A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects

Jinglan Zhang, Véronik Lachance, Adam Schaffner, Xianting Li, Anastasia Fedick, Lauren E. Kaye, Jun Liao, Jill Rosenfeld, Naomi Yachelevich, Mary Lynn Chu, Wendy G. Mitchell, Richard G. Boles, Ellen Moran, Mari Tokita, Elizabeth Gorman, Kaytee Bagley, Wei Zhang, Fan Xia, Magalie Leduc, Yaping YangChristine Eng, Lee Jun Wong, Raphael Schiffmann, George A. Diaz, Ruth Kornreich, Ryan Thummel, Melissa P. Wasserstein, Zhenyu Yue, Lisa Edelmann

Research output: Contribution to journalArticle

16 Citations (Scopus)

Abstract

Genetic leukoencephalopathies (gLEs) are a group of heterogeneous disorders with white matter abnormalities affecting the central nervous system (CNS). The causative mutation in ~50% of gLEs is unknown. Using whole exome sequencing (WES), we identified homozygosity for a missense variant, VPS11: c.2536T>G (p.C846G), as the genetic cause of a leukoencephalopathy syndrome in five individuals from three unrelated Ashkenazi Jewish (AJ) families. All five patients exhibited highly concordant disease progression characterized by infantile onset leukoencephalopathy with brain white matter abnormalities, severe motor impairment, cortical blindness, intellectual disability, and seizures. The carrier frequency of the VPS11: c.2536T>G variant is 1:250 in the AJ population (n = 2,026). VPS11 protein is a core component of HOPS (homotypic fusion and protein sorting) and CORVET (class C core vacuole/endosome tethering) protein complexes involved in membrane trafficking and fusion of the lysosomes and endosomes. The cysteine 846 resides in an evolutionarily conserved cysteine-rich RING-H2 domain in carboxyl terminal regions of VPS11 proteins. Our data shows that the C846G mutation causes aberrant ubiquitination and accelerated turnover of VPS11 protein as well as compromised VPS11-VPS18 complex assembly, suggesting a loss of function in the mutant protein. Reduced VPS11 expression leads to an impaired autophagic activity in human cells. Importantly, zebrafish harboring a vps11 mutation with truncated RING-H2 domain demonstrated a significant reduction in CNS myelination following extensive neuronal death in the hindbrain and midbrain. Thus, our study reveals a defect in VPS11 as the underlying etiology for an autosomal recessive leukoencephalopathy disorder associated with a dysfunctional autophagy-lysosome trafficking pathway.

Original languageEnglish (US)
Article numbere1005848
JournalPLoS Genetics
Volume12
Issue number4
DOIs
StatePublished - Apr 1 2016
Externally publishedYes

Fingerprint

Leukoencephalopathies
defect
mutation
Mutation
endosomes
protein
lysosomes
brain
Endosomes
central nervous system
cysteine
trafficking
Lysosomes
proteins
Cysteine
nervous system
abnormality
myelination
Proteins
Central Nervous System

ASJC Scopus subject areas

  • Ecology, Evolution, Behavior and Systematics
  • Molecular Biology
  • Genetics
  • Genetics(clinical)
  • Cancer Research

Cite this

Zhang, J., Lachance, V., Schaffner, A., Li, X., Fedick, A., Kaye, L. E., ... Edelmann, L. (2016). A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects. PLoS Genetics, 12(4), [e1005848]. https://doi.org/10.1371/journal.pgen.1005848

A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects. / Zhang, Jinglan; Lachance, Véronik; Schaffner, Adam; Li, Xianting; Fedick, Anastasia; Kaye, Lauren E.; Liao, Jun; Rosenfeld, Jill; Yachelevich, Naomi; Chu, Mary Lynn; Mitchell, Wendy G.; Boles, Richard G.; Moran, Ellen; Tokita, Mari; Gorman, Elizabeth; Bagley, Kaytee; Zhang, Wei; Xia, Fan; Leduc, Magalie; Yang, Yaping; Eng, Christine; Wong, Lee Jun; Schiffmann, Raphael; Diaz, George A.; Kornreich, Ruth; Thummel, Ryan; Wasserstein, Melissa P.; Yue, Zhenyu; Edelmann, Lisa.

