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Body Plan (body + plan)
Kinds of Body Plan Selected AbstractsDiffering strategies for forming the arthropod body plan: Lessons from Dpp, Sog and Delta in the fly Drosophila and spider AchaearaneaDEVELOPMENT GROWTH & DIFFERENTIATION, Issue 4 2008Hiroki Oda In the insect Drosophila embryo, establishment of maternal transcription factor gradients, rather than cell,cell interactions, is fundamental to patterning the embryonic axes. In contrast, in the chelicerate spider embryo, cell,cell interactions are thought to play a crucial role in the development of the embryonic axes. A grafting experiment by Holm using spider eggs resulted in duplication of the embryonic axes, similar to the Spemann's organizer experiment using amphibian eggs. Recent work using the house spider Achaearanea tepidariorum has demonstrated that the homologs of decapentaplegic (dpp), short gastrulation (sog) and Delta, which encode a bone morphogenetic protein (BMP)-type ligand, its antagonist and a Notch ligand, respectively, are required in distinct aspects of axis formation. Achaearanea Dpp appears to function as a symmetry-breaking signal, which could account for Holm's results to some extent. Experimental findings concerning Achaearanea sog and Delta have highlighted differences in the mechanisms underlying ventral and posterior development between Drosophila and Achaearanea. Achaearanea ventral patterning essentially depends on sog function, in contrast to the Drosophila patterning mechanism, which is based on the nuclear gradient of Dorsal. Achaearanea posterior (or opisthosomal) patterning relies on the function of the caudal lobe, which develops from cells surrounding the blastopore through progressive activation of Delta-Notch signaling. In this review, we describe the differing strategies for forming the arthropod body plan in the fly and spider, and provide a perspective towards understanding the relationship between the arthropod and vertebrate body plans. [source] Endoderm development in vertebrates: fate mapping, induction and regional specificationDEVELOPMENT GROWTH & DIFFERENTIATION, Issue 6 2005Kimiko Fukuda The formation of the vertebrate body plan begins with the differentiation of cells into three germ layers: ectoderm, mesoderm and endoderm. Cells in the endoderm give rise to the epithelial lining of the digestive tract, associated glands and respiratory system. One of the fundamental problems in developmental biology is to elucidate how these three primary germ layers are established from the homologous population of cells in the early blastomere. To address this question, ectoderm and mesoderm development have been extensively analyzed, but study of endoderm development has only begun relatively recently. In this review, we focus on the ,where', ,when' and ,how' of endoderm development in four vertebrate model organisms: the zebrafish, Xenopus, chick and mouse. We discuss the classical fate mapping of the endoderm and the more recent progress in characterizing its induction, segregation and regional specification. [source] Activin/nodal signaling modulates XPAPC expression during Xenopus gastrulationDEVELOPMENTAL DYNAMICS, Issue 3 2008Xin Lou Abstract Gastrulation is the first obligatory morphogenesis during vertebrate development, by which the body plan is established. Nodal signaling is a key player in many developmental processes, including gastrulation. XPAPC has been found to exert its biological function through modifying the adhesion property of cells and interacting with other several important molecules in embryos. In this report, we show that nodal signaling is necessary and sufficient for XPAPC expression during Xenopus gastrulation. Furthermore, we isolated 4.8 kb upstream DNA sequence of Xenopus XPAPC, and proved that this 4.8-kb genomic contig is sufficient to recapitulate the expression pattern of XPAPC from gastrula to tail bud stage. Transgene and ChIP assays indicate that Activin/nodal signaling participates in regulation of XPAPC expression through a Smad binding element within the XPAPC promoter. Concomitant investigation suggests that the canonical Wnt pathway-activated XPAPC expression requires nodal signaling. Developmental Dynamics 237:683,691, 2008. © 2008 Wiley-Liss, Inc. [source] Evolutionary conservation and divergence of the segmentation process in arthropodsDEVELOPMENTAL DYNAMICS, Issue 6 2007Wim G. M. Damen Abstract A fundamental characteristic of the arthropod body plan is its organization in metameric units along the anterior,posterior axis. The segmental organization is laid down during early embryogenesis. Our view on arthropod segmentation is still strongly influenced by the huge amount of data available from the fruit fly Drosophila melanogaster (the Drosophila paradigm). However, the simultaneous formation of the segments in Drosophila is a derived mode of segmentation. Successive terminal addition of segments from a posteriorly localized presegmental zone is the ancestral mode of arthropod segmentation. This review focuses on the evolutionary conservation and divergence of the genetic mechanisms of segmentation within arthropods. The more downstream levels of the segmentation gene network (e.g., segment polarity genes) appear to be more conserved than the more upstream levels (gap genes, Notch/Delta signaling). Surprisingly, the basally branched arthropod groups also show similarities to mechanisms used in vertebrate somitogenesis. Furthermore, it has become clear that the activation of pair rule gene orthologs is a key step in the segmentation of all arthropods. Important findings of conserved and diverged aspects of segmentation from the last few years now allow us to draw an evolutionary scenario on how the mechanisms of segmentation could have evolved and led to the present mechanisms seen in various insect groups including dipterans like Drosophila. Developmental Dynamics 236:1379,1391, 2007. © 