Plants are a tremendous source of diverse chemicals, including many natural

Plants are a tremendous source of diverse chemicals, including many natural product-derived drugs. to mine genomes for cluster discovery. The roles of H3K27me3 and H2A.Z in repression and activation of single genes in plants are well known. However, our discovery of highly localized operon-like co-regulated regions of chromatin modification is 135459-87-9 manufacture unprecedented in plants. Our findings raise intriguing parallels with groups of physically linked multi-gene complexes in animals and with clustered pathways for specialized metabolism in filamentous fungi. INTRODUCTION The plant kingdom is well known for its great capacity to synthesize diverse specialized metabolites. These natural products have important ecological functions, providing protection against biotic and abiotic stresses such as pest and pathogen attack, ultraviolet radiation and drought. They also provide a rich source of high-value compounds such as agrochemicals and pharmaceuticals, including around 25% of natural product-derived drugs. The ability to produce particular types of natural products is often restricted to narrow taxonomic groupings and is therefore likely to be a reflection of adaptation to different environmental niches. It has recently become apparent that the genes for the biosynthetic pathways for numerous different types of specialized metabolites are organized in clusters in plant genomes (1C3). In eukaryotes genes for multi-step processes are normally dispersed throughout the genome, except for clusters of tandemly duplicated genes [e.g. loci (animals), and disease-resistance genes (plants)]. However, clusters of functionally-related non-homologous genes are known, including the major histocompatibility complex (MHC) locus in animals and specialized metabolic pathways in fungi. Metabolic gene clusters in plants typically consist of three to ten or more co-localized genes encoding different types of biosynthetic enzymes required for the synthesis of a particular compound or group of compounds. They range in size from 35 kb to several hundred kb (1,3). Examples include clusters for the synthesis of agronomically and pharmaceutically important natural products such as anti-tumour alkaloids from opium poppy (noscapine), anti-nutritional steroidal alkaloids from tomato and potato (-tomatine, -solanine/-chaconine) and triterpenes associated with bitterness in cucumber (cucurbitacenes) (4C6). Cluster-derived plant natural products also have key roles as defence compounds in both monocots and eudicots, for example the cyclic hydroxamic acids 2,4-dihydroxy-1, 4-benzoxazin-3-one (DIBOA) and 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one (DIMBOA) in maize; triterpene glycosides known as avenacins in oat; momilactone, phytocassane and oryzalide diterpenes in rice; and cyanogenic glycosides in sorghum, and cassava (7C11). The genes for some of the best known plant natural product pathways such as those for flavonoids and glucosinolates are not clustered. It is not clear why some pathways are clustered and others are not. Intriguingly, clustered plant metabolic pathways have not arisen by horizontal gene transfer from microbes, but have formed relatively recently in evolutionary time by recruitment and neofunctionalization of genes from elsewhere in the genome to Rabbit polyclonal to ZCCHC12 establish co-adapted gene complexes (12,13). The mechanisms of cluster formation are not yet understood. However, clustering presumably reflects extreme selection for the assembly of co-adapted alleles of pathway genes. The genes in these metabolic gene clusters are tightly regulated and are expressed only in particular cell types, at certain stages of development, and/or in response to specific environmental triggers (3). Very little is currently known about how these pathways come to be co-ordinately expressed. So far only two transcription factors have been identified, one implicated in regulation of the cucurbitacin cluster in cucumber and the other in indirect regulation of the rice momilactone and phytocassane/oryzalide diterpene clusters 135459-87-9 manufacture (6,14). Physical clustering has the potential to enable fine tuning of cluster expression, since localized chromatin modifications can influence access of transcription factors to pathway genes (15). This fine tuning may be important in ensuring that newly 135459-87-9 manufacture evolved biosynthetic pathways with potentially maladapted intermediate phenotypes are kept under strict control. Here, we show that metabolic gene clusters in the model plant species are delineated by blocks of two different types of chromatin marks, histone H3 lysine 27 trimethylation (associated with cluster repression) and histone variant H2A.Z (associated with cluster activation) and that these features can be exploited in genome-wide mining approaches for cluster discovery. We further show that cluster-specific chromatin modifications mark metabolic gene clusters not only in but also in oat and maize. Our work opens up new avenues for investigations of specialized metabolism and genome architecture in plants. MATERIALS AND METHODS Plant material and growth conditions All plants used in this study were of the Columbia-0 (Col-0) accession. were kindly provided by Claudia K?hler (16) and (SALK_139371) by Justin Goodrich (17). For analysing the.

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