Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Samara, N., Peleg, S., Frumkin, T., Gold, V., Amir, H., Haikin Herzberger, Einat, Reches, A., Kalma, Y., Ben Yosef, Dalit, Azem, F., Malcov, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
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
_version_ 1784672099837673472
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
work_keys_str_mv AT samaran newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT pelegs newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT frumkint newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT goldv newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT amirh newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT haikinherzbergereinat newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT rechesa newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT kalmay newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT benyosefdalit newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT azemf newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting
AT malcovm newinsightsregardingoriginofmonosomyoccurrenceinearlydevelopingembryosasdemonstratedinpreimplantationgenetictesting