<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE216524" accession="SRP404403">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP404403</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA894167</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE216524</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Analysing the effect of cellular energy levels on codon-specific ribosome occupancy in vivo</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>The aim of this study is to evaluate how cellular energy levels shape codon-specific decoding and affect codon-mediated mRNA degradation. To this end we made use of HT5P-seq (Zhang &amp; Pelechano, 2021, PMID:35474692)  in S. cerevisiae to footprint the ribosome of co-translationally degraded mRNAs in vivo upon swift changes in the concentration of intracellular ATP and other energy metabolites. Overall design: HT5P-seq was performed in 5 different time points (3 replicates each time points), spanning 5 min before and 10 min after the addition of antimycin A to respiring yeast as described in Walther T et al. (PMID: 20087341)</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE216524</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>38491213</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
