Cargando…

Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option

Many asexually-propagating marine invertebrates can survive extreme environmental conditions by developing dormant structures, i.e., morphologically simplified bodies that retain the capacity to completely regenerate a functional adult when conditions return to normal. Here, we examine the environme...

Descripción completa

Detalles Bibliográficos
Autores principales: Hiebert, Laurel S., Scelzo, Marta, Alié, Alexandre, De Tomaso, Anthony W., Brown, Federico D., Tiozzo, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308810/
https://www.ncbi.nlm.nih.gov/pubmed/35871255
http://dx.doi.org/10.1038/s41598-022-16656-8
_version_ 1784753033014411264
author Hiebert, Laurel S.
Scelzo, Marta
Alié, Alexandre
De Tomaso, Anthony W.
Brown, Federico D.
Tiozzo, Stefano
author_facet Hiebert, Laurel S.
Scelzo, Marta
Alié, Alexandre
De Tomaso, Anthony W.
Brown, Federico D.
Tiozzo, Stefano
author_sort Hiebert, Laurel S.
collection PubMed
description Many asexually-propagating marine invertebrates can survive extreme environmental conditions by developing dormant structures, i.e., morphologically simplified bodies that retain the capacity to completely regenerate a functional adult when conditions return to normal. Here, we examine the environmental, morphological, and molecular characteristics of dormancy in two distantly related clonal tunicate species: Polyandrocarpa zorritensis and Clavelina lepadiformis. In both species, we report that the dormant structures are able to withstand harsher temperature and salinity conditions compared to the adults. The dormant structures are the dominant forms these species employ to survive adverse conditions when the zooids themselves cannot survive. While previous work shows C. lepadiformis dormant stage is present in winters in the Atlantic Ocean and summers in the Mediterranean, this study is the first to show a year-round presence of P. zorritensis dormant forms in NW Italy, even in the late winter when all zooids have disappeared. By finely controlling the entry and exit of dormancy in laboratory-reared individuals, we were able to select and characterize the morphology of dormant structures associated with their transcriptome dynamics. In both species, we identified putative stem and nutritive cells in structures that resemble the earliest stages of asexual propagation. By characterizing gene expression during dormancy and regeneration into the adult body plan (i.e., germination), we observed that genes which control dormancy and environmental sensing in other metazoans, notably HIF-α and insulin signaling genes, are also expressed in tunicate dormancy. Germination-related genes in these two species, such as the retinoic acid pathway, are also found in other unrelated clonal tunicates during asexual development. These results are suggestive of repeated co-option of conserved eco-physiological and regeneration programs for the origin of novel dormancy-germination processes across distantly related animal taxa.
format Online
Article
Text
id pubmed-9308810
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-93088102022-07-25 Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option Hiebert, Laurel S. Scelzo, Marta Alié, Alexandre De Tomaso, Anthony W. Brown, Federico D. Tiozzo, Stefano Sci Rep Article Many asexually-propagating marine invertebrates can survive extreme environmental conditions by developing dormant structures, i.e., morphologically simplified bodies that retain the capacity to completely regenerate a functional adult when conditions return to normal. Here, we examine the environmental, morphological, and molecular characteristics of dormancy in two distantly related clonal tunicate species: Polyandrocarpa zorritensis and Clavelina lepadiformis. In both species, we report that the dormant structures are able to withstand harsher temperature and salinity conditions compared to the adults. The dormant structures are the dominant forms these species employ to survive adverse conditions when the zooids themselves cannot survive. While previous work shows C. lepadiformis dormant stage is present in winters in the Atlantic Ocean and summers in the Mediterranean, this study is the first to show a year-round presence of P. zorritensis dormant forms in NW Italy, even in the late winter when all zooids have disappeared. By finely controlling the entry and exit of dormancy in laboratory-reared individuals, we were able to select and characterize the morphology of dormant structures associated with their transcriptome dynamics. In both species, we identified putative stem and nutritive cells in structures that resemble the earliest stages of asexual propagation. By characterizing gene expression during dormancy and regeneration into the adult body plan (i.e., germination), we observed that genes which control dormancy and environmental sensing in other metazoans, notably HIF-α and insulin signaling genes, are also expressed in tunicate dormancy. Germination-related genes in these two species, such as the retinoic acid pathway, are also found in other unrelated clonal tunicates during asexual development. These results are suggestive of repeated co-option of conserved eco-physiological and regeneration programs for the origin of novel dormancy-germination processes across distantly related animal taxa. Nature Publishing Group UK 2022-07-23 /pmc/articles/PMC9308810/ /pubmed/35871255 http://dx.doi.org/10.1038/s41598-022-16656-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Hiebert, Laurel S.
Scelzo, Marta
Alié, Alexandre
De Tomaso, Anthony W.
Brown, Federico D.
Tiozzo, Stefano
Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option
title Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option
title_full Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option
title_fullStr Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option
title_full_unstemmed Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option
title_short Comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option
title_sort comparing dormancy in two distantly related tunicates reveals morphological, molecular, and ecological convergences and repeated co-option
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9308810/
https://www.ncbi.nlm.nih.gov/pubmed/35871255
http://dx.doi.org/10.1038/s41598-022-16656-8
work_keys_str_mv AT hiebertlaurels comparingdormancyintwodistantlyrelatedtunicatesrevealsmorphologicalmolecularandecologicalconvergencesandrepeatedcooption
AT scelzomarta comparingdormancyintwodistantlyrelatedtunicatesrevealsmorphologicalmolecularandecologicalconvergencesandrepeatedcooption
AT aliealexandre comparingdormancyintwodistantlyrelatedtunicatesrevealsmorphologicalmolecularandecologicalconvergencesandrepeatedcooption
AT detomasoanthonyw comparingdormancyintwodistantlyrelatedtunicatesrevealsmorphologicalmolecularandecologicalconvergencesandrepeatedcooption
AT brownfedericod comparingdormancyintwodistantlyrelatedtunicatesrevealsmorphologicalmolecularandecologicalconvergencesandrepeatedcooption
AT tiozzostefano comparingdormancyintwodistantlyrelatedtunicatesrevealsmorphologicalmolecularandecologicalconvergencesandrepeatedcooption