2007 Wiley-Liss, Inc. [source] The emergence of the chordate body plan: some puzzles and problemsACTA ZOOLOGICA, Issue 1 2010Thurston C. Lacalli Abstract Lacalli, T.C. 2010. The emergence of the chordate body plan: some puzzles and problems. ,Acta Zoologica (Stockholm) 91: 4,10 Rather than being sessile filter feeders, ancestral chordates are now thought to have evolved from more active benthic animals, possibly hemichordate-like, that took to swimming, to generate something resembling modern amphioxus. This general picture conceals a number of specific problems that underline how little we understand the transition in detail. I will address three. First, and closest to resolution is the issue of dorsoventral inversion, which has implications for understanding how an internalized brain evolved. This is because the mouth, dorsal after inversion, has first to be moved out of the way. Its migration down the left side of the head during amphioxus development may be a recapitulation of this event. Two other puzzles, both further from resolution are: (1) the significance, if any, of the neurenteric canal, which may be telling us something important about the true nature of deuterostomy, specifically whether hemichordates and echinoderms are deuterostomes for a different reason than chordates, and (2) whether the functional digestive tract of chordates is a secondary replacement of an earlier structure whose fate remains unexplained. Resolving these latter two issues will require a better understanding of molecular level events during development in protochordates and their immediate invertebrate relatives. [source] From genomes to morphology: a view from amphioxusACTA ZOOLOGICA, Issue 1 2010Peter W. H. Holland Abstract Holland, P.W.H. 2010. From genomes to morphology: a view from amphioxus. ,Acta Zoologica (Stockholm) 91: 81,86 As complete genome sequences are determined from an ever-increasing number of animal species, new opportunities are arising for comparative biology. For zoologists interested in the evolution of shape and form, however, there is a problem. The link between genome sequence and morphology is not direct and is obfuscated by complex and evolving genetic pathways, even when conserved regulatory genes are considered. Nonetheless, a large-scale comparison of genome sequences between extant chordates reveals an intriguing parallel between genotypic and phenotypic evolution. Tunicates have highly altered genomes, with loss of ancestral genes and shuffled genetic arrangements, while vertebrate genomes are also derived through gene loss and genome duplication. The recently sequenced amphioxus genome, in contrast, reveals much greater stasis on the cephalochordate lineage, in parallel to a less derived body plan. The opportunities and challenges for relating genome evolution to morphological evolution are discussed. [source] Six major steps in animal evolution: are we derived sponge larvae?EVOLUTION AND DEVELOPMENT, Issue 2 2008Claus Nielsen SUMMARY A review of the old and new literature on animal morphology/embryology and molecular studies has led me to the following scenario for the early evolution of the metazoans. The metazoan ancestor, "choanoblastaea," was a pelagic sphere consisting of choanocytes. The evolution of multicellularity enabled division of labor between cells, and an "advanced choanoblastaea" consisted of choanocytes and nonfeeding cells. Polarity became established, and an adult, sessile stage developed. Choanocytes of the upper side became arranged in a groove with the cilia pumping water along the groove. Cells overarched the groove so that a choanocyte chamber was formed, establishing the body plan of an adult sponge; the pelagic larval stage was retained but became lecithotrophic. The sponges radiated into monophyletic Silicea, Calcarea, and Homoscleromorpha. Homoscleromorph larvae show cell layers resembling true, sealed epithelia. A homoscleromorph-like larva developed an archenteron, and the sealed epithelium made extracellular digestion possible in this isolated space. This larva became sexually mature, and the adult sponge-stage was abandoned in an extreme progenesis. This eumetazoan ancestor, "gastraea," corresponds to Haeckel's gastraea. Trichoplax represents this stage, but with the blastopore spread out so that the endoderm has become the underside of the creeping animal. Another lineage developed a nervous system; this "neurogastraea" is the ancestor of the Neuralia. Cnidarians have retained this organization, whereas the Triploblastica (Ctenophora+Bilateria), have developed the mesoderm. The bilaterians developed bilaterality in a primitive form in the Acoelomorpha and in an advanced form with tubular gut and long Hox cluster in the Eubilateria (Protostomia+Deuterostomia). It is indicated that the major evolutionary steps are the result of suites of existing genes becoming co-opted into new networks that specify new structures. The evolution of the eumetazoan ancestor from a progenetic homoscleromorph larva implies that we, as well as all the other eumetazoans, are derived sponge larvae. [source] Is retinoic acid genetic machinery a chordate innovation?EVOLUTION AND DEVELOPMENT, Issue 5 2006Cristian Cañestro SUMMARY Development of many chordate features depends on retinoic acid (RA). Because the action of RA during development seems to be restricted to chordates, it had been previously proposed that the "invention" of RA genetic machinery, including RA-binding nuclear hormone receptors (Rars), and the RA-synthesizing and RA-degrading enzymes Aldh1a (Raldh) and Cyp26, respectively, was an important step for the origin of developmental mechanisms leading to the chordate body plan. We tested this hypothesis by conducting an exhaustive survey of the RA machinery in genomic databases for twelve deuterostomes. We reconstructed the evolution of these genes in deuterostomes and showed for the first time that RA genetic machinery,that is