ZFIN ID: ZDB-PUB-191022-18
The RNA binding protein fragile X mental retardation protein promotes myelin sheath growth
Doll, C.A., Yergert, K.M., Appel, B.H.
Date: 2019
Source: Glia   68(3): 495-508 (Journal)
Registered Authors: Appel, Bruce, Doll, Caleb
Keywords: RNA binding protein, fragile X mental retardation protein, messenger RNA, myelin, oligodendrocyte, spinal cord, zebrafish
MeSH Terms:
  • Animals
  • Fragile X Mental Retardation Protein/genetics
  • Fragile X Mental Retardation Protein/metabolism*
  • Fragile X Syndrome/genetics
  • Fragile X Syndrome/metabolism
  • Gene Expression Regulation, Developmental/genetics
  • Myelin Sheath/genetics
  • Myelin Sheath/metabolism*
  • Neuronal Plasticity/physiology
  • Neurons/metabolism
  • Oligodendroglia/metabolism*
  • RNA, Messenger/metabolism
  • RNA-Binding Proteins/metabolism*
  • Zebrafish
PubMed: 31626382 Full text @ Glia
ABSTRACT
During development, oligodendrocytes in the central nervous system extend a multitude of processes that wrap axons with myelin. The highly polarized oligodendrocytes generate myelin sheaths on many different axons, which are far removed from the cell body. Neurons use RNA binding proteins to transport, stabilize, and locally translate mRNA in distal domains of neurons. Local synthesis of synaptic proteins during neurodevelopment facilitates the rapid structural and functional changes underlying neural plasticity and avoids extensive protein transport. We hypothesize that RNA binding proteins also regulate local mRNA regulation in oligodendrocytes to promote myelin sheath growth. Fragile X mental retardation protein (FMRP), an RNA binding protein that plays essential roles in the growth and maturation of neurons, is also expressed in oligodendrocytes. To determine whether oligodendrocytes require FMRP for myelin sheath development, we examined fmr1-/- mutant zebrafish and drove FMR1 expression specifically in oligodendrocytes. We found oligodendrocytes in fmr1-/- mutants developed myelin sheaths of diminished length, a phenotype that can be autonomously rescued in oligodendrocytes with FMR1 expression. Myelin basic protein (Mbp), an essential myelin protein, was reduced in myelin tracts of fmr1-/- mutants, but loss of FMRP function did not impact the localization of mbpa transcript in myelin. Finally, expression of FMR1-I304N, a missense allele that abrogates FMRP association with ribosomes, failed to rescue fmr1-/- mutant sheath growth and induced short myelin sheaths in oligodendrocytes of wild-type larvae. Taken together, these data suggest that FMRP promotes sheath growth through local regulation of translation.
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