Akamatsu Yufuko, Kobayashi Takehiko
Division of Cytogenetics, National Institute of Genetics, and Department of Genetics, Sokendai, Mishima, Japan
Mol Cell Biol. 2015 May;35(10):1871-81. doi: 10.1128/MCB.01521-14. Epub 2015 Mar 16.
In S phase, the replication and transcription of genomic DNA need to accommodate each other, otherwise their machineries collide, with chromosomal instability as a possible consequence. Here, we characterized the human replication fork barrier (RFB) that is present downstream from the 47S pre-rRNA gene (ribosomal DNA [rDNA]). We found that the most proximal transcription terminator, Sal box T1, acts as a polar RFB, while the other, Sal box T4/T5, arrests replication forks bidirectionally. The fork-arresting activity at these sites depends on polymerase I (Pol I) transcription termination factor 1 (TTF-1) and a replisome component, TIMELESS (TIM). We also found that the RFB activity was linked to rDNA copies with hypomethylated CpG and coincided with the time that actively transcribed rRNA genes are replicated. Failed fork arrest at RFB sites led to a slowdown of fork progression moving in the opposite direction to rRNA transcription. Chemical inhibition of transcription counteracted this deceleration of forks, indicating that rRNA transcription impedes replication in the absence of RFB activity. Thus, our results reveal a role of RFB for coordinating the progression of replication and transcription activity in highly transcribed rRNA genes.
在S期,基因组DNA的复制和转录需要相互协调,否则它们的机制会发生碰撞,可能导致染色体不稳定。在这里,我们对位于47S前体rRNA基因(核糖体DNA[rDNA])下游的人类复制叉屏障(RFB)进行了表征。我们发现,最靠近近端的转录终止子Sal盒T1作为极性RFB发挥作用,而另一个Sal盒T4/T5则双向阻止复制叉。这些位点的叉捕获活性取决于聚合酶I(Pol I)转录终止因子1(TTF-1)和复制体成分TIMELESS(TIM)。我们还发现,RFB活性与低甲基化CpG的rDNA拷贝相关,并与活跃转录的rRNA基因复制的时间一致。在RFB位点叉捕获失败导致叉前进速度减慢,其方向与rRNA转录相反。转录的化学抑制作用抵消了叉的这种减速,表明在没有RFB活性的情况下,rRNA转录会阻碍复制。因此,我们的结果揭示了RFB在协调高度转录的rRNA基因中复制和转录活性进展方面的作用。