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Mech Dev
2016 Nov 01;142:10-21. doi: 10.1016/j.mod.2016.08.003.
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Regeneration in bipinnaria larvae of the bat star Patiria miniata induces rapid and broad new gene expression.
Oulhen N
,
Heyland A
,
Carrier TJ
,
Zazueta-Novoa V
,
Fresques T
,
Laird J
,
Onorato TM
,
Janies D
,
Wessel G
.
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BACKGROUND: Some metazoa have the capacity to regenerate lost body parts. This phenomenon in adults has been classically described in echinoderms, especially in sea stars (Asteroidea). Sea star bipinnaria larvae can also rapidly and effectively regenerate a complete larva after surgical bisection. Understanding the capacity to reverse cell fates in the larva is important from both a developmental and biomedical perspective; yet, the mechanisms underlying regeneration in echinoderms are poorly understood.
RESULTS: Here, we describe the process of bipinnaria regeneration after bisection in the bat star Patiria miniata. We tested transcriptional, translational, and cell proliferation activity after bisection in anterior and posterior bipinnaria halves as well as expression of SRAP, reported as a sea star regeneration associated protease (Vickery et al., 2001b). Moreover, we found several genes whose transcripts increased in abundance following bisection, including: Vasa, dysferlin, vitellogenin 1 and vitellogenin 2.
CONCLUSION: These results show a transformation following bisection, especially in the anterior halves, of cell fate reassignment in all three germ layers, with clear and predictable changes. These results define molecular events that accompany the cell fate changes coincident to the regenerative response in echinoderm larvae.
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27555501
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Alié,
Somatic stem cells express Piwi and Vasa genes in an adult ctenophore: ancient association of "germline genes" with stemness.
2011, Pubmed
Alié,
Somatic stem cells express Piwi and Vasa genes in an adult ctenophore: ancient association of "germline genes" with stemness.
2011,
Pubmed
Arenas-Mena,
Spatial expression of Hox cluster genes in the ontogeny of a sea urchin.
2000,
Pubmed
,
Echinobase
Balser,
Cloning by Ophiuroid Echinoderm Larvae.
1998,
Pubmed
,
Echinobase
Bely,
Evolution of animal regeneration: re-emergence of a field.
2010,
Pubmed
Cheng,
Calcium signaling in membrane repair.
2015,
Pubmed
Covian-Nares,
Membrane wounding triggers ATP release and dysferlin-mediated intercellular calcium signaling.
2010,
Pubmed
,
Echinobase
Eaves,
Reproduction: widespread cloning in echinoderm larvae.
2003,
Pubmed
,
Echinobase
Fresques,
Selective accumulation of germ-line associated gene products in early development of the sea star and distinct differences from germ-line development in the sea urchin.
2014,
Pubmed
,
Echinobase
GOSS,
KINETICS OF COMPENSATORY GROWTH.
1965,
Pubmed
Haley,
Regulated proteolysis by cortical granule serine protease 1 at fertilization.
2004,
Pubmed
,
Echinobase
Haley,
The cortical granule serine protease CGSP1 of the sea urchin, Strongylocentrotus purpuratus, is autocatalytic and contains a low-density lipoprotein receptor-like domain.
1999,
Pubmed
,
Echinobase
Hinman,
Developmental gene regulatory network evolution: insights from comparative studies in echinoderms.
2014,
Pubmed
,
Echinobase
Hinman,
Developmental gene regulatory network architecture across 500 million years of echinoderm evolution.
2003,
Pubmed
,
Echinobase
Huet,
[The germinal line in echinodermata: the origin and development of the germinal tissue in the course of gonadal regeneration in the sea-star Asterina gibbosa Penn (author's transl)].
1974,
Pubmed
,
Echinobase
Inoue,
Origin of Germ Cells and Early Differentiation of Gonads in the Starfish, Asterina pectinifera: (starfish/germ cells/PGC/gonad/haemal sinus).
