Defective myelination in an RNA polymerase III mutant leukodystrophic mouse
| Autor: | Bridget Shafit-Zagardo, Min Hui Cui, Emilio Merheb, Robyn D. Moir, Maria Gulinello, Ian M. Willis, Juwen C. DuBois, Craig A. Branch |
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| Rok vydání: | 2020 |
| Předmět: |
Male
Lineage (genetic) Protein subunit Growth Biology RNA polymerase III OLIG2 Pathogenesis Mice chemistry.chemical_compound Transcription (biology) RNA polymerase Protein biosynthesis medicine Animals Humans Multidisciplinary Leukodystrophy RNA Polymerase III Biological Sciences medicine.disease Phenotype Mice Mutant Strains Oligodendrocyte Cell biology medicine.anatomical_structure chemistry Mutation Demyelinating Diseases |
| Zdroj: | Proc Natl Acad Sci U S A |
| Popis: | RNA polymerase (Pol) III synthesizes abundant short non-coding 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. 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. Thus, the findings suggest cell-specific roles for Pol III in the development and/or survival of oligodendrocytes as well as their function in myelination.Significance StatementPathogenic mutations in subunits of RNA polymerase (Pol) III cause a prevalent autosomal recessive form of leukodystrophy. However, understanding of the mechanisms of pathogenesis, including how ubiquitously-expressed Pol III mutations affect primarily the central nervous system, has been limited by the absence of an animal model of the disease. We show that conditional knock-in of pathogenic Polr3a mutations in the Olig2 lineage in mice results in growth, neurobehavioral and hypomyelination phenotypes reflecting a subset of clinical features of Pol III-related leukodystrophy patients. Myelination defects in the mice identify neural-specific roles for Pol III transcription. The phenotypes of Pol III-related leukodystrophic mice enable genetic and pharmacological approaches aimed at mitigating the consequences of this disease in humans. |
| Databáze: | OpenAIRE |
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