Jeremy D. Murray
John Innes Centre
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Publication
Featured researches published by Jeremy D. Murray.
Plant Journal | 2008
Vagner A. Benedito; Ivone Torres-Jerez; Jeremy D. Murray; Andry Andriankaja; Stacy N. Allen; Klementina Kakar; Maren Wandrey; Jerome Verdier; Hélène Zuber; Thomas Ott; Sandra Moreau; Andreas Niebel; Tancred Frickey; Georg F. Weiller; Ji He; Xinbin Dai; Patrick Xuechun Zhao; Yuhong Tang; Michael K. Udvardi
Legumes played central roles in the development of agriculture and civilization, and today account for approximately one-third of the worlds primary crop production. Unfortunately, most cultivated legumes are poor model systems for genomic research. Therefore, Medicago truncatula, which has a relatively small diploid genome, has been adopted as a model species for legume genomics. To enhance its value as a model, we have generated a gene expression atlas that provides a global view of gene expression in all major organ systems of this species, with special emphasis on nodule and seed development. The atlas reveals massive differences in gene expression between organs that are accompanied by changes in the expression of key regulatory genes, such as transcription factor genes, which presumably orchestrate genetic reprogramming during development and differentiation. Interestingly, many legume-specific genes are preferentially expressed in nitrogen-fixing nodules, indicating that evolution endowed them with special roles in this unique and important organ. Comparative transcriptome analysis of Medicago versus Arabidopsis revealed significant divergence in developmental expression profiles of orthologous genes, which indicates that phylogenetic analysis alone is insufficient to predict the function of orthologs in different species. The data presented here represent an unparalleled resource for legume functional genomics, which will accelerate discoveries in legume biology.
Annual Review of Genetics | 2011
Giles E. D. Oldroyd; Jeremy D. Murray; Philip S. Poole; J. Allan Downie
Rhizobial bacteria enter a symbiotic association with leguminous plants, resulting in differentiated bacteria enclosed in intracellular compartments called symbiosomes within nodules on the root. The nodules and associated symbiosomes are structured for efficient nitrogen fixation. Although the interaction is beneficial to both partners, it comes with rigid rules that are strictly enforced by the plant. Entry into root cells requires appropriate recognition of the rhizobial Nod factor signaling molecule, and this recognition activates a series of events, including polarized root-hair tip growth, invagination associated with bacterial infection, and the promotion of cell division in the cortex leading to the nodule meristem. The plants command of the infection process has been highlighted by its enforcement of terminal differentiation upon the bacteria within nodules of some legumes, and this can result in a loss of bacterial viability while permitting effective nitrogen fixation. Here, we review the mechanisms by which the plant allows bacterial infection and promotes the formation of the nodule, as well as the details of how this intimate association plays out inside the cells of the nodule where a complex interchange of metabolites and regulatory peptides force the bacteria into a nitrogen-fixing organelle-like state.
Proceedings of the National Academy of Sciences of the United States of America | 2010
Benoit Lefebvre; Ton Timmers; Malick Mbengue; Sandra Moreau; Christine Hervé; Katalin Tóth; Joana Bittencourt-Silvestre; Dörte Klaus; Laurent Deslandes; Laurence Godiard; Jeremy D. Murray; Michael K. Udvardi; Sylvain Raffaele; Sébastien Mongrand; Julie V. Cullimore; Pascal Gamas; Andreas Niebel; Thomas Ott
Remorin proteins have been hypothesized to play important roles during cellular signal transduction processes. Induction of some members of this multigene family has been reported during biotic interactions. However, no roles during host-bacteria interactions have been assigned to remorin proteins until now. We used root nodule symbiosis between Medicago truncatula and Sinorhizobium meliloti to study the roles of a remorin that is specifically induced during nodulation. Here we show that this oligomeric remorin protein attaches to the host plasma membrane surrounding the bacteria and controls infection and release of rhizobia into the host cytoplasm. It interacts with the core set of symbiotic receptors that are essential for perception of bacterial signaling molecules, and thus might represent a plant-specific scaffolding protein.
