Extracellular vesicles mediate the horizontal transfer of an active LINE-1 retrotransposon

J Extracell Vesicles. 2019 Jul 23;8(1):1643214. doi: 10.1080/20013078.2019.1643214. eCollection 2019.

Abstract

Long interspersed element-1 (LINE-1 or L1) retrotransposons replicate through a copy-and-paste mechanism using an RNA intermediate. However, little is known about the physical transmission of retrotransposon RNA between cells. To examine the horizontal transfer of an active human L1 retrotransposon mediated by extracellular vesicles (EVs), human cancer cells were transfected with an expression construct containing a retrotransposition-competent human L1 tagged with a reporter gene. Using this model, active retrotransposition events were detected by screening for the expression of the reporter gene inserted into the host genome by retrotransposition. EVs including exosomes and microvesicles were isolated from cells by differential centrifugation. The enrichment of L1-derived reporter RNA transcripts were detected in EVs isolated from cells expressing active L1 retrotransposition. The delivery of reporter RNA was confirmed in recipient cells, and reporter genes were detected in the genome of recipient cells. Additionally, employing qRT-PCR, we found that host-encoded factors are activated in response to increased exposure to L1-derived RNA transcripts in recipient cells. Our results suggest that the horizontal transfer of retrotransposons can occur through the incorporation of RNA intermediates delivered via EVs and may have important implications for the intercellular regulation of gene expression and gene function.

Keywords: Extracellular vesicles; RNA transport; apolipoprotein; horizontal gene transfer; transposable element.

Grants and funding

This work was supported by Grant-in-Aid for the Project for Cancer Research and Therapeutic Evolution (P-CREATE) from the Japan Agency for Medical Research and Development (AMED; Grant Number 17cm0106402h0002), Grant-in-Aid for Young Scientists (KAKENHI) from the Japan Society for the Promotion of Science (Grant Number 17H04991 and 18J11869).