29 research outputs found
Evaluation of Glycine max mRNA clusters
BACKGROUND: Clustering the ESTs from a large dataset representing a single species is a convenient starting point for a number of investigations into gene discovery, genome evolution, expression patterns, and alternatively spliced transcripts. Several methods have been developed to accomplish this, the most widely available being UniGene, a public domain collection of gene-oriented clusters for over 45 different species created and maintained by NCBI. The goal is for each cluster to represent a unique gene, but currently it is not known how closely the overall results represent that reality. UniGene's build procedure begins with initial mRNA clusters before joining ESTs. UniGene's results for soybean indicate a significant amount of redundancy among some sequences reported to be unique mRNAs. To establish a valid non-redundant known gene set for Glycine max we applied our algorithm to the clustering of only mRNA sequences. The mRNA dataset was run through the algorithm using two different matching stringencies. The resulting cluster compositions were compared to each other and to UniGene. Clusters exhibiting differences among the three methods were analyzed by 1) nucleotide and amino acid alignment and 2) submitting authors conclusions to determine whether members of a single cluster represented the same gene or not. RESULTS: Of the 12 clusters that were examined closely most contained examples of sequences that did not belong in the same cluster. However, neither the two stringencies of PECT nor UniGene had a significantly greater record of accuracy in placing paralogs into separate clusters. CONCLUSION: Our results reveal that, although each method produces some errors, using multiple stringencies for matching or a sequential hierarchical method of increasing stringencies can provide more reliable results and therefore allow greater confidence in the vast majority of clusters that contain only ESTs and no mRNA sequences
Regulation of seed germination and seedling growth by an Arabidopsis phytocystatin isoform, AtCYS6
Phytocystatins are cysteine proteinase inhibitors in plants that are implicated in the endogenous regulation of protein turnover and defense mechanisms against insects and pathogens. A cDNA encoding a phytocystatin called AtCYS6 (Arabidopsis thaliana phytocystatin6) has been isolated. We show that AtCYS6 is highly expressed in dry seeds and seedlings and that it also accumulates in flowers. The persistence of AtCYS6 protein expression in seedlings was promoted by abscisic acid (ABA), a seed germination and post-germination inhibitory phytohormone. This finding was made in transgenic plants bearing an AtCYS6 promoter–β-glucuronidase (GUS) reporter construct, where we found that expression from the AtCYS6 promoter persisted after ABA treatment but was reduced under control conditions and by gibberellin4+7 (GA4+7) treatment during the germination and post-germinative periods. In addition, constitutive over-expression of AtCYS6 retarded germination and seedling growth, whereas these were enhanced in an AtCYS6 knock-out mutant (cys6-2). Additionally, cysteine proteinase activities stored in seeds were inhibited by AtCYS6 in transgenic Arabidopsis. From these data, we propose that AtCYS6 expression is enhanced by the germination inhibitory phytohormone ABA and that it participates in the control of germination rate and seedling growth by inhibiting the activity of stored cysteine proteinases
A nontoxic polypeptide oligomer with a fungicide potency under agricultural conditions which is equal or greater than that of their chemical counterparts
Research ArticleThere are literally hundreds of polypeptides described in the literature which exhibit fungicide
activity. Tens of them have had attempted protection by patent applications but none,
as far as we are aware, have found application under real agricultural conditions. The reasons
behind may be multiple where the sensitivity to the Sun UV radiation can come in first
place. Here we describe a multifunctional glyco-oligomer with 210 kDa which is mainly composed
by a 20 kDa polypeptide termed Blad that has been previously shown to be a stable
intermediary product of β-conglutin catabolism. This oligomer accumulates exclusively in
the cotyledons of Lupinus species, between days 4 and 12 after the onset of germination.
