Shared features of blastula and neural crest stem cells evolved at the base of vertebrates

Joshua R. York, Anjali Rao, Paul B. Huber, Elizabeth N. Schock, Andrew Montequin, Sara Rigney, Carole LaBonne

Research output: Contribution to journalArticlepeer-review

7 Scopus citations

Abstract

The neural crest is a vertebrate-specific stem cell population that helped drive the origin and evolution of vertebrates. A distinguishing feature of these cells is their multi-germ layer potential, which has parallels to another stem cell population—pluripotent stem cells of the vertebrate blastula. Here, we investigate the evolutionary origins of neural crest potential by comparing neural crest and pluripotency gene regulatory networks of a jawed vertebrate, Xenopus, and a jawless vertebrate, lamprey. We reveal an ancient evolutionary origin of shared regulatory factors in these gene regulatory networks that dates to the last common ancestor of extant vertebrates. Focusing on the key pluripotency factor pou5, we show that a lamprey pou5 orthologue is expressed in animal pole cells but is absent from neural crest. Both lamprey and Xenopus pou5 promote neural crest formation, suggesting that pou5 activity was lost from the neural crest of jawless vertebrates or acquired along the jawed vertebrate stem. Finally, we provide evidence that pou5 acquired novel, neural crest-enhancing activity after evolving from an ancestral pou3-like clade. This work provides evidence that both the neural crest and blastula pluripotency networks arose at the base of the vertebrates and that this may be linked to functional evolution of pou5.

Original languageEnglish
Pages (from-to)1680-1692
Number of pages13
JournalNature Ecology and Evolution
Volume8
Issue number9
DOIs
StatePublished - Sep 2024

Bibliographical note

Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Limited 2024.

Funding

We thank S. Miehls and the staff of the Hammond Bay Biological Station for shipment of lampreys. We also thank D. McCauley, D. Medeiros, T. Sauka-Spengler and M. Bronner for clones and reagents; R. Braun for statistical advice; and participants in the Woods Hole Embryology course and members of the LaBonne laboratory for helpful discussions. Funding for the study was received from Life Sciences Research Foundation postdoctoral fellowship (J.R.Y.), National Institutes of Health (grant nos. R01GM116538 (C.L.) and F32DE029113 (E.N.S.)), National Science Foundation (grant no. 1764421 to C.L.) and Simons Foundation (grant no. SFARI 597491-RWC to C.L.). We dedicate this work to Dr. J. Walder (deceased), founder of Integrated DNA Technologies and co-founder of the Walder Foundation, which generously underwrote J.R.Y.’s Life Sciences Research Foundation fellowship.

FundersFunder number
Life Sciences Research Foundation
National Institutes of Health (NIH)R01GM116538, F32DE029113
National Science Foundation Arctic Social Science Program1764421
Simons FoundationSFARI 597491-RWC

    ASJC Scopus subject areas

    • Ecology, Evolution, Behavior and Systematics
    • Ecology

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