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???displayArticle.abstract??? Vasa, a DEAD box helicase, is a germline marker that may also function in multipotent cells. In the embryo of the sea urchin Strongylocentrotus purpuratus, Vasa protein is posttranscriptionally enriched in the small micromere lineage, which results from two asymmetric cleavage divisions early in development. The cells of this lineage are subsequently set aside during embryogenesis for use in constructing the adult rudiment. Although this mode of indirect development is prevalent among echinoderms, early asymmetric cleavage divisions are a derived feature in this phylum. The goal of this study is to explore how vasa is regulated in key members of the phylum with respect to the evolution of the micromere and small micromere lineages. We find that although striking similarities exist between the vasa mRNA expression patterns of several sea urchins and sea stars, the time frame of enriched protein expression differs significantly. These results suggest that a conserved mechanism of vasa regulation was shifted earlier in sea urchin embryogenesis with the derivation of micromeres. These data also shed light on the phenotype of a sea urchin embryo upon removal of the Vasa-positive micromeres, which appears to revert to a basal mechanism used by extant sea stars and pencil urchins to regulate Vasa protein accumulation. Furthermore, in all echinoderms tested here, Vasa protein and/or message is enriched in the larval coelomic pouches, the site of adult rudiment formation, thus suggesting a conserved role for vasa in undifferentiated multipotent cells set aside during embryogenesis for use in juvenile development.
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???displayArticle.pmcLink???PMC3034130 ???displayArticle.link???Evol Dev ???displayArticle.grants???[+]
Altschul,
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
1997, Pubmed
Altschul,
Gapped BLAST and PSI-BLAST: a new generation of protein database search programs.
1997,
Pubmed
Angerer,
Animal-vegetal axis patterning mechanisms in the early sea urchin embryo.
2000,
Pubmed
,
Echinobase
Braat,
Vasa protein expression and localization in the zebrafish.
2000,
Pubmed
Byrne,
Embryogenesis and Larval Development of the Asteroid Patiriella regularis Viewed by Light and Scanning Electron Microscopy.
1991,
Pubmed
,
Echinobase
Cameron,
Macromere cell fates during sea urchin development.
1991,
Pubmed
,
Echinobase
Cameron,
Evolution of the chordate body plan: new insights from phylogenetic analyses of deuterostome phyla.
2000,
Pubmed
Cordin,
The DEAD-box protein family of RNA helicases.
2006,
Pubmed
Cox,
A novel class of evolutionarily conserved genes defined by piwi are essential for stem cell self-renewal.
1998,
Pubmed
DeRenzo,
A clean start: degradation of maternal proteins at the oocyte-to-embryo transition.
2004,
Pubmed
Ettensohn,
The invertebrate deuterostomes: an introduction to their phylogeny, reproduction, development, and genomics.
2004,
Pubmed
Extavour,
Mechanisms of germ cell specification across the metazoans: epigenesis and preformation.
2003,
Pubmed
Forbes,
Nanos and Pumilio have critical roles in the development and function of Drosophila germline stem cells.
1998,
Pubmed
Gruidl,
Multiple potential germ-line helicases are components of the germ-line-specific P granules of Caenorhabditis elegans.
1996,
Pubmed
Hay,
Localization of vasa, a component of Drosophila polar granules, in maternal-effect mutants that alter embryonic anteroposterior polarity.
1990,
Pubmed
Hinman,
Evolutionary plasticity of developmental gene regulatory network architecture.
2007,
Pubmed
,
Echinobase
Hinman,
Developmental gene regulatory network architecture across 500 million years of echinoderm evolution.
2003,
Pubmed
,
Echinobase
Illmensee,
Transplantation of posterior polar plasm in Drosophila. Induction of germ cells at the anterior pole of the egg.
1974,
Pubmed
Inoue,
Germ Cell Differentiation in Starfish: The Posterior Enterocoel as the Origin of Germ Cells in Asterina pectinifera: (starfish/germ cells/PGC/posterior enterocoel/haemal sinus).
1992,
Pubmed
,
Echinobase
Juliano,
Germ line determinants are not localized early in sea urchin development, but do accumulate in the small micromere lineage.
2006,
Pubmed
,
Echinobase
Knaut,
Zebrafish vasa RNA but not its protein is a component of the germ plasm and segregates asymmetrically before germline specification.
2000,
Pubmed
Kobayashi,
Essential role of the posterior morphogen nanos for germline development in Drosophila.
