Delineation of metabolic gene clusters in plant genomes by chromatin signatures

Plants are a tremendous source of diverse chemicals, including many natural product-derived drugs. It has recently become apparent that the genes for the biosynthesis of numerous different types of plant natural products are organized as metabolic gene clusters, thereby unveiling a highly unusual form of plant genome architecture and offering novel avenues for discovery and exploitation of plant specialized metabolism. Here we show that these clustered pathways are characterized by distinct chromatin signatures of histone 3 lysine trimethylation (H3K27me3) and histone 2 variant H2A.Z, associated with cluster repression and activation, respectively, and represent discrete windows of co-regulation in the genome. We further demonstrate that knowledge of these chromatin signatures along with chromatin mutants can be used 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 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.

[1]  M. Kolesnikova,et al.  An effective strategy for exploring unknown metabolic pathways by genome mining. , 2013, Journal of the American Chemical Society.

[2]  M. Freitag,et al.  The Fusarium graminearum Histone H3 K27 Methyltransferase KMT6 Regulates Development and Expression of Secondary Metabolite Gene Clusters , 2013, PLoS genetics.

[3]  D. Kliebenstein,et al.  In Planta Variation of Volatile Biosynthesis: An Alternative Biosynthetic Route to the Formation of the Pathogen-Induced Volatile Homoterpene DMNT via Triterpene Degradation in Arabidopsis Roots , 2015, Plant Cell.

[4]  Cole Trapnell,et al.  TopHat2: accurate alignment of transcriptomes in the presence of insertions, deletions and gene fusions , 2013, Genome Biology.

[5]  Kazunori Okada,et al.  Identification of a Biosynthetic Gene Cluster in Rice for Momilactones* , 2007, Journal of Biological Chemistry.

[6]  Jean YH Yang,et al.  Bioconductor: open software development for computational biology and bioinformatics , 2004, Genome Biology.

[7]  D. Duboule,et al.  Clustering of mammalian Hox genes with other H3K27me3 targets within an active nuclear domain , 2015, Proceedings of the National Academy of Sciences.

[8]  T. Winzer,et al.  A Papaver somniferum 10-Gene Cluster for Synthesis of the Anticancer Alkaloid Noscapine , 2012, Science.

[9]  Hadi Quesneville,et al.  Formation of plant metabolic gene clusters within dynamic chromosomal regions , 2011, Proceedings of the National Academy of Sciences.

[10]  Carla S. Jones,et al.  Minimum Information about a Biosynthetic Gene cluster. , 2015, Nature chemical biology.

[11]  Anne Osbourn,et al.  Regulation of metabolic gene clusters in Arabidopsis thaliana , 2014, The New phytologist.

[12]  Benjamin Leblanc,et al.  Polycomb-Dependent Regulatory Contacts between Distant Hox Loci in Drosophila , 2011, Cell.

[13]  C. Topp,et al.  Repression of Flowering in Arabidopsis Requires Activation of FLOWERING LOCUS C Expression by the Histone Variant H2A.Z[W][OA] , 2007, The Plant Cell Online.

[14]  J. Gershenzon,et al.  Genetic evidence for natural product-mediated plant-plant allelopathy in rice (Oryza sativa). , 2012, The New phytologist.

[15]  Kazunori Okada,et al.  OsTGAP1, a bZIP Transcription Factor, Coordinately Regulates the Inductive Production of Diterpenoid Phytoalexins in Rice* , 2009, The Journal of Biological Chemistry.

[16]  Vincent Colot,et al.  Arabidopsis TFL2/LHP1 Specifically Associates with Genes Marked by Trimethylation of Histone H3 Lysine 27 , 2007, PLoS genetics.

[17]  A. Osbourn,et al.  Gene clustering in plant specialized metabolism. , 2014, Current opinion in biotechnology.

[18]  R. Amasino,et al.  Divergent Roles of a Pair of Homologous Jumonji/Zinc-Finger–Class Transcription Factor Proteins in the Regulation of Arabidopsis Flowering Time , 2004, The Plant Cell Online.

[19]  Joana Sequeira-Mendes,et al.  The Functional Topography of the Arabidopsis Genome Is Organized in a Reduced Number of Linear Motifs of Chromatin States[C][W] , 2014, Plant Cell.

[20]  A. Osbourn,et al.  A gene cluster for secondary metabolism in oat: implications for the evolution of metabolic diversity in plants. , 2004, Proceedings of the National Academy of Sciences of the United States of America.

[21]  Dana J Morrone,et al.  CYP76M7 Is an ent-Cassadiene C11α-Hydroxylase Defining a Second Multifunctional Diterpenoid Biosynthetic Gene Cluster in Rice[W][OA] , 2009, The Plant Cell Online.

[22]  C. Dean,et al.  Detecting histone modifications in plants. , 2014, Methods in molecular biology.

[23]  J. Strauss,et al.  The chromatin code of fungal secondary metabolite gene clusters , 2012, Applied Microbiology and Biotechnology.

[24]  C. Pál,et al.  The evolutionary dynamics of eukaryotic gene order , 2004, Nature Reviews Genetics.

[25]  Erik Splinter,et al.  Looping and interaction between hypersensitive sites in the active beta-globin locus. , 2002, Molecular cell.

[26]  E. Meyerowitz,et al.  A Polycomb-group gene regulates homeotic gene expression in Arabidopsis , 1997, Nature.

