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        <datestamp>2026-09-14T20:09:57Z</datestamp>
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          <dc:title>Dynamic Atlas
and Functional Regulatory Network of
the Whole-Brain Proteome Across 24-Hour Temporal States in Vespertilio sinensis</dc:title>
          <dc:creator>Tianhui Wang (7894490)</dc:creator>
          <dc:creator>Hui Wang (30400)</dc:creator>
          <dc:creator>Xin Li (51274)</dc:creator>
          <dc:creator>Jiang Feng (286772)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Physical Sciences not elsewhere classified</dc:subject>
          <dc:subject>Medicine</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>Ecology</dc:subject>
          <dc:subject>Biological Sciences not elsewhere classified</dc:subject>
          <dc:subject>Inorganic Chemistry</dc:subject>
          <dc:subject>vespertilio sinensis &lt;/</dc:subject>
          <dc:subject>studying diurnal rhythms</dc:subject>
          <dc:subject>revealing partial transcript</dc:subject>
          <dc:subject>proteomic rhythmic analysis</dc:subject>
          <dc:subject>protein rhythmic decoupling</dc:subject>
          <dc:subject>induced metabolic damage</dc:subject>
          <dc:subject>diurnal regulatory landscape</dc:subject>
          <dc:subject>circadian output pathways</dc:subject>
          <dc:subject>based quantitative proteomics</dc:subject>
          <dc:subject>activated sulfur biosynthesis</dc:subject>
          <dc:subject>7652 identified proteins</dc:subject>
          <dc:subject>574 rhythmic proteins</dc:subject>
          <dc:subject>high energy demands</dc:subject>
          <dc:subject>energy metabolic pathways</dc:subject>
          <dc:subject>hour temporal states</dc:subject>
          <dc:subject>hour physiological states</dc:subject>
          <dc:subject>module 9 ).</dc:subject>
          <dc:subject>functional regulatory network</dc:subject>
          <dc:subject>first systematic atlas</dc:subject>
          <dc:subject>brain proteome across</dc:subject>
          <dc:subject>flight energy regulation</dc:subject>
          <dc:subject>upcoming nocturnal activity</dc:subject>
          <dc:subject>energy homeostasis</dc:subject>
          <dc:subject>hour cycle</dc:subject>
          <dc:subject>nocturnal lifestyle</dc:subject>
          <dc:subject>module 3</dc:subject>
          <dc:subject>functional enrichment</dc:subject>
          <dc:subject>dynamic atlas</dc:subject>
          <dc:subject>brain tissues</dc:subject>
          <dc:subject>bat brain</dc:subject>
          <dc:subject>unique models</dc:subject>
          <dc:subject>series clustering</dc:subject>
          <dc:subject>powered flight</dc:subject>
          <dc:subject>performed directdia</dc:subject>
          <dc:subject>parallel transcriptomic</dc:subject>
          <dc:subject>molecular layers</dc:subject>
          <dc:subject>mammals capable</dc:subject>
          <dc:subject>eliminate flight</dc:subject>
          <dc:subject>dna repair</dc:subject>
          <dc:subject>calcium signaling</dc:subject>
          <dc:subject>antioxidant defense</dc:subject>
          <dc:description>As the only mammals capable of powered flight, bats exhibit
extreme
metabolic fluctuations adapted to flight and a nocturnal lifestyle,
making them unique models for studying diurnal rhythms and energy
homeostasis. We performed directDIA-based quantitative proteomics
on whole-brain tissues of &lt;i&gt;Vespertilio sinensis&lt;/i&gt; across
four distinct 24-hour physiological states: Rest, Sleep, Wake, and
Activity. Among the 7652 identified proteins, a total of 643 differentially
expressed proteins (DEPs) were screened via pairwise comparisons across
timepoints. Time-series clustering further resolved two statistically
significant temporal expression modules (Module 3 and Module 9). Combined
with functional enrichment of DEPs and phase set enrichment analysis
(PSEA) of 574 rhythmic proteins, our multi-layered omics results collectively
uncovered stage-specific molecular adaptive patterns. The Active state
upregulated oxidative phosphorylation and thermogenesis for high energy
demands, the Rest state activated immune clearance and autophagy to
eliminate flight-induced metabolic damage, the Sleep state suppressed
global transcription, calcium signaling and DNA repair to reduce neural
energy consumption, and the Wake state (pre-dusk) pre-activated sulfur
biosynthesis, antioxidant defense, and energy metabolic pathways to
prepare for upcoming nocturnal activity. Parallel transcriptomic and
proteomic rhythmic analysis further identified 19 conserved oscillatory
molecules at both molecular layers, revealing partial transcript-protein
rhythmic decoupling in the bat brain and refining the diurnal regulatory
landscape. As the first systematic atlas of the bat whole-brain proteome
across a 24-hour cycle, this study uncovers molecular strategies maintaining
brain homeostasis, providing a foundation for understanding diurnal
physiological adaptation, flight energy regulation, and circadian
output pathways.</dc:description>
          <dc:date>2026-09-14T00:00:00Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.1021/acs.jproteome.6c00330.s006</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Dynamic_Atlas_and_Functional_Regulatory_Network_of_the_Whole-Brain_Proteome_Across_24-Hour_Temporal_States_in_Vespertilio_sinensis/33756272</dc:relation>
          <dc:rights>CC BY-NC 4.0</dc:rights>
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