The Maize Transposable Dsl Element Is Alternatively Spliced from Exon Sequences

REFERENCES

• Augustin, S., M. W. Muller, and R. J. Schweyen. 1990. Reverse self-splicing of group II intron RNAs in vitro. Nature (London) 343:383-386.
   PubMed Web of Science ®Google Scholar
• Cech, T. R. 1990. Self-splicing of group-I introns. Annu. Rev. Biochem. 59:543-568.
   PubMed Web of Science ®Google Scholar
• Colleaux, L., L. D’Auriol, F. Galibert, and B. Dujon. 1988. Recognition and cleavage site of an intron-encoded omega transposase. Proc. Natl. Acad. Sci. USA 85:6022-6026.
   PubMed Web of Science ®Google Scholar
• Dennis, E. S., M. M. Sachs, W. Gerlach, I. Beach, and W. J. Peacock. 1988. The Ds1 transposable element acts as an intron in the mutant allele Adh1-Fm335 and is spliced from the message. Nucleic Acids Res. 16:3315-3328.
   Google Scholar
• Doring, H.-P., M. Freeling, S. Hake, M. A. Johns, R. Kunze, A. Merckelbach, R. Salamini, and P. Starlinger. 1984. A Ds mutation of the Adh1 gene in Zea mays. Mol. Gen. Genet. 193:199-204.
   Google Scholar
• Fedoroff, N., S. Wessler, and M. Shure. 1983. Isolation of the transposable maize controlling elements Ac and Ds. Cell 35:235-242.
   PubMedGoogle Scholar
• Fridell, R. Α., A. M. Pret, and L. L. Searles. 1990. A retrotrans-poson-412 insertion within an exon of the Drosophila melano-gaster vermilion gene is spliced from the precursor RNA. Genes Dev. 4:559-566.
   PubMedGoogle Scholar
• Frohman, Μ. Α., Μ. Dush, and G. R. Martin. 1988. Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc. Natl. Acad. Sci. USA 85:8998-9002.
   PubMed Web of Science ®Google Scholar
• Goodall, G. J., and W. Filipowicz. 1989. The AU-rich sequences present in the introns of plant nuclear pre-mRNAs are required for splicing. Cell 58:473-483.
   PubMedGoogle Scholar
• Hehl, R., and B. Baker. 1989. Induced transposition of Ds by a stable Ac in crosses of transgenic tobacco plants. Mol. Gen. Genet. 217:53-59.
   PubMedGoogle Scholar
• Jacquer, Α., and B. Dujon. 1985. An intron encoded protein is active in a gene conversion process that spreads an intron into a mitochondrial gene. Cell 41:383-394.
   PubMedGoogle Scholar
• Klosgen, R. B., A. Gierl, Z. Schwarz-Sommer, and H. Saedler. 1986. Molecular analysis of the waxy locus of Zea mays. Mol. Gen. Genet. 203:237-244.
   Google Scholar
• Lambowitz, A. M. 1989. Infectious introns. Cell 56:323-326.
   PubMedGoogle Scholar
• McClintock, B. 1948. Mutable loci in maize. Carnegie Inst. Washington Year Book 47:155-169.
   Google Scholar
• McClintock, B. 1951. Mutable loci in maize. Carnegie Inst. Washington Year Book 50:174-181.
   Google Scholar
• McClintock, B. 1963. Further studies of gene-control systems in maize. Carnegie Inst. Washington Year Book 62:486-493.
   Google Scholar
• Menssen, Α., S. Hohmann, W. Martin, P. S. Schnable, P. A. Peterson, H. Saedler, and A. Gierl. 1990. The En/Spm transposable element of Zea mays contains splice sites at the termini generating a novel intron from a dSpm element in the A2 gene? EMBO J. 9:3051-3057.
   PubMedGoogle Scholar
• Morl, M., and C. Schmelzer. 1990. Integration of group II intron bl1 into a foreign RNA by reversal of the self-splicing reaction in vitro. Cell 60:629-636.
   PubMed Web of Science ®Google Scholar
• Nelson, Ο. Ε., and A. S. Klein. 1984. Characterization of an Spm-controlled bronze-mutable allele in maize. Genetics 106:769-779.
   PubMedGoogle Scholar
• Nelson, O. E., and H. W. Rines. 1962. The enzymatic deficiency in the waxy mutant of maize. Biochem. Biophys. Res. Commun. 9:297-300.
   PubMed Web of Science ®Google Scholar
• Osterman, J., and D. Schwartz. 1981. Analysis of a controlling element allele at the adh1 locus of maize. Genetics 99:267-273.
   PubMedGoogle Scholar
• Peacock, W. J., E. S. Dennis, W. L. Gerlach, Μ. Μ. Sachs, and D. Schwartz. 1984. Insertion and excision of Ds controlling elements in maize. Cold Spring Harbor Symp. Quant. Biol. 49:347-354.
   PubMedGoogle Scholar
• Sanger, F., S. Nicklen, and A. R. Coulson. 1977. DNA sequencing with chain-terminating inhibitors. Proc. Natl. Acad. Sci. USA 74:5463-5467.
   PubMed Web of Science ®Google Scholar
• Schiefelbein, J., V. Raboy, N. Fedoroff, and O. Nelson. 1985. Deletions within a defective Suppressor-mutator element in maize affect the frequency and developmental timing of its excision from the bronze locus. Proc. Natl. Acad. Sci. USA 82:4783-4787.
   PubMedGoogle Scholar
• Sharp, P. A. 1985. On the origin of RNA splicing and introns. Cell 42:397-400.
   PubMed Web of Science ®Google Scholar
• Shure, M., S. Wessler, and N. Fedoroff. 1983. Molecular identification and isolation of the waxy locus in maize. Cell 35:225-233.
   PubMed Web of Science ®Google Scholar
• Sutton, W. D., W. L. Gerlach, D. Schwartz, and W. J. Peacock. 1983. Molecular analysis of Ds controlling element mutations at the Adhl locus of maize. Science 223:1265-1268.
   Google Scholar
• Thomas, P. 1980. Hybridization of denatured RNA and small DNA fragments transferred to nitrocellulose. Proc. Natl. Acad. Sci. USA 77:5201-5205.
   PubMed Web of Science ®Google Scholar
• Varagona, M., and S. R. Wessler. 1990. Implications for the cis-requirements for Ds transposition based on the sequence of the wx-B4 Ds element. Mol. Gen. Genet. 220:414-418.
   PubMedGoogle Scholar
• Vieira, J., and J. Messing. 1987. Production of single-stranded plasmid DNA. Methods Enzymol. 153:3-11.
   PubMed Web of Science ®Google Scholar
• Wessler, S. R. 1988. Phenotypic diversity mediated by the maize transposable elements Ac and Spm. Science 242:399-405.
   PubMedGoogle Scholar
• Wessler, S. R., G. Baran, and M. Varagona. 1987. The maize transposable element Ds is spliced from RNA. Science 237:916-918.
   PubMed Web of Science ®Google Scholar
• Wessler, S. R., G. Baran, M. Varagona, and S. L. Dellaporta. 1986. Excision of Ds produces waxy proteins with a range of enzymatic activities? EMBO J. 5:2427-2432.
   PubMedGoogle Scholar