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Hox complex genes control spatial patterning mechanisms in the development of arthropod and vertebrate body plans. Hox genes are all expressed during embryogenesis in these groups, which are all directly developing organisms in that embryogenesis leads at once to formation of major elements of the respective adult body plans. In the maximally indirect development of a large variety of invertebrates, the process of embryogenesis leads only to a free-living, bilaterally organized feeding larva. Maximal indirect development is exemplified in sea urchins. The 5-fold radially symmetric adult body plan of the sea urchin is generated long after embryogenesis is complete, by a separate process occurring within imaginal tissues set aside in the larva. The single Hox gene complex of Strongylocentrotus purpuratus contains 10 genes, and expression of eight of these genes was measured by quantitative methods during both embryonic and larval developmental stages and also in adult tissues. Only two of these genes are used significantly during the entire process of embryogenesis per se, although all are copiously expressed during the stages when the adult body plan is forming in the imaginal rudiment. They are also all expressed in various combinations in adult tissues. Thus, development of a microscopic, free-living organism of bilaterian grade, the larva, does not appear to require expression of the Hox gene cluster as such, whereas development of the adult body plan does. These observations ref lect on mechanisms by which bilaterian metazoans might have arisen in Precambrian evolution.The Hox gene cluster occupies a central position in current conceptions of both the development and evolution of metazoan body plans. Yet systematic evidence regarding the developmental expression of these genes is largely confined to two animal groups, the arthropods and the chordates. These groups are both direct developers, in the sense that major aspects of their adult body plans form immediately during embryogenesis, e.g., the head and the anterior͞posterior body axis, the major mesodermal anlagen, the central nervous system, and metameric body structures (1). Two other organisms for which some information about developmental Hox gene expression exists viz., Caenorhabditis elegans (2) and leech (3, 4), are also direct developers. Expression of the Hox complex has never been examined systematically in any animal that displays maximal indirect development. Here the process of embryogenesis produces a free-living, motile larva capable of feeding and growth, but in structure this larva bears essentially no resemblance to the adult body plan of the species. In maximal indirect development, the adult body plan instead forms within the larva by a complex secondary process from special patches of cells set aside during embryogenesis (1). The larva itself is a small, bilaterally organized metazoan organism that includes mesodermal as well as ectodermal, and endodermal cell types. Thus, it has muscle cells, neurons, gut cells, skeletogenic c...
Hox complex genes control spatial patterning mechanisms in the development of arthropod and vertebrate body plans. Hox genes are all expressed during embryogenesis in these groups, which are all directly developing organisms in that embryogenesis leads at once to formation of major elements of the respective adult body plans. In the maximally indirect development of a large variety of invertebrates, the process of embryogenesis leads only to a free-living, bilaterally organized feeding larva. Maximal indirect development is exemplified in sea urchins. The 5-fold radially symmetric adult body plan of the sea urchin is generated long after embryogenesis is complete, by a separate process occurring within imaginal tissues set aside in the larva. The single Hox gene complex of Strongylocentrotus purpuratus contains 10 genes, and expression of eight of these genes was measured by quantitative methods during both embryonic and larval developmental stages and also in adult tissues. Only two of these genes are used significantly during the entire process of embryogenesis per se, although all are copiously expressed during the stages when the adult body plan is forming in the imaginal rudiment. They are also all expressed in various combinations in adult tissues. Thus, development of a microscopic, free-living organism of bilaterian grade, the larva, does not appear to require expression of the Hox gene cluster as such, whereas development of the adult body plan does. These observations ref lect on mechanisms by which bilaterian metazoans might have arisen in Precambrian evolution.The Hox gene cluster occupies a central position in current conceptions of both the development and evolution of metazoan body plans. Yet systematic evidence regarding the developmental expression of these genes is largely confined to two animal groups, the arthropods and the chordates. These groups are both direct developers, in the sense that major aspects of their adult body plans form immediately during embryogenesis, e.g., the head and the anterior͞posterior body axis, the major mesodermal anlagen, the central nervous system, and metameric body structures (1). Two other organisms for which some information about developmental Hox gene expression exists viz., Caenorhabditis elegans (2) and leech (3, 4), are also direct developers. Expression of the Hox complex has never been examined systematically in any animal that displays maximal indirect development. Here the process of embryogenesis produces a free-living, motile larva capable of feeding and growth, but in structure this larva bears essentially no resemblance to the adult body plan of the species. In maximal indirect development, the adult body plan instead forms within the larva by a complex secondary process from special patches of cells set aside during embryogenesis (1). The larva itself is a small, bilaterally organized metazoan organism that includes mesodermal as well as ectodermal, and endodermal cell types. Thus, it has muscle cells, neurons, gut cells, skeletogenic c...
Interest in preconcentration techniques for the determination of metals at ultratrace levels still continues increasingly because of some disadvantages of flameless atomic absorption spectrometry and the high costs of other sensitive methods in compared to flame atomic absorption spectrometry (FAAS). Among preconcentration techniques, solid‐phase extraction is the most popular because of a number of advantages. In this work, thiol‐containing sulfonamide resin was synthesized, characterized, and applied as a new sorption material for solid phase extraction and determination of lead in natural water samples. The optimization of experimental conditions was performed using the parameters including pH, contact time, and volumes of initial and elution solutions. After preconcentration procedure, FAAS was used for determinations. The synthesized resin exhibits the superiority in compared to the other adsorption reagents because of the fact that there is no necessity of any complexing reagent as well as high sorption capacity. Consequently, 280‐fold improvement in the sensitivity of analytical scheme was achieved by combining the slotted tube atom trap‐atomic absorption spectrometry (STAT‐FAAS) and the developed preconcentration method. The limit of detection was found to be 0.15 ng mL−1. The Pb2+ concentrations in the studied water samples were found to be in the range of 0.9–6.7 ng mL−1.
Background: Echinoderms are a curious group of deuterostomes that forms a clade with hemichordates but has a pentameral body plan. Hox complex plays a pivotal role in axial patterning in bilaterians and often occurs in a cluster on the chromosome. In contrast to hemichordates with an organized Hox cluster, the sea urchin Strongylocentrotus purpuratus has a Hox cluster with an atypical organization. However, the current data on hox expression in sea urchin rudiments are fragmentary. Results: We report a comprehensive examination of hox expression in a sand dollar echinoid. Nine hox genes are expressed in the adult rudiment, which are classified into two groups, but hox11/13b belongs to both: one with linear expression in the coelomic mesoderm and another with radial expression around the adult mouth. The linear genes may endow the coelom/mesentery with axial information to direct postmetamorphic transformation of the digestive tract, whereas the radial genes developmentally correlate with the morphological novelties of echinoderms and/or sea urchins. Recruitment of the radial genes except hox11/13b appears to be accompanied by the loss of ancestral/axial roles. Conclusions: This in toto co-option of the hox genes provides insight into the molecular mechanisms underlying the evolution of echinoderms from a bilateral ancestor.
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