Hua Brian L, Orr-Weaver Terry L
Whitehead Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142.
Department of Biology, Massachusetts Institute of Technology, Cambridge, Massachusetts 02142.
Genetics. 2017 Sep;207(1):29-47. doi: 10.1534/genetics.115.186627.
Proper control of DNA replication is critical to ensure genomic integrity during cell proliferation. In addition, differential regulation of the DNA replication program during development can change gene copy number to influence cell size and gene expression. serves as a powerful organism to study the developmental control of DNA replication in various cell cycle contexts in a variety of differentiated cell and tissue types. Additionally, has provided several developmentally regulated replication models to dissect the molecular mechanisms that underlie replication-based copy number changes in the genome, which include differential underreplication and gene amplification. Here, we review key findings and our current understanding of the developmental control of DNA replication in the contexts of the archetypal replication program as well as of underreplication and differential gene amplification. We focus on the use of these latter two replication systems to delineate many of the molecular mechanisms that underlie the developmental control of replication initiation and fork elongation.
正确控制DNA复制对于确保细胞增殖过程中的基因组完整性至关重要。此外,发育过程中DNA复制程序的差异调节可改变基因拷贝数,从而影响细胞大小和基因表达。作为一种强大的生物体,可用于研究各种分化细胞和组织类型在不同细胞周期背景下DNA复制的发育控制。此外,还提供了几种发育调控的复制模型,以剖析基因组中基于复制的拷贝数变化的分子机制,包括差异不完全复制和基因扩增。在这里,我们回顾了在典型复制程序以及不完全复制和差异基因扩增背景下,关于DNA复制发育控制的关键发现和当前理解。我们重点关注利用后两种复制系统来描绘许多复制起始和叉延伸发育控制背后的分子机制。