Imprinted X‐chromosome inactivation impacts primitive endoderm differentiation in mouse blastocysts. Issue 5 (25th November 2019)

• Record Type: Journal Article
• Authors: Fukuda, Atsushi; Motosugi, Nami; Ando, Mikiko; Kimura, Minoru; Umezawa, Akihiro; Akutsu, Hidenori
• Is Part Of: FEBS letters. Volume 594:Issue 5(2020)
• Page Start: 913
• Page End: 923
• Publication Date: 2019-11-25
• Subjects: imprinted X‐chromosome inactivation -- lineage specification -- sex difference; Biochemistry -- Periodicals; Biophysics -- Periodicals; Molecular biology -- Periodicals; Biochimie -- Périodiques; Biochemistry; Biophysics; Molecular biology; Periodicals; 572.05
• DOI: 10.1002/1873-3468.13676
• Languages: English
• ISSNs: 0014-5793

Abstract

Abstract : Epigenetic and transcriptome alterations are essential for lineage specification, represented by imprinted X‐chromosome inactivation (iXCI) in female mouse preimplantation embryos. However, how various factors affect transcriptome states and lineage commitment remains unclear. We found that in vitro culture duration strongly influences transcriptional variation compared to iXCI loss. Single‐cell analysis of the inner cell mass (ICM) for major transcription and epigenomic factors revealed that sex‐specific differences in expression are diminished by loss of iXCI in the primitive endoderm (PrE) but not in the epiblast. Females had a higher proportion of ICM compared to that in males, and PrE development was affected by iXCI states in female embryos. Our findings provide insight into sex differences and iXCI function in lineage specification. Abstract :