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PRMT5 promotes full-length HTT expression by repressing multiple proximal intronic polyadenylation sites

Title: PRMT5 promotes full-length HTT expression by repressing multiple proximal intronic polyadenylation sites
Authors: Yadav, Manisha; AlQazzaz, Mona A.; Ciamponi, Felipe E.; Ho, Jolene C.; Maron, Maxim I.; Sababi, Aiden M.; MacLeod, Graham; Ahmadi, Moloud; Bullivant, Garrett; Tano, Vincent; Langley, Sarah R.; Sánchez-Osuna, María; Sachamitr, Patty; Kushida, Michelle; Bardile, Costanza Ferrari; Pouladi, Mahmoud A.; Kurtz, Rebecca; Richards, Laura; Pugh, Trevor; Tyers, Mike; Angers, Stephane; Dirks, Peter B.; Bader, Gary D.; Truant, Ray; Massirer, Katlin B.; Barsyte-Lovejoy, Dalia; Shechter, David; Harding, Rachel J.; Arrowsmith, Cheryl H.; Prinos, Panagiotis
Publisher Information: Oxford University Press
Publication Year: 2025
Collection: Cardiff University: ORCA (Online Research @ Cardiff)
Description: Expansion of the CAG trinucleotide repeat tract in exon 1 of the Huntingtin (HTT) gene causes Huntington’s disease (HD) through the expression of a polyglutamine-expanded form of the HTT protein. This mutation triggers cellular and biochemical pathologies, leading to cognitive, motor, and psychiatric symptoms in HD patients. Targeting HTT splicing with small molecule drugs is a compelling approach to lowering HTT protein levels to treat HD, and splice modulators are currently being tested in the clinic. Here, we identify PRMT5 as a novel regulator of HTT messenger RNA (mRNA) splicing and alternative polyadenylation. PRMT5 inhibition disrupts the splicing of HTT introns 9 and 10, leading to the activation of multiple proximal intronic polyadenylation sites within these introns and promoting premature termination, cleavage, and polyadenylation of the HTT mRNA. This suggests that HTT protein levels may be lowered due to this mechanism. We also detected increasing levels of these truncated HTT transcripts across a series of neuronal differentiation samples, which correlated with lower PRMT5 expression. Notably, PRMT5 inhibition in glioblastoma stem cells potently induced neuronal differentiation. We posit that PRMT5-mediated regulation of intronic polyadenylation, premature termination, and cleavage of the HTT mRNA modulates HTT expression and plays an important role during neuronal differentiation.
Document Type: article in journal/newspaper
File Description: application/pdf
Language: English
Relation: https://orca.cardiff.ac.uk/id/eprint/178130/1/gkaf347.pdf; Yadav, Manisha, AlQazzaz, Mona A., Ciamponi, Felipe E., Ho, Jolene C., Maron, Maxim I., Sababi, Aiden M., MacLeod, Graham, Ahmadi, Moloud, Bullivant, Garrett, Tano, Vincent, Langley, Sarah R. https://orca.cardiff.ac.uk/view/cardiffauthors/A2763586Y.html orcid:0000-0003-4419-476X orcid:0000-0003-4419-476X, Sánchez-Osuna, María, Sachamitr, Patty, Kushida, Michelle, Bardile, Costanza Ferrari, Pouladi, Mahmoud A., Kurtz, Rebecca, Richards, Laura, Pugh, Trevor, Tyers, Mike, Angers, Stephane, Dirks, Peter B., Bader, Gary D., Truant, Ray, Massirer, Katlin B., Barsyte-Lovejoy, Dalia, Shechter, David, Harding, Rachel J., Arrowsmith, Cheryl H. and Prinos, Panagiotis 2025. PRMT5 promotes full-length HTT expression by repressing multiple proximal intronic polyadenylation sites. Nucleic Acids Research 53 (8) , gkaf347. 10.1093/nar/gkaf347 https://doi.org/10.1093/nar%2Fgkaf347 file https://orca.cardiff.ac.uk/id/eprint/178130/1/gkaf347.pdf
DOI: 10.1093/nar/gkaf347
Availability: https://orca.cardiff.ac.uk/id/eprint/178130/; https://doi.org/10.1093/nar/gkaf347; https://orca.cardiff.ac.uk/id/eprint/178130/1/gkaf347.pdf
Rights: cc_by_nc_4_0
Accession Number: edsbas.E9170321
Database: BASE