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        <title>EvoDevo - Most accessed articles</title>
        <link>http://www.evodevojournal.com</link>
        <description>The most accessed research articles published by EvoDevo</description>
        <dc:date>2012-01-24T00:00:00Z</dc:date>
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        <title>Lim Homeobox Genes in the Ctenophore Mnemiopsis leidyi: The Evolution of Neural Cell Type Specification</title>
        <description>Background:
Nervous systems are thought to be important to the evolutionary success and diversification of metazoans, yet little is known about the origin of simple nervous systems at the base of the animal tree.  Recent data suggest that ctenophores, a group of macroscopic pelagic marine invertebrates, are the most ancient group of animals that possess a definitive nervous system consisting of a distributed nerve net and an apical statocyst.  This study reports on details of the evolution of the neural cell type specifying transcription factor family of LIM homeobox containing genes (Lhx), which have highly conserved functions in neural specification in bilaterian animals.
Results:
Using next generation sequencing, the first draft of the genome of the ctenophore Mnemiopsis leidyi has been generated.   The Lhx genes in all animals are represented by seven subfamilies (Lhx1/5, Lhx3/4, Lmx, Islet, Lhx2/9, Lhx6/8, and LMO) of which four were found to be represented in the ctenophore lineage (Lhx1/5, Lhx3/4, Lmx, and Islet). Interestingly, the ctenophore Lhx gene complement is more similar to the sponge complement (sponges do not possess neurons) than to either the cnidarian-bilaterian or placozoan Lhx complements.  Using whole mount in situ hybridization, the Lhx gene expression patterns were examined and found to be expressed around the blastopore and in cells that give rise to the apical organ and putative neural sensory cells.
Conclusion:
This research gives us a first look at neural cell type specification in the ctenophore Mnemiopsis leidyi. Within Mnemiopsis leidyi, Lhx genes are expressed in overlapping domains within proposed neural cellular and sensory cell territories.  These data suggest that Lhx genes likely played a conserved role in the patterning of sensory cells in the ancestor of sponges and ctenophores, and may provide a link to the expression of Lhx orthologs in sponge larval photoreceptive cells.  Lhx genes were later co-opted into patterning more diversified complements of neural and non-neural cell types in later evolving animals.</description>
        <link>http://www.evodevojournal.com/content/3/1/2</link>
                <dc:creator>David Simmons</dc:creator>
                <dc:creator>Kevin Pang</dc:creator>
                <dc:creator>Mark Martindale</dc:creator>
                <dc:source>EvoDevo 2012, null:2</dc:source>
        <dc:date>2012-01-13T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-3-2</dc:identifier>
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        <prism:startingPage>2</prism:startingPage>
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        <item rdf:about="http://www.evodevojournal.com/content/3/1/3">
        <title>Development of the larval anterior neurogenic domains of Terebratalia transversa (Brachiopoda) provides insights into the diversification of larval apical organs and the spiralian nervous system</title>
        <description>Background:
Larval features such as the apical organ, apical ciliary tuft, and ciliated bands often complicate the evaluation of hypotheses regarding the origin of the adult bilaterian nervous system.  Understanding how neurogenic domains form within the bilaterian head and larval apical organ requires expression data from animals that exhibit aspects of both centralized and diffuse nervous systems at different life history stages.  Here, we describe the expression of eight neural-related genes during the larval development of the brachiopod, Terebratalia transversa.
