Go to JCI Insight
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact
  • Clinical Research and Public Health
  • Current issue
  • Past issues
  • By specialty
    • COVID-19
    • Cardiology
    • Gastroenterology
    • Immunology
    • Metabolism
    • Nephrology
    • Neuroscience
    • Oncology
    • Pulmonology
    • Vascular biology
    • All ...
  • Videos
    • Conversations with Giants in Medicine
    • Video Abstracts
  • Reviews
    • View all reviews ...
    • Complement Biology and Therapeutics (May 2025)
    • Evolving insights into MASLD and MASH pathogenesis and treatment (Apr 2025)
    • Microbiome in Health and Disease (Feb 2025)
    • Substance Use Disorders (Oct 2024)
    • Clonal Hematopoiesis (Oct 2024)
    • Sex Differences in Medicine (Sep 2024)
    • Vascular Malformations (Apr 2024)
    • View all review series ...
  • Viewpoint
  • Collections
    • In-Press Preview
    • Clinical Research and Public Health
    • Research Letters
    • Letters to the Editor
    • Editorials
    • Commentaries
    • Editor's notes
    • Reviews
    • Viewpoints
    • 100th anniversary
    • Top read articles

  • Current issue
  • Past issues
  • Specialties
  • Reviews
  • Review series
  • Conversations with Giants in Medicine
  • Video Abstracts
  • In-Press Preview
  • Clinical Research and Public Health
  • Research Letters
  • Letters to the Editor
  • Editorials
  • Commentaries
  • Editor's notes
  • Reviews
  • Viewpoints
  • 100th anniversary
  • Top read articles
  • About
  • Editors
  • Consulting Editors
  • For authors
  • Publication ethics
  • Publication alerts by email
  • Advertising
  • Job board
  • Contact

Citations to this article

Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy
Devesh C. Pant, … , Odile Boespflug-Tanguy, Aurora Pujol
Devesh C. Pant, … , Odile Boespflug-Tanguy, Aurora Pujol
Published January 8, 2019
Citation Information: J Clin Invest. 2019;129(3):1240-1256. https://doi.org/10.1172/JCI123959.
View: Text | PDF
Research Article Neuroscience Article has an altmetric score of 82

Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy

  • Text
  • PDF
Abstract

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.

Authors

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

×

Total citations by year

Year: 2025 2024 2023 2022 2021 2020 2019 Total
Citations: 3 8 7 7 9 7 5 46
Citation information
This citation data is accumulated from CrossRef, which receives citation information from participating publishers, including this journal. Not all publishers participate in CrossRef, so this information is not comprehensive. Additionally, data may not reflect the most current citations to this article, and the data may differ from citation information available from other sources (for example, Google Scholar, Web of Science, and Scopus).

Citations to this article (46)

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

← Previous 1 2 Next →

Advertisement

Copyright © 2025 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

Sign up for email alerts

Picked up by 9 news outlets
Posted by 17 X users
On 3 Facebook pages
Referenced in 1 Wikipedia pages
110 readers on Mendeley
See more details