Sphingolipid imbalance is the culprit in a variety of neurological diseases, some affecting the myelin sheath. We have used whole-exome sequencing in patients with undetermined leukoencephalopathies to uncover the endoplasmic reticulum lipid desaturase DEGS1 as the causative gene in 19 patients from 13 unrelated families. Shared features among the cases include severe motor arrest, early nystagmus, dystonia, spasticity, and profound failure to thrive. MRI showed hypomyelination, thinning of the corpus callosum, and progressive thalamic and cerebellar atrophy, suggesting a critical role of DEGS1 in myelin development and maintenance. This enzyme converts dihydroceramide (DhCer) into ceramide (Cer) in the final step of the de novo biosynthesis pathway. We detected a marked increase of the substrate DhCer and DhCer/Cer ratios in patients’ fibroblasts and muscle. Further, we used a knockdown approach for disease modeling in Danio rerio, followed by a preclinical test with the first-line treatment for multiple sclerosis, fingolimod (FTY720, Gilenya). The enzymatic inhibition of Cer synthase by fingolimod, 1 step prior to DEGS1 in the pathway, reduced the critical DhCer/Cer imbalance and the severe locomotor disability, increasing the number of myelinating oligodendrocytes in a zebrafish model. These proof-of-concept results pave the way to clinical translation.
Devesh C. Pant, Imen Dorboz, Agatha Schluter, Stéphane Fourcade, Nathalie Launay, Javier Joya, Sergio Aguilera-Albesa, Maria Eugenia Yoldi, Carlos Casasnovas, Mary J. Willis, Montserrat Ruiz, Dorothée Ville, Gaetan Lesca, Karine Siquier-Pernet, Isabelle Desguerre, Huifang Yan, Jingmin Wang, Margit Burmeister, Lauren Brady, Mark Tarnopolsky, Carles Cornet, Davide Rubbini, Javier Terriente, Kiely N. James, Damir Musaev, Maha S. Zaki, Marc C. Patterson, Brendan C. Lanpher, Eric W. Klee, Filippo Pinto e Vairo, Elizabeth Wohler, Nara Lygia de M. Sobreira, Julie S. Cohen, Reza Maroofian, Hamid Galehdari, Neda Mazaheri, Gholamreza Shariati, Laurence Colleaux, Diana Rodriguez, Joseph G. Gleeson, Cristina Pujades, Ali Fatemi, Odile Boespflug-Tanguy, Aurora Pujol
Title and authors | Publication | Year |
---|---|---|
Regulation of CNS Lipids by Protease Activated Receptor 1
Yoon H, Triplet EM, Wurtz L, Simon WL, Choi CI, Scarisbrick IA |
Journal of neurochemistry | 2025 |
A novel splice site variant in DEGS1 leads to aberrant splicing and loss of DEGS1 enzyme activity, a VUS resolved.
Beale HC, Tse V, Lee JY, Akutagawa J, Mavura Y, Saint-John B, Cheney A, Mulligan DR, Chacaltana G, Gutierrez M, Tenney J, Shieh JT, Martin PM, Yip T, Hodoglugil U, Fay AJ, Brooks AN, Van Ziffle J, Stone MD, Risch N, Sanford JR, Devine P, Saba JD, Vaske OM, Slavotinek A |
medRxiv : the preprint server for health sciences | 2025 |
Deletion Testing of the DEGS1 Gene Should Be Part of the Diagnostic Pipeline for Hypomyelinating Leukodystrophy (HLD18).
Zanobio M, Nardecchia F, Cappuccio G, Onore ME, Di Letto P, Rahman SI, Terrone G, Ugga L, De Giorgi A, Cas MD, Trinchera M, Leuzzi V, Piluso G, Nigro V, Brunetti-Pierri N, Torella A |
Human mutation | 2025 |
Dihydroceramide desaturase governs endoplasmic reticulum and lipid droplet homeostasis to promote glial function in the nervous system.
Zhu Y, Cho K, Lacin H, Zhu Y, DiPaola J, Wilson BA, Patti GJ, Skeath JB |
bioRxiv : the preprint server for biology | 2024 |
GBA1 inactivation in oligodendrocytes affects myelination and induces neurodegenerative hallmarks and lipid dyshomeostasis in mice.