Results:
Radially symmetric gastrulae broadly express Tt-Six3/6 and Tt-hbn in the animal cap ectoderm.  Tt-NK2.1 and Tt-otp are restricted to a central subset of these cells, and Tt-fez and Tt-FoxQ2 expression domains are already asymmetric at this stage.  As gastrulation proceeds, the spatial expression of these genes is split between two anterior ectodermal domains, a more dorsal region comprised of Tt-Six3/6, Tt-fez, Tt-FoxQ2, and Tt-otp expression domains, and an anterior ventral domain demarcated by Tt-hbn and Tt-NK2.1 expression.  More posteriorly, the latter domains are bordered by Tt-FoxG expression in the region of the transverse ciliated band.  Tt-synaptotagmin 1 is expressed throughout the anterior neural ectoderm.  All genes are expressed late into larval development.  The basiepithelial larval nervous system includes three neurogenic domains comprised of the more dorsal apical organ and a ventral cell cluster in the apical lobe as well as a mid-ventral band of neurons in the mantle lobe.  Tt-otp is the only gene expressed in numerous flask-shaped cells of the apical organ and in a subset of neurons in the mantle lobe.
Conclusions:
Our expression data for Tt-Six3/6, Tt-FoxQ2, and Tt-otp confirm some aspects of bilaterian-wide conservation of spatial partitioning within anterior neurogenic domains and also suggest a common origin for central otp-positive cell types within the larval apical organs of spiralians.  However, the field of sensory neurons within the larval apical organ of Terebratalia is broader and composed of more cells relative to those of other spiralian larvae.  These cellular differences are mirrored in the broader spatial and temporal expression patterns of Tt-FoxQ2 and Tt-otp.  Corresponding differences in the expression of Tt-hbn, Tt-NK2.1, and Tt-FoxG are also observed relative to their respective domains within the cerebral ganglia of spiralians.  Based on these data we argue that the anterior region of the bilaterian stem species included Six3/6, NK2.1, otp, hbn, fez, and FoxQ2 expression domains that were subsequently modified within larval and adult neural tissues of protostome and deuterostome animals.</description>
        <link>http://www.evodevojournal.com/content/3/1/3</link>
                <dc:creator>Scott Santagata</dc:creator>
                <dc:creator>Carlee Resh</dc:creator>
                <dc:creator>Andreas Hejnol</dc:creator>
                <dc:creator>Mark Martindale</dc:creator>
                <dc:creator>Yale Passamaneck</dc:creator>
                <dc:source>EvoDevo 2012, null:3</dc:source>
        <dc:date>2012-01-24T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-3-3</dc:identifier>
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        <prism:startingPage>3</prism:startingPage>
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        <item rdf:about="http://www.evodevojournal.com/content/2/1/6">
        <title>Ciliary photoreceptors in the cerebral eyes of a protostome larva </title>
        <description>Background:
Eyes in bilaterian metazoans have been described as being composed of either ciliary or rhabdomeric photoreceptors. Phylogenetic distribution, as well as distinct morphologies and characteristic deployment of different photopigments (ciliary vs. rhabdomeric opsins) and transduction pathways argue for the co-existence of both of these two photoreceptor types in the last common bilaterian ancestor. Both receptor types exist throughout the Bilateria, but only vertebrates are thought to use ciliary photoreceptors for directional light detection in cerebral eyes, while all other invertebrate bilaterians studied utilize rhabdomeric photoreceptors for this purpose. In protostomes, ciliary photoreceptors that express c-opsin have been described only from a non-visual deep-brain photoreceptor. Their homology with vertebrate rods and cones of the human eye has been hypothesized to represent a unique functional transition from non-visual to visual roles in the vertebrate lineage.
Results:
To test the hypothesis that protostome cerebral eyes employ exclusively rhabdomeric photoreceptors, we investigated the ultrastructure of the larval eyes in the brachiopod Terebratalia transversa. We show that these pigment-cup eyes consist of a lens cell and a shading pigment cell, both of which are putative photoreceptors, deploying a modified, enlarged cilium for light perception, and have axonal connections to the larval brain. Our investigation of the gene expression patterns of c-opsin, Pax6 and otx in these eyes confirms that the larval eye spots of brachiopods are cerebral eyes that deploy ciliary type photoreceptors for directional light detection. Interestingly, c-opsin is also expressed during early embryogenesis in all potential apical neural cells, becoming restricted to the anterior neuroectoderm, before expression is initiated in the photoreceptor cells of the eyes. Coincident with the expression of c-opsin in the presumptive neuroectoderm, we found that middle gastrula stage embryos display a positive photoresponse behavior, in the absence of a discrete shading pigment or axonal connections between cells.
