RT Journal Article
SR Electronic
T1 Myc-dependent cell competition and proliferative response requires induction of the ribosome biogenesis regulator Peter Pan
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2020.05.06.080283
DO 10.1101/2020.05.06.080283
A1 Norman Zielke
A1 Anna Vähärautio
A1 Jianping Liu
A1 Jussi Taipale
YR 2020
UL http://biorxiv.org/content/early/2020/05/06/2020.05.06.080283.abstract
AB The transcription factor Myc is activated in most major forms of human cancer. Myc regulates a large set of target genes, and drives cell growth across animal phyla. However, it has not been clear which target genes are required for Myc-induced growth, and whether the targets are individually necessary or act in an additive fashion. Here, we have used comparative functional genomics to identify a core set of Myc target genes whose regulation is conserved between humans and Drosophila melanogaster. Most of these targets are essential genes involved in ribosome biogenesis and ribonucleotide metabolism. To identify Drosophila genes whose upregulation is necessary for Myc induced growth, we deleted the Myc binding sites (E-boxes) in the promoter regions of four genes using CRISPR/Cas9. All mutant flies were homozygous viable, indicating that E-box sequences are not required for basal expression of the Myc target genes. E-Box deletions in RpS20, RpS24 and Nop56 did not cause strong growth phenotypes. However, deletion of the E-box in the rRNA processing factor Peter Pan (ppan) made the flies resistant to Myc-induced cell growth, without affecting Myc-induced apoptosis. Despite their failure to respond to Myc, the ppanEbox−/− flies are healthy and display only a minor developmental delay, suggesting that it may be possible to treat or prevent tumorigenesis by targeting individual downstream targets of Myc.Competing Interest StatementThe authors have declared no competing interest.