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Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update

There is a growing interest in standardizing gene-disease associations for the purpose of facilitating the proper classification of variants in the context of Mendelian diseases. One key line of evidence is the independent observation of pathogenic variants in unrelated individuals with similar phen...

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Autores principales: Maddirevula, Sateesh, Shamseldin, Hanan E., Sirr, Amy, AlAbdi, Lama, Lo, Russell S., Ewida, Nour, Al-Qahtani, Mashael, Hashem, Mais, Abdulwahab, Firdous, Aboyousef, Omar, Kaya, Namik, Monies, Dorota, Salem, May H., Al Harbi, Naffaa, Aldhalaan, Hesham M., Alzaidan, Hamad, Almanea, Hadeel M., Alsalamah, Abrar K., Al Mutairi, Fuad, Ismail, Samira, Abdel-Salam, Ghada M. H., Alhashem, Amal, Asery, Ali, Faqeih, Eissa, AlQassmi, Amal, Al-Hamoudi, Waleed, Algoufi, Talal, Shagrani, Mohammad, Dudley, Aimée M., Alkuraya, Fowzan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806527/
https://www.ncbi.nlm.nih.gov/pubmed/33456446
http://dx.doi.org/10.3389/fgene.2020.580484
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author Maddirevula, Sateesh
Shamseldin, Hanan E.
Sirr, Amy
AlAbdi, Lama
Lo, Russell S.
Ewida, Nour
Al-Qahtani, Mashael
Hashem, Mais
Abdulwahab, Firdous
Aboyousef, Omar
Kaya, Namik
Monies, Dorota
Salem, May H.
Al Harbi, Naffaa
Aldhalaan, Hesham M.
Alzaidan, Hamad
Almanea, Hadeel M.
Alsalamah, Abrar K.
Al Mutairi, Fuad
Ismail, Samira
Abdel-Salam, Ghada M. H.
Alhashem, Amal
Asery, Ali
Faqeih, Eissa
AlQassmi, Amal
Al-Hamoudi, Waleed
Algoufi, Talal
Shagrani, Mohammad
Dudley, Aimée M.
Alkuraya, Fowzan S.
author_facet Maddirevula, Sateesh
Shamseldin, Hanan E.
Sirr, Amy
AlAbdi, Lama
Lo, Russell S.
Ewida, Nour
Al-Qahtani, Mashael
Hashem, Mais
Abdulwahab, Firdous
Aboyousef, Omar
Kaya, Namik
Monies, Dorota
Salem, May H.
Al Harbi, Naffaa
Aldhalaan, Hesham M.
Alzaidan, Hamad
Almanea, Hadeel M.
Alsalamah, Abrar K.
Al Mutairi, Fuad
Ismail, Samira
Abdel-Salam, Ghada M. H.
Alhashem, Amal
Asery, Ali
Faqeih, Eissa
AlQassmi, Amal
Al-Hamoudi, Waleed
Algoufi, Talal
Shagrani, Mohammad
Dudley, Aimée M.
Alkuraya, Fowzan S.
author_sort Maddirevula, Sateesh
collection PubMed
description There is a growing interest in standardizing gene-disease associations for the purpose of facilitating the proper classification of variants in the context of Mendelian diseases. One key line of evidence is the independent observation of pathogenic variants in unrelated individuals with similar phenotypes. Here, we expand on our previous effort to exploit the power of autozygosity to produce homozygous pathogenic variants that are otherwise very difficult to encounter in the homozygous state due to their rarity. The identification of such variants in genes with only tentative associations to Mendelian diseases can add to the existing evidence when observed in the context of compatible phenotypes. In this study, we report 20 homozygous variants in 18 genes (ADAMTS18, ARNT2, ASTN1, C3, DMBX1, DUT, GABRB3, GM2A, KIF12, LOXL3, NUP160, PTRHD1, RAP1GDS1, RHOBTB2, SIGMAR1, SPAST, TENM3, and WASHC5) that satisfy the ACMG classification for pathogenic/likely pathogenic if the involved genes had confirmed rather than tentative links to diseases. These variants were selected because they were truncating, founder with compelling segregation or supported by robust functional assays as with the DUT variant that we present its validation using yeast model. Our findings support the previously reported disease associations for these genes and represent a step toward their confirmation.
