Department of Molecular, Cell, and Developmental Biology, University of California Los Angeles, Los Angeles, California, United States of America.
PLoS Genet. 2012 Jul;8(7):e1002808. doi: 10.1371/journal.pgen.1002808. Epub 2012 Jul 5.
The relationship between epigenetic marks on chromatin and the regulation of DNA replication is poorly understood. Mutations of the H3K27 methyltransferase genes, Arabidopsis trithorax-related protein5 (ATXR5) and ATXR6, result in re-replication (repeated origin firing within the same cell cycle). Here we show that mutations that reduce DNA methylation act to suppress the re-replication phenotype of atxr5 atxr6 mutants. This suggests that DNA methylation, a mark enriched at the same heterochromatic regions that re-replicate in atxr5/6 mutants, is required for aberrant re-replication. In contrast, RNA sequencing analyses suggest that ATXR5/6 and DNA methylation cooperatively transcriptionally silence transposable elements (TEs). Hence our results suggest a complex relationship between ATXR5/6 and DNA methylation in the regulation of DNA replication and transcription of TEs.
染色质上的表观遗传标记与 DNA 复制调控之间的关系还不太清楚。H3K27 甲基转移酶基因 Arabidopsis trithorax-related protein5 (ATXR5) 和 ATXR6 的突变导致了复制(在同一个细胞周期内重复起始)。在这里,我们表明,降低 DNA 甲基化的突变会抑制 atxr5/6 突变体的重复复制表型。这表明 DNA 甲基化(在 atxr5/6 突变体中重复复制的异染色质区域富集的标记)是异常重复复制所必需的。相比之下,RNA 测序分析表明,ATXR5/6 和 DNA 甲基化协同转录沉默转座元件 (TEs)。因此,我们的结果表明,在调节 DNA 复制和 TEs 的转录过程中,ATXR5/6 和 DNA 甲基化之间存在复杂的关系。