The Identification of Nuclear FMRP Isoform Iso6 Partners

• Published in: Cells (Basel, Switzerland) Vol. 12; no. 24; p. 2807
• Main Authors: Ledoux, Nassim, Lelong, Emeline I J, Simard, Alexandre, Hussein, Samer, Adjibade, Pauline, Lambert, Jean-Philippe, Mazroui, Rachid
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.12.2023
• Subjects: Alternative Splicing; Anaphase; Autism; Binding proteins; Causes of; Chromatin remodeling; Chromatography; Chromosomes; DNA - metabolism; DNA biosynthesis; DNA damage; Fibroblasts; Fluorides; FMR1 gene; FMR1 protein; FMRP; Fragile X Mental Retardation Protein - genetics; Fragile X syndrome; Genetic aspects; Genomic instability; GFP-Trap; Health aspects; Identification and classification; Intellectual disabilities; Isoforms; Localization; mass spectrometry; Mass spectroscopy; Microscopy; mRNA; Neurodevelopmental disorders; Paternity; Peptides; Phenotypes; Plasmids; proteasome; Proteasome Endopeptidase Complex - metabolism; Proteasomes; Protein Isoforms - metabolism; Replication; RNA processing; RNA-binding protein; RNA-binding proteins; Canada; United States > US; Germany; proteasome; mass spectrometry; RNA-binding proteins; GFP-Trap; FMRP
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells12242807

A deficiency of FMRP, a canonical RNA-binding protein, causes the development of Fragile X Syndrome (FXS), which is characterised by multiple phenotypes, including neurodevelopmental disorders, intellectual disability, and autism. Due to the alternative splicing of the encoding gene, multiple FMRP isoforms are produced consisting of full-length predominantly cytoplasmic (i.e., iso1) isoforms involved in translation and truncated nuclear (i.e., iso6) isoforms with orphan functions. However, we recently implicated nuclear FMRP isoforms in DNA damage response, showing that they negatively regulate the accumulation of anaphase DNA genomic instability bridges. This finding provided evidence that the cytoplasmic and nuclear functions of FMRP are uncoupled played by respective cytoplasmic and nuclear isoforms, potentially involving specific interactions. While interaction partners of cytoplasmic FMRP have been reported, the identity of nuclear FMRP isoform partners remains to be established. Using affinity purification coupled with mass spectrometry, we mapped the nuclear interactome of the FMRP isoform iso6 in U2OS. In doing so, we found FMRP nuclear interaction partners to be involved in RNA processing, pre-mRNA splicing, ribosome biogenesis, DNA replication and damage response, chromatin remodeling and chromosome segregation. By comparing interactions between nuclear iso6 and cytoplasmic iso1, we report a set of partners that bind specifically to the nuclear isoforms, mainly proteins involved in DNA-associated processes and proteasomal proteins, which is consistent with our finding that proteasome targets the nuclear FMRP iso6. The specific interactions with the nuclear isoform 6 are regulated by replication stress, while those with the cytoplasmic isoform 1 are largely insensitive to such stress, further supporting a specific role of nuclear isoforms in DNA damage response induced by replicative stress, potentially regulated by the proteasome.