UMR 1313 GABI, INRA, AgroParisTech, Université de Saclay, F-78350, Jouy-en-Josas, France; Univ. Limoges, INRA, PEIRENE EA7500, USC1061 GAMAA, F-87000, Limoges, France.
UMR 1313 GABI, INRA, AgroParisTech, Université de Saclay, F-78350, Jouy-en-Josas, France.
Biochem Biophys Res Commun. 2019 Aug 13;516(1):258-263. doi: 10.1016/j.bbrc.2019.06.009. Epub 2019 Jun 21.
DNAJC2 protein, also known as ZRF1 or MPP11, acts both as chaperone and as chromatin regulator. It is involved in stem cell differentiation and its expression is associated with various cancer malignancies. However, the role of Dnajc2 gene during mouse embryogenesis has not been assessed so far. To this aim, we invalidated Dnajc2 gene in FVB/Nj mice using the CrispR/Cas9 approach. We showed that this invalidation leads to the early post-implantation lethality of the nullizygous embryos. Furthermore, using siRNAs against Dnajc2 in mouse 1-cell embryos, we showed that maternal Dnajc2 mRNAs may allow for the early preimplantation development of these embryos. Altogether, these data demonstrate for the first time the requirement of DNAJC2 for early mouse embryogenesis.
DNAJC2 蛋白,也称为 ZRF1 或 MPP11,既作为伴侣蛋白又作为染色质调节因子发挥作用。它参与干细胞分化,其表达与多种癌症恶性肿瘤有关。然而,到目前为止,还没有评估 Dnajc2 基因在小鼠胚胎发生过程中的作用。为此,我们使用 CrispR/Cas9 方法在 FVB/Nj 小鼠中使 Dnajc2 基因失活。我们表明,这种失活导致纯合子胚胎在植入后早期死亡。此外,我们使用针对小鼠 1 细胞胚胎中的 Dnajc2 的 siRNA 表明,母源 Dnajc2 mRNAs 可能允许这些胚胎的早期着床前发育。总之,这些数据首次证明了 DNAJC2 对早期小鼠胚胎发生的必要性。