<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-30T10:20:15Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/26932" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/26932</identifier><datestamp>2026-02-03T11:47:15Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37959</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Benítez-Fuente, Francisco</subfield>
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      <subfield code="a">Amorim-Silva, Vitor</subfield>
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      <subfield code="a">Collado, Javier</subfield>
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      <subfield code="a">Fernández-Busnadiego, Rubén</subfield>
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      <subfield code="a">Botella-Mesa, Miguel Ángel</subfield>
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      <subfield code="c">2023-06</subfield>
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      <subfield code="a">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.</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/26932</subfield>
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      <subfield code="a">Biología molecular - Congresos</subfield>
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      <subfield code="a">Functional characterization of Arabidopsis thaliana Synaptotagmin1 domains using Tricalbin3 chimeras in Saccharomyces cerevisiae</subfield>
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