Plant Physiology | 2007
Michael K. Udvardi; Klementina Kakar; Maren Wandrey; Ombretta Montanari; Jeremy D. Murray; Andry Andriankaja; Ji-Yi Zhang; Vagner A. Benedito; Julie Hofer; Foo Chueng; Christopher D. Town
Transcription factors (TFs) are DNA-binding proteins that interact with other transcriptional regulators, including chromatin remodeling/modifying proteins, to recruit or block access of RNA polymerases to the DNA template. Plant genomes devote approximately 7% of their coding sequence to TFs, which
Trends in Plant Science | 2008
Florian Frugier; Sonja Kosuta; Jeremy D. Murray; Martin Crespi; Krzysztof Szczyglowski
The symbiotic interaction between Rhizobium bacteria and legumes leads to the induction of a new root organ: the nitrogen-fixing nodule. Recent findings have uncovered that cytokinin is instrumental in this developmental process, but they also suggest a broader role for cytokinin in mediating rhizobial infection. In this opinion article, we propose that cytokinin is the key differentiation signal for nodule organogenesis. Furthermore, we discuss a model in which cytokinin might also influence bacterial infection by controlling the expression of NIN (Nodule Inception) and other transcriptional regulators through mechanisms operating both locally and systemically.
Molecular Plant-microbe Interactions | 2011
Jeremy D. Murray
Nodulation of legume roots typically begins with rhizobia attaching to the tip of a growing root-hair cell. The attached rhizobia secrete Nod factors (NF), which are perceived by the plant. This initiates a series of preinfection events that include cytoskeletal rearrangements, curling at the root-hair tip, and formation of radially aligned cytoplasmic bridges called preinfection threads (PIT) in outer cortical cells. Within the root-hair curl, an infection pocket filled with bacteria forms, from which originates a tubular invagination of cell wall and membrane called an infection thread (IT). IT formation is coordinated with nodule development in the underlying root cortex tissues. The IT extends from the infection pocket down through the root hair and into the root cortex, where it passes through PIT and eventually reaches the nascent nodule. As the IT grows, it is colonized by rhizobia that are eventually released into cells within the nodule, where they fix nitrogen. NF can also induce cortical root hairs that appear to originate from PIT and can become infected like normal root hairs. Several genes involved in NF signaling and some of the downstream transcription factors required for infection have been characterized. More recently, several genes with direct roles in infection have been identified, some with roles in actin rearrangement and others with possible roles in protein turnover and secretion. This article provides an overview of the infection process, including the roles of NF signaling, actin, and calcium and the influence of the hormones ethylene and cytokinin.
BMC Bioinformatics | 2009
Ji He; Vagner A. Benedito; Mingyi Wang; Jeremy D. Murray; Patrick Xuechun Zhao; Yuhong Tang; Michael K. Udvardi
BackgroundLegumes (Leguminosae or Fabaceae) play a major role in agriculture. Transcriptomics studies in the model legume species, Medicago truncatula, are instrumental in helping to formulate hypotheses about the role of legume genes. With the rapid growth of publically available Affymetrix GeneChip Medicago Genome Array GeneChip data from a great range of tissues, cell types, growth conditions, and stress treatments, the legume research community desires an effective bioinformatics system to aid efforts to interpret the Medicago genome through functional genomics. We developed the Medicago truncatula Gene Expression Atlas (MtGEA) web server for this purpose.DescriptionThe Medicago truncatula Gene Expression Atlas (MtGEA) web server is a centralized platform for analyzing the Medicago transcriptome. Currently, the web server hosts gene expression data from 156 Affymetrix GeneChip® Medicago genome arrays in 64 different experiments, covering a broad range of developmental and environmental conditions. The server enables flexible, multifaceted analyses of transcript data and provides a range of additional information about genes, including different types of annotation and links to the genome sequence, which help users formulate hypotheses about gene function. Transcript data can be accessed using Affymetrix probe identification number, DNA sequence, gene name, functional description in natural language, GO and KEGG annotation terms, and InterPro domain number. Transcripts can also be discovered through co-expression or differential expression analysis. Flexible tools to select a subset of experiments and to visualize and compare expression profiles of multiple genes have been implemented. Data can be downloaded, in part or full, in a tabular form compatible with common analytical and visualization software. The web server will be updated on a regular basis to incorporate new gene expression data and genome annotation, and is accessible at: http://bioinfo.noble.org/gene-atlas/.ConclusionsThe MtGEA web server has a well managed rich data set, and offers data retrieval and analysis tools provided in the web platform. Its proven to be a powerful resource for plant biologists to effectively and efficiently identify Medicago transcripts of interest from a multitude of aspects, formulate hypothesis about gene function, and overall interpret the Medicago genome from a systematic point of view.
