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      <dc:title>Functional characterization of Arabidopsis thaliana Synaptotagmin1 domains using Tricalbin3 chimeras in Saccharomyces cerevisiae</dc:title>
      <dc:creator>Benítez-Fuente, Francisco</dc:creator>
      <dc:creator>Amorim-Silva, Vitor</dc:creator>
      <dc:creator>Collado, Javier</dc:creator>
      <dc:creator>Fernández-Busnadiego, Rubén</dc:creator>
      <dc:creator>Botella-Mesa, Miguel Ángel</dc:creator>
      <dc:subject>Biología molecular - Congresos</dc:subject>
      <dc:description>Synaptotagmin1 (SYT1) is an Arabidopsis thaliana endoplasmic reticulum (ER)-plasma membrane contact site tether involved in biotic and abiotic stress resistance. These resistance roles have been related to SYT1 tethering and lipid-transport functions. However, the specific contributions of SYT1 domains to these functions and their relevance in stress resistance remain unknown.&#xd;
To efficiently investigate each SYT1 domain in vivo, we carried out domain interchanges in the model organism Saccharomyces cerevisiae (yeast). Tricalbin3 (Tcb3) is a SYT1 homolog in yeast, and it is essential for heat-shock tolerance. Tcb3 also mediates the formation of high-curvature peaks at the ER, which is promotes during heat, and would facilitate lipid homeostasis between the PM and the ER. We generated constructs expressing SYT1/Tcb3 chimeras tagged to fluorescent proteins, transformed them into tcb3Δ yeast cells and studied their subcellular localization and ability to complement the heat-shock hypersensitivity of tcb3Δ. We are further analyzing the ER-peak formation ability of these chimeras by cryo-electron tomography.&#xd;
Our work revealed that SYT1 did not show the localization pattern of Tcb3, nor could complement the heat-shock hypersensitivity of tcb3Δ. However, Tcb3 chimeras containing either SYT1 SMP or C2 domains showed a Tcb3 subcellular pattern and a heat-shock tolerance similar to that of tcb3Δ/Tcb3- GFP complemented strains. Further, Tcb3 N-terminal region was required, although not sufficient, for heat-shock tolerance and localization. Preliminary data suggests that chimeras complementing tcb3Δ heat-shock hypersensitivity also mediate ER peak formation.</dc:description>
      <dc:date>2023-06-12T09:37:24Z</dc:date>
      <dc:date>2023-06-12T09:37:24Z</dc:date>
      <dc:date>2023-06</dc:date>
      <dc:type>conference output</dc:type>
      <dc:identifier>https://hdl.handle.net/10630/26932</dc:identifier>
      <dc:language>eng</dc:language>
      <dc:relation>ICAR 2023</dc:relation>
      <dc:relation>Chiba, Japon</dc:relation>
      <dc:relation>05/06/2023</dc:relation>
      <dc:rights>open access</dc:rights>
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