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DNA methylome reveals cellular origin of cell-free DNA in spent medium of human preimplantation embryos
Yidong Chen, Yuan Gao, Jialin Jia, Liang Chang, Ping Liu, Jie Qiao, Fuchou Tang, Lu Wen, Jin Huang
Yidong Chen, Yuan Gao, Jialin Jia, Liang Chang, Ping Liu, Jie Qiao, Fuchou Tang, Lu Wen, Jin Huang
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Research Article Genetics Reproductive biology

DNA methylome reveals cellular origin of cell-free DNA in spent medium of human preimplantation embryos

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Abstract

The discovery of embryonic cell–free DNA (cfDNA) in spent embryo culture media (SECM) has brought hope for noninvasive preimplantation genetic testing. However, the cellular origins of SECM cfDNA are not sufficiently understood, and methods for determining maternal DNA contamination are limited. Here, we performed whole-genome DNA methylation sequencing for SECM cfDNA. Our results demonstrated that SECM cfDNA was derived from blastocysts, cumulus cells, and polar bodies. We identified the cumulus-specific differentially methylated regions (DMRs) and oocyte/polar body–specific DMRs, and established an algorithm for deducing the cumulus, polar body, and net maternal DNA contamination ratios in SECM. We showed that DNA methylation sequencing accurately detected chromosome aneuploidy in SECM and distinguished SECM samples with low and high false negative rates and gender discordance rates, after integrating the origin analysis. Our work provides insights into the characterization of embryonic DNA in SECM and provides a perspective for noninvasive preimplantation genetic testing in reproductive medicine.

Authors

Yidong Chen, Yuan Gao, Jialin Jia, Liang Chang, Ping Liu, Jie Qiao, Fuchou Tang, Lu Wen, Jin Huang

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Figure 4

Polar body contamination in SECM.

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Polar body contamination in SECM.
(A) Unsupervised hierarchical clusteri...
(A) Unsupervised hierarchical clustering of whole-genome DNA methylation for the SECM samples with no cumulus cell contamination, human preimplantation embryos of different stages, germ cells, and cumulus cells. GV, germinal vesicle oocytes; MII, metaphase II oocytes; PN, pronuclei. (B) A total of 548 regions (O-DMRs) were specifically hypermethylated in the MII oocytes. (C) Chromosome CN profiles of 2 SECM samples clustered with the female pronuclei (upper, S167) or the MII oocytes (lower, S176). The chromosome aneuploidy results of TE biopsy and SECM are indicated, along with the methylation levels of the C-DMRs and the O-DMRs. (D) Correlations between non-CpG (left, CHG; right, CHH) DNA methylation levels and the O-DMR DNA methylation levels. CHG/CHH are short for methylation levels on non-CpG islands; H represents A (adenine) or T (thymine). The 2-tailed Mann-Whitney-Wilcoxon test was used to assess significance.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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