APOBEC3DE Inhibits LINE-1 Retrotransposition by Interacting with ORF1p and Influencing LINE Reverse Transcriptase Activity

  • PLoS One. 2016 Jul 18;11(7):e0157220. doi: 10.1371/journal.pone.0157220.
Weizi Liang  1 Jiwei Xu  1 Wensu Yuan  1 Xuan Song  1 Jianyong Zhang  1 Wei Wei  2  3 Xiao-Fang Yu  1  3 Ying Yang  1
Affiliations
  • 1. School of Life Sciences, Tianjin University, Tianjin, China.
  • 2. First Hospital of Jilin University, Institute of Virology and AIDS Research, Changchun, Jilin Province, China.
  • 3. Department of Molecular Microbiology and Immunology, Johns Hopkins Bloomberg School of Public Health, 615 N. Wolfe Street, Baltimore, MD 21205, United States of America.
Abstract

Human long interspersed elements 1 (LINE-1 or L1) is the only autonomous non-LTR retroelement in humans and has been associated with genome instability, inherited genetic diseases, and the development of Cancer. Certain human APOBEC3 family proteins are known to have LINE-1 restriction activity. The mechanisms by which APOBEC3 affects LINE-1 retrotransposition are not all well characterized; here, we confirm that both A3B and A3DE have a strong ability to inhibit LINE-1 retrotransposition. A3DE interacts with LINE-1 ORF1p to target LINE-1 ribonucleoprotein particles in an RNA-dependent manner. Moreover, A3DE binds to LINE-1 RNA and ORF1 protein in Cell Culture system. Fluorescence microscopy demonstrated that A3DE co-localizes with ORF1p in cytoplasm. Furthermore, A3DE inhibits LINE-1 Reverse Transcriptase activity in LINE-1 ribonucleoprotein particles in a Cytidine deaminase-independent manner. In contrast, A3B has less inhibitory effects on LINE-1 Reverse Transcriptase activity despite its strong inhibition of LINE-1 retrotransposition. This study demonstrates that different A3 proteins have been evolved to inhibit LINE-1 activity through distinct mechanisms.