Conclusions:
Our results indicate that the dichotomy in the deployment of ciliary and rhabdomeric photoreceptors for directional light detection is not as clear-cut as previously thought. Analyses of brachiopod larval eyes demonstrate that the utilization of c-opsin expressing ciliary photoreceptors in cerebral eyes is not limited to vertebrates. The presence of ciliary photoreceptor-based eyes in protostomes suggests that the transition between non-visual and visual functions of photoreceptors has been more evolutionarily labile than previously recognized, and that co-option of ciliary and rhabdomeric photoreceptor cell types for directional light detection has occurred multiple times during animal evolution. In addition, positive photoresponse behavior in gastrula stage embryos suggests that a discrete shading pigment is not requisite for directional photoreception in metazoans. Scanning photoreception of light intensities mediating cell-autonomous changes of ciliary movement may represent an ancient mechanism for regulating locomotory behavior, and is likely to have existed prior to the evolution of eye-mediated directional light detection employing axonal connections to effector cells and a discreet shading pigment.</description>
        <link>http://www.evodevojournal.com/content/2/1/6</link>
                <dc:creator>Yale Passamaneck</dc:creator>
                <dc:creator>Nina Furchheim</dc:creator>
                <dc:creator>Andreas Hejnol</dc:creator>
                <dc:creator>Mark Martindale</dc:creator>
                <dc:creator>Carsten Luter</dc:creator>
                <dc:source>EvoDevo 2011, null:6</dc:source>
        <dc:date>2011-03-01T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-2-6</dc:identifier>
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        <prism:startingPage>6</prism:startingPage>
        <prism:publicationDate>2011-03-01T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.evodevojournal.com/content/3/1/1">
        <title>Developmental plasticity and the evolution of parasitism in an unusual nematode, Parastrongyloides trichosuri.</title>
        <description>Background:
Parasitism is an important life history strategy in many metazoan taxa. This is particularly true of the Phylum Nematoda, in which parasitism has evolved independently at least nine times. The apparent ease with which parasitism has evolved amongst nematodes may, in part, be due to a feature of nematode development acting as a pre-adaptation for the transition from a free-living to a parasitic life history. One candidate pre-adaptive feature for evolution in terrestrial nematodes is the dauer larva, a developmentally arrested morph formed in response to environmental signals.
Results:
We investigated the role of dauer development in the nematode, Parastrongyloides trichosuri, which has retained a complete free-living life cycle in addition to a life cycle as a mammalian gastrointestinal parasite. We show that the developmental switch between these life histories is sensitive to the same environmental cues as dauer arrest in free-living nematodes, including sensitivity to a chemical cue produced by the free-living stages. Furthermore, we show that genetic variation for the sensitivity of the cue(s) exists in natural populations of P. trichosuri, such that we derived inbred lines that were largely insensitive to the cue and other lines that were supersensitive to the cue.
Conclusions:
For this parasitic clade, and perhaps more widely in the phylum, the evolution of parasitism co-opted the dauer switch of a free-living ancestor. This lends direct support to the hypothesis that the switch to developmental arrest in the dauer larva acted as a pre-adaptation for the evolution of parasitism, and suggests that the sensory transduction machinery downstream of the cue may have been similarly co-opted and modified.</description>
        <link>http://www.evodevojournal.com/content/3/1/1</link>
                <dc:creator>Susan Stasiuk</dc:creator>
                <dc:creator>Maxwell Scott</dc:creator>
                <dc:creator>Warwick Grant</dc:creator>
                <dc:source>EvoDevo 2012, null:1</dc:source>
        <dc:date>2012-01-03T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-3-1</dc:identifier>
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                <prism:publicationName>EvoDevo</prism:publicationName>
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        <prism:startingPage>1</prism:startingPage>
        <prism:publicationDate>2012-01-03T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.evodevojournal.com/content/2/1/11">
        <title>Breaking evolutionary and pleiotropic constraints in mammals. 
On sloths, manatees and homeotic mutations.
</title>
        <description>Background:
Mammals as a rule have seven cervical vertebrae, except for sloths and manatees. Bateson proposed that the change in the number of cervical vertebrae in sloths is due to homeotic transformations. A recent hypothesis proposes that the number of cervical vertebrae in sloths is unchanged and that instead the derived pattern is due to abnormal primaxial/abaxial patterning.
Results:
We test the detailed predictions derived from both hypotheses for the skeletal patterns in sloths and manatees for both hypotheses. We find strong support for Bateson&apos;s homeosis hypothesis. The observed vertebral and rib patterns cannot be explained by changes in primaxial/abaxial patterning. Vertebral patterns in sloths and manatees are similar to those in mice and humans with abnormal numbers of cervical vertebrae: incomplete and asymmetric homeotic transformations are common and associated with skeletal abnormalities. In sloths the homeotic vertebral shift involves a large part of the vertebral column. As such, similarity is greatest with mice mutant for genes upstream of Hox.
Conclusions:
We found no skeletal abnormalities in specimens of sister taxa with a normal number of cervical vertebrae. However, we always found such abnormalities in conspecifics with an abnormal number, as in many of the investigated dugongs. These findings strongly support the hypothesis that the evolutionary constraints on changes of the number of cervical vertebrae in mammals is due to deleterious pleitropic effects. We hypothesize that in sloths and manatees low metabolic and activity rates severely reduce the usual stabilizing selection, allowing the breaking of the pleiotropic constraints. This probably also applies to dugongs, although to a lesser extent.</description>
        <link>http://www.evodevojournal.com/content/2/1/11</link>
                <dc:creator>Irma Varela-Lasheras</dc:creator>
                <dc:creator>Alexander Bakker</dc:creator>
                <dc:creator>Steven van der Mije</dc:creator>
                <dc:creator>Johan Metz</dc:creator>
                <dc:creator>Joris van Alphen</dc:creator>
                <dc:creator>Frietson Galis</dc:creator>
                <dc:source>EvoDevo 2011, null:11</dc:source>
        <dc:date>2011-05-06T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-2-11</dc:identifier>
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                <prism:publicationName>EvoDevo</prism:publicationName>
        <prism:issn>2041-9139</prism:issn>
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        <prism:startingPage>11</prism:startingPage>
        <prism:publicationDate>2011-05-06T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.evodevojournal.com/content/2/1/15">
        <title>A study of neural-related microRNAs in the developing amphioxus </title>
        <description>Background:
MicroRNAs are small noncoding RNAs regulating expression of protein coding genes at post-transcriptional level and controlling several biological processes. At present microRNAs have been identified in various metazoans and seem also to be involved in brain development, neuronal differentiation and subtypes specification. An approach to better understand the role of microRNAs in animal gene expression is to determine temporal and tissue-specific expression patterns of microRNAs in different model organisms. Therefore, we have investigated the expression of six neural related microRNAs in amphioxus, an organism having an important phylogenetic position in terms of understanding the origin and evolution of chordates.
Results:
In amphioxus, all the microRNAs we examined are expressed in specific regions of the CNS, and some of them are correlated with specific cell types. In addition, miR-7, miR-137 and miR-184 are also expressed in endodermal and mesodermal tissues. Several potential targets expressed in the nervous system of amphioxus have been identified by computational prediction and some of them are coexpressed with one or more miRNAs.
