PUBLICATION

TGS1 impacts snRNA 3'-end processing, ameliorates survival motor neuron-dependent neurological phenotypes in vivo and prevents neurodegeneration

Authors
Chen, L., Roake, C.M., Maccallini, P., Bavasso, F., Dehghannasiri, R., Santonicola, P., Mendoza-Ferreira, N., Scatolini, L., Rizzuti, L., Esposito, A., Gallotta, I., Francia, S., Cacchione, S., Galati, A., Palumbo, V., Kobin, M.A., Tartaglia, G.G., Colantoni, A., Proietti, G., Wu, Y., Hammerschmidt, M., De Pittà, C., Sales, G., Salzman, J., Pellizzoni, L., Wirth, B., Schiavi, E.D., Gatti, M., Artandi, S.E., Raffa, G.D.
ID
ZDB-PUB-220811-4
Date
2022
Source
Nucleic acids research   50(21): 12400-12424 (Journal)
Registered Authors
Hammerschmidt, Matthias
Keywords
none
MeSH Terms
  • Animals
  • Caenorhabditis elegans/genetics
  • Caenorhabditis elegans/metabolism
  • Drosophila/genetics
  • Drosophila melanogaster/genetics
  • Drosophila melanogaster/metabolism
  • HeLa Cells
  • Humans
  • Methyltransferases*/metabolism
  • Motor Neurons*/metabolism
  • Motor Neurons*/pathology
  • Phenotype
  • RNA, Small Nuclear*/metabolism
PubMed
35947650 Full text @ Nucleic Acids Res.
Abstract
Trimethylguanosine synthase 1 (TGS1) is a highly conserved enzyme that converts the 5'-monomethylguanosine cap of small nuclear RNAs (snRNAs) to a trimethylguanosine cap. Here, we show that loss of TGS1 in Caenorhabditis elegans, Drosophila melanogaster and Danio rerio results in neurological phenotypes similar to those caused by survival motor neuron (SMN) deficiency. Importantly, expression of human TGS1 ameliorates the SMN-dependent neurological phenotypes in both flies and worms, revealing that TGS1 can partly counteract the effects of SMN deficiency. TGS1 loss in HeLa cells leads to the accumulation of immature U2 and U4atac snRNAs with long 3' tails that are often uridylated. snRNAs with defective 3' terminations also accumulate in Drosophila Tgs1 mutants. Consistent with defective snRNA maturation, TGS1 and SMN mutant cells also exhibit partially overlapping transcriptome alterations that include aberrantly spliced and readthrough transcripts. Together, these results identify a neuroprotective function for TGS1 and reinforce the view that defective snRNA maturation affects neuronal viability and function.
Genes / Markers
Figures
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Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping