Research Group Genome Organization and Function, Deutsches Krebsforschungszentrum (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany; Bioquant Center, Im Neuenheimer Feld 267, 69120 Heidelberg, Germany.
Cell Rep. 2015 Jun 16;11(10):1667-78. doi: 10.1016/j.celrep.2015.05.015. Epub 2015 Jun 4.
Non-coding RNAs can modulate histone modifications that, at the same time, affect transcript expression levels. Here, we dissect such a network in mouse embryonic stem cells (ESCs). It regulates the activity of the reverse transcriptase telomerase, which synthesizes telomeric repeats at the chromosome ends. We find that histone H3 serine 10 phosphorylation set by Aurora kinase B (AURKB) in ESCs during the S phase of the cell cycle at centromeric and (sub)telomeric loci promotes the expression of non-coding minor satellite RNA (cenRNA). Inhibition of AURKB induces silencing of cenRNA transcription and establishment of a repressive chromatin state with histone H3 lysine 9 trimethylation and heterochromatin protein 1 accumulation. This process results in a continuous shortening of telomeres. We further show that AURKB interacts with both telomerase and cenRNA and activates telomerase in trans. Thus, in mouse ESCs, telomere maintenance is regulated via expression of cenRNA in a cell-cycle-dependent manner.
非编码 RNA 可以调节组蛋白修饰,而组蛋白修饰同时又会影响转录本的表达水平。在这里,我们在小鼠胚胎干细胞 (ESC) 中解析了这样一个网络。它调控着逆转录酶端粒酶的活性,端粒酶在染色体末端合成端粒重复序列。我们发现,在细胞周期的 S 期,Aurora 激酶 B (AURKB) 在 ESC 中对组蛋白 H3 丝氨酸 10 的磷酸化,促进了着丝粒和(亚)端粒位置上非编码小卫星 RNA (cenRNA) 的表达。AURKB 的抑制会诱导 cenRNA 转录的沉默,并在组蛋白 H3 赖氨酸 9 三甲基化和异染色质蛋白 1 积累的情况下建立抑制性染色质状态。这个过程会导致端粒的持续缩短。我们进一步表明,AURKB 与端粒酶和 cenRNA 相互作用,并在转位中激活端粒酶。因此,在小鼠 ESC 中,端粒维持通过 cenRNA 的表达以细胞周期依赖性的方式进行调控。