Aldh1a, Cyp26, and Rar orthologs,is present in nonchordate deuterostomes. This finding implies that RA genetic machinery was already present during early deuterostome evolution, and therefore, is not a chordate innovation. This new evolutionary viewpoint argues against the hypothesis that the acquisition of gene families underlying RA metabolism and signaling was a key event for the origin of chordates. We propose a new hypothesis in which lineage-specific duplication and loss of RA machinery genes could be related to the morphological radiation of deuterostomes. [source] Transcriptional readthrough of Hox genes Ubx and Antp and their divergent post-transcriptional control during crustacean evolutionEVOLUTION AND DEVELOPMENT, Issue 5 2006Yasuhiro Shiga SUMMARY Hox genes are in principle tandemly arranged in an order colinear with their order of expression along the anterior,posterior axis. Combinations of Hox proteins encode information that specifies the unique characteristics of axial regions in the metazoan body plan. The independent regulation of Hox genes achieved by differential promoter activity is essential for the expression of Hox proteins in distinct territories and thereby creating a full repertoire of Hox codes. Here we report the abundant expression of transcriptional readthrough products of two adjacent Hox genes, Ubx, and Antp, in five crustacean species of Branchiopoda and Malacostraca. Bicistronic mRNA places Antp under the control of the Ubx promoter, which is active in the posterior segments of two branchiopodans Daphnia and Artemia, and would normally reduce the complexity of Hox codes if translated. This does not occur, however, as the translational capability of the bicistronic mRNA is limited. In Daphnia, bicistronic Ubx/Antp mRNA produced no significant level of either UBX or ANTP. In Artemia, on the other hand, the bicistronic mRNA produced only UBX, and replaced the role of monocistronic Ubx mRNA. In this way, multiple post-transcriptional control mechanisms in two extant branchiopodans can be seen as preventing the potentially deleterious consequences of Hox gene fusion. [source] Genomic annotation and transcriptome analysis of the zebrafish (Danio rerio) hox complex with description of a novel member, hoxb13aEVOLUTION AND DEVELOPMENT, Issue 5 2005M. Corredor-Adámez Summary The zebrafish (Danio rerio) is an important model in evolutionary developmental biology, and its study is being revolutionized by the zebrafish genome project. Sequencing is at an advanced stage, but annotation is largely the result of in silico analyses. We have performed genomic annotation, comparative genomics, and transcriptional analysis using microarrays of the hox homeobox-containing transcription factors. These genes have important roles in specifying the body plan. Candidate sequences were located in version Zv4 of the Ensembl genome database by TBLASTN searching with Danio and other vertebrate published Hox protein sequences. Homologies were confirmed by alignment with reference sequences, and by the relative position of genes along each cluster. RT-PCR using adult Tübingen cDNA was used to confirm annotations, to check the genomic sequence and to confirm expression in vivo. Our RT-PCR and microarray data show that all 49 hox genes are expressed in adult zebrafish. Significant expression for all known hox genes could be detected in our microarray analysis. We also find significant expression of hox8 paralogs and hoxb7a in the anti-sense direction. A novel gene, D. rerio hoxb13a, was identified, and a preliminary characterization by in situ hybridization showed expression at 24 hpf at the tip of the developing tail. We are currently characterizing this gene at the functional level. We argue that the oligo design for microarrays can be greatly enhanced by the availability of genomic sequences. [source] Vestigial prototroch in a basal nemertean, Carinoma tremaphoros (Nemertea; Palaeonemertea)EVOLUTION AND DEVELOPMENT, Issue 4 2004S. A. Maslakova Summary Nemerteans have been alleged to belong to a protostome clade called the Trochozoa that includes mollusks, annelids, sipunculids, echiurids, and kamptozoans and is characterized by, among other things, the trochophore larva. The trochophore possesses a prototroch, a preoral belt of specialized ciliary cells, derived from the trochoblast cells. Nemertea is the only trochozoan phylum for which presence of the trochophore larva possessing a prototroch had never been shown. However, so little is known about nemertean larval development that comparing it with development of other trochozoans is difficult. Development in the nemertean clade Pilidiophora is via a highly specialized planktonic larva, the pilidium, and most of the larval body is lost during a drastic metamorphosis. Other nemerteans (hoplonemerteans and palaeonemerteans) lack a pilidium, and their development is direct, forming either an encapsulated or planktonic "planuliform" larva, producing a juvenile without a dramatic change in body plan. We show that early in the development of a member of a basal nemertean assemblage, the palaeonemertean Carinoma tremaphoros, large squamous cells cover the entire larval surface except for the apical and posterior regions. Although apical and posterior cells continue to divide, the large surface cells cleavage arrest and form a contorted preoral belt. Based on its position, cell lineage, and fate, we suggest that this belt corresponds to the prototroch of other trochozoans. Lack of differential ciliation obscures the presence of the prototroch in Carinoma, but differentiation of the trochoblasts is clearly manifested in their permanent cleavage arrest and ultimate degenerative fate. Our results allow a meaningful comparison between the development of nemerteans and other trochozoans. We review previous hypotheses of the evolution of nemertean development and suggest that a trochophore-like larva is plesiomorphic for nemerteans while a