PUBLICATION
Faster embryonic segmentation through elevated Delta-Notch signalling
- Authors
- Liao, B.K., Jörg, D.J., Oates, A.C.
- ID
- ZDB-PUB-160616-4
- Date
- 2016
- Source
- Nature communications 7: 11861 (Journal)
- Registered Authors
- Oates, Andrew
- Keywords
- Biological sciences, Cell biology, Developmental biology
- MeSH Terms
-
- Animals
- Animals, Genetically Modified
- Body Patterning*/genetics
- Central Nervous System/metabolism
- Embryo, Nonmammalian/metabolism*
- Gene Expression Regulation, Developmental
- Homeodomain Proteins/metabolism
- Mesoderm/embryology
- Mesoderm/metabolism
- Models, Biological
- Nerve Tissue Proteins/metabolism*
- Receptor, Notch1/metabolism
- Signal Transduction*
- Somites/embryology
- Somites/metabolism
- Zebrafish/embryology*
- Zebrafish/genetics
- Zebrafish/metabolism*
- Zebrafish Proteins/metabolism*
- PubMed
- 27302627 Full text @ Nat. Commun.
Citation
Liao, B.K., Jörg, D.J., Oates, A.C. (2016) Faster embryonic segmentation through elevated Delta-Notch signalling. Nature communications. 7:11861.
Abstract
An important step in understanding biological rhythms is the control of period. A multicellular, rhythmic patterning system termed the segmentation clock is thought to govern the sequential production of the vertebrate embryo's body segments, the somites. Several genetic loss-of-function conditions, including the Delta-Notch intercellular signalling mutants, result in slower segmentation. Here, we generate DeltaD transgenic zebrafish lines with a range of copy numbers and correspondingly increased signalling levels, and observe faster segmentation. The highest-expressing line shows an altered oscillating gene expression wave pattern and shortened segmentation period, producing embryos with more, shorter body segments. Our results reveal surprising differences in how Notch signalling strength is quantitatively interpreted in different organ systems, and suggest a role for intercellular communication in regulating the output period of the segmentation clock by altering its spatial pattern.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping