The FASTK family proteins fine-tune mitochondrial RNA processing.

Bibliographic Details
Title: The FASTK family proteins fine-tune mitochondrial RNA processing.
Authors: Akira Ohkubo, Lindsey Van Haute, Danielle L Rudler, Maike Stentenbach, Florian A Steiner, Oliver Rackham, Michal Minczuk, Aleksandra Filipovska, Jean-Claude Martinou
Source: PLoS Genetics, Vol 17, Iss 11, p e1009873 (2021)
Publisher Information: Public Library of Science (PLoS), 2021.
Publication Year: 2021
Collection: LCC:Genetics
Subject Terms: Genetics, QH426-470
More Details: Transcription of the human mitochondrial genome and correct processing of the two long polycistronic transcripts are crucial for oxidative phosphorylation. According to the tRNA punctuation model, nucleolytic processing of these large precursor transcripts occurs mainly through the excision of the tRNAs that flank most rRNAs and mRNAs. However, some mRNAs are not punctuated by tRNAs, and it remains largely unknown how these non-canonical junctions are resolved. The FASTK family proteins are emerging as key players in non-canonical RNA processing. Here, we have generated human cell lines carrying single or combined knockouts of several FASTK family members to investigate their roles in non-canonical RNA processing. The most striking phenotypes were obtained with loss of FASTKD4 and FASTKD5 and with their combined double knockout. Comprehensive mitochondrial transcriptome analyses of these cell lines revealed a defect in processing at several canonical and non-canonical RNA junctions, accompanied by an increase in specific antisense transcripts. Loss of FASTKD5 led to the most severe phenotype with marked defects in mitochondrial translation of key components of the electron transport chain complexes and in oxidative phosphorylation. We reveal that the FASTK protein family members are crucial regulators of non-canonical junction and non-coding mitochondrial RNA processing.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1553-7390
1553-7404
Relation: https://doaj.org/toc/1553-7390; https://doaj.org/toc/1553-7404
DOI: 10.1371/journal.pgen.1009873
Access URL: https://doaj.org/article/4c5c70293ada4f08931022703464602a
Accession Number: edsdoj.4c5c70293ada4f08931022703464602a
Database: Directory of Open Access Journals
More Details
ISSN:15537390
15537404
DOI:10.1371/journal.pgen.1009873
Published in:PLoS Genetics
Language:English