pilidium type of development with drastic metamorphosis is derived. [source] Conservation and variation in Ubx expression among cheliceratesEVOLUTION AND DEVELOPMENT, Issue 6 2001Aleksandar Popadi SUMMARY Chelicerates are an ancient arthropod group with a distinct body plan composed of an anterior (prosoma) and a posterior portion (opisthosoma). The expression of the Hox gene Ultrabithorax (Ubx) has been examined in a single representative of the chelicerates, the spider Cupiennius salei. In spiders, Ubx expression starts in the second opisthosomal segment (O2). Because the first opisthosomal segment (O1) in spiders is greatly reduced relative to other chelicerates, we hypothesized that the observed Ubx expression pattern might be secondarily modified. Shifts in the anterior boundary of the expression of Ubx have been correlated with functional shifts in morphology within malacostracan crustaceans. Thus, the boundary of Ubx expression between chelicerates with different morphologies in their anterior opisthosoma could also be variable. To test this prediction, we examined the expression patterns of Ubx and abdominal-A (collectively referred to as UbdA) in two basal chelicerate lineages, scorpions and xiphosurans (horseshoe crabs), which exhibit variation in the morphology of their anterior opisthosoma. In the scorpion Paruroctonus mesaensis, the anterior border of early expression of UbdA is in a few cells in the medial, posterior region of the O2 segment, with a predominant expression in O3 and posterior. Expression later spreads to encompass the whole O2 segment and a ventral, posterior portion of the O1 segment. In the xiphosuran Limulus polyphemus, early expression of UbdA has an anterior boundary in the segment. Later in development, the anterior boundary moves forward one segment to the chilarial (O1) segment. Thus, the earliest expression boundary of UbdA lies within the second opisthosomal segment in all the chelicerates examined. These results suggest that rather than being derived, the spider UbdA expression in O2 likely reflects the ancestral expression boundary. Changes in the morphology of the first opisthosomal segment are either not associated with changes in UbdA expression or correlate with late developmental changes in UbdA expression. [source] Evolution of the echinoderm Hox gene clusterEVOLUTION AND DEVELOPMENT, Issue 5 2001Suzanne Long SUMMARY Extant echinoderms are members of an ancient and highly derived deuterostome phylum. The composition and arrangement of their Hox gene clusters are consequently of interest not only from the perspective of evolution of development, but also in terms of metazoan phylogeny and body plan evolution. Over the last decade numerous workers have reported partial Hox gene sequences from a variety of echinoderms. In this paper we used a combined methods approach to analyze phylogenetic relationships between 68 echinoderm Hox homeodomain fragments, from species of five extant classes,two asteroids, one crinoid, one ophiuroid, one holothuroid, and three echinoids. This analysis strengthens Mito and Endo's (2000) proposition that the ancestral echinoderm's Hox gene cluster contained at least eleven genes, including at least four posterior paralogous group genes. However, representatives of all paralogous groups are not known from all echinoderm classes. In particular, these data suggest that echinoids may have lost a posterior group Hox gene subsequent to the divergence of the echinoderm classes. Evolution of the highly derived echinoderm body plan may have been accompanied by class-specific duplication, diversification and loss of Hox genes. [source] Evolution and development of the primate limb skeletonEVOLUTIONARY ANTHROPOLOGY, Issue 3 2002Chi-Hua Chiu Abstract The order Primates is composed of many closely related lineages, each having a relatively well established phylogeny supported by both the fossil record and molecular data.1 Primate evolution is characterized by a series of adaptive radiations beginning early in the Cenozoic era. Studies of these radiations have uncovered two major trends. One is that substantial amounts of morphological diversity have been produced over short periods of evolutionary time.2 The other is that consistent and repeated patterns (variational tendencies3) are detected. Taxa within clades, such as the strepsirrhines of Madagascar and the platyrrhines of the Neotropics, have diversified in body size, substrate preference, and diet.2, 4,6 The diversification of adaptive strategies within such clades is accompanied by repeated patterns of change in cheiridial proportions7, 8 (Fig. 1) and tooth-cusp morphology.9 There are obvious adaptive, natural-selection based explanations for these patterns. The hands and feet are in direct contact with a substrate, so their form would be expected to reflect substrate preference, whereas tooth shape is related directly to the functional demands of masticating foods having different mechanical properties. What remains unclear, however, is the role of developmental and genetic processes that underlie the evolutionary diversity of the primate body plan. Are variational tendencies a signature of constraints in developmental pathways? What is the genetic basis for similar morphological transformations among closely related species? These are a sampling of the types of questions we believe can be addressed by future research integrating evidence from paleontology, comparative morphology, and developmental genetics. [source] oleed, a medaka Polycomb group gene, regulates ciliogenesis and left,right patterningGENES TO CELLS, Issue 12 2009Daisuke Arai Left-right (LR) patterning is an essential part of the animal body plan. Primary cilia are known to play a pivotal role in this process. In humans, genetic disorders of ciliogenesis cause serious congenital diseases. A comprehensive mechanism that regulates ciliogenesis has not been proposed so far. Here, we show that EED, a