Academic Journal

Loss of FAM111B protease mutated in hereditary fibrosing poikiloderma negatively regulates telomere length

Bibliographic Details
Title: Loss of FAM111B protease mutated in hereditary fibrosing poikiloderma negatively regulates telomere length
Authors: Kliszczak, M, Moralli, D, Jankowska, JD, Bryjka, P, Subha Meem, L, Goncalves, T, Hester, SS, Fischer, R, Clynes, D, Green, CM
Publisher Information: Frontiers Media
Publication Year: 2023
Collection: Oxford University Research Archive (ORA)
Description: Hereditary fibrosing poikiloderma (HFP) is a rare human dominant negative disorder caused by mutations in the FAM111B gene that encodes a nuclear trypsin-like serine protease. HFP patients present with symptoms including skin abnormalities, tendon contractures, myopathy and lung fibrosis. We characterized the cellular roles of human FAM111B using U2OS and MCF7 cell lines and report here that the protease interacts with components of the nuclear pore complex. Loss of FAM111B expression resulted in abnormal nuclear shape and reduced telomeric DNA content suggesting that FAM111B protease is required for normal telomere length; we show that this function is independent of telomerase or recombination driven telomere extension. Even though FAM111B-deficient cells were proficient in DNA repair, they showed hallmarks of genomic instability such as increased levels of micronuclei and ultra-fine DNA bridges. When mutated as in HFP, FAM111B was more frequently localized to the nuclear envelope, suggesting that accumulation of the mutated protease at the nuclear periphery may drive the disease pathology.
Document Type: article in journal/newspaper
Language: English
Relation: https://doi.org/10.3389/fcell.2023.1175069
DOI: 10.3389/fcell.2023.1175069
Availability: https://doi.org/10.3389/fcell.2023.1175069
https://ora.ox.ac.uk/objects/uuid:c6545f55-97e8-4111-bf58-dc1f023bb08d
Rights: info:eu-repo/semantics/openAccess ; CC Attribution (CC BY)
Accession Number: edsbas.6093CEC5
Database: BASE
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