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<prism:publicationName>Development</prism:publicationName>
<prism:issn>0950-1991</prism:issn>
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<title>Development</title>
<url>http://dev.biologists.org/icons/banner/title.gif</url>
<link>http://dev.biologists.org</link>
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<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.022673v1?rss=1">
<title><![CDATA[[Research report] Cell cycle progression is required for zebrafish somite morphogenesis but not segmentation clock function]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.022673v1?rss=1</link>
<description><![CDATA[<b>Lixia Zhang, Christina Kendrick, Dorthe Julich,  and Scott A. Holley</b><br/><br/>
<p><P>
Cell division, differentiation and morphogenesis are coordinated during embryonic development, and frequently are in disarray in pathologies such as cancer. Here, we present a zebrafish mutant that ceases mitosis at the beginning of gastrulation, but that undergoes axis elongation and develops blood, muscle and a beating heart. We identify the mutation as being in <I>early mitotic inhibitor 1</I> (<I>emi1</I>), a negative regulator of the Anaphase Promoting Complex, and use the mutant to examine the role of the cell cycle in somitogenesis. The mutant phenotype indicates that axis elongation during the segmentation period is driven substantially by cell migration. We find that the segmentation clock, which regulates somitogenesis, functions normally in the absence of cell cycle progression, and observe that mitosis is a modest source of noise for the clock. Somite morphogenesis involves the epithelialization of the somite border cells around a core of mesenchyme. As in wild-type embryos, somite boundary...]]></description>
<dc:creator><![CDATA[Zhang, L., Kendrick, C., Julich, D., Holley, S. A.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.022673</dc:identifier>
<dc:title><![CDATA[[Research report] Cell cycle progression is required for zebrafish somite morphogenesis but not segmentation clock function]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Research report</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.021543v1?rss=1">
<title><![CDATA[[Research article] A maternally localised Wnt ligand required for axial patterning in the cnidarian Clytia hemisphaerica]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.021543v1?rss=1</link>
<description><![CDATA[<b>Tsuyoshi Momose, Romain Derelle,  and Evelyn Houliston</b><br/><br/>
<p><P>
Regionalised activation of canonical Wnt signalling via &beta;-catenin stabilisation is a key early step in embryonic patterning in many metazoans, including the basally diverging cnidarians, but the upstream maternal cues appear surprisingly variable. In <I>Clytia</I>, regionalised &beta;-catenin stabilisation defining a presumptive 'oral' territory is determined by two maternally coded Frizzled family Wnt receptors of opposite localisation and function. We have identified a maternally coded ligand, CheWnt3, the RNA of which is localised to the animal cortex (future oral side) of the egg. Antisense morpholino oligonucleotide experiments showed that CheWnt3 is required maternally for regionalised oral &beta;-catenin stabilisation in the early embryo, being only the second clear example of a maternally required Wnt ligand after <I>Xenopus</I> Xwnt11. In line with the determinant role of the maternally localised Frizzleds, CheWnt3 overexpression by RNA injection initially had little effect on establishing the oral domain. Subsequently, however, overexpression had dramatic consequences for axis development,...]]></description>
<dc:creator><![CDATA[Momose, T., Derelle, R., Houliston, E.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.021543</dc:identifier>
<dc:title><![CDATA[[Research article] A maternally localised Wnt ligand required for axial patterning in the cnidarian Clytia hemisphaerica]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.017558v1?rss=1">
<title><![CDATA[[Research article] Ca2+ signals coordinate zygotic polarization and cell cycle progression in the brown alga Fucus serratus]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.017558v1?rss=1</link>
<description><![CDATA[<b>John H.F. Bothwell, Jolanta Kisielewska, Martin J. Genner, Martin R. McAinsh,  and Colin Brownlee</b><br/><br/>
<p><P>
