Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, LA, United States of America.
Department of Embryology, Carnegie Institution for Science, Baltimore, MD, United States of America.
PLoS Genet. 2017 Jun 6;13(6):e1006837. doi: 10.1371/journal.pgen.1006837. eCollection 2017 Jun.
Long interspersed nuclear element-1s (LINE-1s, or L1s) are an active family of retrotransposable elements that continue to mutate mammalian genomes. Despite the large contribution of L1 to mammalian genome evolution, we do not know where active L1 particles (particles in the process of retrotransposition) are located in the cell, or how they move towards the nucleus, the site of L1 reverse transcription. Using a yeast model of LINE retrotransposition, we identified ESCRT (endosomal sorting complex required for transport) as a critical complex for LINE retrotransposition, and verified that this interaction is conserved for human L1. ESCRT interacts with L1 via a late domain motif, and this interaction facilitates L1 replication. Loss of the L1/ESCRT interaction does not impair RNP formation or enzymatic activity, but leads to loss of retrotransposition and reduced L1 endonuclease activity in the nucleus. This study highlights the importance of the ESCRT complex in the L1 life cycle and suggests an unusual mode for L1 RNP trafficking.
长散在核元件-1(LINE-1s,或 L1s)是一类活跃的反转录转座元件家族,它们持续改变哺乳动物的基因组。尽管 L1 对哺乳动物基因组进化有很大的贡献,但我们不知道活性 L1 颗粒(正在反转录的颗粒)在细胞中的位置,也不知道它们如何向细胞核移动,即 L1 逆转录的位点。利用酵母模型的 LINE 反转录转座,我们确定了 ESCRT(内体分选复合物必需的运输)是 LINE 反转录转座的关键复合物,并验证了这种相互作用在人类 L1 中是保守的。ESCRT 通过晚期结构域基序与 L1 相互作用,这种相互作用促进了 L1 的复制。失去 L1/ESCRT 相互作用不会损害 RNP 的形成或酶活性,但会导致反转录转座的丧失和核内 L1 内切酶活性的降低。本研究强调了 ESCRT 复合物在 L1 生命周期中的重要性,并提出了一种 L1 RNP 运输的异常模式。