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        <identifier>oai:ir.soken.ac.jp:00001032</identifier>
        <datestamp>2023-06-20T16:09:40Z</datestamp>
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          <dc:title>Roles of Ric-8 dependent targeting of heterotrimeric G proteins in early embryogenesis of Drosophila</dc:title>
          <dc:title xml:lang="en">Roles of Ric-8 dependent targeting of heterotrimeric G proteins in early embryogenesis of Drosophila</dc:title>
          <jpcoar:creator>
            <jpcoar:creatorName>兼崎, 琢麿</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName>カネサキ, タクマ</jpcoar:creatorName>
          </jpcoar:creator>
          <jpcoar:creator>
            <jpcoar:creatorName xml:lang="en">KANESAKI, Takuma</jpcoar:creatorName>
          </jpcoar:creator>
          <datacite:description descriptionType="Other">Heterotrimeric G protein signaling is involved in various pathways in animal &lt;br /&gt;development. During Drosophila gastrula ion, Ga12 (Cta)mediated signaling &lt;br /&gt;controls the ventral cellular movements of epithelia. Here, I show that G Protein &lt;br /&gt;signaling also regulates the organization of cortical actin cytoskeleton underlining &lt;br /&gt;plasma membrane in the epithelial cells. Multiple Gα subfamilies, Gα12 and &lt;br /&gt;Gαi, are involved in the actin organization, but a known ligand of Gα12, Fog, is &lt;br /&gt;not required. When rie-8, which is required for plasma membrane-targeting of &lt;br /&gt;whole G proteins and their signaling activity, is mutated, the cell surfaces become &lt;br /&gt;unstable and show blebs, and entire cellular movements in gastrulation are &lt;br /&gt;delayed. The mutants for the common cofactors of the Gα's, GB13F and Gγ1, &lt;br /&gt;show the similar phenotypes. Ventral cells also showed blebs like the riｃ-8 &lt;br /&gt;mutant when the cells are treated with inhibitors of actin polymerization. The &lt;br /&gt;disruption of cortical actin in the mutants for G proteins is seen in all epithelial &lt;br /&gt;cells, but the disorganization of the surface occurs only in the moving ventral cells. &lt;br /&gt;This suggests that the organization of cortical actin seems to be required to &lt;br /&gt;endure the stress, which the ventral cells receive when they move during &lt;br /&gt;gastrulation. &lt;br /&gt;   Besides, I also show evidence that heterotrimeric G protein signaling is &lt;br /&gt;involved in the control of the actin dynamics in syncytial blastderm stage. In &lt;br /&gt;this stage, nuclear division is carried out with the assistance of two architectures &lt;br /&gt;of actin cytoskeleton; actin caps in interphase and pseudocleavage &lt;br /&gt;furrow-assembled actin network in mitosis. G protein is colocalized with the caps &lt;br /&gt;and network of actin throughout this stage. In the ric-8mutant, this localization &lt;br /&gt;pattern is lost and actin cytoskeleton shows abnormal morphology. Using &lt;br /&gt;live-imaging technique, it is revealed that the ric-8 mutant shows the delay of the &lt;br /&gt;change of actin morphology. These results suggest that G protein regulates &lt;br /&gt;timing of the dynamic change of actin during mitosis, and provide new insight &lt;br /&gt;into the role of G protein signaling in early embryogenesis of Drosophi7a. &lt;br /&gt;   In addition, here I introduce a novel mutant of ric-8 gene, ric8&lt;sup&gt;atx&lt;/sup&gt;, in which &lt;br /&gt;408th E is substituted to K. The ric8&lt;sup&gt;atx&lt;/sup&gt; mutant embryo shows cta- or fog like &lt;br /&gt;phenotype of gastrulation, which is milder than that of the ric-8 null mutant. &lt;br /&gt;Consistently, the ric8&lt;sup&gt;atx&lt;/sup&gt; mutation results in the Gα12-specific defect of targeting. &lt;br /&gt;Although the role of Ric-8 has been inferred from the results of genetic analyses &lt;br /&gt;and of some in vitro assays in past studies, the true molecular function of this &lt;br /&gt;protein is stil1 unclear. The findings from the analyses of ric8&lt;sup&gt;atx&lt;/sup&gt; promote &lt;br /&gt;elucidating the mysterious function of Ric-8 protein in viva .</datacite:description>
          <datacite:description descriptionType="Other">総研大甲第1061号</datacite:description>
          <dc:language>eng</dc:language>
          <dc:type rdf:resource="http://purl.org/coar/resource_type/c_46ec">thesis</dc:type>
          <jpcoar:identifier identifierType="URI">https://ir.soken.ac.jp/records/1032</jpcoar:identifier>
          <dcndl:degreeName>博士（理学）</dcndl:degreeName>
          <dcndl:dateGranted>2007-03-23</dcndl:dateGranted>
          <jpcoar:degreeGrantor>
            <jpcoar:degreeGrantorName>総合研究大学院大学</jpcoar:degreeGrantorName>
          </jpcoar:degreeGrantor>
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            <jpcoar:URI label="要旨・審査要旨">https://ir.soken.ac.jp/record/1032/files/甲1061_要旨.pdf</jpcoar:URI>
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            <jpcoar:extent>279.3 kB</jpcoar:extent>
            <datacite:date dateType="Available">2016-02-17</datacite:date>
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