Gene Duplication in the Carotenoid Biosynthetic Pathway Preceded Evolution of the Grasses1

Despite ongoing research on carotenoid biosynthesis in model organisms, there is a paucity of information on pathway regulation operating in the grasses (Poaceae), which include plants of world-wide agronomic importance. As a result, efforts to either breed for or metabolically engineer improvements in carotenoid content or composition in cereal crops have led to unexpected results. In comparison to maize (Zea mays), rice (Oryza sativa) accumulates no endosperm carotenoids, despite having a functional pathway in chloroplasts. To better understand why these two related grasses differ in endosperm carotenoid content, we began to characterize genes encoding phytoene synthase (PSY), since this nuclear-encoded enzyme appeared to catalyze a rate-controlling step in the plastid-localized biosynthetic pathway. The enzyme had been previously associated with the maize Y1 locus thought to be the only functional gene controlling PSY accumulation, though function of the Y1 gene product had never been demonstrated. We show that both maize and rice possess and express products from duplicate PSY genes, PSY1 (Y1) and PSY2; PSY1 transcript accumulation correlates with carotenoid-containing endosperm. Using a heterologous bacterial system, we demonstrate enzyme function of PSY1 and PSY2 that are largely conserved in sequence except for N- and C-terminal domains. By database mining and use of ortholog-specific universal PCR primers, we found that the PSY duplication is prevalent in at least eight subfamilies of the Poaceae, suggesting that this duplication event preceded evolution of the Poaceae. These findings will impact study of grass phylogeny and breeding of enhanced carotenoid content in an entire taxonomic group of plant crops critical for global food security.

[1]  P. Mccoon,et al.  Vitamin A value of sweet corn. , 1981, Journal of agricultural and food chemistry.

[2]  E. Wurtzel Use of a Ds Chromosome-Breaking Element to Examine Maize Vp5 Expression , 1992 .

[3]  P. A. Scolnik,et al.  cDNA cloning, expression during development, and genome mapping of PSY2, a second tomato gene encoding phytoene synthase. , 1993, The Journal of biological chemistry.

[4]  P. Matthews,et al.  Maize phytoene desaturase and zeta-carotene desaturase catalyse a poly-Z desaturation pathway: implications for genetic engineering of carotenoid content among cereal crops. , 2003, Journal of experimental botany.

[5]  C. Hunter,et al.  Overexpression of β-carotene hydroxylase enhances stress tolerance in Arabidopsis , 2002, Nature.

[6]  J. Bennetzen,et al.  The y1 gene of maize codes for phytoene synthase. , 1996, Genetics.

[7]  J. Ray,et al.  Using Antisense RNA to Study Gene Function: Inhibition of Carotenoid Biosynthesis in Transgenic Tomatoes , 1991, Bio/Technology.

[8]  G. Heijne,et al.  ChloroP, a neural network‐based method for predicting chloroplast transit peptides and their cleavage sites , 1999, Protein science : a publication of the Protein Society.

[9]  J. Sambrook,et al.  Molecular Cloning: A Laboratory Manual , 2001 .

[10]  G. Giuliano,et al.  Regulation of carotenoid biosynthesis during tomato development. , 1993, The Plant cell.

[11]  B. Burr,et al.  Cloning and characterization of a maize cDNA encoding phytoene desaturase, an enzyme of the carotenoid biosynthetic pathway , 2004, Plant Molecular Biology.

[12]  R. Bone,et al.  Biologic mechanisms of the protective role of lutein and zeaxanthin in the eye. , 2003, Annual review of nutrition.

[13]  D. B. Hand,et al.  Relation between carotenoid content and number of genes per cell in diploid and tetraploid corn. , 1940 .

[14]  R. Wing,et al.  Construction and characterization of two rice bacterial artificial chromosome libraries from the parents of a permanent recombinant inbred mapping population , 1996, Molecular Breeding.

[15]  Michel Georges,et al.  Molecular dissection of a quantitative trait locus: a phenylalanine-to-tyrosine substitution in the transmembrane domain of the bovine growth hormone receptor is associated with a major effect on milk yield and composition. , 2002, Genetics.

