Format

Send to

Choose Destination
Development. 2017 Jan 1;144(1):33-37. doi: 10.1242/dev.142109. Epub 2016 Nov 25.

Tfap2 and Sox1/2/3 cooperatively specify ectodermal fates in ascidian embryos.

Author information

1
Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka 560-0043, Japan imai@bio.sci.osaka-u.ac.jp yutaka@ascidian.zool.kyoto-u.ac.jp.
2
Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka 560-0043, Japan.
3
Department of Zoology, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
4
Department of Zoology, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan imai@bio.sci.osaka-u.ac.jp yutaka@ascidian.zool.kyoto-u.ac.jp.

Abstract

Epidermis and neural tissues differentiate from the ectoderm in animal embryos. Although epidermal fate is thought to be induced in vertebrate embryos, embryological evidence has indicated that no intercellular interactions during early stages are required for epidermal fate in ascidian embryos. To test this hypothesis, we determined the gene regulatory circuits for epidermal and neural specification in the ascidian embryo. These circuits started with Tfap2-r.b and Sox1/2/3, which are expressed in the ectodermal lineage immediately after zygotic genome activation. Tfap2-r.b expression was diminished in the neural lineages upon activation of fibroblast growth factor signaling, which is known to induce neural fate, and sustained only in the epidermal lineage. Tfap2-r.b specified the epidermal fate cooperatively with Dlx.b, which was activated by Sox1/2/3 This Sox1/2/3-Dlx.b circuit was also required for specification of the anterior neural fate. In the posterior neural lineage, Sox1/2/3 activated Nodal, which is required for specification of the posterior neural fate. Our findings support the hypothesis that the epidermal fate is specified autonomously in ascidian embryos.

KEYWORDS:

Ectoderm; Epidermis; Neural induction; Sox1/2/3; TFAP2

PMID:
27888190
DOI:
10.1242/dev.142109
[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for HighWire
Loading ...
Support Center