SUMOylation controls stem cell proliferation and regional cell death through Hedgehog signaling in planarians

  • Manish Thiruvalluvan
  • , Paul G. Barghouth
  • , Assaf Tsur
  • , Limor Broday
  • , Néstor J. Oviedo*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Mechanisms underlying anteroposterior body axis differences during adult tissue maintenance and regeneration are poorly understood. Here, we identify that post-translational modifications through the SUMO (Small Ubiquitin-like Modifier) machinery are evolutionarily conserved in the Lophotrocozoan Schmidtea mediterranea. Disruption of SUMOylation in adult animals by RNA-interference of the only SUMO E2 conjugating enzyme Ubc9 leads to a systemic increase in DNA damage and a remarkable regional defect characterized by increased cell death and loss of the posterior half of the body. We identified that Ubc9 is mainly expressed in planarian stem cells (neoblasts) but it is also transcribed in differentiated cells including neurons. Regeneration in Ubc9(RNAi) animals is impaired and associated with low neoblast proliferation. We present evidence indicating that Ubc9-induced regional cell death is preceded by alterations in transcription and spatial expression of repressors and activators of the Hedgehog signaling pathway. Our results demonstrate that SUMOylation acts as a regional-specific cue to regulate cell fate during tissue renewal and regeneration.

Original languageEnglish
Pages (from-to)1285-1301
Number of pages17
JournalCellular and Molecular Life Sciences
Volume75
Issue number7
DOIs
StatePublished - 1 Apr 2018

Funding

FundersFunder number
National Institute of Health
National Institutes of HealthCA176114
National Cancer Institute
National Institute of General Medical SciencesR15GM109372
Israel Cancer Research Fund14-101-PG
Eunice Kennedy Shriver National Institute of Child Health and Human Development
University of California Merced
Israel Science FoundationISF 1878/15

    Keywords

    • Genomic instability
    • Patched
    • Rad51
    • Regeneration
    • Ubc9

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