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LEUTX regulates porcine embryonic genome activation in somatic cell nuclear transfer embryos.
- Source :
-
Cell reports [Cell Rep] 2024 Jun 25; Vol. 43 (6), pp. 114372. Date of Electronic Publication: 2024 Jun 14. - Publication Year :
- 2024
-
Abstract
- Emerging evidence highlights the regulatory role of paired-like (PRD-like) homeobox transcription factors (TFs) in embryonic genome activation (EGA). However, the majority of PRD-like genes are lost in rodents, thus prompting an investigation into PRD-like TFs in other mammals. Here, we showed that PRD-like TFs were transiently expressed during EGA in human, monkey, and porcine fertilized embryos, yet they exhibited inadequate expression in their cloned embryos. This study, using pig as the research model, identified LEUTX as a key PRD-like activator of porcine EGA through genomic profiling and found that LEUTX overexpression restored EGA failure and improved preimplantation development and cloning efficiency in porcine cloned embryos. Mechanistically, LEUTX opened EGA-related genomic regions and established histone acetylation via recruiting acetyltransferases p300 and KAT2A. These findings reveal the regulatory mechanism of LEUTX to govern EGA in pigs, which may provide valuable insights into the study of early embryo development for other non-rodent mammals.<br />Competing Interests: Declaration of interests The authors declare no competing interests.<br /> (Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Swine
Gene Expression Regulation, Developmental
Homeodomain Proteins metabolism
Homeodomain Proteins genetics
Embryonic Development genetics
Embryo, Mammalian metabolism
Humans
Transcription Factors metabolism
Transcription Factors genetics
Acetylation
Cloning, Organism methods
Histones metabolism
Blastocyst metabolism
Nuclear Transfer Techniques
Genome
Subjects
Details
- Language :
- English
- ISSN :
- 2211-1247
- Volume :
- 43
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Cell reports
- Publication Type :
- Academic Journal
- Accession number :
- 38878289
- Full Text :
- https://doi.org/10.1016/j.celrep.2024.114372