Gregorio I, Russo L, Torretta E, Barbacini P, Contarini G, Pacinelli G, Bizzotto D, Moriggi M, Braghetta P, Papaleo F, Gelfi C, Moro E, Cescon M |
Molecular Neurodegeneration | 2024 |
Loss of function and reduced levels of sphingolipid desaturase DEGS1 variants are both relevant in disease mechanism.
Dei Cas M, Montavoci L, Pasini C, Caretti A, Penati S, Martinelli C, Gianelli U, Casati S, Nardecchia F, Torella A, Brunetti-Pierri N, Trinchera M |
Journal of lipid research | 2024 |
Exome sequencing in four families with neurodevelopmental disorders: genotype-phenotype correlation and identification of novel disease-causing variants in VPS13B and RELN.
Afridi TUK, Fatima A, Satti HS, Akram Z, Yousafzai IK, Naeem WB, Fatima N, Ali A, Iqbal Z, Khan A, Shahzad M, Liu C, Toft M, Zhang F, Tariq M, Davis EE, Khan TN |
Molecular genetics and genomics : MGG | 2024 |
Overview of Neuro-Ophthalmic Findings in Leukodystrophies
Bettinger CM, Dulz S, Atiskova Y, Guerreiro H, Schön G, Guder P, Maier SL, Denecke J, Bley AE |
Journal of Clinical Medicine | 2024 |
Unravelling neuronal and glial differences in ceramide composition, synthesis, and sensitivity to toxicity
McInnis JJ, Sood D, Guo L, Dufault MR, Garcia M, Passaro R, Gao G, Zhang B, Dodge JC |
Communications Biology | 2024 |
Human genetic defects of sphingolipid synthesis
Dubot P, Sabourdy F, Levade T |
Journal of Inherited Metabolic Disease | 2024 |
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population
Kaur N, do Rosario MC, Majethia P, Mascarenhas S, Rao LP, Nair KV, Hunakunti B, Prasannakumar AP, Naik R, Narayanan DL, Nayak SS, Bhat V, Sharma S, Ramesh Bhat Y, Yatheesha BL, Kulkarni R, Patil SJ, Nampoothiri S, Siddiqui S, Girisha KM, Bielas S, Shukla A |
American journal of medical genetics. Part A | 2024 |
DEGS1 deficiency disrupts the mitochondria-associated membrane: implications for human disease
Laura Planas-Serra, Nathalie Launay, Leire Goicoechea, Bénédicte Heron, Cristina Jou, Natalia Juliá-Palacios, Montserrat Ruiz, Stéphane Fourcade, Carlos Casasnovas, Carolina Torre, Antoinette Gelot, Maria Marsal, Pablo Loza-Alvarez, Àngels García-Cazorla, Ali Fatemi, Manel Portero-Otin, Estela Area-Gómez, Aurora Pujol |
Journal of Clinical Investigation | 2023 |
Mutation in PYCR2 gene and hypomyelinating leukodystrophy in children: a case report study
Hosseini SA, Ghelichi-Ghojogh M |
Annals of Medicine and Surgery | 2023 |
Spinal muscular atrophy-like phenotype in a mouse model of acid ceramidase deficiency.
Nagree MS, Rybova J, Kleynerman A, Ahrenhoerster CJ, Saville JT, Xu T, Bachochin M, McKillop WM, Lawlor MW, Pshezhetsky AV, Isaeva O, Budde MD, Fuller M, Medin JA |
Communications biology | 2023 |
Imaging Approaches to Investigate Pathophysiological Mechanisms of Brain Disease in Zebrafish
Turrini L, Roschi L, de Vito G, Pavone FS, Vanzi F |
International journal of molecular sciences | 2023 |
Re-evaluation and re-analysis of 152 research exomes five years after the initial report reveals clinically relevant changes in 18.
