Bracht John R, Wang Xing, Shetty Keerthi, Chen Xiao, Uttarotai Grace J, Callihan Evan C, McCloud Sierra S, Clay Derek M, Wang Jingmei, Nowacki Mariusz, Landweber Laura F
a Department of Biology , American University , Washington, DC , USA.
b Department of Chemistry & Chemical Biology , Rensselaer Polytechnic Institute Troy , NY , USA.
RNA Biol. 2017 May 4;14(5):620-631. doi: 10.1080/15476286.2016.1195940. Epub 2016 Jun 7.
Chromosomal fusions are common in normal and cancer cells and can produce aberrant gene products that promote transformation. The mechanisms driving these fusions are poorly understood, but recurrent fusions are widespread. This suggests an underlying mechanism, and some authors have proposed a possible role for RNA in this process. The unicellular eukaryote Oxytricha trifallax displays an exorbitant capacity for natural genome editing, when it rewrites its germline genome to form a somatic epigenome. This developmental process provides a powerful model system to directly test the influence of small noncoding RNAs on chromosome fusion events during somatic differentiation. Here we show that small RNAs are capable of inducing chromosome fusions in 4 distinct cases (out of 4 tested), including one fusion of 3 chromosomes. We further show that these RNA-mediated chromosome fusions are heritable over multiple sexual generations and that transmission of the acquired fusion is associated with endogenous production of novel piRNA molecules that target the fused junction. We also demonstrate the capacity of a long noncoding RNA (lncRNA) to induce chromosome fusion of 2 distal germline loci. These results underscore the ability of short-lived, aberrant RNAs to act as drivers of chromosome fusion events that can be stably transmitted to future generations.
染色体融合在正常细胞和癌细胞中都很常见,并且可以产生促进细胞转化的异常基因产物。驱动这些融合的机制目前尚不清楚,但重复性融合广泛存在。这表明存在一种潜在机制,一些作者提出RNA在这一过程中可能发挥作用。单细胞真核生物小三毛滴虫在将其生殖系基因组重写成体细胞表观基因组时,展现出了强大的自然基因组编辑能力。这一发育过程提供了一个强大的模型系统,可直接测试小非编码RNA对体细胞分化过程中染色体融合事件的影响。在这里,我们表明小RNA能够在4个不同案例(共测试4个)中诱导染色体融合,包括一次3条染色体的融合。我们进一步表明,这些RNA介导的染色体融合在多个有性世代中是可遗传的,并且获得性融合的传递与靶向融合位点的新型piRNA分子的内源性产生有关。我们还证明了一种长链非编码RNA(lncRNA)能够诱导2个远端生殖系位点的染色体融合。这些结果强调了短寿命的异常RNA作为染色体融合事件驱动因素的能力,这些融合事件可以稳定地传递给后代。