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    <responseDate>2026-10-14T07:44:54Z</responseDate>
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    <identifier>10.57760/sciencedb.33421</identifier>
    <datestamp>2026-04-13T09:25:24Z</datestamp>
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  <dc:date>2026-04-13</dc:date>
  <dc:title>PEMT Couples Methionine Metabolism to Antiviral Defense by Restricting Influenza Virus NS1 mRNA Translation</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.33421</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>A549 cells were infected by IAV (PR8, H1N1) for 12 hrs at MOI=1, and then collected A549 and crosslinked with 1% formaldehyde (10 min) and quenched with 125 mM glycine. Sonicated lysates (Bioruptor Pico, 15 cycles) were incubated overnight with 5 &amp;mu;g anti-PEMT, anti-eIF4G1, or isotype IgG antibodies pre-conjugated to Protein A/G magnetic beads. Following high-stringency washes and reverse crosslinking (65&amp;deg;C, 4 h), RNA was purified via phenol-chloroform extraction and quantified (Qubit). rRNA-depleted libraries (NEBNext Ultra II) were sequenced on an Illumina NovaSeq 4000 (150-bp paired-end). Raw reads were aligned to the human (hg38) and IAV (PR8) genomes using STAR; enriched regions were identified via MACS2 peak calling with an FDR &amp;lt; 0.05.</dc:description>
  <dc:subject>IAV; A549; RNA IP-Sequencing; PEMT; eIF4G1</dc:subject>
  <dc:creator>Ou Qian</dc:creator>
  <dc:rights>EMBARGO</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-sa/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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