Conclusion:
We identified six miRNAs that are expressed in the nervous system of amphioxus in a variety of patterns. miR-124 is found in both differentiating and mature neurons, miR-9 in differentiated neurons, miR-7, miR-137 and miR-184 in restricted CNS regions, and miR-183 in cells of sensory organs. Therefore, such amphioxus miRNAs may play important roles in regional patterning and/or specification of neuronal cell types.</description>
        <link>http://www.evodevojournal.com/content/2/1/15</link>
                <dc:creator>Simona Candiani</dc:creator>
                <dc:creator>Luca Moronti</dc:creator>
                <dc:creator>Davide De Pietri Tonelli</dc:creator>
                <dc:creator>Greta Garbarino</dc:creator>
                <dc:creator>Mario Pestarino</dc:creator>
                <dc:source>EvoDevo 2011, null:15</dc:source>
        <dc:date>2011-07-01T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-2-15</dc:identifier>
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                <prism:publicationName>EvoDevo</prism:publicationName>
        <prism:issn>2041-9139</prism:issn>
        <prism:volume>${item.volume}</prism:volume>
        <prism:startingPage>15</prism:startingPage>
        <prism:publicationDate>2011-07-01T00:00:00Z</prism:publicationDate>
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        <item rdf:about="http://www.evodevojournal.com/content/2/1/1">
        <title>Ancestral and derived attributes of the dlx gene repertoire, cluster structure and expression patterns in an African cichlid fish </title>
        <description>Background:
Cichlid fishes have undergone rapid, expansive evolutionary radiations that are manifested in the diversification of their trophic morphologies, tooth patterning and coloration. Understanding the molecular mechanisms that underlie the cichlids&apos; unique patterns of evolution requires a thorough examination of genes that pattern the neural crest, from which these diverse phenotypes are derived. Among those genes, the homeobox-containing Dlx gene family is of particular interest since it is involved in the patterning of the brain, jaws and teeth.
Results:
In this study, we characterized the dlx genes of an African cichlid fish, Astatotilapia burtoni, to provide a baseline to later allow cross-species comparison within Cichlidae. We identified seven dlx paralogs (dlx1a, -2a, -4a, -3b, -4b, -5a and -6a), whose orthologies were validated with molecular phylogenetic trees. The intergenic regions of three dlx gene clusters (dlx1a-2a, dlx3b-4b, and dlx5a-6a) were amplified with long PCR. Intensive cross-species comparison revealed a number of conserved non-coding elements (CNEs) that are shared with other percomorph fishes. This analysis highlighted additional lineage-specific gains/losses of CNEs in different teleost fish lineages and a novel CNE that had previously not been identified. Our gene expression analyses revealed overlapping but distinct expression of dlx orthologs in the developing brain and pharyngeal arches. Notably, four of the seven A. burtoni dlx genes, dlx2a, dlx3b, dlx4a and dlx5a, were expressed in the developing pharyngeal teeth.
Conclusion:
This comparative study of the dlx genes of A. burtoni has deepened our knowledge of the diversity of the Dlx gene family, in terms of gene repertoire, expression patterns and non-coding elements. We have identified possible cichlid lineage-specific changes, including losses of a subset of dlx expression domains in the pharyngeal teeth, which will be the targets of future functional studies.</description>
        <link>http://www.evodevojournal.com/content/2/1/1</link>
                <dc:creator>Adina Renz</dc:creator>
                <dc:creator>Helen Gunter</dc:creator>
                <dc:creator>Jan Fischer</dc:creator>
                <dc:creator>Huan Qiu</dc:creator>
                <dc:creator>Axel Meyer</dc:creator>
                <dc:creator>Shigehiro Kuraku</dc:creator>
                <dc:source>EvoDevo 2011, null:1</dc:source>
        <dc:date>2011-01-04T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-2-1</dc:identifier>
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        <prism:startingPage>1</prism:startingPage>
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        <item rdf:about="http://www.evodevojournal.com/content/2/1/13">
        <title>Gene expression in bryozoan larvae suggest a fundamental importance of pre-patterned blastemic cells in the bryozoan life-cycle</title>
        <description>Background:
Bryozoa is a clade of aquatic protostomes. The bryozoan life cycle typically comprises a larval stage, which metamorphoses into a sessile adult that proliferates by asexual budding to form colonies. The homology of bryozoan larvae with other protostome larvae is enigmatic. Bryozoan larvae exhibit blastemic tissues that contribute to build the adult during morphogenesis. However, it remains unclear if the cells of these tissues are pre-determined according to their future fate or if the cells are undifferentiated, pluripotent stem cells. Gene expression studies can help to identify molecular patterning of larval and adult tissues and enlighten the evolution of bryozoan life cycle stages.
