Organ-Specific Expression of Maize Adh1 Is Altered After a Mu Transposon Insertion
Open Access
- 1 July 1987
- journal article
- research article
- Published by Oxford University Press (OUP) in Genetics
- Vol. 116 (3) , 469-477
- https://doi.org/10.1093/genetics/116.3.469
Abstract
A new, unstable, organ-specific Adh1 mutant was isolated from a Robertson's mutator line by germinating kernels under partial anaerobic conditions. Families of kernels which showed segregation of a conditional anaerobic lethal phenotype were identified. One mutant, Adh1-3F1124, was shown to express approximately 6% normal levels of ADH1 in seed and anaerobically treated seedlings but expresses normal levels of ADH1 in pollen, the male gametophyte. The ADH1 polypeptide encoded by the mutant allele was found to be indistinguishable from that encoded by the Adh1-3F progenitor but its message levels were lower in seed and seedlings. Robertson's mutator lines are known to carry Mu transposons that cause increased mutation rates. Genomic Southern analysis of Adh1-3F1124 and Adh1-3F showed the presence of a 1.85 kbp insertion at the 5′ region of Adh1. Comparison of the DNA sequences revealed that a Mu1-like element was inserted 31 bp 5′ from the transcriptional start site of Adh1-3F1124gene. The insertion of the Mu element creates an additional TATA box by duplicating the 9 bp genomic sequence—ATATAAATC—at the site of insertion. Consequently, there are two potentially functional TATA sequences, separated by the 1.85 kbp Mu element, 5′ to the transcriptional start site. It is not yet understood how such an arrangement alters the organspecific expression of Adh1.This publication has 26 references indexed in Scilit:
- Independent control elements that determine yolk protein gene expression in alternative Drosophila tissues.Proceedings of the National Academy of Sciences, 1985
- Identification of DNA Sequences Required for the Regulation of Drosophila Alcohol Dehydrogenase Gene ExpressionPublished by Cold Spring Harbor Laboratory ,1985
- DNA insertion in the first intron of maize Adh1 affects message levels: cloning of progenitor and mutant Adh1 alleles.Proceedings of the National Academy of Sciences, 1984
- Nucieotide sequence of the maize transposable elementMulNucleic Acids Research, 1984
- Lambda replacement vectors carrying polylinker sequencesJournal of Molecular Biology, 1983
- cDNA cloning and induction of the alcohol dehydrogenase gene ( Adh1 ) of maizeProceedings of the National Academy of Sciences, 1982
- The anaerobic proteins of maizeCell, 1980
- Rapid isolation of RNA using proteinase K and sodium perchlorateAnalytical Biochemistry, 1979
- Simultaneous induction by anaerobiosis or 2,4-D of multiple enzymes specified by two unlinked genes: Differential Adh1-Adh2 expression in maizeMolecular Genetics and Genomics, 1973
- CHROMOSOME ORGANIZATION AND GENIC EXPRESSIONCold Spring Harbor Symposia on Quantitative Biology, 1951