[16]  P. Bramley,et al.  Biochemical characterization of transgenic tomato plants in which carotenoid synthesis has been inhibited through the expression of antisense RNA to pTOM5 , 1992 .

[17]  G A Colditz,et al.  Intake of carotenoids and retinol in relation to risk of prostate cancer. , 1995, Journal of the National Cancer Institute.

[18]  D. Robertson,et al.  Cloning of carotenoid biosynthetic genes from maize. , 1993, Methods in enzymology.

[19]  P. Beyer,et al.  Engineering the provitamin A (beta-carotene) biosynthetic pathway into (carotenoid-free) rice endosperm. , 2000, Science.

[20]  N. Misawa,et al.  Elucidation of the Erwinia uredovora carotenoid biosynthetic pathway by functional analysis of gene products expressed in Escherichia coli , 1990, Journal of bacteriology.

[21]  Marco Busch,et al.  Functional Analysis of the Early Steps of Carotenoid Biosynthesis in Tobacco , 2002, Plant Physiology.

[22]  E. Gantt,et al.  GENES AND ENZYMES OF CAROTENOID BIOSYNTHESIS IN PLANTS. , 1998, Annual review of plant physiology and plant molecular biology.

[23]  F. Kok,et al.  Lycopene and myocardial infarction risk in the EURAMIC Study. , 1997, American journal of epidemiology.

[24]  Thomas L. Madden,et al.  Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. , 1997, Nucleic acids research.

[25]  M. Kumagai,et al.  Cytoplasmic inhibition of carotenoid biosynthesis with virus-derived RNA. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[26]  O. Sommerburg,et al.  Fruits and vegetables that are sources for lutein and zeaxanthin: the macular pigment in human eyes , 1998, The British journal of ophthalmology.

[27]  Ke,et al.  Seed-specific overexpression of phytoene synthase: increase in carotenoids and other metabolic effects , 1999, The Plant journal : for cell and molecular biology.

[28]  E. Wurtzel,et al.  Surrogate biochemistry: use of Escherichia coli to identify plant cDNAs that impact metabolic engineering of carotenoid accumulation , 2003, Applied Microbiology and Biotechnology.

[29]  M. Morgante,et al.  Contrasting Effects of Selection on Sequence Diversity and Linkage Disequilibrium at Two Phytoene Synthase Loci Online version contains Web-only data. Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.012526. , 2003, The Plant Cell Online.

[30]  N. Misawa,et al.  Molecular cloning and expression in Escherichia coli of a cyanobacterial gene coding for phytoene synthase, a carotenoid biosynthesis enzyme , 1992, FEBS letters.

[31]  P. Beyer,et al.  Transgenic rice (Oryza sativa) endosperm expressing daffodil (Narcissus pseudonarcissus) phytoene synthase accumulates phytoene, a key intermediate of provitamin A biosynthesis. , 1997, The Plant journal : for cell and molecular biology.

[32]  J. Hirschberg,et al.  Carotenoid biosynthesis in flowering plants. , 2001, Current opinion in plant biology.

[33]  Isolation and structural elucidation of (13Z,13'Z,3R,3'R,6'R)-lutein from marigold flowers, kale, and human plasma. , 1999, Journal of agricultural and food chemistry.

[34]  D. Grierson,et al.  Identification and genetic analysis of normal and mutant phytoene synthase genes of tomato by sequencing, complementation and co-suppression , 1993, Plant Molecular Biology.

[35]  P. Beyer,et al.  Phytoene synthase from Narcissus pseudonarcissus: functional expression, galactolipid requirement, topological distribution in chromoplasts and induction during flowering. , 1996, The Plant journal : for cell and molecular biology.

[36]  J. Olson Biological actions of carotenoids. , 1989, The Journal of nutrition.

[37]  P. Matthews,et al.  Metabolic engineering of carotenoid accumulation in Escherichia coli by modulation of the isoprenoid precursor pool with expression of deoxyxylulose phosphate synthase , 2000, Applied Microbiology and Biotechnology.

[38]  H. Kleinig,et al.  Light-dependent regulation of carotenoid biosynthesis occurs at the level of phytoene synthase expression and is mediated by phytochrome in Sinapis alba and Arabidopsis thaliana seedlings. , 1997, The Plant journal : for cell and molecular biology.