[27]  W. Muir,et al.  The CHD3 Remodeler PICKLE Associates with Genes Enriched for Trimethylation of Histone H3 Lysine 271[W][OA] , 2012, Plant Physiology.

[28]  A. Osbourn,et al.  Metabolic Diversification—Independent Assembly of Operon-Like Gene Clusters in Different Plants , 2008, Science.

[29]  A. Aszódi,et al.  H3K27me3 forms BLOCs over silent genes and intergenic regions and specifies a histone banding pattern on a mouse autosomal chromosome. , 2009, Genome research.

[30]  S. Jacobsen,et al.  Epigenetic modifications in plants: an evolutionary perspective. , 2011, Current opinion in plant biology.

[31]  L. Daviet,et al.  The rise of operon-like gene clusters in plants. , 2014, Trends in plant science.

[32]  B. Chadwick,et al.  The insulator factor CTCF controls MHC class II gene expression and is required for the formation of long-distance chromatin interactions , 2008, The Journal of experimental medicine.

[33]  G. Hong,et al.  Nucleic Acids Research , 2015, Nucleic Acids Research.

[34]  P. Majumder,et al.  Regulation of major histocompatibility complex class II genes. , 2011, Current opinion in immunology.

[35]  A. Aharoni,et al.  Biosynthesis of Antinutritional Alkaloids in Solanaceous Crops Is Mediated by Clustered Genes , 2013, Science.

[36]  Seung Y. Rhee,et al.  Genomic Signatures of Specialized Metabolism in Plants , 2014, Science.

[37]  David R. Kelley,et al.  Differential gene and transcript expression analysis of RNA-seq experiments with TopHat and Cufflinks , 2012, Nature Protocols.

[38]  J. A. Jarillo,et al.  Mutations in the Arabidopsis SWC6 gene, encoding a component of the SWR1 chromatin remodelling complex, accelerate flowering time and alter leaf and flower development. , 2008, Journal of experimental botany.

[39]  Y. Reyes-Domínguez,et al.  Chromatin-level regulation of biosynthetic gene clusters. , 2009, Nature chemical biology.

[40]  L. Hennig,et al.  CHD3 Proteins and Polycomb Group Proteins Antagonistically Determine Cell Identity in Arabidopsis , 2009, PLoS genetics.

[41]  Atif Shahab,et al.  Whole-genome mapping of histone H3 Lys4 and 27 trimethylations reveals distinct genomic compartments in human embryonic stem cells. , 2007, Cell stem cell.

[42]  A. Osbourn,et al.  2012 Landes Bioscience. Do not distribute. Order in the playground Formation of plant gene clusters in dynamic chromosomal regions , 2012 .

[43]  A. Osbourn,et al.  Compromised disease resistance in saponin-deficient plants. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[44]  Matteo Pellegrini,et al.  Whole-Genome Analysis of Histone H3 Lysine 27 Trimethylation in Arabidopsis , 2007, PLoS biology.

[45]  Richard Bourgon,et al.  Genome-wide analysis of Polycomb targets in Drosophila melanogaster , 2006, Nature Genetics.

[46]  J. Reyes,et al.  Histone H2A.Z and homologues of components of the SWR1 complex are required to control immunity in Arabidopsis. , 2007, The Plant journal : for cell and molecular biology.

[47]  M Frey,et al.  Analysis of a chemical plant defense mechanism in grasses. , 1997, Science.

[48]  Benjamin M. Bolstad,et al.  affy - analysis of Affymetrix GeneChip data at the probe level , 2004, Bioinform..

[49]  Kirsten Jørgensen,et al.  Genomic clustering of cyanogenic glucoside biosynthetic genes aids their identification in Lotus japonicus and suggests the repeated evolution of this chemical defence pathway. , 2011, The Plant journal : for cell and molecular biology.

[50]  T. Jenuwein,et al.  Silencing by plant Polycomb‐group genes requires dispersed trimethylation of histone H3 at lysine 27 , 2006, The EMBO journal.

[51]  Xiaoquan Qi,et al.  Biosynthesis, regulation, and domestication of bitterness in cucumber , 2014, Science.

[52]  Rongcheng Lin,et al.  The Chromatin-Remodeling Factor PICKLE Integrates Brassinosteroid and Gibberellin Signaling during Skotomorphogenic Growth in Arabidopsis[C][W] , 2014, Plant Cell.

[53]  A. Osbourn,et al.  Modularity of Plant Metabolic Gene Clusters: A Trio of Linked Genes That Are Collectively Required for Acylation of Triterpenes in Oat[W][OA] , 2013, Plant Cell.

[54]  J. Rougemont,et al.  The Dynamic Architecture of Hox Gene Clusters , 2011, Science.

[55]  J. Tena,et al.  An evolutionarily conserved three-dimensional structure in the vertebrate Irx clusters facilitates enhancer sharing and coregulation. , 2011, Nature communications.

[56]  Nathan M. Springer,et al.  Genomic Distribution of Maize Facultative Heterochromatin Marked by Trimethylation of H3K27[W] , 2013, Plant Cell.

[57]  Reuben J. Peters,et al.  Identification of Syn-Pimara-7,15-Diene Synthase Reveals Functional Clustering of Terpene Synthases Involved in Rice Phytoalexin/Allelochemical Biosynthesis1 , 2004, Plant Physiology.