首页> 外文期刊>Journal de la Societe de biologie >Compartiments nucleaires d'heterochromatine et repression genique : le modele de la differentiation hematopoYetique humaine
【24h】

Compartiments nucleaires d'heterochromatine et repression genique : le modele de la differentiation hematopoYetique humaine

机译:异染色质核室和基因抑制:人类造血分化的模型。

获取原文
获取原文并翻译 | 示例
           

摘要

Heterochromatin compartments and gene silencing: human hematopoietic differentiation as a model study.In order to accomplish its differentiation program, the nucleus of a multipotent cell must be sequentially reprogrammed to acquire and maintain new gene expression patterns. When a stem cell is committed to differentiate towards a given lineage, global genome reprogramming involves both repression of non-affiliated genes and selective activation of genes involved in the establishment of the lineage. Accumulating evidence indicates that lineage specific gene expression is determined not only by the availability of specific transcription factors, but also by epigenetic modifications including both local modifications of DNA and chromatin structure, as well as global topological changes in chromosomes and genes positioning in the nucleus. Combined, these different levels of gene regulation allow for fine controls that integrate environmental and intracellular signals to establish appropriate gene expression programs, and hence ultimately determine the identity of the cell. Therefore, epigenetic modifications most likely precede gene activation and play a critical role in the choices of a stem cell to continue to self-renew or to differentiate. However, the cause-effect relationship between chromatin structure, nuclear architecture and cell-fate decisions is still a matter of debate.The pericentromeric heterochromatin compartment will be presented as one of the best studied examples to understand the impact of and positioning of a gene on its transcription. We will set the influence of heterochromatin compartments in the context of hematopoietic differentiation of human multipotent progenitors.
机译:异染色质区室和基因沉默:作为人类造血分化的模型研究。为了完成其分化程序,必须对多能细胞的细胞核进行顺序重编程以获取并维持新的基因表达模式。当干细胞致力于向给定谱系分化时,全局基因组重编程既涉及非亲缘基因的抑制,也包括涉及谱系建立的基因的选择性激活。越来越多的证据表明,谱系特异性基因的表达不仅取决于特异性转录因子的可用性,还取决于表观遗传修饰,包括DNA和染色质结构的局部修饰,以及染色体的整体拓扑变化和基因在细胞核中的定位。结合起来,这些不同水平的基因调控可实现整合环境和细胞内信号的精细控制,以建立适当的基因表达程序,从而最终确定细胞的身份。因此,表观遗传修饰很可能在基因激活之前发生,并在选择干细胞以继续自我更新或分化中起关键作用。然而,染色质结构,核结构和细胞命运决定之间的因果关系仍然是一个争论的话题。着重于着丝粒的异染色质区室将作为研究最好的实例之一,以了解基因对基因的影响和定位。它的转录。我们将在人类多能祖细胞的造血分化背景下设定异染色质区室的影响。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号