core member of the Polycomb group (PcG) genes and a presumed player in many epigenetic processes, is required for ciliogenesis and subsequent LR patterning in the medaka fish, Oryzias latipes. Moderate knockdown of oleed, a medaka homolog of EED, preferentially caused situs inversus. In the affected embryo, the cilia in Kupffer's vesicle showed various defects in their structure, position and motility. Furthermore, we demonstrated that oleed maintains the expression of Noto, which, in mice, regulates ciliogenesis and LR patterning. This study provides the first evidence for the involvement of epigenetic plasticity in LR patterning through ciliogenesis. [source] Generation of a Snail1 (Snai1) conditional null alleleGENESIS: THE JOURNAL OF GENETICS AND DEVELOPMENT, Issue 1 2006Stephen A. Murray Abstract Members of the Snail gene superfamily, which encode zinc finger transcriptional repressors, play critical roles in the establishment of the vertebrate body plan. The Snail1 (Snai1) gene promotes epithelial,mesenchymal transitions during development and disease progression, and Snai1 null mouse embryos exhibit defects in gastrulation. However, the early embryonic lethality of Snai1 null embryos precludes the study of Snai1 function in other developmental contexts or diseases. To overcome this restriction, we generated a Snai1 conditional null allele by flanking the promoter and first two exons of the Snai1 gene with loxP sites. Cre-mediated deletion of the Snai1flox allele generates the Snai1del2 allele, which behaves genetically as a Snai1 null allele. This conditional null allele will enable investigation of Snai1 function in a variety of developmental and pathological contexts. genesis 44:7,11, 2006. © 2006 Wiley-Liss, Inc. [source] The pre-radial history of echinodermsGEOLOGICAL JOURNAL, Issue 3 2005Andrew B. Smith Abstract Gene sequence data now identify a robust phylogeny of deuterostomes and provide a framework within which the evolution of echinoderms can be interpreted. The topology of the molecular tree makes a number of important predictions about the morphological characters of the earliest echinoderm at its split from hemichordates: it possessed gill slits (but not a notochord), had a bilaterally symmetrical body plan in the adult and, less certainly, underwent torsion during development. Carpoids, a highly contentious group of extinct deuterostomes with a plated calcite skeleton that have variously been interpreted as stem- and crown-group chordates, stem-group echinoderms or stem- and crown-group echinoderms, display many of these basal characters and provide critical evidence for how the latest common ancestor of hemichordates and echinoderms was transformed into a pentaradiate crown-group echinoderm. Cinctans have a large atrial opening in addition to mouth and anus, and are interpreted as pharyngeal basket feeders. The paired grooves associated with the mouth indicate the presence of a hydrovascular system, but not necessarily one built along the echinoderm plan (that is, derived from just the left hydrocoel). Stylophorans have a bilateral body plan that is externally masked by torsion and possess gills, either unpaired and external, or paired and internal, opening into an atrial cavity. Their bilateral appendage is a locomotory organ, not an ambulacrum, and there is no evidence that stylophorans ever possessed a well-developed hydrovascular system homologous to the water vascular system of echinoderms and the tentacles of pterobranch hemichordates. Solutes are the most crownward, having a true echinodermal ambulacral system with a single hydropore and no pharyngeal gill openings. Copyright © 2005 John Wiley & Sons, Ltd. [source] Comparison of developmental trajectories in the starlet sea anemone Nematostella vectensis: embryogenesis, regeneration, and two forms of asexual fissionINVERTEBRATE BIOLOGY, Issue 2 2007Adam M. Reitzel Abstract. The starlet sea anemone, Nematostella vectensis, is a small burrowing estuarine animal, native to the Atlantic coast of North America. In recent years, this anemone has emerged as a model system in cnidarian developmental biology. Molecular studies of embryology and larval development in N. vectensis have provided important insights into the evolution of key metazoan traits. However, the adult body plan of N. vectensis may arise via four distinct developmental trajectories: (1) embryogenesis following sexual reproduction, (2) asexual reproduction via physal pinching, (3) asexual reproduction via polarity reversal, and (4) regeneration following bisection through the body column. Here, we compare the ontogenetic sequences underlying alternate developmental trajectories. Additionally, we describe the predictable generation of anomalous phenotypes that can occur following localized injuries to the body column. These studies suggest testable hypotheses on the molecular mechanisms underlying alternate developmental trajectories, and they provoke new questions about the evolution of novel developmental trajectories and their initiation via environmental cues. [source] Regeneration as an evolutionary variableJOURNAL OF ANATOMY, Issue 1-2 2001JEREMY P. BROCKES abstract Regeneration poses a distinctive set of problems for evolutionary biologists, but there has been little substantive progress since these issues were clearly outlined in the monograph of T. H. Morgan (1901). The champions at regeneration among vertebrates are the urodele amphibians such as the newt, and we tend to regard urodele regeneration as an exceptional attribute. The ability to regenerate large sections of the body plan is widespread in metazoan phylogeny, although it is not universal. It is striking that in phylogenetic contexts where regeneration occurs, closely related species are observed which do not possess this ability. It is a challenge to reconcile such variation between species with a conventional selective interpretation of regeneration. The critical hypothesis