<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE128599" accession="SRP188964">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP188964</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA528276</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE128599</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Effect of cycloheximide in the co-translation mRNA degradation pattern in  set2D and rrp6D strains</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>We investigated cryptic transcription start site usage, chromatin organization and post-transcriptional consequences in Saccharomyces cerevisiae. We used 5PSeq approach, which measures ribosome dynamics by sequencing the presence of co-translation mRNA degradation intermediates, to assess if cryptic transcripts are engaged in active translation. Here we assay the effect of Cycloheximide treatment (CHX) in the co-translational degradation profile of using strains where cryptic transcription is enhanced. We study the profiles in set2D and rrp6D, enhanced for the presence of chromatin-sensitive and RNA degradation-sensitive cryptic transcripts respectively. Overall design: We performed 2 biologically independent 5PSeq experiments. All cells were grown in YPD. CHX treated samples were incubated for 10 min and flash frozen in N2.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE128599</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>31740578</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
