A morpholino-based screen to identify novel genes involved in craniofacial morphogenesis
- Authors
- Melvin, V.S., Feng, W., Hernandez-Lagunas, L., Artinger, K.B., and Williams, T.
- ID
- ZDB-PUB-130416-20
- Date
- 2013
- Source
- Developmental Dynamics : an official publication of the American Association of Anatomists 242(7): 817-31 (Journal)
- Registered Authors
- Artinger, Kristin Bruk
- Keywords
- zebrafish, craniofacial development, morpholino, branchial arches, neural crest derived cartilages
- MeSH Terms
-
- Animals
- Calcium-Binding Proteins/genetics
- Calcium-Binding Proteins/metabolism
- Facial Bones/embryology*
- Facial Bones/metabolism*
- PubMed
- 23559552 Full text @ Dev. Dyn.
BACKGROUND: The regulatory mechanisms underpinning facial development are conserved between diverse species. Therefore, results from model systems provide insight into the genetic causes of human craniofacial defects. Previously, we generated a comprehensive dataset examining gene expression during development and fusion of the mouse facial prominences. Here, we used this resource to identify genes that have dynamic expression patterns in the facial prominences, but for which only limited information exists concerning developmental function.
RESULTS: This set of ~80 genes was used for a high throughput functional analysis in the zebrafish system using Morpholino gene knockdown technology. This screen revealed three classes of cranial cartilage phenotypes depending upon whether knockdown of the gene affected the neurocranium, viscerocranium, or both. The targeted genes that produced consistent phenotypes encoded proteins linked to transcription (meis1, meis2a, tshz2, vgll4l), signaling (pkdcc, vlk, macc1, wu:fb16h09), and extracellular matrix function (smoc2). The majority of these phenotypes were not altered by reduction of p53 levels, demonstrating that both p53 dependent and independent mechanisms were involved in the craniofacial abnormalities.
CONCLUSIONS: This Morpholino-based screen highlights new genes involved in development of the zebrafish craniofacial skeleton with wider relevance to formation of the face in other species, particularly mouse and human.
/ 2
