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Transcriptional Regulatory Networks in Embryonic Stem Cells

机译:胚胎干细胞中转录调控网络

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Embryonic stem (ES) cells are characterized by their ability to self-renew and remain pluripotent. Transcription factors havecritical roles in the maintenance of ES cells through specifying an ES-cell-specific gene expression program. Deciphering thetranscriptional regulatory network that describes the specific interactions of these transcription factors with the genomic tem-plate is crucial for understanding the design and key components of this network. Recent advances in genomic technologieshave facilitated genome-wide disclosure of the repertoire of transcription-factor-binding sites. Transcription factor colocal-ization hot spots targeted by multiple transcription factors have been identified. These are sites that integrate the external sig-naling pathways to the transcriptional regulatory circuitry governed by Oct4, Sox2, and Nanog. In addition, these sites mayserve as focal points for the assembly of nucleoprotein complexes known as enhanceosomes. Studying the properties of ES-cell-specific enhanceosomes in different pluripotent cells will shed light on the composition and regulation of their activity.Knowledge of the transcriptional regulatory networks in different pluripotent cells will also help to distinguish the core andperipheral parts of the networks. Collectively, these studies will facilitate the understanding of molecular mechanisms behindtranscription-factor-mediated regulation of pluripotent stem cells.
机译:胚胎茎(ES)细胞的特征在于它们对自我更新和保持多能的能力。通过指定ES细胞特异性基因表达计划,转录因子在维持ES细胞中的维持。解密细分的调节网络,其描述了与基因组Tem-Plate的这些转录因子的具体相互作用对于了解该网络的设计和关键组件至关重要。基因组技术的最新进展促进了转录因子结合位点的曲目的基因组宽的公开。已经鉴定了通过多转录因子靶向的转录因子结具有多个热点。这些是将外部SIG-NALING途径集成到由OCT4,SOX2和NANOG控制的转录调节电路的外部SIG-NALING途径。此外,这些位点可以作为核蛋白络合物组装的焦点,称为增强体。研究不同多能细胞中的ES细胞特异性增强体的性质将在其活性的组成和调节中脱落。在不同多能细胞中的转录调节网络的知识也有助于区分网络的核心和透明部分。总的来说,这些研究将有助于了解分子机制背后的分子机制介导的多能干细胞的调节。

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