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Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease
by
Townsend, StJohn
, Petschnigg, Julia
, Bähler, Jürg
, Minnis, Christopher J.
, Mole, Sara E.
, Russell, Claire
, Tinelli, Elisa
in
631/114/2163
/ 631/208/191
/ 631/208/2490
/ 631/208/325/2484
/ 631/326/193/2541
/ 631/378/1689/1602
/ 631/378/1689/364
/ 692/420/2489/144
/ 692/699/3161
/ 692/699/317
/ 692/699/375
/ BTN1 gene
/ Gene Deletion
/ Genetic analysis
/ Genetic Association Studies
/ Genotypes
/ Homozygote
/ Humanities and Social Sciences
/ Humans
/ Membrane Glycoproteins - genetics
/ Membrane Proteins - genetics
/ Models, Genetic
/ Molecular Chaperones - genetics
/ multidisciplinary
/ Mutation
/ Mutation - genetics
/ Neurodegenerative diseases
/ Neuronal Ceroid-Lipofuscinoses - genetics
/ Neuronal Ceroid-Lipofuscinoses - pathology
/ Phenotypes
/ Precision medicine
/ Schizosaccharomyces - genetics
/ Schizosaccharomyces pombe
/ Schizosaccharomyces pombe Proteins - genetics
/ Science
/ Science (multidisciplinary)
/ Transcription
/ Yeast
2021
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Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease
by
Townsend, StJohn
, Petschnigg, Julia
, Bähler, Jürg
, Minnis, Christopher J.
, Mole, Sara E.
, Russell, Claire
, Tinelli, Elisa
in
631/114/2163
/ 631/208/191
/ 631/208/2490
/ 631/208/325/2484
/ 631/326/193/2541
/ 631/378/1689/1602
/ 631/378/1689/364
/ 692/420/2489/144
/ 692/699/3161
/ 692/699/317
/ 692/699/375
/ BTN1 gene
/ Gene Deletion
/ Genetic analysis
/ Genetic Association Studies
/ Genotypes
/ Homozygote
/ Humanities and Social Sciences
/ Humans
/ Membrane Glycoproteins - genetics
/ Membrane Proteins - genetics
/ Models, Genetic
/ Molecular Chaperones - genetics
/ multidisciplinary
/ Mutation
/ Mutation - genetics
/ Neurodegenerative diseases
/ Neuronal Ceroid-Lipofuscinoses - genetics
/ Neuronal Ceroid-Lipofuscinoses - pathology
/ Phenotypes
/ Precision medicine
/ Schizosaccharomyces - genetics
/ Schizosaccharomyces pombe
/ Schizosaccharomyces pombe Proteins - genetics
/ Science
/ Science (multidisciplinary)
/ Transcription
/ Yeast
2021
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Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease
by
Townsend, StJohn
, Petschnigg, Julia
, Bähler, Jürg
, Minnis, Christopher J.
, Mole, Sara E.
, Russell, Claire
, Tinelli, Elisa
in
631/114/2163
/ 631/208/191
/ 631/208/2490
/ 631/208/325/2484
/ 631/326/193/2541
/ 631/378/1689/1602
/ 631/378/1689/364
/ 692/420/2489/144
/ 692/699/3161
/ 692/699/317
/ 692/699/375
/ BTN1 gene
/ Gene Deletion
/ Genetic analysis
/ Genetic Association Studies
/ Genotypes
/ Homozygote
/ Humanities and Social Sciences
/ Humans
/ Membrane Glycoproteins - genetics
/ Membrane Proteins - genetics
/ Models, Genetic
/ Molecular Chaperones - genetics
/ multidisciplinary
/ Mutation
/ Mutation - genetics
/ Neurodegenerative diseases
/ Neuronal Ceroid-Lipofuscinoses - genetics
/ Neuronal Ceroid-Lipofuscinoses - pathology
/ Phenotypes
/ Precision medicine
/ Schizosaccharomyces - genetics
/ Schizosaccharomyces pombe
/ Schizosaccharomyces pombe Proteins - genetics
/ Science
/ Science (multidisciplinary)
/ Transcription
/ Yeast
2021
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Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease
Journal Article
Global network analysis in Schizosaccharomyces pombe reveals three distinct consequences of the common 1-kb deletion causing juvenile CLN3 disease
2021
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Overview
Juvenile CLN3 disease is a recessively inherited paediatric neurodegenerative disorder, with most patients homozygous for a 1-kb intragenic deletion in
CLN3
. The
btn1
gene is the
Schizosaccharomyces pombe
orthologue of
CLN3
. Here, we have extended the use of synthetic genetic array (SGA) analyses to delineate functional signatures for two different disease-causing mutations in addition to complete deletion of
btn1
. We show that genetic-interaction signatures can differ for mutations in the same gene, which helps to dissect their distinct functional effects. The mutation equivalent to the minor transcript arising from the 1-kb deletion (
btn1
102–208del
) shows a distinct interaction pattern. Taken together, our results imply that the minor 1-kb deletion transcript has three consequences for CLN3: to both lose and retain some inherent functions and to acquire abnormal characteristics. This has particular implications for the therapeutic development of juvenile CLN3 disease. In addition, this proof of concept could be applied to conserved genes for other mendelian disorders or any gene of interest, aiding in the dissection of their functional domains, unpacking the global consequences of disease pathogenesis, and clarifying genotype–phenotype correlations. In doing so, this detail will enhance the goals of personalised medicine to improve treatment outcomes and reduce adverse events.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
Subject
/ Humanities and Social Sciences
/ Humans
/ Membrane Glycoproteins - genetics
/ Membrane Proteins - genetics
/ Molecular Chaperones - genetics
/ Mutation
/ Neuronal Ceroid-Lipofuscinoses - genetics
/ Neuronal Ceroid-Lipofuscinoses - pathology
/ Schizosaccharomyces - genetics
/ Schizosaccharomyces pombe Proteins - genetics
/ Science
/ Yeast
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