- Open Access
Controlled vocabularies for plant anatomical parts optimized for use in data analysis tools and for cross-species studies
© Meskauskiene et al.; licensee BioMed Central Ltd. 2013
- Received: 23 April 2013
- Accepted: 13 July 2013
- Published: 6 August 2013
It is generally accepted that controlled vocabularies are necessary to systematically integrate data from various sources. During the last decade, several plant ontologies have been developed, some of which are community specific or were developed for a particular purpose. In most cases, the practical application of these ontologies has been limited to systematically storing experimental data. Due to technical constraints, complex data structures and term redundancies, it has been difficult to apply them directly into analysis tools.
Here, we describe a simplified and cross-species compatible set of controlled vocabularies for plant anatomy, focussing mainly on monocotypledonous and dicotyledonous crop and model plants. Their content was designed primarily for their direct use in graphical visualization tools. Specifically, we created annotation vocabularies that can be understood by non-specialists, are minimally redundant, simply structured, have low tree depth, and we tested them practically in the frame of Genevestigator.
The application of the proposed ontologies enabled the aggregation of data from hundreds of experiments to visualize gene expression across tissue types. It also facilitated the comparison of expression across species. The described controlled vocabularies are maintained by a dedicated curation team and are available upon request.
- Plant anatomy
- Controlled vocabularies
The wide-spread use of controlled vocabularies to annotate biological experiments holds the promise of full integration and comparability between experiments and databases. It provides the basis for classifying samples more easily into discrete categories and it also facilitates the exchange of information between databases. Ultimately, improved data integration will lead to more powerful tools providing deeper biological insight. Despite these obvious benefits, ontologies have often been perceived as a necessary pain rather than useful instruments. The main drawback has been that ontologies are not easy to use and require some understanding of their semantics. As a result, few databases exist that make systematic use of ontologies, and many biologists still prefer describing their experiments with plain text rather than using controlled vobacularies. In fact, because in many public databases the submission of experiments is carried out by the experimenter and not by a trained curator, the majority of sample annotations is submitted as plain text. The subsequent transformation of this information into systematic annotations is tedious and the use of controlled vocabularies in the first place must be encouraged. This requires the availability of controlled vocabularies that can be easily interpreted and used by experimenters.
Existing ontologies suffer from a number of weaknesses, such as the use of uncommon or abstract terms, excessive tree depth, and term redundancies that cause confusion among users. For example, ‘cardinal organ part’ or ‘collective plant structure’ may be semantically useful terms, but they are not understood by the majority of biological researchers. A further problem is the attempt to incorporate multiple dimensions of an experimental design into a single ontology, such as anatomical parts, stages of organism development, and perturbations. As a result, some of the existing ontologies are very extensive and possess tree depths that can exceed a dozen levels. This depth represents a major handicap for their use in analysis tools alongside a data matrix. The same holds true for term redundancies, which impair a proper clustering of e.g. a data matrix composed of genes and anatomical parts. An example of term redundancy can be found in the current Plant Structure Ontology , in which the term ‘endosperm’ can be found at three locations (in ‘sporophyte/infructescence/fruit/seed/’, in ‘sporophyte/seed/’, and in ‘/tissue/’). This representation is impractical in the context of data analysis because a category may occur multiple times in a given data matrix.
Description of a single dimension of expression (e.g. anatomical parts as representing the spatial dimension).
Minimization of the depth of trees that classify anatomical parts. This constraint is to allow placing an ontology tree next to a results plot (e.g. heat map or scatterplot) on average-sized computer screens, and to improve legibility.
Avoidance of term redundancies to ensure that every expression vector is represented only once in a given data matrix.
Similarity of tree structures between species to facilitate cross-species comparisons.
Use of community-accepted vocabularies.
Target communities and purpose
The aim of this work is to help software developers and database curators build intuitive data annotation systems and user-friendly analysis tools incorporating plant anatomy annotations. We therefore constructed and made available a set of simplified, application-driven controlled vocabularies. The intent is not to propose an alternative to ontologies provided by the Plant Ontology Database , but to make available a set of controlled vocabularies for a specific use case. The level of detail remains at the granularity of sample sizes that are harvested for protein or gene expression profiling. The proposed ontologies were optimized for agronomically relevant crop species and model plants, with a focus on practical applications. It therefore does not aim at giving a general model for plant structure of both flowering and non-flowering plants.