Bartolomaeus T, Hentschel J, Jamra RA, Popp B |
European journal of human genetics : EJHG | 2023 |
3′ UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay
Bi X, Mulhern MS, Spiegel E, Wapner RJ, Levy B, Bain JM, Liao J |
Genes & development | 2023 |
The atypical sphingolipid SPB 18:1(14Z);O2 is a biomarker for DEGS1 related hypomyelinating leukodystrophy
Hülsmeier AJ, Toelle SP, Bellstedt P, Wentzel C, Bahr A, Kolokotronis K, Hornemann T |
Journal of lipid research | 2023 |
Diagnosis of Genetic White Matter Disorders by Singleton Whole-Exome and Genome Sequencing Using Interactome-Driven Prioritization
A Schlüter, A Rodríguez-Palmero, E Verdura, V Vélez-Santamaría, M Ruiz, S Fourcade, L Planas-Serra, J Martínez, C Guilera, M Girós, R Artuch, M Yoldi, M O'Callaghan, A García-Cazorla, J Armstrong, I Marti, E Rezola, C Redin, J Mandel, D Conejo, C Sierra-Córcoles, S Beltrán, M Gut, E Vázquez, M del Toro, M Troncoso, L Pérez-Jurado, L Gutiérrez-Solana, A de Munain, C Casasnovas, S Aguilera-Albesa, A Macaya, A Pujol |
Neurology | 2022 |
Functional Study of TMEM163 Gene Variants Associated with Hypomyelination Leukodystrophy
H Yan, S Yang, Y Hou, S Ali, A Escobar, K Gao, R Duan, T Kubisiak, J Wang, Y Zhang, J Xiao, Y Jiang, T Zhang, Y Wu, M Burmeister, Q Wang, M Cuajungco, J Wang |
Cells | 2022 |
Contribution of specific ceramides to obesity-associated metabolic diseases
Hammerschmidt P, Brüning JC |
Cellular and Molecular Life Sciences | 2022 |
Targeting the Sphingolipid Rheostat in Gliomas.
Zaibaq F, Dowdy T, Larion M |
International journal of molecular sciences | 2022 |
Identification, conservation, and expression of tiered pharmacogenes in zebrafish
Demery-Poulos C, Chambers JM |
PloS one | 2022 |
Chronic oligodendrocyte injury in central nervous system pathologies
Molina-Gonzalez I, Miron VE, Antel JP |
2022 | |
Myelin lipid metabolism and its role in myelination and myelin maintenance
Barnes-Vélez JA, Aksoy Yasar FB, Hu J |
2022 | |
Cholesterol – the devil you know; ceramide – the devil you don’t
TS Tippetts, WL Holland, SA Summers |
Trends in Pharmacological Sciences | 2021 |
Bioinformatic analysis identifies potential key genes of epilepsy
Y Zhu, D Huang, Z Zhao, C Lu, MC Chiang |
PloS one | 2021 |
The multicellular interplay of microglia in health and disease: lessons from leukodystrophy
WM Berdowski, LE Sanderson, TJ van Ham |
Disease models & mechanisms | 2021 |
Stereoselective Synthesis of Novel Sphingoid Bases Utilized for Exploring the Secrets of Sphinx
EM Saied, C Arenz |
International journal of molecular sciences | 2021 |
Ceramide Metabolism Enzymes—Therapeutic Targets against Cancer
A Gomez-Larrauri, UD Adhikari, M Aramburu-Nuñez, A Custodia, A Ouro |
Medicina | 2021 |
Dihydroceramide desaturase promotes the formation of intraluminal vesicles and inhibits autophagy to increase exosome production
CY Wu, JG Jhang, WS Lin, PH Chuang, CW Lin, LA Chu, AS Chiang, HC Ho, CC Chan, SY Huang |
iScience | 2021 |
Comprehensive analysis of LASS6 expression and prognostic value in ovarian cancer
J Xing, J Yi |
Journal of Ovarian Research | 2021 |
Genetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencing
H Yan, H Ji, T Kubisiak, Y Wu, J Xiao, Q Gu, Y Yang, H Xie, T Ji, K Gao, D Li, H Xiong, Z Shi, M Li, Y Zhang, R Duan, X Bao, Y Jiang, M Burmeister, J Wang |
Journal of Human Genetics | 2021 |
Biallelic PI4KA variants cause a novel neurodevelopmental syndrome with hypomyelinating leukodystrophy
