| Literature DB >> 29309036 |
Paolo Mita1, Aleksandra Wudzinska1, Xiaoji Sun1, Joshua Andrade2, Shruti Nayak2, David J Kahler3, Sana Badri4, John LaCava1,5, Beatrix Ueberheide1,2, Chi Y Yun3, David Fenyö1, Jef D Boeke1.
Abstract
LINE-1/L1 retrotransposon sequences comprise 17% of the human genome. Among the many classes of mobile genetic elements, L1 is the only autonomous retrotransposon that still drives human genomic plasticity today. Through its co-evolution with the human genome, L1 has intertwined itself with host cell biology. However, a clear understanding of L1's lifecycle and the processes involved in restricting its insertion and intragenomic spread remains elusive. Here we identify modes of L1 proteins' entrance into the nucleus, a necessary step for L1 proliferation. Using functional, biochemical, and imaging approaches, we also show a clear cell cycle bias for L1 retrotransposition that peaks during the S phase. Our observations provide a basis for novel interpretations about the nature of nuclear and cytoplasmic L1 ribonucleoproteins (RNPs) and the potential role of DNA replication in L1 retrotransposition.Entities:
Keywords: LINE-1; MCM proteins; PCNA; cell biology; cell cycle; evolutionary biology; genomics; human; retrotransposition; retrotransposons; virus
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Year: 2018 PMID: 29309036 PMCID: PMC5821460 DOI: 10.7554/eLife.30058
Source DB: PubMed Journal: Elife ISSN: 2050-084X Impact factor: 8.140