Ermakova V V, Aleksandrova E V, Kuzmin A A, Tomilin A N
Institute of Cytology, Russian Academy of Sciences, St. Petersburg, 194064 Russia.
Acta Naturae. 2025 Apr-Jun;17(2):64-74. doi: 10.32607/actanaturae.27596.
The gene encodes the Oct4 protein, one of the key transcription factors required for maintaining the pluripotent state of epiblast cells and the viability of germ cells. However, functional genetics provides convincing evidence that has a broader range of functions in mouse ontogeny, including suppression of atherosclerotic processes. Related studies have primarily focused on the functions of the Oct4 protein, while the regulatory sequences within the gene have not been considered. In this study, we have developed a genetic model which is based on mouse embryonic stem cells (ESCs) for assessing the roles of the gene promoter in the transcriptional regulation of neighboring genes within the major histocompatibility complex (MHC) locus. We have demonstrated that deletion of this promoter affects the expression of selected genes within this locus neither in ESCs nor in the trophoblast derivatives of these cells. A notable exception is the gene, which is upregulated upon promoter deletion and might be associated with the atherosclerosis pathology due to its pro-inflammatory activity. The developed genetic model will pave the way for future studies into the functional contribution of the -regulatory association of , and, possibly, other genes with the atherosclerotic phenotype previously reported for mice carrying the promoter deletion in vascular endothelial and smooth muscle cells.
该基因编码Oct4蛋白,它是维持外胚层细胞多能状态和生殖细胞活力所需的关键转录因子之一。然而,功能遗传学提供了令人信服的证据,表明其在小鼠个体发育中具有更广泛的功能,包括抑制动脉粥样硬化进程。相关研究主要集中在Oct4蛋白的功能上,而该基因内的调控序列尚未得到考虑。在本研究中,我们基于小鼠胚胎干细胞(ESC)开发了一种遗传模型,用于评估该基因启动子在主要组织相容性复合体(MHC)位点内相邻基因转录调控中的作用。我们已经证明,该启动子的缺失在ESC中以及这些细胞的滋养层衍生物中均不影响该位点内选定基因的表达。一个显著的例外是该基因,它在启动子缺失后会上调,并且由于其促炎活性可能与动脉粥样硬化病理相关。所开发的遗传模型将为未来研究该基因与其他基因的调控关联对先前报道的在血管内皮和平滑肌细胞中携带该启动子缺失的小鼠动脉粥样硬化表型的功能贡献铺平道路。