E Verdura, A Rodríguez-Palmero, V Vélez-Santamaria, L Planas-Serra, I de la Calle, M Raspall-Chaure, A Roubertie, M Benkirane, F Saettini, L Pavinato, G Mandrile, M OLeary, E OHeir, E Barredo, A Chacón, V Michaud, C Goizet, M Ruiz, A Schlüter, I Rouvet, J Sala-Coromina, C Fossati, M Iascone, F Canonico, A Marcé-Grau, P de Souza, DR Adams, C Casasnovas, HL Rehm, HC Mefford, LG Gutierrez-Solana, A Brusco, M Koenig, A Macaya, A Pujol |
Brain | 2021 |
The failure of microglia to digest developmental apoptotic cells contributes to the pathology of RNASET2‐deficient leukoencephalopathy
N Hamilton, HA Rutherford, JJ Petts, HM Isles, T Weber, M Henneke, J Gärtner, MJ Dunning, SA Renshaw |
Glia | 2020 |
Selective autophagy: the rise of the zebrafish model
DC Pant, TY Nazarko |
Autophagy | 2020 |
Precision Medicine for Lysosomal Disorders
FP e Vairo, DR Málaga, F Kubaski, CF de Souza, F de Oliveira Poswar, G Baldo, R Giugliani |
Biomolecules | 2020 |
Impact of integrated translational research on clinical exome sequencing
EW Klee, MA Cousin, FP e Vairo, JA Morales-Rosado, EL Macke, WG Jenkinson, A Ferrer, LE Schultz-Rogers, RJ Olson, GR Oliver, AN Sigafoos, TL Schwab, MT Zimmermann, RA Urrutia, C Kaiwar, A Gupta, PR Blackburn, NJ Boczek, CA Prochnow, RJ Lowy, LA Mulvihill, TM McAllister, SL Aoudia, TM Kruisselbrink, LB Gunderson, JL Kemppainen, LJ Fisher, JM Tarnowski, MM Hager, SA Kroc, NL Bertsch, KE Agre, JL Jackson, SK Macklin-Mantia, MI Murphree, LM Rust, JM Bolster, SA Beck, PS Atwal, MS Ellingson, SS Barnett, KJ Rasmussen, CA Lahner, Z Niu, L Hasadsri, MJ Ferber, CA Marcou, KJ Clark, PN Pichurin, DR Deyle, E Morava-Kozicz, RH Gavrilova, R Dhamija, KJ Wierenga, BC Lanpher, D Babovic-Vuksanovic, G Farrugia, LA Schimmenti, AK Stewart, KN Lazaridis |
Genetics in Medicine | 2020 |
A novel hypomorphic splice variant in EIF2B5 gene is associated with mild ovarioleukodystrophy
A RodríguezPalmero, A Schlüter, E Verdura, M Ruiz, JJ Martínez, I Gourlaouen, C Ka, R Lobato, C Casasnovas, GL Gac, S Fourcade, A Pujol |
Annals of Clinical and Translational Neurology | 2020 |
Case Report: Benign Infantile Seizures Temporally Associated With COVID-19
M García-Howard, M Herranz-Aguirre, L Moreno-Galarraga, M Urretavizcaya-Martínez, J Alegría-Echauri, N Gorría-Redondo, L Planas-Serra, A Schlüter, M Gut, A Pujol, S Aguilera-Albesa |
Frontiers in Pediatrics | 2020 |
Biosynthesis of long chain base in sphingolipids in animals, plants and fungi
R Mashima, T Okuyama, M Ohira |
Future Science OA | 2020 |
Rare DEGS1 variant significantly alters de novo ceramide synthesis pathway
NB Blackburn, LF Michael, PJ Meikle, JM Peralta, M Mosior, S McAhren, HH Bui, MA Bellinger, C Giles, S Kumar, AC Leandro, M Almeida, JM Weir, MC Mahaney, TD Dyer, L Almasy, JL VandeBerg, S Williams-Blangero, DC Glahn, R Duggirala, M Kowala, J Blangero, JE Curran |
Journal of lipid research | 2019 |
Use of preclinical models to identify markers of type 2 diabetes susceptibility and novel regulators of insulin secretion – A step towards precision medicine
B Thorens, A Rodriguez, C Cruciani-Guglielmacci, L Wigger, M Ibberson, C Magnan |
Molecular Metabolism | 2019 |
The Link between Gaucher Disease and Parkinson’s Disease Sheds Light on Old and Novel Disorders of Sphingolipid Metabolism
R Indellicato, M Trinchera |
International journal of molecular sciences | 2019 |
DEGS1 variant causes neurological disorder
V Dolgin, R Straussberg, R Xu, I Mileva, Y Yogev, R Khoury, O Konen, Y Barhum, A Zvulunov, C Mao, OS Birk |
European Journal of Human Genetics | 2019 |
Monitoring the Sphingolipid de novo Synthesis by Stable-Isotope Labeling and Liquid Chromatography-Mass Spectrometry
D Wigger, E Gulbins, B Kleuser, F Schumacher |
Frontiers in Cell and Developmental Biology | 2019 |