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New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing
INTRODUCTION: Analyses of miscarriage products indicate that the majority of aneuploidies in early developing embryos derive from errors occurring during maternal meiosis and the paternal contribution is less than 10%. Our aim was to assess the aneuploidy (mainly monosmies) frequencies at the earlie...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935781/ https://www.ncbi.nlm.nih.gov/pubmed/35313946 http://dx.doi.org/10.1186/s13039-022-00582-5 |
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author | Samara, N. Peleg, S. Frumkin, T. Gold, V. Amir, H. Haikin Herzberger, Einat Reches, A. Kalma, Y. Ben Yosef, Dalit Azem, F. Malcov, M. |
author_facet | Samara, N. Peleg, S. Frumkin, T. Gold, V. Amir, H. Haikin Herzberger, Einat Reches, A. Kalma, Y. Ben Yosef, Dalit Azem, F. Malcov, M. |
author_sort | Samara, N. |
collection | PubMed |
description | INTRODUCTION: Analyses of miscarriage products indicate that the majority of aneuploidies in early developing embryos derive from errors occurring during maternal meiosis and the paternal contribution is less than 10%. Our aim was to assess the aneuploidy (mainly monosmies) frequencies at the earliest stages of embryo development, 3 days following fertilization during In vitro fertilization (IVF) treatments and to elucidate their parental origin. Later, we compared monosomies rates of day 3 to those of day 5 as demonstrated from Preimplantation Genetic Testing for Structural chromosomal Rearrangement (PGT-SR) results. METHODS: For a retrospective study, we collected data of 210 Preimplantation Genetic Testing for Monogenic Disorder (PGT-M) cycles performed between years 2008 and 2019.This study includes 2083 embryos, of 113 couples. It also included 432 embryos from 90 PGT-SR cycles of other 45 patients, carriers of balanced translocations. Defining the parental origin of aneuploidy in cleavage stage embryos was based on haplotypes analysis of at least six informative markers flanking the analyzed gene. For comprehensive chromosomal screening (CCS), chromosomal microarray (CMA) and next generation sequencing (NGS) was used. RESULTS: We inspected haplotype data of 40 genomic regions, flanking analyzed genes located on 9 different chromosomes.151 (7.2%) embryos presented numerical alterations in the tested chromosomes. We found similar paternal and maternal contribution to monosomy at cleavage stage. We demonstrated paternal origin in 51.5% of the monosomy, and maternal origin in 48.5% of the monosomies cases. CONCLUSION: In our study, we found equal parental contribution to monosomies in cleavage-stage embryos. Comparison to CCS analyses of PGT-SR patients revealed a lower rate of monosomy per chromosome in embryos at day 5 of development. This is in contrast to the maternal dominancy described in studies of early miscarriage. Mitotic errors and paternal involvement in chemical pregnancies and IVF failure should be re-evaluated. Our results show monosomies are relatively common and may play a role in early development of ART embryos. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13039-022-00582-5. |
format | Online Article Text |
id | pubmed-8935781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-89357812022-03-23 New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing Samara, N. Peleg, S. Frumkin, T. Gold, V. Amir, H. Haikin Herzberger, Einat Reches, A. Kalma, Y. Ben Yosef, Dalit Azem, F. Malcov, M. Mol Cytogenet Research INTRODUCTION: Analyses of miscarriage products indicate that the majority of aneuploidies in early developing embryos derive from errors occurring during maternal meiosis and the paternal contribution is less than 10%. Our aim was to assess the aneuploidy (mainly monosmies) frequencies at the earliest stages of embryo development, 3 days following fertilization during In vitro fertilization (IVF) treatments and to elucidate their parental origin. Later, we compared monosomies rates of day 3 to those of day 5 as demonstrated from Preimplantation Genetic Testing for Structural chromosomal Rearrangement (PGT-SR) results. METHODS: For a retrospective study, we collected data of 210 Preimplantation Genetic Testing for Monogenic Disorder (PGT-M) cycles performed between years 2008 and 2019.This study includes 2083 embryos, of 113 couples. It also included 432 embryos from 90 PGT-SR cycles of other 45 patients, carriers of balanced translocations. Defining the parental origin of aneuploidy in cleavage stage embryos was based on haplotypes analysis of at least six informative markers flanking the analyzed gene. For comprehensive chromosomal screening (CCS), chromosomal microarray (CMA) and next generation sequencing (NGS) was used. RESULTS: We inspected haplotype data of 40 genomic regions, flanking analyzed genes located on 9 different chromosomes.151 (7.2%) embryos presented numerical alterations in the tested chromosomes. We found similar paternal and maternal contribution to monosomy at cleavage stage. We demonstrated paternal origin in 51.5% of the monosomy, and maternal origin in 48.5% of the monosomies cases. CONCLUSION: In our study, we found equal parental contribution to monosomies in cleavage-stage embryos. Comparison to CCS analyses of PGT-SR patients revealed a lower rate of monosomy per chromosome in embryos at day 5 of development. This is in contrast to the maternal dominancy described in studies of early miscarriage. Mitotic errors and paternal involvement in chemical pregnancies and IVF failure should be re-evaluated. Our results show monosomies are relatively common and may play a role in early development of ART embryos. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13039-022-00582-5. BioMed Central 2022-03-21 /pmc/articles/PMC8935781/ /pubmed/35313946 http://dx.doi.org/10.1186/s13039-022-00582-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Samara, N. Peleg, S. Frumkin, T. Gold, V. Amir, H. Haikin Herzberger, Einat Reches, A. Kalma, Y. Ben Yosef, Dalit Azem, F. Malcov, M. New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing |
title | New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing |
title_full | New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing |
title_fullStr | New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing |
title_full_unstemmed | New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing |
title_short | New insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing |
title_sort | new insights regarding origin of monosomy occurrence in early developing embryos as demonstrated in preimplantation genetic testing |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935781/ https://www.ncbi.nlm.nih.gov/pubmed/35313946 http://dx.doi.org/10.1186/s13039-022-00582-5 |
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