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Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis

Glycosphingolipids are ubiquitous constituents of eukaryotic plasma membranes, and their sialylated derivatives, gangliosides, are the major class of glycoconjugates expressed by neurons. Deficiencies in their catabolic pathways give rise to a large and well-studied group of inherited disorders, the...

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Autores principales: Harlalka, Gaurav V., Lehman, Anna, Chioza, Barry, Baple, Emma L., Maroofian, Reza, Cross, Harold, Sreekantan-Nair, Ajith, Priestman, David A., Al-Turki, Saeed, McEntagart, Meriel E., Proukakis, Christos, Royle, Louise, Kozak, Radoslaw P., Bastaki, Laila, Patton, Michael, Wagner, Karin, Coblentz, Roselyn, Price, Joy, Mezei, Michelle, Schlade-Bartusiak, Kamilla, Platt, Frances M., Hurles, Matthew E., Crosby, Andrew H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859217/
https://www.ncbi.nlm.nih.gov/pubmed/24103911
http://dx.doi.org/10.1093/brain/awt270
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author Harlalka, Gaurav V.
Lehman, Anna
Chioza, Barry
Baple, Emma L.
Maroofian, Reza
Cross, Harold
Sreekantan-Nair, Ajith
Priestman, David A.
Al-Turki, Saeed
McEntagart, Meriel E.
Proukakis, Christos
Royle, Louise
Kozak, Radoslaw P.
Bastaki, Laila
Patton, Michael
Wagner, Karin
Coblentz, Roselyn
Price, Joy
Mezei, Michelle
Schlade-Bartusiak, Kamilla
Platt, Frances M.
Hurles, Matthew E.
Crosby, Andrew H.
author_facet Harlalka, Gaurav V.
Lehman, Anna
Chioza, Barry
Baple, Emma L.
Maroofian, Reza
Cross, Harold
Sreekantan-Nair, Ajith
Priestman, David A.
Al-Turki, Saeed
McEntagart, Meriel E.
Proukakis, Christos
Royle, Louise
Kozak, Radoslaw P.
Bastaki, Laila
Patton, Michael
Wagner, Karin
Coblentz, Roselyn
Price, Joy
Mezei, Michelle
Schlade-Bartusiak, Kamilla
Platt, Frances M.
Hurles, Matthew E.
Crosby, Andrew H.
author_sort Harlalka, Gaurav V.
collection PubMed
description Glycosphingolipids are ubiquitous constituents of eukaryotic plasma membranes, and their sialylated derivatives, gangliosides, are the major class of glycoconjugates expressed by neurons. Deficiencies in their catabolic pathways give rise to a large and well-studied group of inherited disorders, the lysosomal storage diseases. Although many glycosphingolipid catabolic defects have been defined, only one proven inherited disease arising from a defect in ganglioside biosynthesis is known. This disease, because of defects in the first step of ganglioside biosynthesis (GM3 synthase), results in a severe epileptic disorder found at high frequency amongst the Old Order Amish. Here we investigated an unusual neurodegenerative phenotype, most commonly classified as a complex form of hereditary spastic paraplegia, present in families from Kuwait, Italy and the Old Order Amish. Our genetic studies identified mutations in B4GALNT1 (GM2 synthase), encoding the enzyme that catalyzes the second step in complex ganglioside biosynthesis, as the cause of this neurodegenerative phenotype. Biochemical profiling of glycosphingolipid biosynthesis confirmed a lack of GM2 in affected subjects in association with a predictable increase in levels of its precursor, GM3, a finding that will greatly facilitate diagnosis of this condition. With the description of two neurological human diseases involving defects in two sequentially acting enzymes in ganglioside biosynthesis, there is the real possibility that a previously unidentified family of ganglioside deficiency diseases exist. The study of patients and animal models of these disorders will pave the way for a greater understanding of the role gangliosides play in neuronal structure and function and provide insights into the development of effective treatment therapies.
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spelling pubmed-38592172013-12-11 Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis Harlalka, Gaurav V. Lehman, Anna Chioza, Barry Baple, Emma L. Maroofian, Reza Cross, Harold Sreekantan-Nair, Ajith Priestman, David A. Al-Turki, Saeed McEntagart, Meriel E. Proukakis, Christos Royle, Louise Kozak, Radoslaw P. Bastaki, Laila Patton, Michael Wagner, Karin Coblentz, Roselyn Price, Joy Mezei, Michelle Schlade-Bartusiak, Kamilla Platt, Frances M. Hurles, Matthew E. Crosby, Andrew H. Brain Original Articles Glycosphingolipids are ubiquitous constituents of eukaryotic plasma membranes, and their sialylated derivatives, gangliosides, are the major class of glycoconjugates expressed by neurons. Deficiencies in their catabolic pathways give rise to a large and well-studied group of inherited disorders, the lysosomal storage diseases. Although many glycosphingolipid catabolic defects have been defined, only one proven inherited disease arising from a defect in ganglioside biosynthesis is known. This disease, because of defects in the first step of ganglioside biosynthesis (GM3 synthase), results in a severe epileptic disorder found at high frequency amongst the Old Order Amish. Here we investigated an unusual neurodegenerative phenotype, most commonly classified as a complex form of hereditary spastic paraplegia, present in families from Kuwait, Italy and the Old Order Amish. Our genetic studies identified mutations in B4GALNT1 (GM2 synthase), encoding the enzyme that catalyzes the second step in complex ganglioside biosynthesis, as the cause of this neurodegenerative phenotype. Biochemical profiling of glycosphingolipid biosynthesis confirmed a lack of GM2 in affected subjects in association with a predictable increase in levels of its precursor, GM3, a finding that will greatly facilitate diagnosis of this condition. With the description of two neurological human diseases involving defects in two sequentially acting enzymes in ganglioside biosynthesis, there is the real possibility that a previously unidentified family of ganglioside deficiency diseases exist. The study of patients and animal models of these disorders will pave the way for a greater understanding of the role gangliosides play in neuronal structure and function and provide insights into the development of effective treatment therapies. Oxford University Press 2013-12 2013-10-06 /pmc/articles/PMC3859217/ /pubmed/24103911 http://dx.doi.org/10.1093/brain/awt270 Text en © The Author (2013). Published by Oxford University Press on behalf of the Guarantors of Brain. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Harlalka, Gaurav V.
Lehman, Anna
Chioza, Barry
Baple, Emma L.
Maroofian, Reza
Cross, Harold
Sreekantan-Nair, Ajith
Priestman, David A.
Al-Turki, Saeed
McEntagart, Meriel E.
Proukakis, Christos
Royle, Louise
Kozak, Radoslaw P.
Bastaki, Laila
Patton, Michael
Wagner, Karin
Coblentz, Roselyn
Price, Joy
Mezei, Michelle
Schlade-Bartusiak, Kamilla
Platt, Frances M.
Hurles, Matthew E.
Crosby, Andrew H.
Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis
title Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis
title_full Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis
title_fullStr Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis
title_full_unstemmed Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis
title_short Mutations in B4GALNT1 (GM2 synthase) underlie a new disorder of ganglioside biosynthesis
title_sort mutations in b4galnt1 (gm2 synthase) underlie a new disorder of ganglioside biosynthesis
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3859217/
https://www.ncbi.nlm.nih.gov/pubmed/24103911
http://dx.doi.org/10.1093/brain/awt270
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