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        <datestamp>2026-09-28T17:53:27Z</datestamp>
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          <dc:title>&lt;p&gt;Analysis of nuclear metabolic enzymes across the &lt;i&gt;T. cruzi&lt;/i&gt; cell cycle.&lt;/p&gt;</dc:title>
          <dc:creator>Ana Paula Menezes (25132835)</dc:creator>
          <dc:creator>Camila Gachet-Castro (11579152)</dc:creator>
          <dc:creator>Suzanne McGill (11916067)</dc:creator>
          <dc:creator>Richard Burchmore (178746)</dc:creator>
          <dc:creator>Ariel Silber (25132838)</dc:creator>
          <dc:creator>Maria Carolina Elias (9906069)</dc:creator>
          <dc:creator>Júlia P. C. da Cunha (25132841)</dc:creator>
          <dc:subject>Biophysics</dc:subject>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Physical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Genetics</dc:subject>
          <dc:subject>Molecular Biology</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Chemical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Hematology</dc:subject>
          <dc:subject>Computational  Biology</dc:subject>
          <dc:subject>unique cellular features</dc:subject>
          <dc:subject>transition using hydroxyurea</dc:subject>
          <dc:subject>regulating fundamental processes</dc:subject>
          <dc:subject>pyruvate kinase activities</dc:subject>
          <dc:subject>maintaining genomic integrity</dc:subject>
          <dc:subject>hu ), followed</dc:subject>
          <dc:subject>cd ), represents</dc:subject>
          <dc:subject>specific expression patterns</dc:subject>
          <dc:subject>previously underappreciated role</dc:subject>
          <dc:subject>gene expression regulation</dc:subject>
          <dc:subject>canonical regulatory mechanisms</dc:subject>
          <dc:subject>&gt;, potentially influencing</dc:subject>
          <dc:subject>trypanosoma cruzi &lt;/</dc:subject>
          <dc:subject>purified nuclear fraction</dc:subject>
          <dc:subject>metabolic enzymes including</dc:subject>
          <dc:subject>gene expression</dc:subject>
          <dc:subject>metabolic enzymes</dc:subject>
          <dc:subject>cruzi &lt;/</dc:subject>
          <dc:subject>pivotal role</dc:subject>
          <dc:subject>variant histones</dc:subject>
          <dc:subject>valuable model</dc:subject>
          <dc:subject>temporal compartmentalization</dc:subject>
          <dc:subject>specialized organelles</dc:subject>
          <dc:subject>revealing distinct</dc:subject>
          <dc:subject>results suggest</dc:subject>
          <dc:subject>provide insights</dc:subject>
          <dc:subject>proteins involved</dc:subject>
          <dc:subject>proteins identified</dc:subject>
          <dc:subject>protein synthesis</dc:subject>
          <dc:subject>nucleoside metabolisms</dc:subject>
          <dc:subject>nuclear region</dc:subject>
          <dc:subject>nuclear proteome</dc:subject>
          <dc:subject>nuclear division</dc:subject>
          <dc:subject>microtubule dynamics</dc:subject>
          <dc:subject>increased levels</dc:subject>
          <dc:subject>immunofluorescence supported</dc:subject>
          <dc:subject>identified 2</dc:subject>
          <dc:subject>eukaryotic models</dc:subject>
          <dc:subject>etiological agent</dc:subject>
          <dc:subject>dna replication</dc:subject>
          <dc:subject>diverging eukaryotes</dc:subject>
          <dc:subject>citrate synthase</dc:subject>
          <dc:subject>chromosome condensation</dc:subject>
          <dc:description>&lt;p&gt;Proportion of nuclear proteins associated with metabolism (5.96%) identified using GO terms related to key metabolic processes, including “cellular amino acid metabolic process” (GO:0006520), “carbohydrate metabolic process” (GO:0005975), “pyruvate metabolic process” (GO:0006090), “ATP metabolic process” (GO:00046034), “nucleotide metabolic process” (GO:0009116), “nucleoside metabolic process” (GO:0009117), “lipid metabolic process” (GO:0006629), and “generation of precursor metabolites and energy” (GO:0006091). &lt;b&gt;(B)&lt;/b&gt; KEGG pathway enrichment analysis of the metabolic enzymes identified in &lt;b&gt;(A)&lt;/b&gt;, performed using TriTrypDB’s tool with a Bonferroni-corrected p-value cutoff of 0.05. Enriched pathways are shown according to fold enrichment. &lt;b&gt;(C)&lt;/b&gt; Venn diagram comparing the nuclear proteins identified in this study (CC_PN) with those present in the nuclear proteome (CC_PT) (De Castro Moreira Dos Santos et al., 2015) and those at chromatin proteome (Chr_P) (De Jesus et al., 2017). &lt;b&gt;(D)&lt;/b&gt; Hierarchical clustering analysis of all protein expression profiles across different cell cycle phases. The protein data abundance was normalized before clustering by the Euclidean distance ratio. &lt;b&gt;(E)&lt;/b&gt; Venn diagram between the nuclear cell cycle proteins identified in this study (CC_NP) and the Cell cycle proteome (CC_P) (Santos Júnior et al., 2021). &lt;b&gt;(F)&lt;/b&gt; Box plots representing the relative abundance (%) of nuclear metabolic proteins found in (A) and ribosomal proteins across cell cycle phases.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T17:59:59Z</dc:date>
          <dc:type>Image</dc:type>
          <dc:type>Figure</dc:type>
          <dc:identifier>10.1371/journal.pntd.0013299.g004</dc:identifier>
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