Defective myelination in an RNA polymerase III mutant leukodystrophic mouse.
Emilio MerhebMin-Hui CuiJuwen C DuBoisCraig A BranchMaria E GulinelloBridget Shafit-ZagardoRobyn D MoirIan M WillisPublished in: Proceedings of the National Academy of Sciences of the United States of America (2021)
RNA polymerase (Pol) III synthesizes abundant short noncoding RNAs that have essential functions in protein synthesis, secretion, and other processes. Despite the ubiquitous functions of these RNAs, mutations in Pol III subunits cause Pol III-related leukodystrophy, an early-onset neurodegenerative disease. The basis of this neural sensitivity and the mechanisms of disease pathogenesis are unknown. Here we show that mice expressing pathogenic mutations in the largest Pol III subunit, Polr3a , specifically in Olig2-expressing cells, have impaired growth and developmental delay, deficits in cognitive, sensory, and fine sensorimotor function, and hypomyelination in multiple regions of the cerebrum and spinal cord. These phenotypes reflect a subset of clinical features seen in patients. In contrast, the gross motor defects and cerebellar hypomyelination that are common features of severely affected patients are absent in the mice, suggesting a relatively mild form of the disease in this conditional model. Our results show that disease pathogenesis in the mice involves defects that reduce both the number of mature myelinating oligodendrocytes and the ability of these cells to produce a myelin sheath of normal thickness. The findings suggest unique sensitivities of oligodendrogenesis and myelination to perturbations of Pol III transcription.
Keyphrases
- early onset
- end stage renal disease
- spinal cord
- newly diagnosed
- ejection fraction
- induced apoptosis
- wild type
- high fat diet induced
- magnetic resonance
- traumatic brain injury
- cell cycle arrest
- prognostic factors
- metabolic syndrome
- magnetic resonance imaging
- skeletal muscle
- late onset
- neuropathic pain
- multiple sclerosis
- type diabetes
- transcription factor
- patient reported