A homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly.

TitleA homozygous MRPL24 mutation causes a complex movement disorder and affects the mitoribosome assembly.
Publication TypeJournal Article
Year of Publication2020
AuthorsDi Nottia, M, Marchese, M, Verrigni, D, Mutti, C, Torraco, A, Oliva, R, Fernandez-Vizarra, E, Morani, F, Trani, G, Rizza, T, Ghezzi, D, Ardissone, A, Nesti, C, Vasco, G, Zeviani, M, Minczuk, M, Bertini, E, Santorelli, FMaria, Carrozzo, R
JournalNeurobiol Dis
Pagination104880
Date Published2020 Apr 25
ISSN1095-953X
Abstract

Mitochondrial ribosomal protein large 24 (MRPL24) is 1 of the 82 protein components of mitochondrial ribosomes, playing an essential role in the mitochondrial translation process. We report here on a baby girl with cerebellar atrophy, choreoathetosis of limbs and face, intellectual disability and a combined defect of complexes I and IV in muscle biopsy, caused by a homozygous missense mutation identified in MRPL24. The variant predicts a Leu91Pro substitution at an evolutionarily conserved site. Using human mutant cells and the zebrafish model, we demonstrated the pathological role of the identified variant. In fact, in fibroblasts we observed a significant reduction of MRPL24 protein and of mitochondrial respiratory chain complex I and IV subunits, as well a markedly reduced synthesis of the mtDNA-encoded peptides. In zebrafish we demonstrated that the orthologue gene is expressed in metabolically active tissues, and that gene knockdown induced locomotion impairment, structural defects and low ATP production. The motor phenotype was complemented by human WT but not mutant cRNA. Moreover, sucrose density gradient fractionation showed perturbed assembly of large subunit mitoribosomal proteins, suggesting that the mutation leads to a conformational change in MRPL24, which is expected to cause an aberrant interaction of the protein with other components of the 39S mitoribosomal subunit.

DOI10.1016/j.nbd.2020.104880
Alternate JournalNeurobiol. Dis.
Citation Key10.1016/j.nbd.2020.104880
PubMed ID32344152