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Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents

BACKGROUND: Inactivating mutations of the hypothalamic transcription factor singleminded1 (SIM1) have been shown as a cause of early-onset severe obesity. However, to date, the contribution of SIM1 mutations to the obesity phenotype has only been studied in a few populations. In this study, we scree...

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Autores principales: Stanikova, Daniela, Buzga, Marek, Krumpolec, Patrik, Skopkova, Martina, Surova, Martina, Ukropcova, Barbara, Ticha, Lubica, Petrasova, Miroslava, Gabcova, Dominika, Huckova, Miroslava, Piskorova, Lucie, Bozensky, Jan, Mokan, Marian, Ukropec, Jozef, Zavacka, Ivona, Klimes, Iwar, Stanik, Juraj, Gasperikova, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417716/
https://www.ncbi.nlm.nih.gov/pubmed/28472148
http://dx.doi.org/10.1371/journal.pone.0177222
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author Stanikova, Daniela
Buzga, Marek
Krumpolec, Patrik
Skopkova, Martina
Surova, Martina
Ukropcova, Barbara
Ticha, Lubica
Petrasova, Miroslava
Gabcova, Dominika
Huckova, Miroslava
Piskorova, Lucie
Bozensky, Jan
Mokan, Marian
Ukropec, Jozef
Zavacka, Ivona
Klimes, Iwar
Stanik, Juraj
Gasperikova, Daniela
author_facet Stanikova, Daniela
Buzga, Marek
Krumpolec, Patrik
Skopkova, Martina
Surova, Martina
Ukropcova, Barbara
Ticha, Lubica
Petrasova, Miroslava
Gabcova, Dominika
Huckova, Miroslava
Piskorova, Lucie
Bozensky, Jan
Mokan, Marian
Ukropec, Jozef
Zavacka, Ivona
Klimes, Iwar
Stanik, Juraj
Gasperikova, Daniela
author_sort Stanikova, Daniela
collection PubMed
description BACKGROUND: Inactivating mutations of the hypothalamic transcription factor singleminded1 (SIM1) have been shown as a cause of early-onset severe obesity. However, to date, the contribution of SIM1 mutations to the obesity phenotype has only been studied in a few populations. In this study, we screened the functional regions of SIM1 in severely obese children of Slovak and Moravian descent to determine if genetic variants within SIM1 may influence the development of obesity in these populations. METHODS: The SIM1 promoter region, exons and exon-intron boundaries were sequenced in 126 unrelated obese children and adolescents (2–18 years of age) and 41 adult lean controls of Slovak and Moravian origin. Inclusion criteria for the children and adolescents were a body mass index standard deviation score higher than 2 SD for an appropriate age and sex, and obesity onset at less than 5 years of age. The clinical phenotypes of the SIM1 variant carriers were compared with clinical phenotypes of 4 MC4R variant carriers and with 27 unrelated SIM1 and MC4R mutation negative obese controls that were matched for age and gender. RESULTS: Seven previously described SIM1 variants and one novel heterozygous variant p.D134N were identified. The novel variant was predicted to be pathogenic by 7 in silico software analyses and is located at a highly conserved position of the SIM1 protein. The p.D134N variant was found in an 18 year old female proband (BMI 44.2kg/m(2); +7.5 SD), and in 3 obese family members. Regardless of early onset severe obesity, the proband and her brother (age 16 years) did not fulfill the criteria of metabolic syndrome. Moreover, the variant carriers had significantly lower preferences for high sugar (p = 0.02) and low fat, low carbohydrate, high protein (p = 0.02) foods compared to the obese controls. CONCLUSIONS: We have identified a novel SIM1 variant, p.D134N, in 4 obese individuals from a single pedigree which is also associated with lower preference for certain foods.
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spelling pubmed-54177162017-05-14 Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents Stanikova, Daniela Buzga, Marek Krumpolec, Patrik Skopkova, Martina Surova, Martina Ukropcova, Barbara Ticha, Lubica Petrasova, Miroslava Gabcova, Dominika Huckova, Miroslava Piskorova, Lucie Bozensky, Jan Mokan, Marian Ukropec, Jozef Zavacka, Ivona Klimes, Iwar Stanik, Juraj Gasperikova, Daniela PLoS One Research Article BACKGROUND: Inactivating mutations of the hypothalamic transcription factor singleminded1 (SIM1) have been shown as a cause of early-onset severe obesity. However, to date, the contribution of SIM1 mutations to the obesity phenotype has only been studied in a few populations. In this study, we screened the functional regions of SIM1 in severely obese children of Slovak and Moravian descent to determine if genetic variants within SIM1 may influence the development of obesity in these populations. METHODS: The SIM1 promoter region, exons and exon-intron boundaries were sequenced in 126 unrelated obese children and adolescents (2–18 years of age) and 41 adult lean controls of Slovak and Moravian origin. Inclusion criteria for the children and adolescents were a body mass index standard deviation score higher than 2 SD for an appropriate age and sex, and obesity onset at less than 5 years of age. The clinical phenotypes of the SIM1 variant carriers were compared with clinical phenotypes of 4 MC4R variant carriers and with 27 unrelated SIM1 and MC4R mutation negative obese controls that were matched for age and gender. RESULTS: Seven previously described SIM1 variants and one novel heterozygous variant p.D134N were identified. The novel variant was predicted to be pathogenic by 7 in silico software analyses and is located at a highly conserved position of the SIM1 protein. The p.D134N variant was found in an 18 year old female proband (BMI 44.2kg/m(2); +7.5 SD), and in 3 obese family members. Regardless of early onset severe obesity, the proband and her brother (age 16 years) did not fulfill the criteria of metabolic syndrome. Moreover, the variant carriers had significantly lower preferences for high sugar (p = 0.02) and low fat, low carbohydrate, high protein (p = 0.02) foods compared to the obese controls. CONCLUSIONS: We have identified a novel SIM1 variant, p.D134N, in 4 obese individuals from a single pedigree which is also associated with lower preference for certain foods. Public Library of Science 2017-05-04 /pmc/articles/PMC5417716/ /pubmed/28472148 http://dx.doi.org/10.1371/journal.pone.0177222 Text en © 2017 Stanikova et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Stanikova, Daniela
Buzga, Marek
Krumpolec, Patrik
Skopkova, Martina
Surova, Martina
Ukropcova, Barbara
Ticha, Lubica
Petrasova, Miroslava
Gabcova, Dominika
Huckova, Miroslava
Piskorova, Lucie
Bozensky, Jan
Mokan, Marian
Ukropec, Jozef
Zavacka, Ivona
Klimes, Iwar
Stanik, Juraj
Gasperikova, Daniela
Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents
title Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents
title_full Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents
title_fullStr Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents
title_full_unstemmed Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents
title_short Genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents
title_sort genetic analysis of single-minded 1 gene in early-onset severely obese children and adolescents
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5417716/
https://www.ncbi.nlm.nih.gov/pubmed/28472148
http://dx.doi.org/10.1371/journal.pone.0177222
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