Dual regulation of lin28a by Myc is necessary during zebrafish retina regeneration.
Soumitra MitraPoonam SharmaSimran KaurMohammad Anwar KhursheedShivangi GuptaMansi ChaudharyAkshai J KurupRajesh RamachandranPublished in: The Journal of cell biology (2019)
Cellular reprogramming leading to induction of Muller glia-derived progenitor cells (MGPCs) with stem cell characteristics is essential for zebrafish retina regeneration. Although several regeneration-specific genes are characterized, the significance of MGPC-associated Mycb induction remains unknown. Here, we show that early expression of Mycb induces expression of genes like ascl1a, a known activator of lin28a in MGPCs. Notably, mycb is simultaneously activated by Ascl1a and repressed by Insm1a in regenerating retina. Here, we unravel a dual role of Mycb in lin28a expression, both as an activator through Ascl1a in MGPCs and a repressor in combination with Hdac1 in neighboring cells. Myc inhibition reduces the number of MGPCs and abolishes normal regeneration. Myc in collaboration with Hdac1 inhibits her4.1, an effector of Delta-Notch signaling. Further, we also show the repressive role of Delta-Notch signaling on lin28a expression in post-injured retina. Our studies reveal mechanistic understanding of Myc pathway during zebrafish retina regeneration, which could pave way for therapeutic intervention during mammalian retina regeneration.
Keyphrases
- stem cells
- poor prognosis
- diabetic retinopathy
- optic nerve
- transcription factor
- genome wide
- randomized controlled trial
- binding protein
- wound healing
- long non coding rna
- dendritic cells
- oxidative stress
- nuclear factor
- single cell
- cell cycle arrest
- bone marrow
- dna methylation
- cell proliferation
- cell death
- mesenchymal stem cells
- case control