ZC3H4—a novel Cys-Cys-Cys-His-type zinc finger protein—is essential for early embryogenesis in mice. Issue 2 (27th November 2020)

• Record Type: Journal Article
• Authors: Su, Jianmin; Miao, Xiaosu; Archambault, Danielle; Mager, Jesse; Cui, Wei
• Is Part Of: Biology of reproduction. Volume 104:Issue 2(2021)
• Page Start: 325
• Page End: 335
• Publication Date: 2020-11-27
• Subjects: Blastocyst embryo -- inner cell mass -- cell lineage specification -- epiblast -- DNA break; Reproduction -- Periodicals; Biology; Reproduction; Reproduction; Electronic journals; Periodicals; Periodicals; 571.805
• DOI: 10.1093/biolre/ioaa215
• Languages: English
• ISSNs: 0006-3363

Abstract

Abstract: Zinc finger domains of the Cys-Cys-Cys-His (CCCH) class are evolutionarily conserved proteins that bind nucleic acids and are involved in various biological processes. Nearly 60 CCCH-type zinc finger proteins have been identified in humans and mice, most have not been functionally characterized. Here, we provide the first in vivo functional characterization of ZC3H4—a novel CCCH-type zinc finger protein. Our results show that although Zc3h4 mutant embryos exhibit normal morphology at E3.5 blastocyst stage, they cannot be recovered at E7.5 early post-gastrulation stage, suggesting implantation failure. Outgrowth assays reveal that mutant blastocysts either fail to hatch from the zona pellucida, or can hatch but do not form a typical inner cell mass colony, the source of embryonic stem cells (ESCs). Although there is no change in levels of reactive oxygen species, Zc3h4 mutants display severe DNA breaks and reduced cell proliferation. Analysis of lineage specification reveals that both epiblast and primitive endoderm lineages are compromised with severe reductions in cell number and/or specification in the mutant blastocysts. In summary, these findings demonstrate the essential role of ZC3H4 during early mammalian embryogenesis. Abstract : ZC3H4 is essential during early embryo development in vivo, loss of ZC3H4 results in defective epiblast and primitive endoderm lineages, severe DNA breaks, reduced cell proliferation, and failure to develop beyond blastocyst formation.