Abstract
We have cloned and sequenced a 1.7-kb Mu element from a Mutator line of maize and compared its structure to Mu1, a 1.4-kb element. With the exception of a 385-bp block of DNA present in the 1.7-kb element, these transposable elements are structurally similar, sharing terminally inverted and internal direct repeated sequences. Derivation of 1.4-kb elements from the 1.7-kb class via deletion of internal sequence is suggested by the finding that a portion of the extra DNA in Mu1.7 is part of a truncated direct repeat sequence in the 1.4-kb element. An abundant poly(A)+ RNA homologous to a portion of this extra DNA is present in several tissues of both Mutator and non-Mutator lines. Analysis of transcripts from an unstable mutant bronze 1 (bz) allele containing a Mu1.7 element inserted in an exon of the gene detects three species of poly(A)+ RNA that hybridize to a Bz1 (Bronze) gene probe: the largest contains the entire Mu1.7 element in the Bz1 gene transcript; another appears to be a spliced, chimeric transcript; the smallest is normal size Bz1 mRNA. The latter is most likely encoded by the normal-size alleles detected by Southern analysis of tissue expressing purple pigment, suggesting that normal gene function is restored by excision of the Mu1.7 element.
MeSH Terms
Base Sequence
Cloning, Molecular
DNA/genetics,isolation & purification
DNA Restriction Enzymes
DNA Transposable Elements
Molecular Sequence Data
Mutation
Nucleic Acid Hybridization
Nucleotide Mapping
Plants/genetics
RNA/genetics,isolation & purification
Zea mays/genetics
Chemicals
DNA Transposable Elements
RNA
DNA
DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Taylor L P
Department of Biological Sciences, Stanford University, California 94305.
Walbot V
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