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Human L1 retrotransposon encodes a conserved endonuclease required for retrotransposition
Author(s): Feng QH, Moran JV, Kazazian HH, Boeke JD
Source: CELL    Volume: 87    Issue: 5    Pages: 905-916    Published: NOV 29 1996  
Times Cited: 386     References: 58     
Abstract: Human L1 elements are highly abundant poly(A) (non-LTR) 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.
Document Type: Article
Language: English
Addresses:
1. JOHNS HOPKINS UNIV, DEPT MOL BIOL & GENET, SCH MED, BALTIMORE, MD 21205 USA
2. UNIV PENN, SCH MED, DEPT GENET, PHILADELPHIA, PA 19104 USA
Publisher: CELL PRESS, 1050 MASSACHUSETTES AVE, CIRCULATION DEPT, CAMBRIDGE, MA 02138
Subject Category: Biochemistry & Molecular Biology; Cell Biology
IDS Number: VV774
ISSN: 0092-8674
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