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Let-7 represses Nr6a1 and a mid-gestation developmental program in adult fibroblasts

机译:Let-7抑制Nr6a1和成年成纤维细胞的妊娠中期发育程序

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摘要

MicroRNAs (miRNAs) are critical to proliferation, differentiation, and development. Here, we characterize gene expression in murine Dicer-null adult mesenchymal stem cell lines, a fibroblast cell type. Loss of Dicer leads to derepression of let-7 targets at levels that exceed 10-fold to 100-fold with increases in transcription. Direct and indirect targets of this miRNA belong to a mid-gestation embryonic program that encompasses known oncofetal genes as well as oncogenes not previously associated with an embryonic state. Surprisingly, this mid-gestation program represents a distinct period that occurs between the pluripotent state of the inner cell mass at embryonic day 3.5 (E3.5) and the induction of let-7 upon differentiation at E10.5. Within this mid-gestation program, we characterize the let-7 target Nr6a1, an embryonic transcriptional repressor that regulates gene expression in adult fibroblasts following miRNA loss. In total, let-7 is required for the continual suppression of embryonic gene expression in adult cells, a mechanism that may underlie its tumor-suppressive function.
机译:MicroRNA(miRNA)对于增殖,分化和发育至关重要。在这里,我们表征鼠Dicer空的成人间充质干细胞系,成纤维细胞类型中的基因表达。 Dicer的缺失会导致let-7靶标的抑制降低,其转录水平会超过10倍至100倍。此miRNA的直接和间接靶标属于妊娠中期胚胎程序,该程序包含已知的癌胚基因以及以前与胚胎状态不相关的癌基因。出乎意料的是,该中期妊娠程序代表了在胚胎第3.5天(E3.5)的内细胞团的多能状态与在E10.5分化时诱导let-7之间发生的不同时期。在这个中期妊娠计划中,我们表征了let-7靶标Nr6a1,这是一种胚胎转录阻遏物,可调节miRNA缺失后成年成纤维细胞中的基因表达。总的来说,let-7是持续抑制成年细胞中胚胎基因表达所必需的,这可能是其抑制肿瘤功能的机制。

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