XRCC3 loss leads to midgestational embryonic lethality in mice Journal Article
| Authors: | Prakash, R.; Freyer, L.; Saiz, N.; Gavrilov, S.; Wang, R. Q.; Romanienko, P. J.; Lacy, E.; Hadjantonakis, A. K.; Jasin, M. |
| Article Title: | XRCC3 loss leads to midgestational embryonic lethality in mice |
| Abstract: | RAD51 paralogs are key components of the homologous recombination (HR) machinery. Mouse mutants have been reported for four of the canonical RAD51 paralogs, and each of these mutants exhibits embryonic lethality, although at different gestational stages. However, the phenotype of mice deficient in the fifth RAD51 paralog, XRCC3, has not been reported. Here we report that Xrcc3 knockout mice exhibit midgestational lethality, with mild phenotypes beginning at about E8.25 but severe developmental abnormalities evident by E9.0–9.5. The most obvious phenotypes are small size and a failure of the embryo to turn to a fetal position. A knockin mutation at a key ATPase residue in the Walker A box results in embryonic lethality at a similar stage. Death of knockout mice can be delayed a few days for some embryos by homozygous or heterozygous Trp53 mutation, in keeping with an important role for XRCC3 in promoting genome integrity. Given that XRCC3 is a unique member of one of two RAD51 paralog complexes with RAD51C, these results demonstrate that both RAD51 paralog complexes are required for mouse development. © 2021 Elsevier B.V. |
| Keywords: | mouse embryogenesis; xrcc3; atpase mutant; rad51 paralog; walker a box mutation |
| Journal Title: | DNA Repair |
| Volume: | 108 |
| ISSN: | 1568-7864 |
| Publisher: | Elsevier Inc. |
| Date Published: | 2021-12-01 |
| Start Page: | 103227 |
| Language: | English |
| DOI: | 10.1016/j.dnarep.2021.103227 |
| PROVIDER: | scopus |
| PUBMED: | 34601382 |
| PMCID: | PMC8783620 |
| DOI/URL: | |
| Notes: | Article -- Source: Scopus |
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14Prakash -
249Jasin -
74Lacy -
13Romanienko -
191Hadjantonakis -
5
Wang -
4
Gavrilov -
3Freyer
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