1991,
Pubmed
,
Echinobase
Inoue,
Germ Cell Differentiation in Starfish: The Posterior Enterocoel as the Origin of Germ Cells in Asterina pectinifera: (starfish/germ cells/PGC/posterior enterocoel/haemal sinus).
1992,
Pubmed
,
Echinobase
Janies,
EchinoDB, an application for comparative transcriptomics of deeply-sampled clades of echinoderms.
2016,
Pubmed
,
Echinobase
Juliano,
An evolutionary transition of Vasa regulation in echinoderms.
2009,
Pubmed
,
Echinobase
Katoh,
MAFFT multiple sequence alignment software version 7: improvements in performance and usability.
2013,
Pubmed
Livak,
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.
2001,
Pubmed
Livingston,
Lithium evokes expression of vegetal-specific molecules in the animal blastomeres of sea urchin embryos.
1989,
Pubmed
,
Echinobase
McCauley,
Expression of wnt and frizzled genes during early sea star development.
2013,
Pubmed
,
Echinobase
Mladenov,
Mechanisms of arm-tip regeneration in the sea star, Leptasterias hexactis.
1989,
Pubmed
,
Echinobase
Mochizuki,
Universal occurrence of the vasa-related genes among metazoans and their germline expression in Hydra.
2001,
Pubmed
Oulhen,
Dysferlin is essential for endocytosis in the sea star oocyte.
2014,
Pubmed
,
Echinobase
Pek,
A role for vasa in regulating mitotic chromosome condensation in Drosophila.
2011,
Pubmed
Pfister,
Flatworm stem cells and the germ line: developmental and evolutionary implications of macvasa expression in Macrostomum lignano.
2008,
Pubmed
Reich,
Phylogenomic analyses of Echinodermata support the sister groups of Asterozoa and Echinozoa.
2015,
Pubmed
,
Echinobase
Renault,
vasa is expressed in somatic cells of the embryonic gonad in a sex-specific manner in Drosophila melanogaster.
2012,
Pubmed
Sánchez Alvarado,
Rethinking differentiation: stem cells, regeneration, and plasticity.
2014,
Pubmed
Schmittgen,
Quantitative reverse transcription-polymerase chain reaction to study mRNA decay: comparison of endpoint and real-time methods.
2000,
Pubmed
Schupbach,
Germline autonomy of maternal-effect mutations altering the embryonic body pattern of Drosophila.
1986,
Pubmed
Stamatakis,
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies.
2014,
Pubmed
Swartz,
Localization of Vasa mRNA during early cleavage of the snail Ilyanassa.
2008,
Pubmed
Technau,
Evolutionary crossroads in developmental biology: Cnidaria.
2011,
Pubmed
Tomczyk,
Hydra, a powerful model for aging studies.
2015,
Pubmed
Towbin,
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
1979,
Pubmed
Vaughn,
Predators induce cloning in echinoderm larvae.
2008,
Pubmed
,
Echinobase
Vickery,
Utilization of a novel deuterostome model for the study of regeneration genetics: molecular cloning of genes that are differentially expressed during early stages of larval sea star regeneration.
2001,
Pubmed
,
Echinobase
Vickery,
Morphogenesis and organogenesis in the regenerating planktotrophic larvae of asteroids and echinoids.
2002,
Pubmed
,
Echinobase
Wessel,
Use of sea stars to study basic reproductive processes.
2010,
Pubmed
,
Echinobase
Wessel,
Origin and development of the germ line in sea stars.
2014,
Pubmed
,
Echinobase
Winer,
Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytes in vitro.
1999,
Pubmed
Yajima,
Essential elements for translation: the germline factor Vasa functions broadly in somatic cells.
2015,
Pubmed
,
Echinobase
Yajima,
The DEAD-box RNA helicase Vasa functions in embryonic mitotic progression in the sea urchin.
2011,
Pubmed
,
Echinobase
Zhou,
Characterization and expression analysis of a trypsin-like serine protease from planarian Dugesia japonica.
2012,
Pubmed