Zygotes of the fucoid brown algae provide excellent models for addressing fundamental questions about zygotic symmetry breaking. Although the acquisition of polarity is tightly coordinated with the timing and orientation of the first asymmetric division - with zygotes having to pass through a G1/S-phase checkpoint before the polarization axis can be fixed - the mechanisms behind the interdependence of polarization and cell cycle progression remain unclear. In this study, we combine in vivo Ca<SUP>2+</SUP> imaging, single cell monitoring of S-phase progression and multivariate analysis of high-throughput intracellular Ca<SUP>2+</SUP> buffer loading to demonstrate that Ca<SUP>2+</SUP> signals coordinate polarization and cell cycle progression in the <I>Fucus serratus</I> zygote. Consistent with earlier studies on this organism, and in contrast to animal models, we observe no fast Ca<SUP>2+</SUP> wave following fertilization. Rather, we show distinct slow localized Ca<SUP>2+</SUP> elevations associated with both fertilization and S-phase progression, and we show that both S-phase and zygotic...]]></description>
<dc:creator><![CDATA[Bothwell, J. H.F., Kisielewska, J., Genner, M. J., McAinsh, M. R., Brownlee, C.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.017558</dc:identifier>
<dc:title><![CDATA[[Research article] Ca2+ signals coordinate zygotic polarization and cell cycle progression in the brown alga Fucus serratus]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.017459v1?rss=1">
<title><![CDATA[[Research article] Activation of {beta}-catenin signaling programs embryonic epidermis to hair follicle fate]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.017459v1?rss=1</link>
<description><![CDATA[<b>Yuhang Zhang, Thomas Andl, Steven H. Yang, Monica Teta, Fei Liu, John T. Seykora, John W. Tobias, Stefano Piccolo, Ruth Schmidt-Ullrich, Andras Nagy, Makoto M. Taketo, Andrzej A. Dlugosz,  and Sarah E. Millar</b><br/><br/>
<p><P>
&beta;-Catenin signaling is required for hair follicle development, but it is unknown whether its activation is sufficient to globally program embryonic epidermis to hair follicle fate. To address this, we mutated endogenous epithelial &beta;-catenin to a dominant-active form in vivo. Hair follicle placodes were expanded and induced prematurely in activated &beta;-catenin mutant embryos, but failed to invaginate or form multilayered structures. Eventually, the entire epidermis adopted hair follicle fate, broadly expressing hair shaft keratins in place of epidermal stratification proteins. Mutant embryonic skin was precociously innervated, and displayed prenatal pigmentation, a phenomenon never observed in wild-type controls. Thus, &beta;-catenin signaling programs the epidermis towards placode and hair shaft fate at the expense of epidermal differentiation, and activates signals directing pigmentation and innervation. In transcript profiling experiments, we identified elevated expression of <I>Sp5</I>, a direct &beta;-catenin target and transcriptional repressor. We show that <I>Sp5</I> normally localizes to hair follicle placodes and...]]></description>
<dc:creator><![CDATA[Zhang, Y., Andl, T., Yang, S. H., Teta, M., Liu, F., Seykora, J. T., Tobias, J. W., Piccolo, S., Schmidt-Ullrich, R., Nagy, A., Taketo, M. M., Dlugosz, A. A., Millar, S. E.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.017459</dc:identifier>
<dc:title><![CDATA[[Research article] Activation of {beta}-catenin signaling programs embryonic epidermis to hair follicle fate]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.016378v1?rss=1">
<title><![CDATA[[Research article] Cell-autonomous requirement for {beta}1 integrin in endothelial cell adhesion, migration and survival during angiogenesis in mice]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.016378v1?rss=1</link>
<description><![CDATA[<b>Timothy R. Carlson, Huiqing Hu, Rickmer Braren, Yung Hae Kim,  and Rong A. Wang</b><br/><br/>
<p><P>
&beta;1 integrin (encoded by <I>Itgb1</I>) is established as a regulator of angiogenesis based upon the phenotypes of complete knockouts of &beta;1 heterodimer partners or ligands and upon antibody inhibition studies in mice. Its direct function in endothelial cells (ECs) in vivo has not been determined because <I>Itgb1<SUP>-/-</SUP></I> embryos die before vascular development. Excision of <I>Itgb1</I> from ECs and a subset of hematopoietic cells, using <I>Tie2-Cre</I>, resulted in abnormal vascular development by embryonic day (e) 8.5 and lethality by e10.5. <I>Tie1-Cre</I> mediated a more restricted excision of <I>Itgb1</I> from ECs and hematopoietic cells and resulted in embryonic lethal vascular defects by e11.5. Capillaries of the yolk sacs were disorganized, and the endothelium of major blood vessels and of the heart was frequently discontinuous in mutant embryos. We also found similar vascular morphogenesis defects characterized by EC disorganization in embryonic explants and isolated ECs. <I>Itgb1</I>-null ECs were deficient in adhesion and migration...]]></description>
<dc:creator><![CDATA[Carlson, T. R., Hu, H., Braren, R., Kim, Y. H., Wang, R. A.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.016378</dc:identifier>
