Literature DB >> 30443691

Chromosome constitution of equal-sized three-cell embryos using next-generation sequencing technology.

Minyue Ma1, Shihui Zhang1, Chongzhao Lu1, Shuling Wang1, Yuanqing Yao1, Hongmei Peng2.   

Abstract

PURPOSE: To study the chromosome constitution of equal-sized three-cell embryo.
METHODS: We determined the chromosome constitution of 105 blastomeres from 35 embryos using multiple annealing and looping-based amplification cycles (MALBAC) together with NGS sequencing technology. Chromosomal copy number variation (CNV) analysis was successfully performed in 27 embryos. We also analyzed radius, perimeter, area, and volume of each blastomere to explore the possibility of selecting the normal embryos.
RESULTS: Majority of the embryos (77.8%, 21/27) studied were mosaic or aneuploid, and only 22.2% (6/27) had normal chromosome numbers. The aneuploid chromosomes spread across all chromosomes and the most frequent aneuploidies were for chromosomes 1, 16, and 18 followed by 13, 19, and 21. Statistical analyses showed no significant difference between euploid and aneuploid embryos regarding radius, perimeter, area, and volume of their blastomeres.
CONCLUSIONS: Our results showed that majority of the equal-sized three-cell embryos were chromosomally abnormal and could not be distinguished by morphology observation, so they should be given lower priority at selection for transfer.

Keywords:  Aneuploidy; Assisted reproduction; Chromosome constitution; Equal-sized three-cell embryos; Next-generation sequencing

Mesh:

Year:  2018        PMID: 30443691      PMCID: PMC6420552          DOI: 10.1007/s10815-018-1362-7

Source DB:  PubMed          Journal:  J Assist Reprod Genet        ISSN: 1058-0468            Impact factor:   3.412


  28 in total

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8.  Time-lapse cleavage rating predicts human embryo viability.

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10.  Comprehensive chromosomal analysis of human preimplantation embryos using whole genome amplification and single cell comparative genomic hybridization.

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