The proposed controlled vocabularies were developed for monocotyledonous (monocot) and dicotyledonous (dicot) species. Each set of controlled vocabularies is structured as a tree, with parent nodes representing structures that contain multiple organs, tissues or cell types. To ensure cross-species comparability, we developed three basic types of trees: a cross-monocotyledonous tree, a cross-dicotyledonous tree, and a generic plant (angiosperm) anatomy tree that provides the overal basic structure for both monocots and dicots.
Cross-monocotyledonous tree structure
In species-specific and the generalized ‘monocot’ trees, it was tried to avoid redundancies such as placing an anatomical structure under more than one parent category. However, identical anatomical structures found in several different organs were placed under the respective parent structures. For example, the mesocotyl, stem internodes, and all root types (primary, lateral, nodal) contain an epidermis. Epidermis is therefore a child category of several parent categories, meaning e.g. ‘epidermis of a primary root’, ‘epidermis of a lateral root’, ‘epidermis of a crown root’, ‘epidermis of a stem internode’, etc. The anatomical structures present in at least one of the four species are basically included in the ‘monocot’ tree. For instance, the ‘monocot’ tree contains pulvinus of stem internode, husk leaf, and brace root although these structures, present in maize, are not found in rice, wheat, or barley (Figure 1). However, the ‘monocot’ tree does not include the male and female inflorescence branches present in the maize-specific anatomy tree. The reason for this is to avoid redundancies such as having e.g. stamen twice in the anatomy tree: once in the male-inflorescence branch and once in the male-female inflorescence branch.
Cross-dicotyledonous tree structure
The tree of anatomical parts for dicots (Figure 1) was built by identifying common structures between earlier versions of the Genevestigator anatomy trees for Arabidopsis, soybean, tomato, and tobacco. The basic principles are the same as for species-specific and ‘monocot’ anatomy trees: 1. The hierarchical tree reflects a dicot plant with child structures being part of the parent structure except for various root types. 2. Redundancies are avoided with the exception of anatomical structures/tissues/cell-types that are found in several different plant organs. 3. A few anatomical categories that do not exist in plants but are required for experiment-annotation are added. 4. Anatomical structures that are present in at least one of the four species (e.g. nodule, which is only present in soybean) are included, as long as this does not lead to unnecessary redundancies. One exception from this rule is that the dicot tree does not contain the tobacco-specific categories (Primings, Lugs, Cutters, Leaves and Tips), which indicate the position of a leaf on the stalk, and which are used for tobacco experiment annotation (see case study below).
Extending and merging tree structures
With the increasing number of published transcriptome studies and the accumulation of such data in proprietary and public databases, it has become imperative to integrate all experiments using controlled vocabularies. Organizing these vocubularies in trees rather than simple lists of keywords is an important step towards facilitating data interpretation. In fact, the visualization of results for individual tissues in their larger spatial context helps understanding their biological regulation and function.
Burley and Flue-cured: primings, lugs, cutters, leaves, tips
Oriental: the stalk anatomy of an Oriental tobacco is quite different, however an equivalence is now widely accepted and the leaf positions are matched to the Burley and Flue-Cured terminology with the exception of primings that do not exist in Oriental varieties.
For each leaf position the ontology includes the subsequent descriptors ‘auxillary bud’ or ‘leaf’ (except for primings where only ‘leaf’ is meaningful), then ‘petiole’ or ‘blade(lamina)’ and finally ‘trichome’ or ‘midrib’ or ‘lateral vein’.
For tobacco, some specificities were included to also describe the curing process, that is part of the tobacco processing after harvest. This aspect was added, as the curing is a key step in studying valued properties of tobacco leaves. It has to be also noted that several microarray experiments () revealed a gene transcription activity long after ripping. Also greenhouse conditions (e.g lighting, temperature, fertilization, humidity) have been described. The genotype list includes commercial tobacco cultivars from the PMI germplasm collection as well as N. tabacum ancestors and other Nicotiana species.
