Skip to main content

Advertisement

Log in

A candidate-gene approach to clone the sorghum Brown midrib gene encoding caffeic acid O-methyltransferase

  • Original Paper
  • Published:
Molecular Genetics and Genomics Aims and scope Submit manuscript

Abstract

The brown midrib (bmr) mutants of sorghum have brown vascular tissue in the leaves and stem as a result of changes in lignin composition. The bmr mutants were generated via chemical mutagenesis with diethyl sulfate (DES) and resemble the brown midrib (bm) mutants of maize. The maize and sorghum brown midrib mutants are of particular value for the comparison of lignin biosynthesis across different, yet evolutionarily related, species. Although the sorghum brown midrib mutants were first described in 1978, none of the Brown midrib genes have been cloned. We have used a candidate-gene approach to clone the first Brown midrib gene from sorghum. Based on chemical analyses of the allelic mutants bmr12, bmr18 and bmr26, we hypothesized that these mutants had reduced activity of the lignin biosynthetic enzyme caffeic acid O-methyltransferase (COMT). After a northern analysis revealed strongly reduced expression of the COMT gene, the gene was cloned from the mutants and the corresponding wild types using PCR. In all three mutants, point mutations resulting in premature stop codons were identified: bmr12, bmr18 and bmr26 are therefore mutant alleles of the gene encoding COMT. RT-PCR indicated that all three mutants express the mutant allele, but at much lower levels relative to the wild-type controls. Molecular markers were developed for each of the three mutant alleles to facilitate the use of these mutant alleles in genetic studies and breeding programs.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1A–D.
Fig. 2A, B.
Fig. 3.
Fig. 4.
Fig. 5A, B.
Fig. 6.
Fig. 7A–C.

Similar content being viewed by others

References

  • Akin DE, Hanna WW, Snook ME, Himmelsbach DS, Barton FE, Windham WR (1986) Normal-12 and brown midrib-12 sorghum. II. Chemical variation and digestibility. Agron J 78:832–837

    CAS  Google Scholar 

  • Bennetzen JL, Freeling M (1997) The unified grass genome: synergy in synteny. Genome Res 7:301–306

    CAS  PubMed  Google Scholar 

  • Bittinger TS, Cantrell RP, Axtell JD (1981) Allelism tests of the brown-midrib mutants of sorghum. J Hered 72:147–148

    Google Scholar 

  • Boudet A-M (2000) Lignins and lignification: selected issues. Plant Physiol Biochem 38:91–96

    Google Scholar 

  • Campbell MM, Sederoff RR (1996) Variation in lignin content and composition. Plant Physiol 110:3–13

    CAS  Google Scholar 

  • Carpita NC, Gibeaut DM (1993) Structural models of the primary cell walls in flowering plants: consistency of molecular structure with the physical properties of the wall during growth. Plant J 3:1–30

    CAS  PubMed  Google Scholar 

  • Chang S, Puryear J, Cairney, J (1993) A simple and efficient method for isolating RNA from pine trees. Plant Mol Biol Rep 11:113–116

    CAS  Google Scholar 

  • Chen M, Sanmiguel P, deOliveira AC, Woo SS, Zhang H, Wing RA, Bennetzen J (1997) Microlinearity of the sh-2 homologous regions of the maize, rice and sorghum genomes. Proc Natl Acad Sci USA 94:3431–3435

    CAS  PubMed  Google Scholar 

  • Cobb BD, Clarkson JM (1994) A simple procedure for optimising the polymerase chain reaction (PCR) using modfied Taguchi methods. Nucleic Acids Res 22:3801–3805

    CAS  PubMed  Google Scholar 

  • Davin LB, Lewis NG (2000) Dirigent proteins and dirigent sites explain the mystery of specificity of radical precursor coupling in lignan and lignin biosynthesis. Plant Phys 123:453–461

    Article  CAS  PubMed  Google Scholar 

  • Devos KM, Gale MD (2000) Genome relationships: the grass model in current research. Plant Cell 12:637–646

