Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition

Qinghua Feng, John V. Moran, Haig H. Kazazian, Jef D. Boeke

    Research output: Contribution to journalArticle

    Abstract

    Human L1 elements are highly abundant poly(A) (nonLTR) retrotransposons whose second open reading frame (ORF2) encodes a reverse transcriptase (RT). We have identified an endonuclease (EN) domain at the L1 ORF2 N-terminus that is highly conserved among poly(A) retrotransposons and resembles the apurinic/apyrimidinic (AP) endonucleases. Purified L1 EN protein (L1 ENp) makes 5'-PO4, 3'-OH nicks in supercoiled plasmids, shows no preference for AP sites, and preferentially cleaves sequences resembling L1 in vivo target sequences. Mutations in conserved amino acid residues of L1 EN abolish its nicking activity and eliminate L1 retrotransposition. We propose that L1 EN cleaves the target site for L1 insertion and primes reverse transcription.

    Original languageEnglish (US)
    Pages (from-to)905-916
    Number of pages12
    JournalCell
    Volume87
    Issue number5
    DOIs
    StatePublished - Nov 29 1996

      Fingerprint

    ASJC Scopus subject areas

    • Biochemistry, Genetics and Molecular Biology(all)

    Cite this