Ncbp1 deficiency affects morula-to-blastocyst transition through lipid metabolic dysregulation

基因敲除 细胞生物学 生物 信使核糖核酸 胚泡 核糖核酸 胚胎发生 合子 卵母细胞 胚胎干细胞 RNA结合蛋白 胚胎 小干扰RNA 基因表达 调解人 基因表达调控 体细胞 RNA干扰 转录组 脂质代谢 重编程 小RNA 母子转换 表型 核糖核蛋白 基因沉默 小RNA 蛋白质亚单位
作者
Yu Liu,Yiming He,Xiangfei Wang,N. Wang,Xiaomeng Wang,Yuqian Wang,Lu Chen,Xiaohui Zhu,Jie Qiao,Peng Yuan,Liying Yan
出处
期刊:Reproduction [Bioscientifica]
卷期号:171 (2)
标识
DOI:10.1093/reprod/xaaf020
摘要

Preimplantation embryogenesis requires precise synchronization of transcriptional activation, mRNA export and translation, and metabolic reprogramming to sustain developmental requirements. Nuclear cap-binding protein 1 (NCBP1), a conserved subunit of the cap-binding complex, has established roles in mRNA processing and export in somatic cells, but its potential functions in preimplantation embryogenesis remain undefined. The spatiotemporal expression dynamics of Ncbp1 were explored on multiple levels. After microinjecting interfering RNA at zygotic stage to knockdown Ncbp1, embryonic developmental competence was evaluated. Co-injection of small interfering RNA and in vitro transcribed Ncbp1 mRNA into the zygote was used to rescue the knockdown phenotype. Further, poly-adenylated RNA-fluorescence in situ hybridization, RNA sequencing, and quantitative proteomics were used to investigate the effects of Ncbp1 knockdown. In addition, oleic acid (OA) supplementation was used to rescue developmental abnormalities. NCBP1 exhibited dynamic spatiotemporal expression coinciding with nuclear-to-cytoplasmic translocation of protein from morula stage. Depletion of Ncbp1 caused morula arrest or fragmentation, accompanied by nuclear poly-adenylated RNA retention and down-regulation of lipid metabolic pathways, notably, stearoyl-CoA desaturase 1 (SCD1), a key enzyme generating monounsaturated OA. Exogenous OA supplementation partially rescued blastocyst formation, implicating NCBP1 in the regulation of SCD1-OA-mediated metabolic homeostasis during morula-to-blastocyst transition. This study illustrates NCBP1 as a mediator that regulates RNA export and lipid homeostasis during early mouse embryo development. Especially NCBP1 regulates the SCD1-OA metabolic pathways, ensuring metabolic flexibility essential for successful morula-to-blastocyst transition, thereby providing new insights into the molecular basis of embryonic developmental competence.

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