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Published on April 10, 2009; 10.1104/pp.109.136408

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Received January 29, 2009
Accepted April 6, 2009

A nonsense mutation in a cinnamyl alcohol dehydrogenase gene is responsible for the sorghum brown midrib 6 phenotype

Scott E. Sattler *, Aaron J. Saathoff , Eric J. Haas , Nathan A. Palmer , Deanna L. Funnell-Harris , Gautam Sarath , and Jeffrey F. Pedersen

Grain, Forage and Bioenergy Research Unit, USDA-ARS; Dept. of Agronomy and Horticulture; Dept. of Plant Pathology, University of Nebraska-Lincoln, Lincoln, NE 68583-0739 USA; Department of Chemistry, Creighton University, 2500 California Plaza, Omaha, NE 68178

* Corresponding author; email: Scott.Sattler{at}ars.usda.gov.

brown midrib 6 (bmr6) affects phenylpropanoid metabolism resulting in reduced lignin concentrations and altered lignin composition in Sorghum bicolor. Recently, bmr6 plants were shown to have limited cinnamyl alcohol dehydrogenase activity (CAD; EC 1.1.1.195), the enzyme that catalyzes the conversion of hydroxycinnamoyl aldehydes (monolignals) to monolignols. A candidate gene approach was taken to identify Bmr6. Two CAD genes (Sb02g024190 and Sb04g005950) were identified in the sorghum genome based on similarity to known CAD genes and through DNA sequencing a nonsense mutation was discovered in Sb04g005950 that results in a truncated protein lacking the NADPH-binding and C-terminal catalytic domains. Immunoblotting confirmed that the Bmr6 protein was absent in protein extracts from bmr6 plants. Phylogenetic analysis indicated that Bmr6 is a member of an evolutionarily conserved group of CAD proteins, which function in lignin biosynthesis. In addition, Bmr6 is distinct from the other CAD-like proteins in sorghum including SbCAD4 (Sb02g024190). Although both Bmr6 and SbCAD4 are expressed in sorghum internodes, an examination of enzymatic activity of recombinant Bmr6 and SbCAD4 showed that Bmr6 had 1-2 orders of magnitude greater activity for monolignol substrates. Modeling of Bmr6 and SbCAD4 protein structures showed differences in the amino acid composition of the active site that could explain the difference in enzyme activity. These differences include His57, which is unique to Bmr6 and other grass CADs. In summary, Bmr6 encodes the major CAD protein involved in lignin synthesis in Sorghum bicolor, and the bmr6 mutant is a null allele.






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