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spelling pubmed-78065272021-01-15 Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update Maddirevula, Sateesh Shamseldin, Hanan E. Sirr, Amy AlAbdi, Lama Lo, Russell S. Ewida, Nour Al-Qahtani, Mashael Hashem, Mais Abdulwahab, Firdous Aboyousef, Omar Kaya, Namik Monies, Dorota Salem, May H. Al Harbi, Naffaa Aldhalaan, Hesham M. Alzaidan, Hamad Almanea, Hadeel M. Alsalamah, Abrar K. Al Mutairi, Fuad Ismail, Samira Abdel-Salam, Ghada M. H. Alhashem, Amal Asery, Ali Faqeih, Eissa AlQassmi, Amal Al-Hamoudi, Waleed Algoufi, Talal Shagrani, Mohammad Dudley, Aimée M. Alkuraya, Fowzan S. Front Genet Genetics There is a growing interest in standardizing gene-disease associations for the purpose of facilitating the proper classification of variants in the context of Mendelian diseases. One key line of evidence is the independent observation of pathogenic variants in unrelated individuals with similar phenotypes. Here, we expand on our previous effort to exploit the power of autozygosity to produce homozygous pathogenic variants that are otherwise very difficult to encounter in the homozygous state due to their rarity. The identification of such variants in genes with only tentative associations to Mendelian diseases can add to the existing evidence when observed in the context of compatible phenotypes. In this study, we report 20 homozygous variants in 18 genes (ADAMTS18, ARNT2, ASTN1, C3, DMBX1, DUT, GABRB3, GM2A, KIF12, LOXL3, NUP160, PTRHD1, RAP1GDS1, RHOBTB2, SIGMAR1, SPAST, TENM3, and WASHC5) that satisfy the ACMG classification for pathogenic/likely pathogenic if the involved genes had confirmed rather than tentative links to diseases. These variants were selected because they were truncating, founder with compelling segregation or supported by robust functional assays as with the DUT variant that we present its validation using yeast model. Our findings support the previously reported disease associations for these genes and represent a step toward their confirmation. Frontiers Media S.A. 2020-12-31 /pmc/articles/PMC7806527/ /pubmed/33456446 http://dx.doi.org/10.3389/fgene.2020.580484 Text en Copyright © 2020 Maddirevula, Shamseldin, Sirr, AlAbdi, Lo, Ewida, Al-Qahtani, Hashem, Abdulwahab, Aboyousef, Kaya, Monies, Salem, Al Harbi, Aldhalaan, Alzaidan, Almanea, Alsalamah, Al Mutairi, Ismail, Abdel-Salam, Alhashem, Asery, Faqeih, AlQassmi, Al-Hamoudi, Algoufi, Shagrani, Dudley and Alkuraya. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Maddirevula, Sateesh
Shamseldin, Hanan E.
Sirr, Amy
AlAbdi, Lama
Lo, Russell S.
Ewida, Nour
Al-Qahtani, Mashael
Hashem, Mais
Abdulwahab, Firdous
Aboyousef, Omar
Kaya, Namik
Monies, Dorota
Salem, May H.
Al Harbi, Naffaa
Aldhalaan, Hesham M.
Alzaidan, Hamad
Almanea, Hadeel M.
Alsalamah, Abrar K.
Al Mutairi, Fuad
Ismail, Samira
Abdel-Salam, Ghada M. H.
Alhashem, Amal
Asery, Ali
Faqeih, Eissa
AlQassmi, Amal
Al-Hamoudi, Waleed
Algoufi, Talal
Shagrani, Mohammad
Dudley, Aimée M.
Alkuraya, Fowzan S.
Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update
title Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update
title_full Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update
title_fullStr Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update
title_full_unstemmed Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update
title_short Exploiting the Autozygome to Support Previously Published Mendelian Gene-Disease Associations: An Update
title_sort exploiting the autozygome to support previously published mendelian gene-disease associations: an update
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7806527/
https://www.ncbi.nlm.nih.gov/pubmed/33456446
http://dx.doi.org/10.3389/fgene.2020.580484
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