TY - JOUR
T1 - SLK is mutated in individuals with a neurodevelopmental disorder
AU - SYNAPS Study Group
AU - Queen Square Genomics
AU - Alabdi, Lama
AU - Altuwaijri, Norah
AU - Zhu, Jun yi
AU - Efthymiou, Stephanie
AU - Lee, Hangnoh
AU - Duan, Jianli
AU - Salem, Israa
AU - Yu, Piao
AU - Abdullah, Nor Linda
AU - Alzahrani, Fatema
AU - Xu, Qing
AU - Felemban, Mashael M.
AU - Alfaifi, Abdullah
AU - Rahman, Fatima
AU - Christoforou, Marilena
AU - Maqbool, Shazia
AU - Martinez-Agosto, Julian A.
AU - Alsaif, Hessa S.
AU - Hashem, Mais
AU - Helaby, Rana
AU - Alsulaiman, Ahood
AU - Groppa, Stanislav
AU - Marinova Karashova, Blagovesta
AU - Nachbauer, Wolfgang
AU - Boesch, Sylvia
AU - Arning, Larissa
AU - Timmann, Dagmar
AU - Cormand, Bru
AU - Pérez-Dueñas, Belen
AU - Di Rosa, Gabriella
AU - Goraya, Jatinder S.
AU - Sultan, Tipu
AU - Mine, Jun
AU - Avdjieva, Daniela
AU - Kathom, Hadil
AU - Tincheva, Radka
AU - Banu, Selina
AU - Pineda-Marfa, Mercedes
AU - Veggiotti, Pierangelo
AU - Ferrari, Michel D.
AU - Verrotti, Alberto
AU - Marseglia, Giangluigi
AU - Savasta, Salvatore
AU - García-Silva, Mayte
AU - Macaya Ruiz, Alfons
AU - Garavaglia, Barbara
AU - Borgione, Eugenia
AU - Ibrahim, Shahnaz
AU - Kirmani, Salman
AU - Baig, Shahid
N1 - Publisher Copyright:
© 2025 The Author(s)
PY - 2025/6
Y1 - 2025/6
N2 - Background: Key to neuronal cell polarization and maturation is proper cytoskeletal organization and function that endows the bipolar neuronal cell with mature dendrites, axons, and functional synapses. Ste20-like kinase (SLK) has been shown to have various cytoskeletal roles. SLK regulates the polarity of microtubules, and its deficiency in the developing murine cortex leads to major defects including impaired development of the distal dendritic tree. No neurodevelopmental phenotypes in humans, however, have been linked to SLK. Methods: Clinical phenotyping, positional mapping, exome sequencing and functional analyses using patient-derived cells, SLK knock down cell lines, as well as a Drosophila model of Slik deficiency (the orthologue of SLK). Findings: We identified three individuals from three families (two are consanguineous) in whom a neurodevelopmental disorder (NDD) is linked to biallelic variants in SLK. The deleterious nature of these variants is confirmed by their failure to rescue the abnormal synapse maturation and locomotor defects phenotype in a Drosophila model of Slik deficiency. We also recapitulated the previously published abnormal cytoskeletal phenotype using patient cells, which showed abnormal organization of the cytoskeleton with accompanying impairment of migration and polarization. Furthermore, transdifferentiated neurons from patient fibroblasts displayed immature neuronal-like morphology with reduced dendritic arborization. Interpretation: Our results support an autosomal recessive SLK-related NDD and suggest abnormal cytoskeleton-mediated neuronal maturation as the underlying mechanism. Funding: MRC (MR/S01165X/1, MR/S005021/1, G0601943, MR/S005021/1), The National Institute for Health Research University College London Hospitals Biomedical Research Centre, Rosetree Trust, Ataxia UK, MSA Trust, Brain Research UK, Sparks GOSH Charity, Muscular Dystrophy UK (MDUK), Muscular Dystrophy Association (MDA USA). National Institutes of Health (NIH) grants HL134940 and DK098410. King Abdullah University of Science and Technology (KAUST) through the baseline fund to STA and LI as well as to STA and LI, and the KAUST Center of Excellence for Smart Health (KCSH), under award number 5932.
AB - Background: Key to neuronal cell polarization and maturation is proper cytoskeletal organization and function that endows the bipolar neuronal cell with mature dendrites, axons, and functional synapses. Ste20-like kinase (SLK) has been shown to have various cytoskeletal roles. SLK regulates the polarity of microtubules, and its deficiency in the developing murine cortex leads to major defects including impaired development of the distal dendritic tree. No neurodevelopmental phenotypes in humans, however, have been linked to SLK. Methods: Clinical phenotyping, positional mapping, exome sequencing and functional analyses using patient-derived cells, SLK knock down cell lines, as well as a Drosophila model of Slik deficiency (the orthologue of SLK). Findings: We identified three individuals from three families (two are consanguineous) in whom a neurodevelopmental disorder (NDD) is linked to biallelic variants in SLK. The deleterious nature of these variants is confirmed by their failure to rescue the abnormal synapse maturation and locomotor defects phenotype in a Drosophila model of Slik deficiency. We also recapitulated the previously published abnormal cytoskeletal phenotype using patient cells, which showed abnormal organization of the cytoskeleton with accompanying impairment of migration and polarization. Furthermore, transdifferentiated neurons from patient fibroblasts displayed immature neuronal-like morphology with reduced dendritic arborization. Interpretation: Our results support an autosomal recessive SLK-related NDD and suggest abnormal cytoskeleton-mediated neuronal maturation as the underlying mechanism. Funding: MRC (MR/S01165X/1, MR/S005021/1, G0601943, MR/S005021/1), The National Institute for Health Research University College London Hospitals Biomedical Research Centre, Rosetree Trust, Ataxia UK, MSA Trust, Brain Research UK, Sparks GOSH Charity, Muscular Dystrophy UK (MDUK), Muscular Dystrophy Association (MDA USA). National Institutes of Health (NIH) grants HL134940 and DK098410. King Abdullah University of Science and Technology (KAUST) through the baseline fund to STA and LI as well as to STA and LI, and the KAUST Center of Excellence for Smart Health (KCSH), under award number 5932.
KW - Focal adhesion
KW - Neurodevelopmental disorder
KW - SLK
KW - Transdifferentiation
UR - https://www.scopus.com/pages/publications/105004707160
U2 - 10.1016/j.ebiom.2025.105725
DO - 10.1016/j.ebiom.2025.105725
M3 - Article
AN - SCOPUS:105004707160
SN - 2352-3964
VL - 116
JO - eBioMedicine
JF - eBioMedicine
M1 - 105725
ER -