1996,
Pubmed
Komiya,
Isolation and characterization of a novel gene of the DEAD box protein family which is specifically expressed in germ cells of Xenopus laevis.
1994,
Pubmed
Lasko,
Posterior localization of vasa protein correlates with, but is not sufficient for, pole cell development.
1990,
Pubmed
Lasko,
The product of the Drosophila gene vasa is very similar to eukaryotic initiation factor-4A.
1988,
Pubmed
Letunic,
SMART 5: domains in the context of genomes and networks.
2006,
Pubmed
Liu,
Fat facets interacts with vasa in the Drosophila pole plasm and protects it from degradation.
2003,
Pubmed
Markussen,
Translational control of oskar generates short OSK, the isoform that induces pole plasma assembly.
1995,
Pubmed
Minokawa,
Expression patterns of four different regulatory genes that function during sea urchin development.
2004,
Pubmed
,
Echinobase
Mochizuki,
Universal occurrence of the vasa-related genes among metazoans and their germline expression in Hydra.
2001,
Pubmed
Pehrson,
The fate of the small micromeres in sea urchin development.
1986,
Pubmed
,
Echinobase
Peterson,
Set-aside cells in maximal indirect development: evolutionary and developmental significance.
1997,
Pubmed
Pfister,
Flatworm stem cells and the germ line: developmental and evolutionary implications of macvasa expression in Macrostomum lignano.
2008,
Pubmed
Ransick,
Postembryonic segregation of the germ line in sea urchins in relation to indirect development.
1996,
Pubmed
,
Echinobase
Rebscher,
Vasa unveils a common origin of germ cells and of somatic stem cells from the posterior growth zone in the polychaete Platynereis dumerilii.
2007,
Pubmed
Rebscher,
The germ plasm component Vasa allows tracing of the interstitial stem cells in the cnidarian Hydractinia echinata.
2008,
Pubmed
Reddien,
Fundamentals of planarian regeneration.
2004,
Pubmed
Schultz,
SMART, a simple modular architecture research tool: identification of signaling domains.
1998,
Pubmed
Styhler,
vasa is required for GURKEN accumulation in the oocyte, and is involved in oocyte differentiation and germline cyst development.
1998,
Pubmed
Suzuki,
Functional redundancy among Nanos proteins and a distinct role of Nanos2 during male germ cell development.
2007,
Pubmed
Tam,
The allocation of epiblast cells to ectodermal and germ-line lineages is influenced by the position of the cells in the gastrulating mouse embryo.
1996,
Pubmed
Tanaka,
Study of the Lineage and Cell Cycle of Small Micromeres in Embryos of the Sea Urchin, Hemicentrotus pulcherrimus: (small micromeres/cell cycle/cell lineage/unequal cleavage/sea urchin).
1990,
Pubmed
,
Echinobase
Tanaka,
The mouse homolog of Drosophila Vasa is required for the development of male germ cells.
2000,
Pubmed
Tomancak,
Oocyte polarity depends on regulation of gurken by Vasa.
1998,
Pubmed
Toyooka,
Expression and intracellular localization of mouse Vasa-homologue protein during germ cell development.
2000,
Pubmed
Tsuda,
Conserved role of nanos proteins in germ cell development.
2003,
Pubmed
Voronina,
Vasa protein expression is restricted to the small micromeres of the sea urchin, but is inducible in other lineages early in development.
2008,
Pubmed
,
Echinobase
Wada,
Phylogenetic relationships among extant classes of echinoderms, as inferred from sequences of 18S rDNA, coincide with relationships deduced from the fossil record.
1994,
Pubmed
,
Echinobase
Wang,
Nanos maintains germline stem cell self-renewal by preventing differentiation.
2004,
Pubmed
Wolke,
Multiple levels of posttranscriptional control lead to germ line-specific gene expression in the zebrafish.
2002,
Pubmed
Wray,
The origin of spicule-forming cells in a 'primitive' sea urchin (Eucidaris tribuloides) which appears to lack primary mesenchyme cells.
1988,
Pubmed
,
Echinobase
Wray,
The evolution of echinoderm development is driven by several distinct factors.
1994,
Pubmed
,
Echinobase
Wylie,
Germ cells.
1999,
Pubmed
Yoon,
Zebrafish vasa homologue RNA is localized to the cleavage planes of 2- and 4-cell-stage embryos and is expressed in the primordial germ cells.
1997,
Pubmed