The Plant Cell | 2014
Andrew Breakspear; Chengwu Liu; Sonali Roy; Nicola Stacey; Christian Rogers; Martin Trick; Giulia Morieri; Kirankumar S. Mysore; Jiangqi Wen; Giles E. D. Oldroyd; J. Allan Downie; Jeremy D. Murray
Transcriptome profiling of M. truncatula root hairs during the initial stages of rhizobial infection helps to interpret two decades of research on Medicago and provides a foundation for future studies on host-symbiont interactions in the rhizosphere. Nitrogen-fixing rhizobia colonize legume roots via plant-made intracellular infection threads. Genetics has identified some genes involved but has not provided sufficient detail to understand requirements for infection thread development. Therefore, we transcriptionally profiled Medicago truncatula root hairs prior to and during the initial stages of infection. This revealed changes in the responses to plant hormones, most notably auxin, strigolactone, gibberellic acid, and brassinosteroids. Several auxin responsive genes, including the ortholog of Arabidopsis thaliana Auxin Response Factor 16, were induced at infection sites and in nodule primordia, and mutation of ARF16a reduced rhizobial infection. Associated with the induction of auxin signaling genes, there was increased expression of cell cycle genes including an A-type cyclin and a subunit of the anaphase promoting complex. There was also induction of several chalcone O-methyltransferases involved in the synthesis of an inducer of Sinorhizobium meliloti nod genes, as well as a gene associated with Nod factor degradation, suggesting both positive and negative feedback loops that control Nod factor levels during rhizobial infection. We conclude that the onset of infection is associated with reactivation of the cell cycle as well as increased expression of genes required for hormone and flavonoid biosynthesis and that the regulation of auxin signaling is necessary for initiation of rhizobial infection threads.
Proceedings of the National Academy of Sciences of the United States of America | 2012
F. Xie; Jeremy D. Murray; Jiyoung Kim; Anne B. Heckmann; Anne Edwards; Giles E. D. Oldroyd; J. A. Downie
To allow rhizobial infection of legume roots, plant cell walls must be locally degraded for plant-made infection threads (ITs) to be formed. Here we identify a Lotus japonicus nodulation pectate lyase gene (LjNPL), which is induced in roots and root hairs by rhizobial nodulation (Nod) factors via activation of the nodulation signaling pathway and the NIN transcription factor. Two Ljnpl mutants produced uninfected nodules and most infections arrested as infection foci in root hairs or roots. The few partially infected nodules that did form contained large abnormal infections. The purified LjNPL protein had pectate lyase activity, demonstrating that this activity is required for rhizobia to penetrate the cell wall and initiate formation of plant-made infection threads. Therefore, we conclude that legume-determined degradation of plant cell walls is required for root infection during initiation of the symbiotic interaction between rhizobia and legumes.
Plant Journal | 2011
Jeremy D. Murray; RajaSekhara Reddy Duvvuru Muni; Ivone Torres-Jerez; Yuhong Tang; Stacy N. Allen; Megan Andriankaja; Guangming Li; Ashverya Laxmi; Xiaofei Cheng; Jiangqi Wen; David Vaughan; Michael Schultze; Jongho Sun; Myriam Charpentier; Giles E. D. Oldroyd; Million Tadege; Pascal Ratet; Kirankumar S. Mysore; Rujin Chen; Michael K. Udvardi
Intracellular invasion of root cells is required for the establishment of successful endosymbioses in legumes of both arbuscular mycorrhizal (AM) fungi and rhizobial bacteria. In both interactions a requirement for successful entry is the activation of a common signalling pathway that includes five genes required to generate calcium oscillations and two genes required for the perception of the calcium response. Recently, it has been discovered that in Medicago truncatula, the Vapyrin (VPY) gene is essential for the establishment of the arbuscular mycorrhizal symbiosis. Here, we show by analyses of mutants that the same gene is also required for rhizobial colonization and nodulation. VPY encodes a protein featuring a Major Sperm Protein domain, typically featured on proteins involved in membrane trafficking and biogenesis, and a series of ankyrin repeats. Plants mutated in this gene have abnormal rhizobial infection threads and fewer nodules, and in the case of interactions with AM fungi, epidermal penetration defects and aborted arbuscule formation. Calcium spiking in root hairs in response to supplied Nod factors is intact in the vpy-1 mutant. This, and the elevation of VPY transcripts upon application of Nod factors which we show to be dependent on NFP, DMI1, and DMI3, indicates that VPY acts downstream of the common signalling pathway.