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相关概念视频

Chromatin Modification in iPS Cells01:32

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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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Before a cell can divide, it must accurately replicate all of its chromosomes, including the DNA and its associated histone and non-histone proteins.  This process begins at numerous origins of replication during the S phase of the cell cycle in each of a cell’s chromosomes simultaneously. Certain nucleotides can act as origins of replication, but these sequences are not well defined - especially in complex, multi-cellular, eukaryotic species. The length of DNA that spans an origin...
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Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012...
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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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In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
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How does a complex organism such as a human develop from a single cell? It all starts from a single fertilized egg which gives rise to a vast array of cell types, such as nerve cells, muscle cells, and epithelial cells that characterize the adult? Throughout development and adulthood, cellular differentiation leads cells to assume their final morphology and physiology. Differentiation is the process by which unspecialized cells become specialized to carry out distinct functions.
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基因组复制的发育变化 多能与差异化人类细胞的复制进展.

Sunil Kumar Pradhan1, Teresa Lozoya1, Paulina Prorok1

  • 1Cell Biology and Epigenetics, Department of Biology, Technical University of Darmstadt, 64287 Darmstadt, Germany.

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概括

人类细胞在发育过程中表现出不同的DNA复制模式. 与差异化细胞相比,多能干细胞表现出独特的复制分叉速度和起源变异性,rDNA重复时间发生显著变化.

关键词:
中心的中心 (centromere)染色体压缩的压缩方式基因组复制的进展.人类细胞是人类细胞.诱导多能干细胞的诱导干细胞.多能胚胎干细胞多能胚胎干细胞rDNADNA 的意思是爬行动物 - 鱼类

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科学领域:

  • 细胞生物学 细胞生物学
  • 基因组学就是基因组学.
  • 发展生物学 发展生物学

背景情况:

  • 基因复制对于细胞分裂期间的基因组维护至关重要,特别是在早期发育过程中.
  • 了解不同的人类细胞类型的复制动力学是发育生物学的关键.

研究的目的:

  • 为了比较人类胚胎干细胞,诱导多能干细胞和分化细胞中的基因组复制进展.
  • 为了研究时空复制模式,色素影响,并在人类发育过程中重复元素的时间.

主要方法:

  • 单细胞显微镜和超高分辨率成像用于绘制基因组复制图.
  • 对色素痕迹和紧缩水平的分析.
  • 结合的核酸和复合体活动的比度分析.

主要成果:

  • 大多数基因组重复的复制时间在多能和差异化状态中保持一致.
  • 在核糖体DNA (rDNA) 重复的复制时间中观察到发育变化.
  • 与体细胞相比,多能细胞显示出更高的起源变异性和明显的复制分叉速度.

结论:

  • 人类细胞在整个发育状态中表现出保存和独特的DNA复制程序.
  • 复制时间和分叉动力学在多能细胞和分化细胞之间有所不同,突出显示出发育调节.
  • 研究结果提供了对人类发育过程中基因组维护策略的见解.