通过p53介导的DNA损伤反应限制了重编程,以确保iPS细胞的基因组完整性
Rosa M Marión1, Katerina Strati, Han Li
1Telomeres and Telomerase Group, Molecular Oncology Program, Spanish National Cancer Research Centre (CNIO), Melchor Fernández Almagro 3, Madrid E-28029, Spain.
Nature
|August 12, 2009
概括
瘤抑制剂p53防止从受损细胞中产生诱导多能干细胞 (iPS). 阻止p53允许产生具有DNA损伤和染色体异常的iPS细胞.
科学领域:
- 细胞生物学 细胞生物学
- 遗传学 遗传学是一种遗传学.
- 干细胞研究 干细胞研究
背景情况:
- 将分化细胞重新编程成诱导多能干细胞 (iPS) 是无效的.
- 短端粒的细胞对重编程具有抗性,这表明存在"重编程障碍".
- 这些障碍可能与未封闭的端粒和DNA损伤有关.
研究的目的:
- 为了研究p53在防止从DNA受损的细胞中重新编程iPS细胞中的作用.
- 要确定p53是否作为重编程细胞的障碍,以各种形式的DNA损伤.
主要方法:
- 使用了诱导DNA损伤的小鼠和人类细胞模型 (短端粒,修复缺陷,外源性损伤).
- 评估了具有或没有 p53 功能活动的重编程效率.
- 分析生成的iPS细胞以检测DNA损伤和染色体稳定性.
主要成果:
- 由DNA损伤反应触发的p53激活,通过亡来中止重编程.
- 取消p53的功能可以有效地重新编程受损的细胞.
- 缺乏功能性p53的生成的iPS细胞表现出持续的DNA损伤和染色体异常.
结论:
- 细胞在重新编程过程中表现出增加的DNA损伤不耐受性.
- p53对于防止从不理想的父细胞生成多能细胞至关重要.
- p53作为一种重要的保护措施,防止产生具有基因组不稳定的iPS细胞.
相关概念视频
DNA Damage can Stall the Cell Cycle
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
DNA Damage Can Stall the Cell Cycle
In response to DNA damage, cells can pause the cell cycle to assess and repair the breaks. However, the cell must check the DNA at certain critical stages during the cell cycle. If the cell cycle pauses before DNA replication, the cells will contain twice the amount of DNA. On the other hand, if cells arrest after DNA replication but before mitosis, they will contain four times the normal amount of DNA. With a host of specialized proteins at their disposal,cells must use the right protein at...
Abnormal Proliferation
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the daughter...
Somatic to iPS Cell Reprogramming
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 for this...
Negative Regulator Molecules
Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
Chromatin Modification in iPS Cells
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.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...


