Leukodystrophy-associated POLR3A mutations down-regulate the RNA polymerase III transcript and important regulatory RNA BC200
| Autor: | Benoit Coulombe, Elisabeth Meloche, Geneviève Bernard, Raphael Schiffmann, Claudia L. Kleinman, Marc R. Fabian, Marie-Josée Dicaire, Martin Teichmann, Karine Choquet, Adeline Vanderver, Diane Forget, Bernard Brais |
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| Rok vydání: | 2019 |
| Předmět: |
0301 basic medicine
RNA polymerase III leukodystrophy Down-Regulation Genes Recessive Biology Biochemistry Transcriptome 03 medical and health sciences chemistry.chemical_compound CRISPR/Cas proteomics brain cytoplasmic 200 RNA (BCYRN1) Transcription (biology) Translational regulation Humans RNA Messenger Molecular Biology Gene 030102 biochemistry & molecular biology RNA Molecular Bases of Disease Cell Biology Cell biology transfer RNA (tRNA) myelin Hereditary Central Nervous System Demyelinating Diseases 030104 developmental biology chemistry Mutation Transfer RNA RNA Long Noncoding RNA-seq transcription oligodendrocyte DNA HeLa Cells |
| Zdroj: | The Journal of Biological Chemistry |
| ISSN: | 0021-9258 |
| DOI: | 10.1074/jbc.ra118.006271 |
| Popis: | RNA polymerase III (Pol III) is an essential enzyme responsible for the synthesis of several small noncoding RNAs, a number of which are involved in mRNA translation. Recessive mutations in POLR3A, encoding the largest subunit of Pol III, cause POLR3-related hypomyelinating leukodystrophy (POLR3–HLD), characterized by deficient central nervous system myelination. Identification of the downstream effectors of pathogenic POLR3A mutations has so far been elusive. Here, we used CRISPR-Cas9 to introduce the POLR3A mutation c.2554A→G (p.M852V) into human cell lines and assessed its impact on Pol III biogenesis, nuclear import, DNA occupancy, transcription, and protein levels. Transcriptomic profiling uncovered a subset of transcripts vulnerable to Pol III hypofunction, including a global reduction in tRNA levels. The brain cytoplasmic BC200 RNA (BCYRN1), involved in translation regulation, was consistently affected in all our cellular models, including patient-derived fibroblasts. Genomic BC200 deletion in an oligodendroglial cell line led to major transcriptomic and proteomic changes, having a larger impact than those of POLR3A mutations. Upon differentiation, mRNA levels of the MBP gene, encoding myelin basic protein, were significantly decreased in POLR3A-mutant cells. Our findings provide the first evidence for impaired Pol III transcription in cellular models of POLR3–HLD and identify several candidate effectors, including BC200 RNA, having a potential role in oligodendrocyte biology and involvement in the disease. |
| Databáze: | OpenAIRE |
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