Results:
We investigated the spatial expression of 13 developmental genes in the larval stage of the gymnolaemate bryozoan Bugula neritina. We found most genes expressed in discrete regions in larval blastemic tissues that form definitive components of the adult body plan. Only two of the 13 genes, BnTropomyosin and BnFoxAB, were exclusively expressed in larval tissues that are discarded during metamorphosis.
Conclusions:
Our results suggest that the larval blastemas in Bugula are pre-patterned according to their future fate in the adult. The gene expression patterns indicate that some of the bryozoan blastemas can be interpreted to correspond to homologous adult tissues of other animals. This study challenges an earlier proposed view that metazoan larvae share homologous undifferentiated &quot;set-aside cells&quot;, and instead points to an independent origin of the bryozoan larval stage with respect to other lophotrochozoans.</description>
        <link>http://www.evodevojournal.com/content/2/1/13</link>
                <dc:creator>Judith Fuchs</dc:creator>
                <dc:creator>Mark Martindale</dc:creator>
                <dc:creator>Andreas Hejnol</dc:creator>
                <dc:source>EvoDevo 2011, null:13</dc:source>
        <dc:date>2011-06-06T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-2-13</dc:identifier>
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                <prism:publicationName>EvoDevo</prism:publicationName>
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        <prism:startingPage>13</prism:startingPage>
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        <item rdf:about="http://www.evodevojournal.com/content/2/1/21">
        <title>Heterochrony and developmental modularity of cranial osteogenesis in lipotyphlan mammals</title>
        <description>Background:
Here we provide the most comprehensive study to date on the cranial ossification sequence in Lipotyphla, the group which includes shrews, moles and hedgehogs. This unique group, which encapsulates diverse ecological modes, such as terrestrial, subterranean, and aquatic lifestyles, is used to examine the evolutionary lability of cranial osteogenesis and to investigate the modularity of development.
Results:
An acceleration of developmental timing of the vomeronasal complex has occurred in the common ancestor of moles. However, ossification of the nasal bone has shifted late in the more terrestrial shrew mole. Among the lipotyphlans, sequence heterochrony shows no significant association with modules derived from developmental origins (that is, neural crest cells vs. mesoderm derived parts) or with those derived from ossification modes (that is, dermal vs. endochondral ossification).