The N. tabacum ontology was used within Philip Morris International (PMI) to annotate and describe gene expression experiments for a total of 216 microarrays, as well as for other types of analyses.
organ specific (e.g. trichome) studies
variety comparison (fields and greenhouse)
transcription activity during the curing process (time-course experiment)
impact of the cadmium content in soil on the gene signatures
cold shock treatment effect on seedlings
Nicotiana species comparison (e.g. N. rustica)
Mapping to existing ontologies from POC
To meet community standards, the terms used to describe anatomical structures were mapped to the corresponding POC identifiers. In case of multiple options, the most suitable POC entities were chosen, i.e. our controlled vocabulary terms were mapped to those POC entities where the description applies best. Detailed mappings are available in Additional file 3 and Additional file 4.
In this work, we focused primarily on plant species of agricultural and biotechnological interest. The proposed ontologies were therefore optimized for cereal crops and for dicotyledonous species like Arabidopsis, soybean and tobacco. The choice of using hierarchical trees rather than a more general directed acyclic graph (DAG) was imposed by plot visualization constraints and the need to minimize redundancies. Existing ontologies, such as the Plant Structure Ontology  focused primarily on their use to search terms and associated annotations, to identify samples of interest or to associate the expression of particular genes with anatomical parts. Our use case is different, and the adaptations made resulted in ontologies that are slim and purpose-specific, and they work well for the agronomically relevant species described here. As correctly pointed out by Ilic et al. , however, for some plant species where a given tissue type can be part of different structures, using a hierarchical system would inevitably result in redundancies. This is rarely the case for the monocotyledonous and dicotyledonous species described here. Therefore, the simplification of a DAG to a hierarchical tree greatly facilitates the implementation of a tree within a tool without causing such undesired redundancies.
The further simplification of the anatomy tree to remove nodes that do not represent physical entities that can be harvested (e.g. terms such as ‘cardinal part’ or ‘collective organ part structure’) resulted in a shallow tree with minimal width. This was essential to facilitate the representation of measurement results in a plot or heat map that is displayed next to the tree. Figure 2 shows the characteristics of the monocot, dicot and general angiosperm tree in terms of tree depth. In contrast to the Plant Structure Ontology , which have depths of up to 15 and the most populated depths being 5 and 6, the proposed ontologies have a maximum depth of 8, with the most populated depth being 3 for the dicot model and 4 for the monocot model. Despite this lower depth, the proposed ontologies are sufficiently fine-granular to represent all biological samples that can currently be harvested and genomically profiled. As newer methods of harvesting get closer to single-cell analytics, the granularity will increase while we move from organs to tissues to cell types. The anatomy ontology model described here is extensible and can accomodate new levels. The advent of single-cell profiling is not expected to extend the depth by more than two or three levels.
Currently, the anatomy ontology contains organs and tissues that underwent normal development. It is possible that the same tree structure be used to create a phenotype ontology to capture morphologic variations (quantitative or qualitative). Alternatively, it is conceivable that phenotypic variations get depicted in the same ontology, alongside the corresponding normal anatomical structures to allow direct, side-by-side comparison of gene expression between such structures. Here, we do not impose one or the other way of capturing phenotypic variation into an ontology.
The ontologies described here have been tested and used practically in the context of a database and analysis tools, namely Genevestigator. The chosen level of structure and granularity has been optimized over several years and provide a robust framework to build user-friendly databases and analysis tools for genomic data. The proposed ontologies are freely available upon request.
To build a controlled vocabulary for plant anatomy the following sources were used: Plant Ontology Consortium (POC) [2, 3], Gramene , MaizeGDB , TAIR , Food and Agriculture Organization of the United Nations (FAO, www.fao.org), together with other relevant publications [10–12]. For individual plant anatomy trees, terms were chosen according to specificity and acceptance within the respective communities to enable a precise experiment annotation and/or - analysis. For generalized trees (dicots and monocots), however, a more general terminology was applied to facilitate the analysis across different species.
We acknowledge support of our research from the European Union (EU Framework Program 6, AGRONOMICS (LSHG-CT-2006-037704); EU-KBBE Program, 3TO4 (289582)), CTI (Swiss Innovation Promotion Agency) project 9428.1 PFLSLS, ETH Zurich, and Philip Morris International.
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