<dc:title><![CDATA[[Research article] Cell-autonomous requirement for {beta}1 integrin in endothelial cell adhesion, migration and survival during angiogenesis in mice]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.015990v1?rss=1">
<title><![CDATA[[Research article] Gli3 coordinates three-dimensional patterning and growth of the tectum and cerebellum by integrating Shh and Fgf8 signaling]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.015990v1?rss=1</link>
<description><![CDATA[<b>Sandra Blaess, Daniel Stephen,  and Alexandra L. Joyner</b><br/><br/>
<p><P>
The coordination of anterior-posterior (AP) and dorsal-ventral (DV) patterning of the mesencephalon (mes) and rhombomere 1 (r1) is instrumental for the development of three distinct brain structures: the tectum and cerebellum dorsally and the tegmentum ventrally. Patterning of the mes/r1 is primarily mediated by signaling molecules secreted from two organizers: sonic hedgehog (Shh) from the floor plate (DV) and Fgf8 from the isthmus (AP). Gli3, a zinc-finger transcription factor in the Shh signaling pathway, has been implicated in regulating <I>Fgf8</I> expression and is therefore a potential candidate for coordinating the action of the two organizers. By inactivating mouse <I>Gli3</I> at successive embryonic time points in vivo, we uncovered the extent and the underlying mechanism of Gli3 function in the mes/r1. We demonstrate that before E9.0, <I>Gli3</I> is required for establishing a distinct posterior tectum, isthmus and cerebellum, but does not play a role in the development of the tegmentum. Between...]]></description>
<dc:creator><![CDATA[Blaess, S., Stephen, D., Joyner, A. L.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.015990</dc:identifier>
<dc:title><![CDATA[[Research article] Gli3 coordinates three-dimensional patterning and growth of the tectum and cerebellum by integrating Shh and Fgf8 signaling]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.015719v1?rss=1">
<title><![CDATA[[Research article] Expression of multiple slow myosin heavy chain genes reveals a diversity of zebrafish slow twitch muscle fibres with differing requirements for Hedgehog and Prdm1 activity]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.015719v1?rss=1</link>
<description><![CDATA[<b>Stone Elworthy, Murray Hargrave, Robert Knight, Katharina Mebus,  and Philip W. Ingham</b><br/><br/>
<p><P>
The zebrafish embryo develops a series of anatomically distinct slow twitch muscle fibres that characteristically express genes encoding lineage-specific isoforms of sarcomeric proteins such as MyHC and troponin. We show here that different subsets of these slow fibres express distinct members of a tandem array of slow MyHC genes. The first slow twitch muscle fibres to differentiate, which are specified by the activity of the transcription factor Prdm1 (also called Ubo or Blimp1) in response to Hedgehog (Hh) signalling, express the <I>smyhc1</I> gene<I>.</I> Subsequently, secondary slow twitch fibres differentiate in most cases independently of Hh activity. We find that although some of these later-forming fibres also express <I>smyhc1</I>, others express <I>smyhc2</I> or <I>smyhc3</I>. We show that the <I>smyhc1</I>-positive fibres express the <I>ubo</I> (<I>prdm1</I>) gene and adopt fast twitch fibre characteristics in the absence of Prdm1 activity, whereas those that do not express <I>smyhc1</I> can differentiate independently of Prdm1 function. Conversely,...]]></description>
<dc:creator><![CDATA[Elworthy, S., Hargrave, M., Knight, R., Mebus, K., Ingham, P. W.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.015719</dc:identifier>
<dc:title><![CDATA[[Research article] Expression of multiple slow myosin heavy chain genes reveals a diversity of zebrafish slow twitch muscle fibres with differing requirements for Hedgehog and Prdm1 activity]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.014498v1?rss=1">
<title><![CDATA[[Review] Tracheal branching morphogenesis in Drosophila: new insights into cell behaviour and organ architecture]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.014498v1?rss=1</link>
<description><![CDATA[<b>Markus Affolter and Emmanuel Caussinus</b><br/><br/>
<p><P>
Our understanding of the molecular control of morphological processes has increased tremendously over recent years through the development and use of high resolution in vivo imaging approaches, which have enabled cell behaviour to be linked to molecular functions. Here we review how such approaches have furthered our understanding of tracheal branching morphogenesis in <I>Drosophila</I>, during which the control of cell invagination, migration, competition and rearrangement is accompanied by the sequential secretion and resorption of proteins into the apical luminal space, a vital step in the elaboration of the trachea's complex tubular network. We also discuss the similarities and differences between flies and vertebrates in branched organ formation that are becoming apparent from these studies.</P>
