of a subset of these elements remains preserved among these two lineages. Taken together with our recent investigations, it is proposed here that during vertebrate evolution the Gli3 expression control acquired multiple, independently acting, intronic enhancers for spatiotemporal patterning of CNS, limbs, craniofacial structures and internal organs.