Denoising inferred functional association networks obtained by gene fusion analysis.

BACKGROUND: Gene fusion detection - also known as the 'Rosetta Stone' method - involves the identification of fused composite genes in a set of reference genomes, which indicates potential interactions between its un-fused counterpart genes in query genomes. The precision of this method typically improves with an ever-increasing number of reference genomes. RESULTS: In order to explore the usefulness and scope of this approach for protein interaction prediction and generate a high-quality, non-redundant set of interacting pairs of proteins across a wide taxonomic range, we have exhaustively performed gene fusion analysis for 184 genomes using an efficient variant of a previously developed protocol. By analyzing interaction graphs and applying a threshold that limits the maximum number of possible interactions within the largest graph components, we show that we can reduce the number of implausible interactions due to the detection of promiscuous domains. With this generally applicable approach, we generate a robust set of over 2 million distinct and testable interactions encompassing 696,894 proteins in 184 species or strains, most of which have never been the subject of high-throughput experimental proteomics. We investigate the cumulative effect of increasing numbers of genomes on the fidelity and quantity of predictions, and show that, for large numbers of genomes, predictions do not become saturated but continue to grow linearly, for the majority of the species. We also examine the percentage of component (and composite) proteins with relation to the number of genes and further validate the functional categories that are highly represented in this robust set of detected genome-wide interactions. CONCLUSION: We illustrate the phylogenetic and functional diversity of gene fusion events across genomes, and their usefulness for accurate prediction of protein interaction and function

Epigenetic chromatin modifiers in barley: IV. The study of barley Polycomb group (PcG) genes during seed development and in response to external ABA

<p>Abstract</p> <p>Background</p> <p>Epigenetic phenomena have been associated with the regulation of active and silent chromatin states achieved by modifications of chromatin structure through DNA methylation, and histone post-translational modifications. The latter is accomplished, in part, through the action of PcG (Polycomb group) protein complexes which methylate nucleosomal histone tails at specific sites, ultimately leading to chromatin compaction and gene silencing. Different PcG complex variants operating during different developmental stages have been described in plants. In particular, the so-called FIE/MEA/FIS2 complex governs the expression of genes important in embryo and endosperm development in <it>Arabidopsis</it>. In our effort to understand the epigenetic mechanisms regulating seed development in barley (<it>Hordeum vulgare</it>), an agronomically important monocot plant cultivated for its endosperm, we set out to characterize the genes encoding barley PcG proteins.</p> <p>Results</p> <p>Four barley <it>PcG </it>gene homologues, named <it>HvFIE</it>, <it>HvE(Z), HvSu(z)12a</it>, and <it>HvSu(z)12b </it>were identified and structurally and phylogenetically characterized. The corresponding genes <it>HvFIE</it>, <it>HvE(Z), HvSu(z)12a</it>, and <it>HvSu(z)12b </it>were mapped onto barley chromosomes 7H, 4H, 2H and 5H, respectively. Expression analysis of the <it>PcG </it>genes revealed significant differences in gene expression among tissues and seed developmental stages and between barley cultivars with varying seed size. Furthermore, <it>HvFIE </it>and <it>HvE(Z) </it>gene expression was responsive to the abiotic stress-related hormone abscisic acid (ABA) known to be involved in seed maturation, dormancy and germination.</p> <p>Conclusion</p> <p>This study reports the first characterization of the <it>PcG </it>homologues, <it>HvFIE, HvE(Z)</it>, <it>HvSu(z)12a </it>and <it>HvSu(z)12b </it>in barley. All genes co-localized with known chromosomal regions responsible for malting quality related traits, suggesting that they might be used for developing molecular markers to be applied in marker assisted selection. The <it>PcG </it>differential expression pattern in different tissues and seed developmental stages as well as in two barley cultivars with different seed size is suggestive of a role for these genes in barley seed development. <it>HvFIE </it>and <it>HvE(Z) </it>were also found to be induced by the plant hormone ABA implying an association with ABA-mediated processes during seed development, germination and stress response.</p

Application of the ITS2 region for barcoding plants of the genus Triticum L. and Aegilops L.

Molecular taxonomic studies have been performed in the past in order to identify different wheat species and construct a molecular phylogeny. These were based on universal but sufficiently divergent sequences from both the nuclear and chloroplastic genomes of wheat. They included two short plastid sequences from the plastid genes rbcL and matK which have been proposed as the core “barcode” sequences by the “barcoding” guidelines for general plant identification. Historically, in molecular plant taxonomy, plastidic sequences had been favored over nuclear sequences, due to their uniparental inheritance and consequently lower intra-molecular recombination. However recently, the short nuclear sequence from the internal transcribed spacer 2 (ITS2) has been used successfully for the accurate identification of many medicinal and other plant species. Herein, we have used the plastidic matK, rbcL trnL, and the nuclear ITS2 region for the identification of different wheat species of Triticum L. and goatgrass species of Aegilops L. We have successfully discriminated all species that were examined from both genera, thus, validating the ITS2 region as a ‘barcode tool’ for accurate distinction of plants in the genus Triticum L. and Aegilops L. The success rate of PCR amplification and sequencing of the ITS2 region was 100%. We report also that matK, rbcL and trnL regions could not discriminate all species in contrast to the ITS2 region which demonstrated full discriminatory capacity

The nab1 gene product is important for light-induced state transitions in Chlamydomonas reinhardtii

Mussgnug JH, Kapazoglou A, Mullineaux CW, Nixon PJ, Kruse O. The nab1 gene product is important for light-induced state transitions in Chlamydomonas reinhardtii. In: Photosynthesis: Fundamental aspects to global perspectives, 13th International Congress on Photosynthesis, Montreal, Alliance Communication Group. Alliance Communication Group; 2004

Epigenetic chromatin modifiers in barley: I. Cloning, mapping and expression analysis of the plant specific HD2 family of histone deacetylases from barley, during seed development and after hormonal treatment

Epigenetic phenomena have been associated with modifications of chromatin structure. These are achieved, in part, by histone post-translational modifications including acetylations and deacetylations, the later being catalyzed by histone deacetylaces (HDACs). Eukaryotic HDACs are grouped into three major families, RPD3/HDA1, SIR2 and the plant-specific HD2. HDAC genes have been analyzed from model plants such as arabidopsis,rice and maize and have been shown to be involved in various cellular processes including seed development, vegetative and reproductive growth and responses to abiotic and biotic stress, but reports on HDACs from other crops are limited. In this work two full-length cDNAs (HvHDAC2-1 and HvHDAC2-2) encoding two members of the plant-specific HD2 family, respectively, were isolated and characterized from barley (Hordeum vulgare), an agronomically important cereal crop.HvHDAC2-1 andHvHDAC2-2 were mapped on barley chromosomes 1H and 3H, respectively, which could prove useful in developing markers for marker-assisted selection in breeding programs. Expression analysis of the barley HD2 genes demonstrated that they are expressed in all tissues and seed developmental stages examined.Significant differences were observed among tissues and seed stages, andbetween cultivars with varying seed size, suggesting an association of thesegenes with seed development. Furthermore, the HD2 genes from barley werefound to respond to treatments with plant stress-related hormones such asjasmonic acid (JA), abscisic acid (ABA) and salicylic acid (SA) implying anassociation of these genes with plant resistance to biotic and abiotic stress.The expression pattern of HD2 genes suggests a possible role for these genesin the epigenetic regulation of seed development and stress response