Key Laboratory of Animal Resistance Research, Shandong Provincial Key Laboratory of Animal Resistance Biology, College of Life Science, Shandong Normal University, No.88 East Wenhua Road, Jinan, 250014, Shandong, China.
Department of Obstetrics, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, Jinan, 250011, Shandong, China.
Cell Tissue Res. 2022 Sep;389(3):559-572. doi: 10.1007/s00441-022-03655-4. Epub 2022 Jun 17.
UV-damaged DNA-binding protein 1 (DDB1) and cullin 4-associated factor 2 (DCAF2, also known as DTL or CDT2) is an evolutionarily highly conserved substrate recognition factor in the cullin 4 RING E3 ubiquitin ligase (CRL4) complex. This complex degrades multiple DNA replication and cell cycle-associated proteins to maintain genome stability. To clarify the function of DCAF2 in vivo, we used Cre recombinase driven by the Elf5 promoter to generate knockout mouse model that was specifically deleted Dcaf2 in the trophoblast lineage (Elf5-Cre; Dcaf2, Dcaf2 cKO). Here, we show that mice with the genotype Elf5-Cre; Dcaf2 are normal and fertile. However, after mating of Elf5-Cre; Dcaf2 mice with Dcaf2, no Dcaf2 cKO pups were born. Timed pregnancy studies have shown that Dcaf2 cKO mice developed abnormally on embryonic day 5.5 and died at gastrulation stage. It is worth noting that the extraembryonic ectoderm of Dcaf2 cKO mice is severely reduced or missing and leading to embryonic death. We also proved that stronger DNA damage accumulated in the trophoblastic cells of Dcaf2 cKO mice at E8.5. In addition, higher expression of Caspase-3 was found in the embryonic and trophoblastic cells of these cKO mice. In general, our research shows that the placental DCAF2 is crucial to the formation of gastrula.
紫外线损伤 DNA 结合蛋白 1(DDB1)和环指蛋白 4 相关因子 2(DCAF2,也称为 DTL 或 CDT2)是在环指蛋白 4 环 E3 泛素连接酶(CRL4)复合物中进化上高度保守的底物识别因子。该复合物降解多种与 DNA 复制和细胞周期相关的蛋白质,以维持基因组稳定性。为了阐明 DCAF2 在体内的功能,我们使用 Elf5 启动子驱动的 Cre 重组酶在滋养层谱系中特异性敲除 Dcaf2(Elf5-Cre;Dcaf2,Dcaf2 cKO)生成了敲除小鼠模型。在这里,我们表明具有 Elf5-Cre;Dcaf2 基因型的小鼠是正常且可育的。然而,当 Elf5-Cre;Dcaf2 小鼠与 Dcaf2 交配时,没有出生 Dcaf2 cKO 幼崽。定时妊娠研究表明,Dcaf2 cKO 小鼠在胚胎第 5.5 天发育异常,并在原肠胚形成阶段死亡。值得注意的是,Dcaf2 cKO 小鼠的胚外外胚层严重减少或缺失,导致胚胎死亡。我们还证明,Dcaf2 cKO 小鼠的滋养层细胞中积累了更强的 DNA 损伤。此外,在这些 cKO 小鼠的胚胎和滋养层细胞中发现 Caspase-3 的表达更高。总的来说,我们的研究表明胎盘 DCAF2 对于原肠胚的形成至关重要。