Medusa Development Research Articles

Coevolution of the Tlx homeobox gene with medusa development (Cnidaria: Medusozoa)

Cnidarians display a wide diversity of life cycles. Among the main cnidarian clades, only Medusozoa possesses a swimming life cycle stage called the medusa, alternating with a benthic polyp stage. The medusa stage was repeatedly lost during medusozoan evolution, notably in the most diverse medusozoan class, Hydrozoa. Here, we show that the presence of the homeobox gene Tlx in Cnidaria is correlated with the presence of the medusa stage, the gene having been lost in clades that ancestrally lack a medusa (anthozoans, endocnidozoans) and in medusozoans that secondarily lost the medusa stage. Our characterization of Tlx expression indicate an upregulation of Tlx during medusa development in three distantly related medusozoans, and spatially restricted expression patterns in developing medusae in two distantly related species, the hydrozoan Podocoryna carnea and the scyphozoan Pelagia noctiluca. These results suggest that Tlx plays a key role in medusa development and that the loss of this gene is likely linked to the repeated loss of the medusa life cycle stage in the evolution of Hydrozoa.

Patterns of Wnt signaling in the life cycle of Podocoryna carnea and its implications for medusae evolution in Hydrozoa (Cnidaria).

Hydrozoans are known for their complex life cycles, alternating between benthic, asexually reproducing polyps and pelagic, sexually reproducing medusae. Although patterning in hydrozoan polyps has been well studied, little is known about the signaling mechanisms governing medusa development. In order to investigate the role of Wnt signaling in medusa development, we use RNA-Seq data collected from three discrete life cycle stages of Podocoryna carnea to assemble, annotate, and assess enrichment and differential expression (DE) of Wnt pathway elements in P. carnea's transcriptome. Enrichment analyses revealed a statistically significant enrichment of DE Wnt signaling transcripts in the transcriptome of P. carnea, of which, the vast majority of these were significantly up-regulated in developing and adult medusae stages. Whole mount in situ hybridization (ISH) reveals co-expression of the Wnt ligand, Wnt3, and a membrane bound Wnt receptor, frizzled3, at the distal and oral ends of the developmental axes of medusae and polyps in P. carnea. DE and ISH results presented here reveal expression of Wnt signaling components consistent with it playing a role in medusa development. Specifically, Wnt ligand expression in the oral region suggests that the Wnt pathway may play a role in medusa patterning, similar to that of polyps. Previous Wnt expression studies in hydrozoan taxa with reduced medusa have failed to detect co-expression of Wnt3 and a frizzled receptor at their truncated developmental axes, suggesting that down regulation of Wnt pathway elements may play a key role in the loss of the medusa life cycle stage in hydrozoan evolution.

Expression of Wnt pathway genes in polyps and medusa‐like structures of Ectopleura larynx (Cnidaria: Hydrozoa)

The canonical Wnt signaling pathway is conserved in its role in axial patterning throughout Metazoa. In some hydrozoans (Phylum Cnidaria), Wnt signaling is implicated in oral-aboral patterning of the different life cycle stages-the planula, polyp and medusa. Unlike most hydrozoans, members of Aplanulata lack a planula larva and the polyp instead develops directly from a brooded or encysted embryo. The Aplanulata species Ectopleura larynx broods such embryos within gonophores. These gonophores are truncated medusae that remain attached to the polyps from which they bud, and retain evolutionary remnants of medusa structures. In E. larynx, gonophores differ between males and females in their degree of medusa truncation, making them an ideal system for examining truncated medusa development. Using next-generation sequencing, we isolated genes from Wnt signaling pathways and examined their expression in E. larynx. Our data are consistent with the Wnt pathway being involved in axial patterning of the polyp and truncated medusa. Changes in the spatial expression of Wnt pathway genes are correlated with the development of different oral structures in male and female gonophores. The absence of expression of components of the Wnt pathway and presence of a Wnt pathway antagonist SFRP in the developing anterior end of the gonophore suggest that downregulation of the Wnt pathway could play a role in medusa reduction in E. larynx.

