Prediction model for aneuploidy in early human embryo development revealed by single-cell analysis
Aneuploidies are prevalent in the human embryo and impair proper development, leading to cell cycle arrest. Recent advances in imaging and molecular and genetic analyses are postulated as promising strategies to unveil the mechanisms involved in aneuploidy generation. Here we combine time-lapse, com...
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Published in: | Nature communications Vol. 6; no. 1; p. 7601 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
London
Nature Publishing Group UK
07-07-2015
Nature Publishing Group Nature Pub. Group |
Subjects: | |
Online Access: | Get full text |
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Summary: | Aneuploidies are prevalent in the human embryo and impair proper development, leading to cell cycle arrest. Recent advances in imaging and molecular and genetic analyses are postulated as promising strategies to unveil the mechanisms involved in aneuploidy generation. Here we combine time-lapse, complete chromosomal assessment and single-cell RT–qPCR to simultaneously obtain information from all cells that compose a human embryo until the approximately eight-cell stage (
n
=85). Our data indicate that the chromosomal status of aneuploid embryos (
n
=26), including those that are mosaic (
n
=3), correlates with significant differences in the duration of the first mitotic phase when compared with euploid embryos (
n
=28). Moreover, gene expression profiling suggests that a subset of genes is differentially expressed in aneuploid embryos during the first 30 h of development. Thus, we propose that the chromosomal fate of an embryo is likely determined as early as the pronuclear stage and may be predicted by a 12-gene transcriptomic signature.
Aneuploidy may be fatal for the embryo, hence predicting its occurrence is important for successful
in vitro
fertilization. Here the authors monitor development of human preimplantation embryos in real-time and correlate the blastomere ploidy with cleavage dynamics and gene expression, identifying 12-transcript signature that determines ploidy. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present address: Division of Reproductive and Developmental Sciences, Oregon National Primate Research Center, Beaverton, Oregon 97006, USA. Department of Obstetrics and Gynecology, Oregon Health and Science University, Beaverton, Oregon 97006, USA or Department Physiology and Pharmacology, Oregon Health and Science University, Beaverton, Oregon 97006, USA Present address: Department of Cell Biology and Neurosciences, Montana State University, Bozeman, Montana 59717, USA or Department of Chemistry and Biochemistry, Montana State University, Bozeman, Montana 59717, USA |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/ncomms8601 |