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相关概念视频

Maintenance of the ES Cell State01:14

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The cells of the blastocyst inner cell mass only remain pluripotent for a short time. This state of pluripotency and self-renewal can be maintained in embryonic stem (ES) cell culture by adding specific chemicals or growth factors to ensure the cells can continue dividing and later differentiate into different cell types. In some cases, the cells are grown on a feeder layer of differentiated cells, which provides the growth factors and extracellular matrix components necessary for stem cell...
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The gene expression in cells is regulated at different stages: (i) transcription, (ii) RNA processing, (iii) RNA localization, and (iv) translation. Transcriptional regulation is mediated by regulatory proteins such as transcription factors, activators, or repressors—these control gene expression by initiating or inhibiting the transcription of genes. Once a precursor or pre-mRNA is produced, it undergoes post-transcriptional modification, including 5' capping, splicing, and the...
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In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
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Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
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All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
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相关实验视频

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Author Spotlight: Exploring the Frontier of mRNA Research with Poly A Tail Analysis Techniques
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多A) 干细胞的尾部调节和早期发育.

Xiaosu Miao1, Guang Hu2

  • 1Epigenetics and RNA Biology Laboratory, National Institute of Environmental Health Sciences, Research Triangle Park, Durham, NC, 27709, USA.

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概括

多甲尾通过控制mRNA稳定性和翻译来调节基因表达. 新的测序方法和对多尾调节器的理解正在推动干细胞命运和胚胎发育的研究.

关键词:
死亡化 死亡化胚胎发育的时间波利 (Poly) 尾巴 (A) 是一个多重的尾巴.聚亚脱化 聚亚脱化转录后的监管 转录后的监管干细胞是一种干细胞.

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科学领域:

  • 分子生物学分子生物学
  • 基因规则 基因规则
  • 发展生物学 发展生物学

背景情况:

  • 细胞信使RNAs (mRNAs) 在它们的3'-末端具有多A尾.
  • 多A尾对转录后基因调节至关重要,影响mRNA稳定性和翻译.
  • 动态调节多样性尾的长度对于细胞过程至关重要.

研究的目的:

  • 描述生物过程和蛋白质因子,控制多 (A) 尾的合成和缩短.
  • 审查最近在多种尾部测序技术方面的进展.
  • 讨论多种A尾调节器在干细胞命运和胚胎发育中的作用.

主要方法:

  • 关于控制多 (A) 尾动态的生物过程的文献综述.
  • 讨论涉及多尾新陈代谢的关键蛋白质因素.
  • 概述高通量聚合物 (A) 尾部测序方法.

主要成果:

  • 详细描述聚甲尾合成和降解途径.
  • 突出了创新的测序技术,以准确地测量多种类型的尾巴长度.
  • 识别关键的多项监管机制.

结论:

  • 多的尾巴长度是基因表达的一个关键决定因素.
  • 测序的进步使得可以精确地分析poly (A) 尾动力学.
  • 多元A尾调节显著影响干细胞多能性和胚胎模式.