The life cycle of Gastroblasta raffaelei (Cnidaria, Hydrozoa, Leptomedusae, Campanulariidae) and a review of the genus Gastroblasta

The genus Gastroblasta was proposed by Keller in 1883 for a campanulariid medusa from the Red Sea, G. timida, with round umbrella, multiple radial canals and multiple manubria. A second species, G. raffaelei, with elliptic umbrella, multiple manubria and radial canals, and a great tendency to fission, was subsequently described from the Mediterranean Sea by Lang in 1886. A third species with multiple manubria was described by Mayer in 1900 from Tortugas: Multioralis ovalis (currently ascribed to Gastroblasta). The complete life cycle of a species of Gastroblasta, whose polyp stage was collected inside sponges from the Ligurian Sea and the Ionian and Adriatic Seas, is described. The first stage of medusa development is a typical Clytia with four radial canals and four tentacles, then the medusa becomes similar to G. ovale, to subsequently acquire the typical morphology of G. raffaelei. The species G. timida and G. raffaelei are considered as valid representatives of the genus, sharing the characters of multiple manubria and radial canals. The medusa of G. ovale has a diagonal canal system, instead of multiple radial canals, sharing with Gastroblasta the presence of multiple manubria only: it is proposed to resurrect the genus Multioralis to accommodate it.

BMP2/4 and BMP5-8 in jellyfish development and transdifferentiation

Bone morphogenetic proteins (BMPs) have key roles in gastrulation, mesoderm induction and axial patterning. The multitude of bilaterian BMPs employed in these morphogenetic processes contrasts starkly with the scarcity of BMPs in Cnidaria, the most basal eumetazoan phylum. In coral, sea anemone and hydra species, BMPs have been found to be associated with larval and polyp axial patterning. In the hydrozoan jellyfish Podocoryne (Hydractinia) carnea the BMP2/4 and BMP5-8 genes are expressed unilaterally in the larva, corroborating a possible role in larval axial development. With the focal area of BMP expression in the anterior region, however, the jellyfish larva may have a developmental reversal of spatial polarity compared to the anthozoan larva. In medusa development, BMP genes are expressed in divergent expression territories within the presumptive radial canals and in various parts of the endoderm, indicative of an involvement in mesoderm patterning and gastrovascular system formation reminiscent of bilaterian BMP functions. In addition, the BMP2/4 and BMP5-8 genes may play roles in wound response and dedifferentiation or S-phase re-entry, respectively, as the former is expressed in striated muscle cells immediately after excision from the bell and the latter in the initial phase of muscle cell transdifferentiation.

Variations on a theme? Polyp and medusa development in Podocoryna carnea

Variations on a theme? Polyp and medusa development in Podocoryna carnea

Evolutionary aspects of developmentally regulated helix-loop-helix transcription factors in striated muscle of jellyfish

The function of basic helix-loop-helix (bHLH) proteins in cell differentiation was shown to be conserved from Drosophila to vertebrates, exemplified by the function of MyoD in striated muscle differentiation. In phylogeny striated muscle tissue appears first in jellyfish and the question of its evolutionary position is controversially discussed. For this reason we have studied the developmental role of myogenic bHLH genes in medusa development. Based on their dimerization ability, four genes of the bHLH family of transcription factors were isolated from the hydrozoan jellyfish Podocoryne carnea. While the proteins Id and Ash group with cognate family members from bilaterians, Net-like and JellyD1 could not be unequivocally classified. Id is expressed during the medusa budding process and in the adult medusa, Ash and Net-like are expressed in all life cycle stages from egg to adult medusa and JellyD1 is expressed in the blastula and gastrula stages, the planula larva, and in late medusa bud stages. The dimerization specificity, the expression pattern, and the conservation of two residues specific for a MyoD bHLH domain suggest that JellyD1 is related to an ancestral MyoD gene. Id, Net-like, and JellyD1 are either expressed in the entocodon or its derived tissues, the striated and smooth muscle of the bell. These findings strengthen the hypothesis that the entocodon is a mesoderm-like structure and that the common ancestor of Cnidaria and Bilateria was more complex in cell-type architecture and body organization than commonly thought.

Development and biology of Periphylla periphylla (Scyphozoa: Coronatae) in a Norwegian fjord

