<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="A-Myb" center_name="Umass Medical School" accession="SRP008820">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP008820</PRIMARY_ID>
      <SUBMITTER_ID namespace="Umass Medical School">A-Myb</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>The Transcription Factor A-Myb Initiates Pachytene piRNA Production During Mouse Spermatogenesis</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>In animals, germ cells require PIWI-interacting RNAs (piRNAs), small silencing RNAs that suppress transposons and enable gamete maturation. In mammals, transposon-silencing piRNAs accumulate early in spermatogenesis, whereas pachytene piRNAs are produced later in sperm development and account for &gt;95% of all piRNAs in adult mouse testes. Without pachytene piRNAs, mice fail to produce functional sperm , but neither the molecular function nor the trigger for pachytene piRNA production is known. Here, we show that the transcription factor A-Myb initiates pachytene piRNAs production. A-Myb drives transcription of both pachytene piRNA precursor RNAs and the mRNA encoding Miwi, the Argonaute protein through which pachytene piRNAs function. Together, A-Myb and Miwi create a conserved feed-forward loop that ensures the rapid accumulation of pachytene piRNAs.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME/>
      <STUDY_DESCRIPTION>Small RNA, ChIP-Seq, and RNA-Seq libraries used in publication</STUDY_DESCRIPTION>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
