Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, 02215, USA; Broad Institute of Harvard and MIT, Cambridge, MA, 02142, USA.
Department of Molecular Biology, Center for Regenerative Science and Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Dev Biol. 2024 Dec;516:47-58. doi: 10.1016/j.ydbio.2024.07.019. Epub 2024 Jul 31.
CMTR2 is an mRNA cap methyltransferase with poorly understood physiological functions. It catalyzes 2'-O-ribose methylation of the second transcribed nucleotide of mRNAs, potentially serving to mark RNAs as "self" to evade the cellular innate immune response. Here we analyze the consequences of Cmtr2 deficiency in mice. We discover that constitutive deletion of Cmtr2 results in mouse embryos that die during mid-gestation, exhibiting defects in embryo size, placental malformation and yolk sac vascularization. Endothelial cell deletion of Cmtr2 in mice results in vascular and hematopoietic defects, and perinatal lethality. Detailed characterization of the constitutive Cmtr2 KO phenotype shows an activation of the p53 pathway and decreased proliferation, but no evidence of interferon pathway activation. In summary, our study reveals the essential roles of Cmtr2 in mammalian cells beyond its immunoregulatory function.
CMTR2 是一种 mRNA 帽甲基转移酶,其生理功能尚不清楚。它催化 mRNA 第二个转录核苷酸的 2'-O-核糖甲基化,可能有助于将 RNA 标记为“自身”,以逃避细胞固有免疫反应。在这里,我们分析了 Cmtr2 缺乏对小鼠的影响。我们发现 Cmtr2 的组成性缺失导致小鼠胚胎在妊娠中期死亡,表现出胚胎大小、胎盘畸形和卵黄囊血管化缺陷。内皮细胞中 Cmtr2 的缺失导致血管和造血缺陷以及围产期致死。对组成型 Cmtr2 KO 表型的详细特征分析表明,p53 途径的激活和增殖减少,但没有干扰素途径激活的证据。总之,我们的研究揭示了 Cmtr2 在哺乳动物细胞中的重要作用,超出了其免疫调节功能。