PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensis

Abstract Background Pax genes are a family of conserved transcription factors that regulate many aspects of developmental morphogenesis, notably the development of ectodermal sensory structures including eyes. Nematostella vectensis, the starlet sea anemone, has numerous Pax orthologs, many of which...

Full description

Bibliographic Details
Main Authors: Leslie S. Babonis, Mark Q. Martindale
Format: Article
Language:English
Published: BMC 2017-09-01
Series:EvoDevo
Subjects:
Online Access:http://link.springer.com/article/10.1186/s13227-017-0077-7
_version_ 1819023167396511744
author Leslie S. Babonis
Mark Q. Martindale
author_facet Leslie S. Babonis
Mark Q. Martindale
author_sort Leslie S. Babonis
collection DOAJ
description Abstract Background Pax genes are a family of conserved transcription factors that regulate many aspects of developmental morphogenesis, notably the development of ectodermal sensory structures including eyes. Nematostella vectensis, the starlet sea anemone, has numerous Pax orthologs, many of which are expressed early during embryogenesis. The function of Pax genes in this eyeless cnidarian is unknown. Results Here, we show that PaxA, but not PaxC, plays a critical role in the development of cnidocytes in N. vectensis. Knockdown of PaxA results in a loss of developing cnidocytes and downregulation of numerous cnidocyte-specific genes, including a variant of the transcription factor Mef2. We also demonstrate that the co-expression of Mef2 in a subset of the PaxA-expressing cells is associated with the development with a second lineage of cnidocytes and show that knockdown of the neural progenitor gene SoxB2 results in downregulation of expression of PaxA, Mef2, and several cnidocyte-specific genes. Because PaxA is not co-expressed with SoxB2 at any time during cnidocyte development, we propose a simple model for cnidogenesis whereby a SoxB2-expressing progenitor cell population undergoes division to give rise to PaxA-expressing cnidocytes, some of which also express Mef2. Discussion The role of PaxA in cnidocyte development among hydrozoans has not been studied, but the conserved role of SoxB2 in regulating the fate of a progenitor cell that gives rise to neurons and cnidocytes in Nematostella and Hydractinia echinata suggests that this SoxB2/PaxA pathway may well be conserved across cnidarians.
first_indexed 2024-12-21T04:34:35Z
format Article
id doaj.art-ec835f1daea0442784736ea6aea3b2cc
institution Directory Open Access Journal
issn 2041-9139
language English
last_indexed 2024-12-21T04:34:35Z
publishDate 2017-09-01
publisher BMC
record_format Article
series EvoDevo
spelling doaj.art-ec835f1daea0442784736ea6aea3b2cc2022-12-21T19:15:53ZengBMCEvoDevo2041-91392017-09-018112010.1186/s13227-017-0077-7PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensisLeslie S. Babonis0Mark Q. Martindale1Whitney Laboratory for Marine Bioscience, University of FloridaWhitney Laboratory for Marine Bioscience, University of FloridaAbstract Background Pax genes are a family of conserved transcription factors that regulate many aspects of developmental morphogenesis, notably the development of ectodermal sensory structures including eyes. Nematostella vectensis, the starlet sea anemone, has numerous Pax orthologs, many of which are expressed early during embryogenesis. The function of Pax genes in this eyeless cnidarian is unknown. Results Here, we show that PaxA, but not PaxC, plays a critical role in the development of cnidocytes in N. vectensis. Knockdown of PaxA results in a loss of developing cnidocytes and downregulation of numerous cnidocyte-specific genes, including a variant of the transcription factor Mef2. We also demonstrate that the co-expression of Mef2 in a subset of the PaxA-expressing cells is associated with the development with a second lineage of cnidocytes and show that knockdown of the neural progenitor gene SoxB2 results in downregulation of expression of PaxA, Mef2, and several cnidocyte-specific genes. Because PaxA is not co-expressed with SoxB2 at any time during cnidocyte development, we propose a simple model for cnidogenesis whereby a SoxB2-expressing progenitor cell population undergoes division to give rise to PaxA-expressing cnidocytes, some of which also express Mef2. Discussion The role of PaxA in cnidocyte development among hydrozoans has not been studied, but the conserved role of SoxB2 in regulating the fate of a progenitor cell that gives rise to neurons and cnidocytes in Nematostella and Hydractinia echinata suggests that this SoxB2/PaxA pathway may well be conserved across cnidarians.http://link.springer.com/article/10.1186/s13227-017-0077-7PaxAPaxCMef2SoxB2Cell differentiationNovelty
spellingShingle Leslie S. Babonis
Mark Q. Martindale
PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensis
EvoDevo
PaxA
PaxC
Mef2
SoxB2
Cell differentiation
Novelty
title PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensis
title_full PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensis
title_fullStr PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensis
title_full_unstemmed PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensis
title_short PaxA, but not PaxC, is required for cnidocyte development in the sea anemone Nematostella vectensis
title_sort paxa but not paxc is required for cnidocyte development in the sea anemone nematostella vectensis
topic PaxA
PaxC
Mef2
SoxB2
Cell differentiation
Novelty
url http://link.springer.com/article/10.1186/s13227-017-0077-7
work_keys_str_mv AT lesliesbabonis paxabutnotpaxcisrequiredforcnidocytedevelopmentintheseaanemonenematostellavectensis
AT markqmartindale paxabutnotpaxcisrequiredforcnidocytedevelopmentintheseaanemonenematostellavectensis