| Literature DB >> 36192632 |
Tatyana D Larionova1, Soniya Bastola2, Tatiana E Aksinina1, Ksenia S Anufrieva3,4, Jia Wang5, Victoria O Shender1,3,4, Dmitriy E Andreev1,6, Tatiana F Kovalenko1, Georgij P Arapidi1,3,4, Polina V Shnaider3,4, Anastasia N Kazakova4, Yaroslav A Latyshev7, Victor V Tatarskiy8, Alexander A Shtil9, Pascale Moreau10, Francis Giraud10, Chaoxi Li11, Yichan Wang5, Maria P Rubtsova1,6, Olga A Dontsova1,6,12, Michael Condro2, Benjamin M Ellingson13,14,15,16, Mikhail I Shakhparonov1, Harley I Kornblum17, Ichiro Nakano18, Marat S Pavlyukov19,20.
Abstract
Glioblastoma (GBM) is characterized by exceptionally high intratumoral heterogeneity. However, the molecular mechanisms underlying the origin of different GBM cell populations remain unclear. Here, we found that the compositions of ribosomes of GBM cells in the tumour core and edge differ due to alternative RNA splicing. The acidic pH in the core switches before messenger RNA splicing of the ribosomal gene RPL22L1 towards the RPL22L1b isoform. This allows cells to survive acidosis, increases stemness and correlates with worse patient outcome. Mechanistically, RPL22L1b promotes RNA splicing by interacting with lncMALAT1 in the nucleus and inducing its degradation. Contrarily, in the tumour edge region, RPL22L1a interacts with ribosomes in the cytoplasm and upregulates the translation of multiple messenger RNAs including TP53. We found that the RPL22L1 isoform switch is regulated by SRSF4 and identified a compound that inhibits this process and decreases tumour growth. These findings demonstrate how distinct GBM cell populations arise during tumour growth. Targeting this mechanism may decrease GBM heterogeneity and facilitate therapy.Entities:
Year: 2022 PMID: 36192632 DOI: 10.1038/s41556-022-00994-w
Source DB: PubMed Journal: Nat Cell Biol ISSN: 1465-7392 Impact factor: 28.213