The globally distributed coronate scyphomedusa Periphyllaperiphylla (Peron and Lesueur, 1809) occurs in permanent and extremely high abundance in some Norwegian fjords. Studies on the species in Lurefjorden, 40 km north of Bergen, have revealed a holopelagic life cycle with direct development. We distinguished 14 successive developmental stages, characterised by size and morphology. Eggs and early stages are non-mobile, neutrally buoyant, and found mainly at intermediate depths. Rearing studies indicated a development time of 2–3 months from fertilisation to stage 9, when the medusa starts feeding and becomes motile. The fjord population usually shows a strong diel vertical migration, with aggregations at shallower depths during the night. The development includes a gradual increase in pigmentation (porphyrins), starting with the stomach, and thereafter extending to tentacles and the whole exumbrella. This pigment is photodegraded by natural light. Rearing experiments in the laboratory have shown a lethal effect of light. Here, development stops at stage 5. Pigments become visible in stage 7. Older medusae are severely damaged and killed within a few days by exposure to daylight. All stages of P. periphylla are bioluminescent, with this capacity increasing with growth, probably in connection with the development of the nervous net. The light reaction starts at the point of stimulation and spreads at two different speeds corresponding to the two nerve nets of the medusae. The coronal furrow has a central function in transmission of the reaction. It is hypothesised that the bioluminescence is used mainly as a warning to some potential predators, signalling that the porphyrin-containing medusa is unpalatable. P. periphylla has the same two categories of nematocysts as other coronates, with a total of six different types. Nematocyst abundance, distribution and morphology indicate their function. The giant euryteles (capsule up to 100 µm and tubule up to 1160 µm) are the largest ones known among Scyphozoa, and are unique in that this size increases during medusa development.

Phylogeny of Medusozoa and the evolution of cnidarian life cycles

Abstract To investigate the evolution of cnidarian life cycles, data from the small subunit of the ribosome are used to derive a phylogenetic hypothesis for Medusozoa. These data indicate that Cnidaria is monophyletic and composed of Anthozoa and Medusozoa. While Cubozoa and Hydrozoa are well supported clades, Scyphozoa appears to be paraphyletic. Stauromedusae is possibly the sister group of either Cubozoa or all other medusozoans. The phylogenetic results suggest that: the polyp probably preceded the medusa in the evolution of Cnidaria; within Hydrozoa, medusa development involving the entocodon is ancestral; within Trachylina, the polyp was lost and subsequently regained in the parasitic narcomedusans; within Siphonophorae, the float originated prior to swimming bells; stauromedusans are not likely to be descended from ancestors that produced medusae by strobilation; and cubozoan polyps are simplified from those of their ancestors, which possessed polyps with gastric septa and four mesogleal muscle bands and peristomial pits.

Conservation of Brachyury, Mef2, and Snail in the myogenic lineage of jellyfish: a connection to the mesoderm of bilateria.

One major difference between simple metazoans such as cnidarians and all the bilaterian animals is thought to involve the invention of mesoderm. The terms diploblasts and triploblasts are therefore, often used to group prebilaterian and bilaterian animals, respectively. However, jellyfish contain well developed striated and smooth muscle tissues that derive from the entocodon, a mesoderm-like tissue formed during medusa development. We investigated the hypothesis, that the entocodon could be homologous to the third germ layer of bilaterians by analyzing the structures and expression patterns of the homologues of Brachyury, Mef2, and Snail in the jellyfish Podocoryne carnea. These are regulatory genes from the T-box, MADS-box and zinc finger families known to play important roles in bilaterian mesoderm patterning and muscle differentiation. The sequence and expression data demonstrate that the genes are structurally and functionally conserved and even more similar to humans or other deuterostomes than to protostome model organisms such as Drosophila or Caenorhabditis elegans. Based on these data we conclude that the common ancestor of the cnidarians and bilaterians not only shared genes that play a role in regulating myogenesis but already used them to develop and differentiate muscle systems similar to those of triploblasts.

INTEGRIN AND TALIN IN THE JELLYFISH PODOCORYNE CARNEA

We have isolated an integrin-β and -α subunit from Podocoryne carnea (Cnidaria, Hydrozoa) and studied their expression in the life-cycle and during cell migration, in vitro transdifferentiation and regeneration. Comparison of the integrin expression pattern with a Podocoryne talin homologue by RT-PCR demonstrates that all three genes are maternal messages and continuously expressed in the life-cycle, in medusa development and in all medusae tissues. In situ hybridisation experiments confirm co-expression of both integrin subunits in the different life-stages. Integrin expression was furthermore studied in isolated striated muscle induced to transdifferentiate to new cell types, or grafted on ECM where the muscle adheres and migrates. Integrin expression was maintained continuously throughout both processes. These results suggest that in Podocoryne carnea processes such as cell migration and differentiation are not controlled by up- or downregulation of alternative integrin subunits, but by a single integrin heterodimer which activates different downstream signalling cascades.

