TY - JOUR
T1 - More active human L1 retrotransposons produce longer insertions
AU - Farley, Alexander H.
AU - Luning Park, Eline T.
AU - Kazazian, Haig H.
N1 - Funding Information:
We thank John Moran and members of the Kazazian and Luning Prak laboratories for their thoughtful comments on the manuscript. We thank the reviewers of this work for helpful suggestions and Chatima Noi Talchi for statistical analyses. This work was supported in part by NIH K08 CA83977 to E.L.P., a Nassau Fund grant to A.F. and RO1 GM45398 to H.K.
PY - 2004
Y1 - 2004
N2 - The vast majority of L1 insertions are 5′ truncated and thus inactive. Yet, the mechanism of 5′ truncation is unknown. To examine whether the frequency of L1 retrotransposition is directly correlated with the length of genomic L1 insertions, we used a cell culture assay to measure retrotransposition frequency and a PCR-based assay to measure L1 insertion length. We tested five full-length human L1 elements that retrotranspose at different frequencies: LRE3, L1RP, L1.3, L1.2A and L1.2B. Our data suggest that L1 insertion length correlates with L1 retrotransposition frequency for insertions >1 kb in length. For two elements, L1RP and L1.2A, we found that swapping the reverse transcriptase domains had little effect. Instead, we found that genomic insertion length and retrotransposition frequency are substantially affected by amino acid substitutions at positions 363, 1220 and 1259 in ORF2. We suggest that the region containing residues 1220 and 1259 may be important in the binding of ORF2p to L1 RNA to facilitate reverse transcription.
AB - The vast majority of L1 insertions are 5′ truncated and thus inactive. Yet, the mechanism of 5′ truncation is unknown. To examine whether the frequency of L1 retrotransposition is directly correlated with the length of genomic L1 insertions, we used a cell culture assay to measure retrotransposition frequency and a PCR-based assay to measure L1 insertion length. We tested five full-length human L1 elements that retrotranspose at different frequencies: LRE3, L1RP, L1.3, L1.2A and L1.2B. Our data suggest that L1 insertion length correlates with L1 retrotransposition frequency for insertions >1 kb in length. For two elements, L1RP and L1.2A, we found that swapping the reverse transcriptase domains had little effect. Instead, we found that genomic insertion length and retrotransposition frequency are substantially affected by amino acid substitutions at positions 363, 1220 and 1259 in ORF2. We suggest that the region containing residues 1220 and 1259 may be important in the binding of ORF2p to L1 RNA to facilitate reverse transcription.
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U2 - 10.1093/nar/gkh202
DO - 10.1093/nar/gkh202
M3 - Article
C2 - 14742665
AN - SCOPUS:1342264711
SN - 0305-1048
VL - 32
SP - 502
EP - 510
JO - Nucleic acids research
JF - Nucleic acids research
IS - 2
ER -