Elsevier

Developmental Biology

Volume 394, Issue 1, 1 October 2014, Pages 170-180
Developmental Biology

Evolution of Developmental Control Mechanisms
Ephrin-mediated restriction of ERK1/2 activity delimits the number of pigment cells in the Ciona CNS

https://doi.org/10.1016/j.ydbio.2014.07.010Get rights and content
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Highlights

  • Live-imaging of the melanocyte lineage during Ciona neurulation.

  • The melanocyte lineage undergoes a previously unrecognized cell division.

  • Differential ERK1/2 activity during four successive A–P oriented cell divisions.

  • Eph signal inhibition results in ectopic ERK activity and supernumerary pigment cells.

Abstract

Recent evidence suggests that ascidian pigment cells are related to neural crest-derived melanocytes of vertebrates. Using live-imaging, we determine a revised cell lineage of the pigment cells in Ciona intestinalis embryos. The neural precursors undergo successive rounds of anterior–posterior (A–P) oriented cell divisions, starting at the blastula 64-cell stage. A previously unrecognized fourth A–P oriented cell division in the pigment cell lineage leads to the generation of the post-mitotic pigment cell precursors. We provide evidence that MEK/ERK signals are required for pigment cell specification until approximately 30 min after the final cell division has taken place. Following each of the four A–P oriented cell divisions, ERK1/2 is differentially activated in the posterior sister cells, into which the pigment cell lineage segregates. Eph/ephrin signals are critical during the third A–P oriented cell division to spatially restrict ERK1/2 activation to the posterior daughter cell. Targeted inhibition of Eph/ephrin signals results in, at neurula stages, anterior expansion of both ERK1/2 activation and a pigment cell lineage marker and subsequently, at larval stages, supernumerary pigment cells. We discuss the implications of these findings with respect to the evolution of the vertebrate neural crest.

Keywords

Melanocyte
Pigment cell
Ascidian
Neural crest
Oriented cell division

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These authors contributed equally to this work.