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The Majority of Resorptions in Old Mice Are Euploid
Chromosomal abnormality is a leading cause of aging-related infertility, spontaneous abortion and congenital birth defects in humans. Karyotype analyses of spontaneously aborted human fetuses reveal high proportions (~50%) being chromosomal abnormal with the majority being trisomies of various chrom...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670076/ https://www.ncbi.nlm.nih.gov/pubmed/26636341 http://dx.doi.org/10.1371/journal.pone.0143360 |
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author | Tao, Yong Liu, X. Johné |
author_facet | Tao, Yong Liu, X. Johné |
author_sort | Tao, Yong |
collection | PubMed |
description | Chromosomal abnormality is a leading cause of aging-related infertility, spontaneous abortion and congenital birth defects in humans. Karyotype analyses of spontaneously aborted human fetuses reveal high proportions (~50%) being chromosomal abnormal with the majority being trisomies of various chromosomes. As a model organism, mice are widely used for studies of reproduction and reproductive aging. Like older women, older mice exhibit high incidences of early embryo death. However, it is not known if aneuploidy is prevalent amongst resorptions in older mice. We have karyotyped 65 retarded/resorbed fetuses in 10-month-old C57BL/6 mice, and found that 55 (84.6%±8.8%, with 95% confidence) were euploid. Similarly, of 40 such fetuses from 17 month-old C57BL/6 mice, we found 38 (95±7%, with 95% confidence 95%) being euploid. Therefore, aneuploidy is not a leading cause of embryo death in older mice. |
format | Online Article Text |
id | pubmed-4670076 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46700762015-12-10 The Majority of Resorptions in Old Mice Are Euploid Tao, Yong Liu, X. Johné PLoS One Research Article Chromosomal abnormality is a leading cause of aging-related infertility, spontaneous abortion and congenital birth defects in humans. Karyotype analyses of spontaneously aborted human fetuses reveal high proportions (~50%) being chromosomal abnormal with the majority being trisomies of various chromosomes. As a model organism, mice are widely used for studies of reproduction and reproductive aging. Like older women, older mice exhibit high incidences of early embryo death. However, it is not known if aneuploidy is prevalent amongst resorptions in older mice. We have karyotyped 65 retarded/resorbed fetuses in 10-month-old C57BL/6 mice, and found that 55 (84.6%±8.8%, with 95% confidence) were euploid. Similarly, of 40 such fetuses from 17 month-old C57BL/6 mice, we found 38 (95±7%, with 95% confidence 95%) being euploid. Therefore, aneuploidy is not a leading cause of embryo death in older mice. Public Library of Science 2015-12-04 /pmc/articles/PMC4670076/ /pubmed/26636341 http://dx.doi.org/10.1371/journal.pone.0143360 Text en © 2015 Tao, Liu http://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 properly credited. |
spellingShingle | Research Article Tao, Yong Liu, X. Johné The Majority of Resorptions in Old Mice Are Euploid |
title | The Majority of Resorptions in Old Mice Are Euploid |
title_full | The Majority of Resorptions in Old Mice Are Euploid |
title_fullStr | The Majority of Resorptions in Old Mice Are Euploid |
title_full_unstemmed | The Majority of Resorptions in Old Mice Are Euploid |
title_short | The Majority of Resorptions in Old Mice Are Euploid |
title_sort | majority of resorptions in old mice are euploid |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670076/ https://www.ncbi.nlm.nih.gov/pubmed/26636341 http://dx.doi.org/10.1371/journal.pone.0143360 |
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