]]></description>
<dc:creator><![CDATA[Affolter, M., Caussinus, E.]]></dc:creator>
<dc:date>2008-05-14</dc:date>
<dc:identifier>info:doi/10.1242/dev.014498</dc:identifier>
<dc:title><![CDATA[[Review] Tracheal branching morphogenesis in Drosophila: new insights into cell behaviour and organ architecture]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-05-14</prism:publicationDate>
<prism:section>Review</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.020099v1?rss=1">
<title><![CDATA[[Research article] Early patterning of the chorion leads to the trilaminar trophoblast cell structure in the placental labyrinth]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.020099v1?rss=1</link>
<description><![CDATA[<b>David G. Simmons, David R.C. Natale, Valerie Begay, Martha Hughes, Achim Leutz,  and James C. Cross</b><br/><br/>
<p><P>
The labyrinth of the rodent placenta contains villi that are the site of nutrient exchange between mother and fetus. They are covered by three trophoblast cell types that separate the maternal blood sinusoids from fetal capillaries - a single mononuclear cell that is a subtype of trophoblast giant cell (sinusoidal or S-TGC) with endocrine function and two multinucleated syncytiotrophoblast layers, each resulting from cell-cell fusion, that function in nutrient transport. The developmental origins of these cell types have not previously been elucidated. We report here the discovery of cell-layer-restricted genes in the mid-gestation labyrinth (E12.5-14.5) including <I>Ctsq</I> in S-TGCs (also <I>Hand1-</I>positive), <I>Syna</I> in syncytiotrophoblast layer I (SynT-I), and <I>Gcm1</I>, <I>Cebpa</I> and <I>Synb</I> in syncytiotrophoblast layer II (SynT-II). These genes were also expressed in distinct layers in the chorion as early as E8.5, prior to villous formation. Specifically, <I>Hand1</I> was expressed in apical cells lining maternal blood spaces (<I>Ctsq</I> is not...]]></description>
<dc:creator><![CDATA[Simmons, D. G., Natale, D. R.C., Begay, V., Hughes, M., Leutz, A., Cross, J. C.]]></dc:creator>
<dc:date>2008-04-30</dc:date>
<dc:identifier>info:doi/10.1242/dev.020099</dc:identifier>
<dc:title><![CDATA[[Research article] Early patterning of the chorion leads to the trilaminar trophoblast cell structure in the placental labyrinth]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-04-30</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

<item rdf:about="http://dev.biologists.org/cgi/content/short/dev.018200v1?rss=1">
<title><![CDATA[[Research article] Activation of Eklf expression during hematopoiesis by Gata2 and Smad5 prior to erythroid commitment]]></title>
<link>http://dev.biologists.org/cgi/content/short/dev.018200v1?rss=1</link>
<description><![CDATA[<b>Felix Lohmann and James J. Bieker</b><br/><br/>
<p><P>
The hierarchical progression of stem and progenitor cells to their more-committed progeny is mediated through cell-to-cell signaling pathways and intracellular transcription factor activity. However, the mechanisms that govern the genetic networks underlying lineage fate decisions and differentiation programs remain poorly understood. Here we show how integration of Bmp4 signaling and Gata factor activity controls the progression of hematopoiesis, as exemplified by the regulation of <I>Eklf</I> during establishment of the erythroid lineage. Utilizing transgenic reporter assays in differentiating mouse embryonic stem cells as well as in the murine fetal liver, we demonstrate that Eklf expression is initiated prior to erythroid commitment during hematopoiesis. Applying phylogenetic footprinting and in vivo binding studies in combination with newly developed loss-of-function technology in embryoid bodies, we find that Gata2 and Smad5 cooperate to induce <I>Eklf</I> in a progenitor population, followed by a switch to Gata1-controlled regulation of <I>Eklf</I> transcription upon erythroid commitment. This stage- and...]]></description>
<dc:creator><![CDATA[Lohmann, F., Bieker, J. J.]]></dc:creator>
<dc:date>2008-04-30</dc:date>
<dc:identifier>info:doi/10.1242/dev.018200</dc:identifier>
<dc:title><![CDATA[[Research article] Activation of Eklf expression during hematopoiesis by Gata2 and Smad5 prior to erythroid commitment]]></dc:title>
<dc:publisher>Company of Biologists</dc:publisher>
<prism:publicationDate>2008-04-30</prism:publicationDate>
<prism:section>Research article</prism:section>
</item>

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