Natural variation in maize architecture is mediated by allelic differences at the PINOID co-ortholog barren inflorescence2

Plant J. 2009 May;58(4):618-28. doi: 10.1111/j.1365-313X.2009.03802.x. Epub 2009 Jan 19.

Abstract

We characterized allelic variation at barren inflorescence2 (bif2), a maize co-ortholog of the Arabidopsis PINOID protein kinase (PID), and tested for trait associations with bif2 in both an association mapping population of 277 diverse maize inbreds and in the inter-mated B73 x Mo17 (IBM) linkage population. Results from the quantitative analyses were compared with previous reports of bif2 phenotypes in mutagenesis studies. All three approaches (association, linkage, and mutagenesis) detect a significant effect of bif2 on tassel architecture. Association mapping implicates bif2 in an unexpectedly wide range of traits including plant height, node number, leaf length, and flowering time. Linkage mapping finds a significant interaction effect for node number between bif2 and other loci, in keeping with previous reports that bif2;spi1 and Bif2;Bif1 double mutants produce fewer phytomers. The Mo17 allele is associated with a reduced tassel branch zone and shows lower expression than the B73 allele in hybrid B73-Mo17 F(1) inflorescences, consistent with the complete absence of tassel branches in the bif2 knockout mutant. Overall, these data suggest that allelic variation at bif2 affects maize architecture by modulating auxin transport during vegetative and inflorescence development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Arabidopsis Proteins
  • Base Sequence
  • DNA, Plant / genetics
  • Flowers / genetics
  • Flowers / growth & development*
  • Flowers / metabolism
  • Gene Expression Regulation, Plant
  • Genes, Plant
  • Genetic Variation
  • Indoleacetic Acids / metabolism
  • Linkage Disequilibrium
  • Molecular Sequence Data
  • Phenotype
  • Plant Proteins / genetics
  • Plant Proteins / metabolism*
  • Protein Serine-Threonine Kinases / genetics
  • Protein Serine-Threonine Kinases / metabolism*
  • Quantitative Trait, Heritable
  • Sequence Alignment
  • Sequence Analysis, DNA
  • Zea mays / enzymology
  • Zea mays / genetics*
  • Zea mays / growth & development

Substances

  • Arabidopsis Proteins
  • DNA, Plant
  • Indoleacetic Acids
  • Plant Proteins
  • PINOID protein, Arabidopsis
  • Protein Serine-Threonine Kinases