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Matthias Lange / Curated_wheat_historical_phenotypic_data_from_European_Genebanks
Creative Commons Attribution 4.0 InternationalUpdated -
Kevin Schneider / Maus_Microbiom
Creative Commons Attribution 4.0 InternationalUpdated -
Usadellab / Cold_salt_stress_Capsicum
Creative Commons Attribution 4.0 InternationalUpdated -
Differential analysis of lpa2 mutant Chlamy complexome
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CEPLAS / VonDahlen-2023
Creative Commons Attribution 4.0 InternationalGlobal expression patterns of R-genes in tomato and potato
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ARC_templates / Genomics_ARC
Creative Commons Attribution 4.0 InternationalUpdated -
SFB1535_MibiNet / Sankaranarayanan-2023
Creative Commons Attribution 4.0 InternationalFungal pathogens depend on sophisticated gene expression programs for successful infection. A crucial component is RNA regulation mediated by RNA-binding proteins (RBPs). However, little is known about the spatiotemporal RNA control mechanisms during fungal pathogenicity. Here, we discover that the RBP Khd4 defines a distinct mRNA regulon to orchestrate membrane trafficking during pathogenic development of Ustilago maydis. By establishing hyperTRIBE for fungal RBPs, we generated a comprehensive transcriptome-wide map of Khd4 interactions in vivo. We identify a defined set of target mRNAs enriched for regulatory proteins involved, e.g., in GTPase signaling. Khd4 controls the stability of target mRNAs via its cognate regulatory element AUACCC present in their 3′ untranslated regions. Studying individual examples reveals a unique link between Khd4 and vacuole maturation. Thus, we uncover a distinct role for an RNA stability factor defining a specific mRNA regulon for membrane trafficking during pathogenicity.
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