Abstract
The maize Bronze-2 (Bz2) gene, whose product acts late in the anthocyanin biosynthetic pathway, has been cloned and its transcript has been mapped. We have developed a general procedure for reconstructing wild-type alleles from transposable element-induced mutants. An existing transposon-containing clone, bz2::mu1 [McLaughlin, M., and Walbot, V. (1987). Genetics 117, 771-776], was modified by replacing the region of bz2::mu1 containing the transposon with the corresponding polymerase chain reaction-amplified sequence from the progenitor allele that has no Mu insertion. Particle gun delivery of the reconstructed Bz2 gene to embryonic scutellar tissue lacking a functional Bz2 gene complemented the bz2 mutant phenotype, as demonstrated by the production of purple spots. Having cloned the wild-type allele, we then analyzed the Bz2 transcript, whose features include an 82-nucleotide 5'-untranslated leader, one small intron (78 base pairs) within the coding region, and multiple polyadenylation sites. Four Mutator transposon insertions that eliminate gene function were mapped within the 850-nucleotide transcription unit. We found that variable levels of unspliced Bz2 RNA are present in purple husk tissue; this finding may indicate that the expression of Bz2 is regulated in part at the level of transcript processing.
MeSH Terms
Alleles
Base Sequence
Cloning, Molecular
DNA Transposable Elements/genetics
Introns/genetics
Molecular Sequence Data
Plant Proteins/genetics
Polymerase Chain Reaction
RNA Splicing/genetics
RNA, Messenger/genetics,metabolism
Recombinant Fusion Proteins/genetics
Transcription, Genetic/genetics
Zea mays/genetics
Chemicals
DNA Transposable Elements
Plant Proteins
RNA, Messenger
Recombinant Fusion Proteins
BZ2 protein, Zea mays
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Nash J
Department of Biological Sciences, Stanford University, California 94305-5020.
Luehrsen K R
Walbot V
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