Citation:
Lambowitz AM, Zimmerly S. Mobile group II introns. Annu Rev Genet. 38 :1-35.
Publications
The Neurospora crassa CYT-18 protein C-terminal RNA-binding domain helps stabilize interdomain tertiary interactions in group I introns.
Citation:
Chen X, Mohr G, Lambowitz AM. The Neurospora crassa CYT-18 protein C-terminal RNA-binding domain helps stabilize interdomain tertiary interactions in group I introns. RNA. 10 (4) :634-44.
Use of computer-designed group II introns to disrupt Escherichia coli DExH/D-box protein and DNA helicase genes.
Citation:
Perutka J, Wang W, Goerlitz D, Lambowitz AM. Use of computer-designed group II introns to disrupt Escherichia coli DExH/D-box protein and DNA helicase genes. J Mol Biol. 336 (2) :421-39.
Effects of maturase binding and Mg2+ concentration on group II intron RNA folding investigated by UV cross-linking.
Citation:
Noah JW, Lambowitz AM. Effects of maturase binding and Mg2+ concentration on group II intron RNA folding investigated by UV cross-linking. Biochemistry. 42 (43) :12466-80.
Genetic manipulation of Lactococcus lactis by using targeted group II introns: generation of stable insertions without selection.
Citation:
Frazier CL, San Filippo J, Lambowitz AM, Mills DA. Genetic manipulation of Lactococcus lactis by using targeted group II introns: generation of stable insertions without selection. Appl Environ Microbiol. 69 (2) :1121-8.
Group II intron mobility using nascent strands at DNA replication forks to prime reverse transcription.
Citation:
Zhong J, Lambowitz AM. Group II intron mobility using nascent strands at DNA replication forks to prime reverse transcription. EMBO J. 22 (17) :4555-65.
Mobility of the Sinorhizobium meliloti group II intron RmInt1 occurs by reverse splicing into DNA, but requires an unknown reverse transcriptase priming mechanism.
Citation:
Muñoz-Adelantado E, San Filippo J, Martínez-Abarca F, García-Rodríguez FM, Lambowitz AM, Toro N. Mobility of the Sinorhizobium meliloti group II intron RmInt1 occurs by reverse splicing into DNA, but requires an unknown reverse transcriptase priming mechanism. J Mol Biol. 327 (5) :931-43.
The pathway for DNA recognition and RNA integration by a group II intron retrotransposon.
Citation:
Aizawa Y, Xiang Q, Lambowitz AM, Pyle AM. The pathway for DNA recognition and RNA integration by a group II intron retrotransposon. Mol Cell. 11 (3) :795-805.
Putative proteins related to group II intron reverse transcriptase/maturases are encoded by nuclear genes in higher plants.
Citation:
Mohr G, Lambowitz AM. Putative proteins related to group II intron reverse transcriptase/maturases are encoded by nuclear genes in higher plants. Nucleic Acids Res. 31 (2) :647-52.
Targeted and random bacterial gene disruption using a group II intron (targetron) vector containing a retrotransposition-activated selectable marker.
Citation:
Zhong J, Karberg M, Lambowitz AM. Targeted and random bacterial gene disruption using a group II intron (targetron) vector containing a retrotransposition-activated selectable marker. Nucleic Acids Res. 31 (6) :1656-64.
