<?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>2026-04-14T09:30:54Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:2445/143332" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:2445/143332</identifier><datestamp>2025-12-10T00:59:46Z</datestamp><setSpec>com_2072_1057</setSpec><setSpec>col_2072_478917</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>A Plasmodium falciparum C-mannosyltransferase is dispensable for parasite asexual blood stage development</dc:title>
   <dc:creator>López Gutiérrez, Borja</dc:creator>
   <dc:creator>Cova, Marta</dc:creator>
   <dc:creator>Izquierdo Lázaro, Luis</dc:creator>
   <dc:subject>Plasmodium falciparum</dc:subject>
   <dc:subject>Paràsits</dc:subject>
   <dc:subject>Parasites</dc:subject>
   <dc:description>C-mannosylation was recently identified in the thrombospondin-related anonymous protein&#xd;
(TRAP) from Plasmodium falciparum salivary gland sporozoites. A candidate P. falciparum&#xd;
C-mannosyltransferase (Pf DPY-19) was demonstrated to modify thrombospondin type 1&#xd;
repeat (TSR) domains in vitro, exhibiting a different acceptor specificity than their mammalian counterparts. According to the described minimal acceptor of Pf DPY19, several TSR&#xd;
domain-containing proteins of P. falciparum could be C-mannosylated in vivo. However,&#xd;
the relevance of this protein modification for the parasite viability remains unknown. In&#xd;
the present study, we used CRISPR/Cas9 technology to generate a Pf DPY19 null mutant,&#xd;
demonstrating that this glycosyltransferase is not essential for the asexual blood development&#xd;
of the parasite. Pf DPY19 gene disruption was not associated with a growth phenotype, not&#xd;
even under endoplasmic reticulum-stressing conditions that could impair protein folding.&#xd;
The data presented in this work strongly suggest that Pf DPY19 is unlikely to play a critical&#xd;
role in the asexual blood stages of the parasite, at least under in vitro conditions.</dc:description>
   <dc:date>2019-10-29T11:23:53Z</dc:date>
   <dc:date>2019-10-29T11:23:53Z</dc:date>
   <dc:date>2019-09-27</dc:date>
   <dc:date>2019-10-25T18:00:30Z</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>0031-1820</dc:identifier>
   <dc:identifier>https://hdl.handle.net/2445/143332</dc:identifier>
   <dc:identifier>31559936</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Reproducció del document publicat a: http://dx.doi.org/10.1017/S0031182019001380</dc:relation>
   <dc:relation>Parasitology, 2019</dc:relation>
   <dc:relation>http://dx.doi.org/10.1017/S0031182019001380</dc:relation>
   <dc:rights>cc by (c) Cambridge University Press, 2019</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>6 p.</dc:format>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Cambridge University Press</dc:publisher>
   <dc:source>Articles publicats en revistes (ISGlobal)</dc:source>
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