from phylogenetic analysis is that regeneration is a basic, primordial attribute of metazoans rather than a mechanism which has evolved independently in a variety of contexts. In order to explain its absence in closely related species, it is postulated to be lost secondarily for reasons which are not understood. Our approach to this question is to compare a differentiated newt cell with its mammalian counterpart in respect of the plasticity of differentiation. [source] Embryonic development of Galloisiana yuasai Asahina, with special reference to external morphology (Insecta: Grylloblattodea)JOURNAL OF MORPHOLOGY, Issue 2 2005Toshiki Uchifune Abstract The embryogenesis of Grylloblattodea, one of the most primitive of the polyneopteran orders, is described using Galloisiana yuasai with special reference to external morphology. The egg membranes are characterized by an endochorion crossed by numerous vertical aeropyles and a fairly thin vitelline membrane, features shared by Mantophasmatodea. The inner layer formation is of the fault type. Serosal elements in the amnioserosal fold differentiate into hydropylar cells, to function in water absorption together with specialized amniotic structures, i.e., an amniotic strand and a thickened amnion. The germ band is of the short germ type. The germ band immerses deep into the yolk after its full elongation along the egg surface, and in this respect blastokinesis closely resembles that of Mantophasmatodea. The embryological features, i.e., those on egg membranes and blastokinesis, may suggest a closer affinity of Grylloblattodea and Mantophasmatodea. Appendages, ectodermal invaginations, and sternal and pleural sclerites are discussed in the light of serial homology, to provide a new basis for elucidating the insect body plan. Appendages are divided into the proximal coxopodite and distal telopodite, the former being divided further into the subcoxa and coxa. Subcoxal and coxal elements are identified in the mandible as well as in the abdominal appendages. The subcoxa is divided into the epimeron and episternum by the pleural suture in thoracic segments. Likewise, in the abdominal segments the subcoxa is divided into two, although the homologs of the epimeron and episternum are not sclerotized, and in the labial segment the subcoxal derivative or the postmentum is divided into the submentum and mentum. Two coxal endites bulge out from the medial side of the gnathal appendages. The mandibular molar and incisor, maxillary lacinia and galea, and labial glossa and paraglossa are serially homologous with each other. In the thoracic segments the original embryonic sternum or "protosternum" is largely replaced by subcoxal elements, and merely remains as a small anterior presternum and a posterior spinasternum. A major part of the venter is represented by the derivatives of the episternum such as an extensive basisternum, katepisternum, and trochantin and the medial element of the epimeron. The pleuron is derived from the episternal elements or the anepisternum and preepisternum, which bears a spiracle in the mesothorax and metathorax, and the lateral element of the epimeron. The homolog of the preepisternum in the prothorax is the cervical sclerite, but with no spiracle developed. A median ventral invagination arises in the thoracic segments as a spina, and the homolog of the spina develops into the eversible sac in the first abdominal segment. J. Morphol. © 2005 Wiley-Liss, Inc. [source] Anatomy and lifestyles of Early Cambrian priapulid worms exemplified by Corynetis and Anningvermis from the Maotianshan Shale (SW China)LETHAIA, Issue 1 2004DI-YING HUANG Accurate information on the anatomy and ecology of worms from the Cambrian Lagerstätten of SW China is sparse. The present study of two priapulid worms Anningvermis n. gen. and Corynetis Luo & Hu, 1999 from the Lower Cambrian Maotianshan Shale biota brings new information concerning the anatomical complexity, functional morphology and lifestyles of the Early Cambrian priapulids. Comparisons are made with Recent priapulids from Sweden (live observations, SEM). The cuspidate pharyngeal teeth of Anningvermis (circumoral pentagons) and the most peculiar radiating oral crown of Corynetis added to the very elongate pharynx of these two forms are interpreted as two different types of grasping apparatus possibly involved in the capture of small prey. Corynetis and Anningvermis are two representative examples of the Early Cambrian endobenthic communities largely dominated by priapulid worms (more than ten species in the Maotianshan Shale biota) and to a much lesser extent by brachiopods. Corynetis and Anningvermis were probably active mud-burrowers and predators of small meiobenthic animals. Likewise predator priapulid worms exploited the interface layer between the seawater and bottom sediment, where meiobenthic organisms were abundant and functioned as prey. This implies that complex prey-predator relationship between communities already existed in the Early Cambrian. This study also shows that the circumoral pentagonal teeth and caudal appendage were present in the early stages of the evolutionary history of the group and were important features of the priapulid body plan already in the Early Cambrian. Two new families, one new genus and new species are introduced and described in the appendix. [source] New anomalocaridid appendages from the Burgess Shale, CanadaPALAEONTOLOGY, Issue 4 2010ALLISON C. DALEY Abstract:, The complex history of description of the anomalocaridids has partly been caused by the fragmentary nature of these fossils. Frontal appendages and mouth parts are more readily preserved than whole-body assemblages, so the earliest work on these animals examined these structures in isolation. After several decades of research, these disarticulated elements were assembled together to reconstruct the anomalocaridid body plan, and a total of three Burgess Shale genera, Anomalocaris, Laggania