Distinct regulation of Snail in two muscle lineages of the ascidian embryo achieves temporal coordination of muscle development.
Miki TokuokaKenji KobayashiYutaka SatouPublished in: Development (Cambridge, England) (2018)
The transcriptional repressor Snail is required for proper differentiation of the tail muscle of ascidian tadpole larvae. Two muscle lineages (B5.1 and B6.4) contribute to the anterior tail muscle cells, and are consecutively separated from a transcriptionally quiescent germ cell lineage at the 16- and 32-cell stages. Concomitantly, cells of these lineages begin to express Tbx6.b (Tbx6-r.b) at the 16- and 32-cell stages, respectively. Meanwhile, Snail expression begins in these two lineages simultaneously at the 32-cell stage. Here, we show that Snail expression is regulated differently between these two lineages. In the B5.1 lineage, Snail was activated through Tbx6.b, which is activated by maternal factors, including Zic-r.a. In the B6.4 lineage, the MAPK pathway was cell-autonomously activated by a constitutively active form of Raf, enabling Zic-r.a to activate Snail independently of Tbx6.b As a result, Snail begins to be expressed at the 32-cell stage simultaneously in these two lineages. Such shortcuts might be required for coordinating developmental programs in embryos in which cells become separated progressively from stem cells, including germline cells.
Keyphrases
- epithelial mesenchymal transition
- single cell
- induced apoptosis
- stem cells
- cell therapy
- skeletal muscle
- cell cycle arrest
- signaling pathway
- poor prognosis
- oxidative stress
- endoplasmic reticulum stress
- public health
- transcription factor
- gene expression
- mesenchymal stem cells
- pregnant women
- zika virus
- bone marrow
- pregnancy outcomes
- dna repair