The Mesoderm Specification Factor Twist in the Life Cycle of Jellyfish

The basic helix-loop-helix (bHLH) transcription factor Twist is highly conserved from Drosophila to vertebrates and plays a major role in mesoderm specification of triploblasts. The presence of a Twist homologue in diploblasts such as the cnidarian Podocoryne carnea raises questions on the evolution of mesoderm, the third cell layer characteristic for triploblasts. Podocoryne Twist is expressed in the early embryo until the myoepithelial cells of the larva differentiate and then again during medusa development. There, the gene is detected first when the myoepithelial cells of the polyp dedifferentiate to form the medusa bud and later Twist is found transiently in the entocodon, a mesoderm-like cell layer which differentiates into the smooth muscle and striated muscle of the bell. On the other hand, in later bud stages and the medusa, expression is seen where non-muscle tissues differentiate. Experimental analysis of in vitro transdifferentiation and regeneration demonstrates that Twist activity is not needed when isolated striated muscle regenerate medusa organs. Developmental roles of Twist are discussed with respect to early animal evolution from a common ancestor of cnidarians and bilaterians.

The HOX-like gene Cnox2-Pc is expressed at the anterior region in all life cycle stages of the jellyfish Podocoryne carnea.

The marine jellyfish Podocoryne carnea (Cnidaria, Hydrozoa) has a metagenic life cycle consisting of a larva, a colonial polyp and a free-swimming jellyfish (medusa). To study the function of HOX genes in primitive diploblastic animals we screened a library of P. carnea cDNA using PCR primers derived from the most conserved regions in helix 1 and helix 3 of the homeobox. A novel gene, Cnox2-Pc, has been isolated and characterized. Cnox2-Pc is a HOX cluster-like gene, and its homeodomain shows similarity to the Deformed subfamily of HOM-C/HOX genes. In situ hybridization revealed that Cnox2-Pc is expressed in the anterior region of the larva, the polyp head, and the most apical ectoderm of the differentiating bud during medusa development. In adult medusa expression is restricted to the gastrovascular entoderm. The results suggest that Cnox2-Pc is involved in establishment of an anterior-posterior axis during development in primitive metazoans.

Life stage specific expression of a myosin heavy chain in the hydrozoan Podocoryne carnea

Abstract In order to study life stage specific gene-expression and also to investigate the molecular components of jellyfish muscle we cloned a tissue specifically expressed cDNA of the metagenetic hydrozoan Podocoryne carnea. A monoclonal antibody was made that reacts with the filaments of striated muscle of the medusa stage. The mAb detects a protein of 220 kDa in Western blots. The antibody was used to clone a cDNA from an expression library. Sequence analysis showed that the clone codes for the rod part of a myosing heavy chain (MHC). Surprisingly, the sequence is more similar to MHCs from striated muscle than to smooth muscle or non-muscle MHCs from either invertebrates or vertebrates. A particularly well conserved region, which may be correlated to a function in striated muscle, was found. Expression studies showed that the corresponding RNA is only present in the striated muscle cells of the medusa. During medusa development, the transcript became detectable at the same time as muscle differentiation becomes visible in the electron microscops.

Life stage specific expression of a myosin heavy chain in the hydrozoan Podocoryne carnea

Abstract In order to study life stage specific gene-expression and also to investigate the molecular components of jellyfish muscle we cloned a tissue specifically expressed cDNA of the metagenetic hydrozoan Podocoryne carnea. A monoclonal antibody was made that reacts with the filaments of striated muscle of the medusa stage. The mAb detects a protein of 220 kDa in Western blots. The antibody was used to clone a cDNA from an expression library. Sequence analysis showed that the clone codes for the rod part of a myosing heavy chain (MHC). Surprisingly, the sequence is more similar to MHCs from striated muscle than to smooth muscle or non-muscle MHCs from either invertebrates or vertebrates. A particularly well conserved region, which may be correlated to a function in striated muscle, was found. Expression studies showed that the corresponding RNA is only present in the striated muscle cells of the medusa. During medusa development, the transcript became detectable at the same time as muscle differentiation becomes visible in the electron microscops.

An electron microscopic study of early developmental stages, myogenesis, oogenesis and cnidogenesis in the anthomedusa, Podocoryne carnea M. Sars.

This descriptive electron microscopic study of the blastogenetic medusa development of Podocoryne carnea focuses on the earliest stages of primordium formation, myogenesis, oogenesis and cnidogenesis. The events which take place at the cellular level prior to the formation of stage 1 (Frey, '68), which are characterized by ecto- and entodermal accumulations of undifferentiated I-cells and the beginning of transdifferentiation of epithelial cells, have been subdivided into four distinct stages (U1-U4). The genealogy of cells participating in medusa differentiation indicates that some cell types of the medusa are derived by transdifferentiation from the polyp's epithelial cells, while others originate by differentiation from I-cells. The myogenesis of the subumbrellar muscle cells resembles vertebrate myocardiac differentiation in many respects.