and Hurdia, were described in full. Here we present new frontal appendage material of additional anomalocaridid taxa from the ,Middle' Cambrian (Series 3) Burgess Shale Formation in Canada, showing that the diversity of anomalocaridids in this locality is even higher than previously thought. Material includes Amplectobelua stephenensis sp. nov., the first known occurrence of this genus outside of China; Caryosyntrips serratus gen. et sp. nov., which is similar to the Anomalocaris appendage but has a straighter outline and a different arrangement of spines; and an appendage that may be either the Laggania appendage or a third morph of the Hurdia appendage. The new anomalocaridid material is contemporaneous with the previously described taxa Anomalocaris, Laggania, and Hurdia, and the differences in morphology between the frontal appendages may reflect different feeding strategies. The stratigraphically lowest locality, S7 on Mount Stephen, yields material from all anomalocaridid taxa, but the assemblages in the younger quarries on Fossil Ridge are dominated by Anomalocaris and Hurdia only. [source] Developmental anatomy of seedlings of Indodalzellia gracilis (Podostemaceae)PLANT BIOLOGY, Issue 5 2010S. Koi Abstract In Tristichoideae, aquatic angiosperms in the family Podostemaceae, Terniopsis, Tristicha, Indotristicha and Cussetia have creeping roots with flanking (sub)cylindrical shoots, while Dalzellia is rootless and has crustose shoots. Indodalzellia gracilis, sister to a clade of Dalzellia zeylanica and Indotristicha ramosissima, has subcrustose shoots on the side of creeping roots, suggesting that I. gracilis may be a key species to reveal how saltational evolution of the body plan occurred in these three species. We investigated developmental morphology of I. gracilis seedlings grown in culture, using scanning electron microscopy and semi-thin serial sections. As in D. zeylanica, the plumular apical meristem in the seedling gives rise to two shoot apical meristems, which develop into horizontal subcrustose shoots with dorsal and marginal leaves. Neither radicle nor adventitious root is produced from the hypocotyl, but an adventitious root arises endogenously from the juvenile shoot and from some shoots of adult plants. These results, together with the phylogenetic relationships, suggest that the Indodalzellia seedling evolved by loss of the adventitious root derived from the hypocotyl, appearance of shoots in the axil of cotyledons, and appearance of adventitious roots from adventitious shoots. The difference in place of origin of the root between Indodalzellia and I. ramosissima suggests differing evolutionary origin of the root in Tristichoideae. [source] Moss Systems Biology en Route: Phytohormones in Physcomitrella DevelopmentPLANT BIOLOGY, Issue 3 2006E. L. Decker Abstract: The moss Physcomitrella patens has become a powerful model system in modern plant biology. Highly standardized cell culture techniques, as well as the necessary tools for computational biology, functional genomics and proteomics have been established. Large EST collections are available and the complete moss genome will be released soon. A simple body plan and the small number of different cell types in Physcomitrella facilitate the study of developmental processes. In the filamentous juvenile moss tissue, developmental decisions rely on the differentiation of single cells. Developmental steps are controlled by distinct phytohormones and integration of environmental signals. Especially the phytohormones auxin, cytokinin, and abscisic acid have distinct effects on early moss development. In this article, we review current knowledge about phytohormone influences on early moss development in an attempt to fully unravel the complex regulatory signal transduction networks underlying the developmental decisions of single plant cells in a holistic systems biology approach. [source] Laser capture microdissection for the analysis of gene expression during embryogenesis of ArabidopsisTHE PLANT JOURNAL, Issue 1 2005Stuart Casson Summary It is during embryogenesis that the body plan of the developing plant is established. Analysis of gene expression during embryogenesis has been limited due to the technical difficulty of accessing the developing embryo. Here we demonstrate that laser capture microdissection can be applied to the analysis of embryogenesis. We show how this technique can be used in concert with DNA microarray for the large-scale analysis of gene expression in apical and basal domains of the globular-stage and heart-stage embryo, respectively, when critical events of polarity, symmetry and biochemical differentiation are established. This high resolution spatial analysis shows that up to approximately 65% of the genome is expressed in the developing embryo, and that differential expression of a number of gene classes can be detected. We discuss the validity of this approach for the functional analysis of both published and previously uncharacterized essential genes. [source] In vitro culture of Arabidopsis embryos within their ovulesTHE PLANT JOURNAL, Issue 5 2004Michael Sauer Summary Embryogenesis of flowering plants establishes a basic body plan with apical,basal, radial and bilateral patterns from the single-celled zygote. Arabidopsis embryogenesis exhibits a nearly invariant cell division pattern and therefore is an ideal system for studies of early plant development. However, plant embryos are difficult to access for experimental manipulation, as they develop deeply inside maternal tissues. Here we present a method for the culture of zygotic Arabidopsis embryos in vitro. The technique omits excision of the embryo by culturing the entire ovule, thus greatly facilitating the time and effort involved. It enables external manipulation of embryo development and culture from the earliest developmental stages up to maturity. Administration of various chemical treatments as well as the use of