    Google Scholar 

  • Finlayson SA, Lee I-J, Mullet JE, Morgan PW (1999) The mechanism of rhythmic ethylene production in sorghum. The role of phytochrome B and simulated shading. Plant Physiol 119:1083–1089

    Article  CAS  PubMed  Google Scholar 

  • Franke R, Humphreys JM, Hemm MR, Denault JW, Ruegger MO, Cusumano JC, Chapple C (2002) The Arabidopsis REF8 gene encodes the 3-hydroxylase of phenylpropanoid metabolism. Plant J 30:33–45

    Article  CAS  PubMed  Google Scholar 

  • Hatfield R, Vermerris W (2001) Lignin formation in plants: the dilemma of linkage specificity. Plant Physiol 126:1351–1357

    Article  CAS  PubMed  Google Scholar 

  • Hatfield RD, Ralph J, Grabber JH (1998) Cell wall cross-linking by ferulates and diferulates in grasses. J Sci Food Agric 79:403–407

    Article  Google Scholar 

  • Humphreys JM, Chapple C (2002) Rewriting the lignin road map. Curr Opin Plant Biol 5:224–229

    Article  CAS  PubMed  Google Scholar 

  • Humphreys JM, Hemm MR, Chapple C (1999) New routes for lignin biosythesis defined by biochemical characterization of recombinant ferulate 5-hydroxylase, a multifunctional cytochrome P450-dependent monooxygenase. Proc Natl Acad Sci USA 96:10045–10050

    CAS  PubMed  Google Scholar 

  • Inoue K, Sewalt VJH, Ballance GM, Ni W, Stürzer C, Dixon RA (1998) Developmental expression and substrate specificities of alfalfa caffeic acid 3-O-methyltransferase and caffeoyl coenzyme A 3-O-methyltransferase in relation to lignification. Plant Physiol 117:761–770

    Article  CAS  PubMed  Google Scholar 

  • Kenrick P, Crane PR (1997) The origin and early evolution of plants on land. Nature 389:33–39

    Article  CAS  Google Scholar 

  • Konieczny A, Ausubel F (1993) A procedure for mapping Arabidopsis mutations using co-dominant ecotype-specific PCR-based markers. Plant J 4:403–410

    CAS  PubMed  Google Scholar 

  • Mango SE (2001) Stop making nonSense: the C. elegans smg genes. Trends Genet 17:646–653

    Article  CAS  PubMed  Google Scholar 

  • Maquat LE, Carmichael GG (2001) Quality control of mRNA function. Cell 104:173–176

    CAS  PubMed  Google Scholar 

  • Melake Berhan A, Hulbert SH, Butler LG, Bennetzen JL (1993) Structure and evolution of the genomes of Sorghum bicolor and Zea mays. Theor Appl Genet 86:598–604

    CAS  Google Scholar 

  • Mulder MM, Van der Hage ERE, Boon JJ (1992) Analytical in source pyrolytic methylation electron impact mass spectrometry of phenolic acids in biological matrices. Phytochem Anal 3:165–172

    CAS  Google Scholar 

  • Ohtsubo H, Kumekawa N, Ohtsubo E (1999) RIRE2, a novel gypsy-type retrtransposon from rice. Genes Genet Syst 74:83–91

    CAS  PubMed  Google Scholar 

  • Osakabe K, Tsao CC, Li L, Popko JL, Umezawa T, Carraway DT, Smeltzer RH, Joshi CP, Chiang VL (1999) Coniferyl aldehyde 5-hydroxylation and methylation direct syringyl lignin biosynthesis in angiosperms. Proc Natl Acad Sci USA 96:8955–8960

    CAS  PubMed  Google Scholar 

  • Petracek ME, Nuygen T, Thompson WF, Dickey LF (2000) Premature termination codons destabilize ferredoxin-1 mRNA when ferredoxin-1 is translated. Plant J 563–569

  • Pflieger S, Lefebvre V, Causse M (2001) The candidate gene approach in plant genetics: a review. Mol Breed 7:275–291

    Article  CAS  Google Scholar 

  • Porter KS, Axtell JD, Lechtenberg VL, Colenbrander VF (1978) Phenotype, fiber composition, and in vitro dry matter disappearance of chemically induced brown midrib (bmr) mutants of sorghum. Crop Sci 18:205–209