Blad-oligomer reveals a plethora of biochemical properties, like lectin and catalytic activities,
which are not unusual per si, but are remarkable when found to coexist in the same protein
molecule. With this vast range of chemical characteristics, antifungal activity arises
almost as a natural consequence. The biological significance and potential technological
applications of Blad-oligomer as a plant fungicide to agriculture, its uniqueness stems from
being of polypeptidic in nature, and with efficacies which are either equal or greater than the
top fungicides currently in the market are addressedinfo:eu-repo/semantics/publishedVersio
PCR cloning and expression analysis of cDNAs encoding cysteine proteinases from germinating seeds of Vicia sativa L.
Biochemical and immunocytochemical localization of a BAPAase in developing and mature lupin cotyledons
Influence of various factors on individual radiation exposure from the chernobyl disaster
<p>Abstract</p> <p>Background</p> <p>The explosion at the Chernobyl Nuclear Power Plant was one of the greatest known nuclear disasters of the 20th century. To reduce individual exposure to ionizing radiation the Soviet Union government introduced a number of counter-measures. This article presents a description of how historical events conspired to disrupt these efforts and affect residents in exposed areas.</p> <p>Methods</p> <p>This study employed an extensive review of data on radionuclide deposition, contamination patterns and lifestyle characteristics. Data were obtained from the Ukraine Ministry of Health and the Ukraine Research Center for Radiation Medicine.</p> <p>Results</p> <p>Data are presented on annual contamination rates in selected locales as well as data on local food consumption patterns. Historical factors including economic and political circumstances are also highlighted. Results show the diminution of individual doses between 1987 and 1991 and then an increase between 1991 and 1994 and the relationship between this increase and changes in the lifestyle of the local population.</p> <p>Conclusion</p> <p>A number of factors played direct and indirect roles in contributing to the populace's cumulative radiation exposure. Future post-contamination studies need to consider these factors when estimating individual exposures.</p
The unique biosynthetic route from Lupinus Beta-conglutin gene to blad
Background: During seed germination, b-conglutin undergoes a major cycle of limited proteolysis in which many of its
constituent subunits are processed into a 20 kDa polypeptide termed blad. Blad is the main component of a glycooligomer,
accumulating exclusively in the cotyledons of Lupinus species, between days 4 and 12 after the onset of germination.
Principal Findings: The sequence of the gene encoding b-conglutin precursor (1791 nucleotides) is reported. This gene,
which shares 44 to 57% similarity and 20 to 37% identity with other vicilin-like protein genes, includes several features in
common with these globulins, but also specific hallmarks. Most notable is the presence of an ubiquitin interacting motif
(UIM), which possibly links the unique catabolic route of b-conglutin to the ubiquitin/proteasome proteolytic pathway.
Significance: Blad forms through a unique route from and is a stable intermediary product of its precursor, b-conglutin, the
major Lupinus seed storage protein. It is composed of 173 amino acid residues, is encoded by an intron-containing, internal
fragment of the gene that codes for b-conglutin precursor (nucleotides 394 to 913) and exhibits an isoelectric point of 9.6
and a molecular mass of 20,404.85 Da. Consistent with its role as a storage protein, blad contains an extremely high
proportion of the nitrogen-rich amino acidsinfo:eu-repo/semantics/publishedVersio
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Modeling based on the structure of vicilins predicts a histidine cluster in the active site of oxalate oxidase
It is known that germin, which is a marker of the onset of growth in germinating wheat, is an oxalate oxidase, and also that germins possess sequence similarity with legumin and vicilin seed storage proteins. These two pieces of information have been combined in order to generate a 3D model of germin based on the structure of vicilin and to examine the model with regard to a potential oxalate oxidase active site. A cluster of three histidine residues has been located within the conserved beta-barrel structure. While there is a relatively low level of overall sequence similarity between the model and the vicilin structures, the conservation of amino acids important in maintaining the scaffold of the beta-barrel lends confidence to the juxtaposition of the histidine residues. The cluster is similar structurally to those found in copper amine oxidase and other proteins, leading to the suggestion that it defines a metal-binding location within the oxalate oxidase active site. It is also proposed that the structural elements involved in intermolecular interactions in vicilins may play a role in oligomer formation in germin/oxalate oxidase
