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Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18

Insulin and insulin-like growth factor signaling (IIS) is an anabolic pathway conserved among humans and Caenorhabditis elegans . In humans, the tumour suppressor protein Phosphatase and Tensin Homolog (PTEN) inhibits IIS, preventing excessive growth. PTEN variants are associated with disease, but h...

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Autores principales: Ermakova, Glafira, Hou, Chadwick, Boudreau, Jeffrey, Bendena, William G, Chin-Sang, Ian D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748723/
https://www.ncbi.nlm.nih.gov/pubmed/36530472
http://dx.doi.org/10.17912/micropub.biology.000689
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author Ermakova, Glafira
Hou, Chadwick
Boudreau, Jeffrey
Bendena, William G
Chin-Sang, Ian D
author_facet Ermakova, Glafira
Hou, Chadwick
Boudreau, Jeffrey
Bendena, William G
Chin-Sang, Ian D
author_sort Ermakova, Glafira
collection PubMed
description Insulin and insulin-like growth factor signaling (IIS) is an anabolic pathway conserved among humans and Caenorhabditis elegans . In humans, the tumour suppressor protein Phosphatase and Tensin Homolog (PTEN) inhibits IIS, preventing excessive growth. PTEN variants are associated with disease, but how they affect PTEN function is not well understood. Here, we characterized variants of unknown significance (VUSs) implicated in autism spectrum disorder by studying homologous mutations in the C. elegans protein DAF-18 to infer how they play a role in human disease.We found that variants D66E and L115V are likely benign, H168Q is intermediate while variants H138R and T176I are likely pathogenic.
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spelling pubmed-97487232022-12-15 Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18 Ermakova, Glafira Hou, Chadwick Boudreau, Jeffrey Bendena, William G Chin-Sang, Ian D MicroPubl Biol New Finding Insulin and insulin-like growth factor signaling (IIS) is an anabolic pathway conserved among humans and Caenorhabditis elegans . In humans, the tumour suppressor protein Phosphatase and Tensin Homolog (PTEN) inhibits IIS, preventing excessive growth. PTEN variants are associated with disease, but how they affect PTEN function is not well understood. Here, we characterized variants of unknown significance (VUSs) implicated in autism spectrum disorder by studying homologous mutations in the C. elegans protein DAF-18 to infer how they play a role in human disease.We found that variants D66E and L115V are likely benign, H168Q is intermediate while variants H138R and T176I are likely pathogenic. Caltech Library 2022-11-28 /pmc/articles/PMC9748723/ /pubmed/36530472 http://dx.doi.org/10.17912/micropub.biology.000689 Text en Copyright: © 2022 by the authors https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle New Finding
Ermakova, Glafira
Hou, Chadwick
Boudreau, Jeffrey
Bendena, William G
Chin-Sang, Ian D
Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18
title Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18
title_full Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18
title_fullStr Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18
title_full_unstemmed Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18
title_short Characterizing Variants of Unknown Significance of the PTEN tumour suppressorHomolog DAF-18
title_sort characterizing variants of unknown significance of the pten tumour suppressorhomolog daf-18
topic New Finding
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9748723/
https://www.ncbi.nlm.nih.gov/pubmed/36530472
http://dx.doi.org/10.17912/micropub.biology.000689
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