In: PLoS Genetics, Vol. 12, No. 4, e1005848, 01.04.2016.

Research output: Contribution to journalArticle

Zhang, J, Lachance, V, Schaffner, A, Li, X, Fedick, A, Kaye, LE, Liao, J, Rosenfeld, J, Yachelevich, N, Chu, ML, Mitchell, WG, Boles, RG, Moran, E, Tokita, M, Gorman, E, Bagley, K, Zhang, W, Xia, F, Leduc, M, Yang, Y, Eng, C, Wong, LJ, Schiffmann, R, Diaz, GA, Kornreich, R, Thummel, R, Wasserstein, MP, Yue, Z & Edelmann, L 2016, 'A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects', PLoS Genetics, vol. 12, no. 4, e1005848. https://doi.org/10.1371/journal.pgen.1005848
Zhang, Jinglan ; Lachance, Véronik ; Schaffner, Adam ; Li, Xianting ; Fedick, Anastasia ; Kaye, Lauren E. ; Liao, Jun ; Rosenfeld, Jill ; Yachelevich, Naomi ; Chu, Mary Lynn ; Mitchell, Wendy G. ; Boles, Richard G. ; Moran, Ellen ; Tokita, Mari ; Gorman, Elizabeth ; Bagley, Kaytee ; Zhang, Wei ; Xia, Fan ; Leduc, Magalie ; Yang, Yaping ; Eng, Christine ; Wong, Lee Jun ; Schiffmann, Raphael ; Diaz, George A. ; Kornreich, Ruth ; Thummel, Ryan ; Wasserstein, Melissa P. ; Yue, Zhenyu ; Edelmann, Lisa. / A Founder Mutation in VPS11 Causes an Autosomal Recessive Leukoencephalopathy Linked to Autophagic Defects. In: PLoS Genetics. 2016 ; Vol. 12, No. 4.
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abstract = "Genetic leukoencephalopathies (gLEs) are a group of heterogeneous disorders with white matter abnormalities affecting the central nervous system (CNS). The causative mutation in ~50{\%} of gLEs is unknown. Using whole exome sequencing (WES), we identified homozygosity for a missense variant, VPS11: c.2536T>G (p.C846G), as the genetic cause of a leukoencephalopathy syndrome in five individuals from three unrelated Ashkenazi Jewish (AJ) families. All five patients exhibited highly concordant disease progression characterized by infantile onset leukoencephalopathy with brain white matter abnormalities, severe motor impairment, cortical blindness, intellectual disability, and seizures. The carrier frequency of the VPS11: c.2536T>G variant is 1:250 in the AJ population (n = 2,026). VPS11 protein is a core component of HOPS (homotypic fusion and protein sorting) and CORVET (class C core vacuole/endosome tethering) protein complexes involved in membrane trafficking and fusion of the lysosomes and endosomes. The cysteine 846 resides in an evolutionarily conserved cysteine-rich RING-H2 domain in carboxyl terminal regions of VPS11 proteins. Our data shows that the C846G mutation causes aberrant ubiquitination and accelerated turnover of VPS11 protein as well as compromised VPS11-VPS18 complex assembly, suggesting a loss of function in the mutant protein. Reduced VPS11 expression leads to an impaired autophagic activity in human cells. Importantly, zebrafish harboring a vps11 mutation with truncated RING-H2 domain demonstrated a significant reduction in CNS myelination following extensive neuronal death in the hindbrain and midbrain. Thus, our study reveals a defect in VPS11 as the underlying etiology for an autosomal recessive leukoencephalopathy disorder associated with a dysfunctional autophagy-lysosome trafficking pathway.",
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AU - Wong, Lee Jun

AU - Schiffmann, Raphael

AU - Diaz, George A.

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