4.5 Article

Wdhd1 is essential for early mouse embryogenesis

Journal

Publisher

ELSEVIER
DOI: 10.1016/j.bbamcr.2021.119011

Keywords

Mouse; Embryogenesis; Wdhd1; Proliferation; CRISPR/Cas9; DNA replication

Funding

  1. Ministry of Science and Technology [107-2320-B-002-059, 108-2320-B-002-021]

Ask authors/readers for more resources

The study indicates that Wdhd1 plays a critical role in mouse embryonic development, with Wdhd1 homozygous null mutation resulting in reduced cell proliferation, affecting embryonic growth and viability.
WD repeat and HMG-box DNA binding protein 1 (Wdhd1) is the mouse ortholog of budding yeast Chromosome Transmission Fidelity 4 (CTF4), the protein product of which integrates the MCM2-7 helicase and DNA polymerase alpha/primase complex to initiate DNA replication. Previous work in fruit flies, Xenopus egg extracts, and human cell lines suggest that Wdhd1 is required for efficient DNA synthesis. However, rigorous in vivo functional studies on Wdhd1 in mammals are unavailable. In the present study, we have successfully generated a Wdhd1 null allele in mice through CRISPR/Cas9-mediated genome editing to investigate the role of Wdhd1 in embryogenesis in vivo. We characterized Wdhd1 expression using quantitative reverse-transcription polymerase chain reaction, and assessed embryonic cell proliferation by histology in both pre- and peri-implantation embryos. While Wdhd1 heterozygous mutant mice were grossly normal and fertile, we observed a reduction in cell proliferation by the gastrulation stage in Wdhd1 homozygous null mutant embryos which severely hampered their growth and viability. These results indicate that Wdhd1 plays a major role in cell proliferation during embryogenesis in mice.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available