Divergent mechanisms regulate conserved cardiopharyngeal development and gene expression in distantly related ascidians
Abstract
Ascidians present a striking dichotomy between conserved phenotypes and divergent genomes: embryonic cell lineages and gene expression patterns are conserved between distantly related species. Much research has focused on Ciona or Halocynthia spp. but development in other ascidians remains poorly characterized. Here we surveyed the multipotent myogenic B7.5 lineage in Molgula spp. Comparisons to the homologous lineage in Ciona revealed identical cell division and fate specification events that result in segregation of larval, cardiac, and pharyngeal muscle progenitors. Moreover, the expression patterns of key regulators are conserved, but cross-species transgenic assays uncovered incompatibility, or "unintelligibility", of orthologous cis-regulatory sequences between Molgula and Ciona. These sequences drive identical expression patterns that are not recapitulated in cross-species assays. We show that this unintelligibility is likely due to changes in both cis- and trans-actingelements, hinting at widespread and frequent turnover of regulatory mechanisms underlying otherwise conserved aspects of ascidian embryogenesis.
Article and author information
Author details
Reviewing Editor
- Margaret Buckingham, Institut Pasteur, France
Version history
- Received: June 18, 2014
- Accepted: September 5, 2014
- Accepted Manuscript published: September 10, 2014 (version 1)
- Version of Record published: September 30, 2014 (version 2)
Copyright
© 2014, Stolfi et al.
This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.
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Further reading
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- Developmental Biology
- Physics of Living Systems
Geometric criteria can be used to assess whether cell intercalation is active or passive during the convergent extension of tissue.
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- Computational and Systems Biology
- Developmental Biology
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