Genome-wide analysis of Musashi-2 targets reveals novel functions in governing epithelial cell migration

Christopher G. Bennett, Kent Riemondy, Douglas A. Chapnick, Eric Bunker, Xuedong Liu, Scott Kuersten, Rui Yi*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

41 Scopus citations


The Musashi-2 (Msi2) RNA-binding protein maintains stem cell self-renewal and promotes oncogenesis by enhancing cell proliferation in hematopoietic and gastrointestinal tissues. However, it is unclear how Msi2 recognizes and regulates mRNA targets in vivo and whether Msi2 primarily controls cell growth in all cell types. Here we identified Msi2 targets with HITS-CLIP and revealed that Msi2 primarily recognizes mRNA 3′UTRs at sites enriched in multiple copies of UAG motifs in epithelial progenitor cells. RNA-seq and ribosome profiling demonstrated that Msi2 promotes targeted mRNA decay without affecting translation efficiency. Unexpectedly, the most prominent Msi2 targets identified are key regulators that govern cell motility with a high enrichment in focal adhesion and extracellular matrix-receptor interaction, in addition to regulators of cell growth and survival. Loss of Msi2 stimulates epithelial cell migration, increases the number of focal adhesions and also compromises cell growth. These findings provide new insights into the molecular mechanisms of Msi2's recognition and repression of targets and uncover a key function of Msi2 in restricting epithelial cell migration.

Original languageEnglish (US)
Pages (from-to)3788-3800
Number of pages13
JournalNucleic acids research
Issue number8
StatePublished - May 5 2016

ASJC Scopus subject areas

  • Genetics


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