different molecular markers is demonstrated together with standard techniques for visualizing gene expression and protein localization in in vitro cultivated embryos. The presented set of techniques allows for so far unavailable molecular physiology approaches in the study of early plant development. [source] Organizing chordates with an organizerBIOESSAYS, Issue 7 2007Jordi Garcia-Fernàndez Understanding how the chordate body plan originated and evolved is still controversial. The discovery by Spemann and Mangold in 1924 of the vertebrate organizer and its inductive properties in patterning the AP and DV axis was followed by a long gap until the 1960s when scientists started characterizing the molecular events responsible for such inductions. However, the evolutionary origin of the organizer itself remained obscure until very recently; did it appear together with the origin and radiation of vertebrates, or was it a chordate affair? A recent study by Yu and collaborators,1 which analyses the expression of several organizer-specific genes in amphioxus together with recent phylogenetic data that reversed the position of invertebrate extant chordates (e.g. urochordates and cephalochordates), indicates that the organizer probably appeared in early chordates. It likely had separate signalling centres generating BMP and Wnt signalling gradients along the DV and AP axis. The organizer was then lost in the urochordate lineage, most probably as an adaptation to a rapid and determinate development. BioEssays 29:619,624, 2007. © 2007 Wiley Periodicals, Inc. [source] Vetulicolians,are they deuterostomes? chordates?BIOESSAYS, Issue 3 2002Thurston C. Lacalli A recent paper by Shu et al.(1) reinterprets the fossil Vetulicola and related forms, all from the Lower Cambrian, as basal deuterostomes, assigning them their own phylum, Vetulicolia. Their conclusion is based on the presence of structures resembling gill slits and a trunk-like region that shows evidence of segmentation. This report summarizes the fossil evidence for their interpretation and evaluates a possible alternative, that vetulicolians may instead be tunicate-like chordates. Implications for our understanding of the nature of the primitive deuterostome (and chordate) body plan are discussed. BioEssays 24:208,211, 2002. © 2002 Wiley Periodicals, Inc.; DOI 10.1002/bies.10064 [source] Differing strategies for forming the arthropod body plan: Lessons from Dpp, Sog and Delta in the fly Drosophila and spider AchaearaneaDEVELOPMENT GROWTH & DIFFERENTIATION, Issue 4 2008Hiroki Oda In the insect Drosophila embryo, establishment of maternal transcription factor gradients, rather than cell,cell interactions, is fundamental to patterning the embryonic axes. In contrast, in the chelicerate spider embryo, cell,cell interactions are thought to play a crucial role in the development of the embryonic axes. A grafting experiment by Holm using spider eggs resulted in duplication of the embryonic axes, similar to the Spemann's organizer experiment using amphibian eggs. Recent work using the house spider Achaearanea tepidariorum has demonstrated that the homologs of decapentaplegic (dpp), short gastrulation (sog) and Delta, which encode a bone morphogenetic protein (BMP)-type ligand, its antagonist and a Notch ligand, respectively, are required in distinct aspects of axis formation. Achaearanea Dpp appears to function as a symmetry-breaking signal, which could account for Holm's results to some extent. Experimental findings concerning Achaearanea sog and Delta have highlighted differences in the mechanisms underlying ventral and posterior development between Drosophila and Achaearanea. Achaearanea ventral patterning essentially depends on sog function, in contrast to the Drosophila patterning mechanism, which is based on the nuclear gradient of Dorsal. Achaearanea posterior (or opisthosomal) patterning relies on the function of the caudal lobe, which develops from cells surrounding the blastopore through progressive activation of Delta-Notch signaling. In this review, we describe the differing strategies for forming the arthropod body plan in the fly and spider, and provide a perspective towards understanding the relationship between the arthropod and vertebrate body plans. [source] Invertebrate immune systems , not homogeneous, not simple, not well understoodIMMUNOLOGICAL REVIEWS, Issue 1 2004Eric S Loker Summary:, The approximate 30 extant invertebrate phyla have diversified along separate evolutionary trajectories for hundreds of millions of years. Although recent work understandably has emphasized the commonalities of innate defenses, there is also ample evidence, as from completed genome studies, to suggest that even members of the same invertebrate order have taken significantly different approaches to internal defense. These data suggest that novel immune capabilities will be found among the different phyla. Many invertebrates have intimate associations with symbionts that may play more of a role in internal defense than generally appreciated. Some invertebrates that are either long lived or have colonial body plans may diversify components of their defense systems via somatic mutation. Somatic diversification following pathogen exposure, as seen in plants, has been investigated little in invertebrates. Recent molecular studies of sponges, cnidarians, shrimp, mollusks, sea urchins, tunicates, and lancelets have found surprisingly diversified immune molecules, and a model is presented that supports the adaptive value of diversified non-self recognition molecules in invertebrates. Interactions between invertebrates and viruses also remain poorly understood. As we are in the midst of alarming losses of coral reefs, increased pathogen challenge to invertebrate aquaculture, and rampant invertebrate-transmitted parasites of humans and domestic animals, we need a better understanding of invertebrate immunology. [source] | ||||||||||||||||||||||||||||