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    <responseDate>2026-10-11T03:36:43Z</responseDate>
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    <identifier>10.57760/sciencedb.31947</identifier>
    <datestamp>2026-07-02T16:11:51Z</datestamp>
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<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" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2026-07-02</dc:date>
  <dc:title>The genotoxic stress-inducible gene GEI1(Orf19.3109) is a repressor of virulence in Candida albicans</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.31947</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Transcriptional reprogramming under genotoxic stress is essential for the survival and pathogenesis of Candida albicans. While many DNA damage response (DDR) genes are well-characterized, the functions of pathogen-specific, stress-inducible genes remain enigmatic. Here, we characterized GEI1 (Orf19.3109), a gene robustly induced by genotoxic agents and oxidative stress, which lacks a discernible ortholog in Saccharomyces cerevisiae. Unexpectedly, although GEI1 expression is triggered by DNA damage, its deletion does not impair genotoxin tolerance. Instead, the gei1&amp;Delta;/&amp;Delta; mutant exhibits a striking increase in resistance to oxidative stress, characterized by reduced intracellular reactive oxygen species (ROS) accumulation and attenuated apoptosis. Furthermore, loss of GEI1 leads to massive hyper-secretion of extracellular aspartyl proteases (Saps) and displays an extreme hypervirulence phenotype in the Galleria mellonella infection model. Integrated transcriptomic profiling and CRISPR-interference (CRISPRi) assays revealed that GEI1 functions as a negative regulator of the antioxidant-defense axis and proteolytic enzyme secretion. We demonstrate that the hypervirulence of the gei1&amp;Delta;/&amp;Delta; strain is primarily driven by the transcriptional de-repressions of SAP1, SAP3 and SAP5 and the putative alcohol dehydrogenase ADH4. Repression of these downstream effectors in the gei1&amp;Delta;/&amp;Delta; background successfully restricted protease hyper-secretion and restored fungal virulence to wild-type levels. Our findings uncouple transcriptional induction from conventional DNA repair functions and reveal a novel regulatory checkpoint where GEI1 links genotoxic stress signaling to the suppression of key pathogenic traits in C. albicans.</dc:description>
  <dc:subject>Candida albicans; GEI1; virulence</dc:subject>
  <dc:creator>Yi Zhou</dc:creator>
  <dc:creator>Wenxia Gao</dc:creator>
  <dc:creator>Yuting Feng</dc:creator>
  <dc:creator>Xingyi Tang</dc:creator>
  <dc:creator>Yutong Jin</dc:creator>
  <dc:creator>Jinrong Feng</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
</oai_dc:dc>

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