Conclusions:
The drastic acceleration of vomeronasal development in moles is most likely coupled with the increased importance of the rostrum for digging and its use as a specialized tactile surface, both fossorial adaptations. The late development of the nasal in shrew moles, a condition also displayed by hedgehogs and shrews, is suggested to be the result of an ecological reversal to terrestrial lifestyle and reduced functional importance of the rostrum. As an overall pattern in lipotyphlans, our results reject the hypothesis that ossification sequence heterochrony occurs in modular fashion when considering the developmental patterns of the skull. We suggest that shifts in the cranial ossification sequence are not evolutionarily constrained by developmental origins or mode of ossification.</description>
        <link>http://www.evodevojournal.com/content/2/1/21</link>
                <dc:creator>Daisuke Koyabu</dc:creator>
                <dc:creator>Hideki Endo</dc:creator>
                <dc:creator>Christian Mitgutsch</dc:creator>
                <dc:creator>Gen Suwa</dc:creator>
                <dc:creator>Kenneth Catania</dc:creator>
                <dc:creator>Christoph Zollikofer</dc:creator>
                <dc:creator>Sen-ichi Oda</dc:creator>
                <dc:creator>Kazuhiko Koyasu</dc:creator>
                <dc:creator>Motokazu Ando</dc:creator>
                <dc:creator>Marcelo Sanchez-Villagra</dc:creator>
                <dc:source>EvoDevo 2011, null:21</dc:source>
        <dc:date>2011-11-01T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-2-21</dc:identifier>
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                <prism:publicationName>EvoDevo</prism:publicationName>
        <prism:issn>2041-9139</prism:issn>
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        <prism:startingPage>21</prism:startingPage>
        <prism:publicationDate>2011-11-01T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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        <title>Expression of FoxA and GATA transcription factors correlates with regionalized gut development in two lophotrochozoan marine worms: Chaetopterus (Annelida) and Themiste lageniformis (Sipuncula)</title>
        <description>Background:
A through gut is present in almost all metazoans, and most likely represents an ancient innovation that enabled bilaterian animals to exploit a wide range of habitats. Molecular developmental studies indicate that Fox and GATA regulatory genes specify tissue regions along the gut tube in a broad diversity of taxa, although little is known about gut regionalization within the Lophotrochozoa. In this study, we isolated FoxA and GATA456 orthologs and used whole mount in situ hybridization during larval gut formation in two marine worms: the segmented, polychaete annelid Chaetopterus, which develops a planktotrophic larva with a tripartite gut, and the non-segmented sipunculan Themiste lageniformis, which develops a lecithotrophic larva with a U-shaped gut.
Results:
FoxA and GATA456 transcripts are predominantly restricted to gut tissue, and together show regional expression spanning most of the alimentary canal in each of these lophotrochozoans, although neither FoxA nor GATA456 is expressed in the posterior intestine of Chaetopterus. In both species, FoxA is expressed at the blastula stage, transiently in presumptive endoderm before formation of a definitive gut tube, and throughout early larval development in discrete foregut and hindgut domains. GATA456 genes are expressed during endoderm formation, and in endoderm and mesoderm associated with the midgut in each species. Several species-specific differences were detected, including an overlap of FoxA and GATA456 expression in the intestinal system of Themiste, which is instead complimentary in Chaetopterus. Other differences include additional discrete expression domains of FoxA in ectodermal trunk cells in Themiste but not Chaetopterus, and expression of GATA456 in anterior ectoderm and midgut cells unique to Chaetopterus.
Conclusions:
This study of gene expression in a sipunculan contributes new comparative developmental insights from lophotrochozoans, and shows that FoxA and GATA456 transcription factors are part of an ancient patterning mechanism that was deployed during early evolution of the metazoan through gut. The common utilization of FoxA and GATA456 throughout gut formation by species with contrasting life history modes indicates that both genes are core components of a gut-specific gene regulatory network in spiralians. Despite a highly conserved pattern of early development, and probably similar ontogenic origins of gut tissue, there are molecular differences in gut regionalization between lophotrochozoan species.</description>
        <link>http://www.evodevojournal.com/content/1/1/2</link>
                <dc:creator>Michael Boyle</dc:creator>
                <dc:creator>Elaine Seaver</dc:creator>
                <dc:source>EvoDevo 2010, null:2</dc:source>
        <dc:date>2010-07-05T00:00:00Z</dc:date>
        <dc:identifier>doi:10.1186/2041-9139-1-2</dc:identifier>
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                <prism:publicationName>EvoDevo</prism:publicationName>
        <prism:issn>2041-9139</prism:issn>
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        <prism:startingPage>2</prism:startingPage>
        <prism:publicationDate>2010-07-05T00:00:00Z</prism:publicationDate>
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                <cc:license rdf:resource="http://creativecommons.org/licenses/by/2.0/" />
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