[SLFN14 inhibits LINE-1 transposition activity]

Yi Chuan. 2020 Jul 20;42(7):669-679. doi: 10.16288/j.yczz.20-081.
[Article in Chinese]

Abstract

Long interspersed nuclear element-1 (LINE-1) is the only active autonomous transposon in the human genome. Its transposition frequently induces host genome instability, leading to a variety of genetic diseases, including cancers. The host factors play important roles in inhibiting LINE-1 retrotransposition. As an important component of the immune system, the host factor SLFN14 has antiviral activity. Our laboratory shows that SLFN14 possesses potent inhibitory activity against LINE-1 retrotransposition. To explore the potential mechanism of SLFN14 inhibition, we analyzed its effects on transcription, translation, reverse transcription and insertion in the LINE-1 replication cycle. We confirmed that SLFN14 could suppress the LINE-1 mRNA level by affecting its transcription and degradation, thereby diminishing the protein and cDNA levels of LINE-1, which eventually block the LINE-1 retrotransposition. Further, by mapping the active domains of SLFN14, we found its inhibitory activity on LINE-1 being closely related to its endoribonuclease and ribosome binding domains. These results demonstrate the mechanism of SLFN14 in regulating LINE-1 replication, which further provide new insights for improving the regulation network of host factors for controlling genomic instability caused by LINE-1 replication.

长散在核重复序列1 (long interspersed nuclear element-1, LINE-1)是迄今为止发现的人体基因组中唯一具有自主转座活性的逆转录转座子,其转座常引起宿主基因组不稳定,从而导致包括癌症在内的各种严重基因疾病的发生。宿主因子在宿主抗LINE-1转座中发挥着重要作用。宿主因子SLFN14作为免疫系统重要组成员,具有抗病毒活性。本实验室研究发现SLFN14对于LINE-1的转座具有抑制作用。为进一步探究其具体的作用机制,通过对LINE-1复制周期中的转录、翻译、逆转录、整合环节进行实验分析,证实SLFN14能够通过影响LINE-1 mRNA转录过程及其半衰期,降低LINE-1 mRNA的水平,从而影响LINE-1蛋白及cDNA表达水平,最终导致LINE-1复制受阻。同时,通过对SLFN14活性中心的定位,本研究还发现SLFN14的抗LINE-1活性与其核糖核酸内切酶结构域和核糖体结合结构域密切相关。上述研究结果展示了SLFN14调控LINE-1复制的机制,进一步完善了宿主因子调控网络,为控制因LINE-1复制引起的基因组不稳定提供了新思路。.

Keywords: 5 ?-UTR internal promotor region;; LINE-1; SLFN14; retrotransposon; transposition.

MeSH terms

  • Endoribonucleases* / physiology
  • Genome, Human*
  • Genomic Instability
  • Humans
  • Long Interspersed Nucleotide Elements* / genetics
  • RNA, Messenger
  • Reverse Transcription

Substances

  • RNA, Messenger
  • Endoribonucleases
  • SLFN14 protein, human