    CAS  Google Scholar 

  • Ralph J, Hatfield RD (1991) Pyrolysis-GC-MS characterization of forage materials. J Agr Food Chem 39:1426–1437

    CAS  Google Scholar 

  • Ralph J, Hatfield RD, Quideau S, Helm RF, Grabber JH, Jung H-JG (1994) Pathway of p-coumaric acid incorporation into maize lignin as revealed by NMR. J Am Chem Soc 116:9448–9456

    CAS  Google Scholar 

  • Ralph J, et al (2001) Elucidation of new structures in lignins of CAD- and COMT-deficient plants by NMR. Phytochemistry 57:993–1003

    Article  CAS  PubMed  Google Scholar 

  • Schoch G, Goepfert S, Morant M, Hehn A, Meyer D, Ullmann P, Werck-Reichhart D (2001) CYP98A3 from Arabidopsis thaliana is a 3´-hydroxylase of phenolic esters, a missing link in the phenylpropanoid pathway. J Biol Chem 276:36566–36574

    Article  CAS  PubMed  Google Scholar 

  • Shields R (1993) Pastoral synteny. Nature 365:297–298

    Google Scholar 

  • Siebert PD, Chenchik A, Kellogg DE, Lukyanov KA, Lukyanov SA (1995) An improved PCR method for walking uncloned genomic DNA. Nucleic Acid Res 23:1087–1088

    CAS  PubMed  Google Scholar 

  • Suzuki S, Lam TBT, Iiyama K (1997) 5-Hydroxyguaiacyl nuclei as aromatic constituents of native lignin. Phytochemistry 46:695–700

    Article  CAS  Google Scholar 

  • Ugozzolli L, Wallace RB (1991) Allele-specific polymerase chain reaction. Methods 2:42–48

    CAS  Google Scholar 

  • Van Hoof A, Green P (1996) Premature nonsense codons decrease the stability of the phytohemagglutinin mRNA in a position-dependent manner. Plant J 10:415–424

    Article  PubMed  Google Scholar 

  • Vermerris W, Boon JJ (2001) Tissue-specific patterns of lignification are disturbed in the brown midrib2 mutant of maize (Zea mays L.). J Agric. Food Chem 49:721–728

    Article  CAS  Google Scholar 

  • Vermerris W, Thompson KJ, McIntyre LM, Axtell JD (2002) Evidence for an evolutionary conserved interaction between cell wall biogenesis and plant development in maize and sorghum. BMC Evolutionary Biology 2:2 (http://www.biomedcentral.com/1471–2148/2/2)

    Google Scholar 

  • Vignols F, Rigau J, Torres MA, Capellades M, Puigdomènech P (1995) The brown-midrib3 (bm3) mutation in maize occurs in the gene encoding caffeic acid O-methyl transferase. Plant Cell 7:407–416

    Article  CAS  PubMed  Google Scholar 

  • Wilusz CJ, Wang W, Peltz SW (2001) Curbing the nonsense: the activation and regulation of mRNA surveillance. Genes Dev 15:2781–2785

    CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors would like to thank Dr. Gebisa Ejeta for providing the bmr26 mutant, Terry Lemming for excellent care of the plants, Adam Hoagland and Suzanne Cunningham for assistance with the northern analyses, and Dr. Jeff Denault for technical assistance with the Py-GC-MS analyses. We are grateful for financial support from the Showalter Foundation for the acquisition of the Py-GC-MS equipment. This article is paper no. 16999 in the Purdue Agricultural Experiment Station Series

The sorghum COMT sequence has been submitted to GenBank under the Accession No. AY217766.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to W. Vermerris.

Additional information

Communicated by R. Hagemann

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bout, S., Vermerris, W. A candidate-gene approach to clone the sorghum Brown midrib gene encoding caffeic acid O-methyltransferase. Mol Gen Genomics 269, 205–214 (2003). https://doi.org/10.1007/s00438-003-0824-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00438-003-0824-4

Keywords

Navigation