Mabb Angela M, Simon Jeremy M, King Ian F, Lee Hyeong-Min, An Lin-Kun, Philpot Benjamin D, Zylka Mark J
Department of Cell Biology and Physiology, UNC Neuroscience Center, Carolina Institute for Developmental Disabilities, The University of North Carolina, Chapel Hill, North Carolina, United States of America.
Neuroscience Institute, Georgia State University, Atlanta, Georgia, United States of America.
PLoS One. 2016 May 27;11(5):e0156439. doi: 10.1371/journal.pone.0156439. eCollection 2016.
Topoisomerase 1 (TOP1) inhibitors, including camptothecin and topotecan, covalently trap TOP1 on DNA, creating cleavage complexes (cc's) that must be resolved before gene transcription and DNA replication can proceed. We previously found that topotecan reduces the expression of long (>100 kb) genes and unsilences the paternal allele of Ube3a in neurons. Here, we sought to evaluate overlap between TOP1cc-dependent and -independent gene regulation in neurons. To do this, we utilized Top1 conditional knockout mice, Top1 knockdown, the CRISPR-Cas9 system to delete Top1, TOP1 catalytic inhibitors that do not generate TOP1cc's, and a TOP1 mutation (T718A) that stabilizes TOP1cc's. We found that topotecan treatment significantly alters the expression of many more genes, including long neuronal genes, immediate early genes, and paternal Ube3a, when compared to Top1 deletion. Our data show that topotecan has a stronger effect on neuronal transcription than Top1 deletion, and identifies TOP1cc-dependent and -independent contributions to gene expression.
拓扑异构酶1(TOP1)抑制剂,包括喜树碱和拓扑替康,可将TOP1共价捕获在DNA上,形成切割复合物(cc's),在基因转录和DNA复制能够进行之前,这些复合物必须得到解决。我们之前发现拓扑替康会降低长基因(>100 kb)的表达,并使神经元中Ube3a的父本等位基因去沉默。在此,我们试图评估神经元中TOP1cc依赖性和非依赖性基因调控之间的重叠情况。为此,我们利用了Top1条件性敲除小鼠、Top1敲低、CRISPR-Cas9系统来删除Top1、不会产生TOP1cc的TOP1催化抑制剂以及一种可稳定TOP1cc的TOP1突变体(T718A)。我们发现,与Top1缺失相比,拓扑替康处理会显著改变更多基因的表达,包括长神经元基因、即早基因和父本Ube3a。我们的数据表明,拓扑替康对神经元转录的影响比Top1缺失更强,并确定了TOP1cc对基因表达的依赖性和非依赖性作用。