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Effect of AGG Interruptions on FMR1 Maternal Transmissions
There are four classes of CGG repeat alleles in the FMR1 gene: normal alleles have up to 44 repeats; patients with Fragile X Syndrome have more than 200 repeats; those between 55 and 200 CGGs are considered FMR1 premutation alleles, because they are associated with maternal expansions of the number...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381193/ https://www.ncbi.nlm.nih.gov/pubmed/32766278 http://dx.doi.org/10.3389/fmolb.2020.00135 |
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author | Villate, Olatz Ibarluzea, Nekane Maortua, Hiart de la Hoz, Ana Belén Rodriguez-Revenga, Laia Izquierdo-Álvarez, Silvia Tejada, María Isabel |
author_facet | Villate, Olatz Ibarluzea, Nekane Maortua, Hiart de la Hoz, Ana Belén Rodriguez-Revenga, Laia Izquierdo-Álvarez, Silvia Tejada, María Isabel |
author_sort | Villate, Olatz |
collection | PubMed |
description | There are four classes of CGG repeat alleles in the FMR1 gene: normal alleles have up to 44 repeats; patients with Fragile X Syndrome have more than 200 repeats; those between 55 and 200 CGGs are considered FMR1 premutation alleles, because they are associated with maternal expansions of the number of CGGs in the next generation and finally, alleles between 45 and 54 CGGs are called intermediate or gray zone alleles. In these last categories, the stability depends on the presence of AGG interruptions, which usually occurs between 9 and 10 CGGs. In this context, we have studied retrospectively 66 women with CGG repeats between 45 and 65, and their offspring. In total 87 transmissions were analyzed with triplet repeat primed PCR using AmplideX® FMR1 PCR (Asuragen, Austin, TX, USA) and we found that alleles with CGG repeats between 45 and 58 do not expand in the next generation except two cases with 56 repeats and 0 AGG interruptions. Furthermore, we have found four females with alleles with more than 59 CGG repeats and 2 AGG interruptions that do not expand either. Alleles from 56 CGG repeats without AGGs expand in all cases. In light of these results and those of the literature, we consider that the risk of unstable transmissions should be based on the presence or absence of AGG interruptions and not on the classical cutoffs which define each category of FMR1 alleles. The application of these results in the genetic and reproductive counseling is essential and AGG interruptions should always be studied. |
format | Online Article Text |
id | pubmed-7381193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73811932020-08-05 Effect of AGG Interruptions on FMR1 Maternal Transmissions Villate, Olatz Ibarluzea, Nekane Maortua, Hiart de la Hoz, Ana Belén Rodriguez-Revenga, Laia Izquierdo-Álvarez, Silvia Tejada, María Isabel Front Mol Biosci Molecular Biosciences There are four classes of CGG repeat alleles in the FMR1 gene: normal alleles have up to 44 repeats; patients with Fragile X Syndrome have more than 200 repeats; those between 55 and 200 CGGs are considered FMR1 premutation alleles, because they are associated with maternal expansions of the number of CGGs in the next generation and finally, alleles between 45 and 54 CGGs are called intermediate or gray zone alleles. In these last categories, the stability depends on the presence of AGG interruptions, which usually occurs between 9 and 10 CGGs. In this context, we have studied retrospectively 66 women with CGG repeats between 45 and 65, and their offspring. In total 87 transmissions were analyzed with triplet repeat primed PCR using AmplideX® FMR1 PCR (Asuragen, Austin, TX, USA) and we found that alleles with CGG repeats between 45 and 58 do not expand in the next generation except two cases with 56 repeats and 0 AGG interruptions. Furthermore, we have found four females with alleles with more than 59 CGG repeats and 2 AGG interruptions that do not expand either. Alleles from 56 CGG repeats without AGGs expand in all cases. In light of these results and those of the literature, we consider that the risk of unstable transmissions should be based on the presence or absence of AGG interruptions and not on the classical cutoffs which define each category of FMR1 alleles. The application of these results in the genetic and reproductive counseling is essential and AGG interruptions should always be studied. Frontiers Media S.A. 2020-07-14 /pmc/articles/PMC7381193/ /pubmed/32766278 http://dx.doi.org/10.3389/fmolb.2020.00135 Text en Copyright © 2020 Villate, Ibarluzea, Maortua, de la Hoz, Rodriguez-Revenga, Izquierdo-Álvarez and Tejada. 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 | Molecular Biosciences Villate, Olatz Ibarluzea, Nekane Maortua, Hiart de la Hoz, Ana Belén Rodriguez-Revenga, Laia Izquierdo-Álvarez, Silvia Tejada, María Isabel Effect of AGG Interruptions on FMR1 Maternal Transmissions |
title | Effect of AGG Interruptions on FMR1 Maternal Transmissions |
title_full | Effect of AGG Interruptions on FMR1 Maternal Transmissions |
title_fullStr | Effect of AGG Interruptions on FMR1 Maternal Transmissions |
title_full_unstemmed | Effect of AGG Interruptions on FMR1 Maternal Transmissions |
title_short | Effect of AGG Interruptions on FMR1 Maternal Transmissions |
title_sort | effect of agg interruptions on fmr1 maternal transmissions |
topic | Molecular Biosciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7381193/ https://www.ncbi.nlm.nih.gov/pubmed/32766278 http://dx.doi.org/10.3389/fmolb.2020.00135 |
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