Map-based cloning and expression analysis of BMR-6 in sorghum

J Genet. 2015 Sep;94(3):445-52. doi: 10.1007/s12041-015-0550-9.

Abstract

Brown midrib mutants in sorghum are associated with reduced lignin content and increased cell wall digestibility. In this study, we characterized a bmr-6 sorghum mutant, which shows reddish pigment in the midrib and stem after the fifth-leaf stage. Compared to wild type, Kalson lignin content of bmr-6 is decreased significantly. We used histological analysis to determine that the mutant exhibited a modified pattern of lignin staining and found an increased polysaccharide content. We cloned BMR-6 gene, a gene encoded a cinnamyl alcohol dehydrogenase (CAD), using a map-based cloning approach. Genetic complementation confirmed that CAD is responsible for the BMR-6 phenotype. BMR-6 gene was expressed in all tested sorghum tissues, with the highest being in midrib and stem. Transient expression assays in Nicotiana benthamiana leaves demonstrated cytomplasmic localization of BMR-6. We found that the expression level of bmr-6 was significantly decreased in the mutant but expression of SbCAD3 and SbCAD5 were significantly increased. Our results indicate that BMR-6 not only affects the distribution of lignin but also the biosynthesis of lignin in sorghum.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Chromosome Mapping*
  • Chromosome Segregation / genetics
  • Cloning, Molecular / methods*
  • Crosses, Genetic
  • Gene Expression Regulation, Plant
  • Genes, Plant*
  • Genetic Complementation Test
  • Genetic Loci
  • Molecular Sequence Data
  • Phenotype
  • Plant Proteins / genetics*
  • Plant Proteins / metabolism
  • Plants, Genetically Modified
  • Quantitative Trait, Heritable
  • Reproducibility of Results
  • Sorghum / cytology
  • Sorghum / genetics*
  • Subcellular Fractions / metabolism

Substances

  • Plant Proteins