A PATO-compliant zebrafish screening database (MODB): management of morpholino knockdown screen information
© Knowlton et al; licensee BioMed Central Ltd. 2008
Received: 28 April 2007
Accepted: 07 January 2008
Published: 07 January 2008
The zebrafish is a powerful model vertebrate amenable to high throughput in vivo genetic analyses. Examples include reverse genetic screens using morpholino knockdown, expression-based screening using enhancer trapping and forward genetic screening using transposon insertional mutagenesis. We have created a database to facilitate web-based distribution of data from such genetic studies.
The MOrpholino DataBase is a MySQL relational database with an online, PHP interface. Multiple quality control levels allow differential access to data in raw and finished formats. MODBv1 includes sequence information relating to almost 800 morpholinos and their targets and phenotypic data regarding the dose effect of each morpholino (mortality, toxicity and defects). To improve the searchability of this database, we have incorporated a fixed-vocabulary defect ontology that allows for the organization of morpholino affects based on anatomical structure affected and defect produced. This also allows comparison between species utilizing Phenotypic Attribute Trait Ontology (PATO) designated terminology. MODB is also cross-linked with ZFIN, allowing full searches between the two databases. MODB offers users the ability to retrieve morpholino data by sequence of morpholino or target, name of target, anatomical structure affected and defect produced.
MODB data can be used for functional genomic analysis of morpholino design to maximize efficacy and minimize toxicity. MODB also serves as a template for future sequence-based functional genetic screen databases, and it is currently being used as a model for the creation of a mutagenic insertional transposon database.
Advances in scientific technology and the availability of genomic sequence for an increasing number of species have led to a paradigm shift from identifying sequence to gene product function. Large functional genetic screens are becoming increasingly prevalent and require a new way of thinking about data to facilitate cross-species comparison and deciphering gene product function in different organisms. Zebrafish are particularly amenable to large screens as they have a tremendous ability to reproduce, and their embryos finish the development of most organ rudiments by 2 days post-fertilization . Their semi-transparent embryos and the ready availability of transgenic lines facilitate functional annotation of the many genes required for numerous organ systems and pathways. While historically their most common use in genetic screenings has been primarily restricted to ENU mutagenesis screens [2–4] and retroviral mutagenesis , the availability of morpholinos , antisense knockdown oligonucleotides, and insertional mutagenic transposons  have opened new avenues for functional genetic research.
Recently, several morpholino screens have been published in collaboration with the Ekker laboratory [8, 9]. The largest among them, the Secretome Screen [9, 10], identified likely secreted genes from available transcriptome databases using a bioinformatics approach. The Vertebrate Secretome DataBase (VSDB)  was established to identify co-translationally translocated (CTT) proteins in several model organism species . Using a combination of signal sequence, transmembrane domain, and initiation site predictors as well as homology to known secreted proteins, a subset of zebrafish CTT genes were identified (0.3× genome coverage based on zebrafish loaded and predicted protein sequences in the CTTome database and Genescan gene prediction estimates of the zebrafish genome [4, 5]). 150 gene targets were selected at random for morpholino design, carried out using an Assisted MOrpholino Design tool (AMOD) [11, 12]. Each gene was knocked down in zebrafish via morpholino-injection then screened for defects in general morphology and several organ systems including ocular, renal, pigment, vascular, hematopoietic, cranio-facial, and motor . A second morpholino knockdown screen, the Hematopoietic Stem Cell Screen, was conducted using zebrafish homologues of human genes differentially expressed in hematopoietic stem cell differentiation by microarray analysis .
Currently, the zebrafish community stores published and sequence-related results on several web-based databases. The principal database for zebrafish-related research is the Zebrafish Information Network (ZFIN) [13, 14]. Ensembl , likewise, stores sequences targeted by published morpholinos. Ensembl is limited in its ability to store and display experimental data, and while ZFIN contains a wealth of information on published results it lacks specific information such as dosage and searchable phenotype data for published morpholinos and phenotypic data for largely unpublished morpholinos.
Many model organism communities have developed online databases to access results from mutagenic, knock-down/out and over-expression studies. While mouse knockout mutant [15, 16] and C. elegans RNAi [17, 18] experimental result databases with phenotypic content exist, the only morpholino-specific database available is for a pilot Xenopus morpholino screen in which 202 genes were targeted and subsequent phenotypes displayed on a webpage [19, 20]. The Xenopus tropicalis Morpholino Screen database is a flat format website that allows for records to be accessed and viewed by gene targeted, synphenotype group or specific defect. Notably this database does not include search functions and does not offer a means for further input by outside sources. However, the intent of this database as stated by the authors is to display the results from their specific screen [19, 20].
Given the intent of our database to display the large amount of data generated from our on-going collaborative screens, we have developed of a scalable, centralized yet easily accessible worldwide, MOrpholino DataBase (MODB)  to store and facilitate retrieval of zebrafish morpholino screening results. Additional access has been provided by active links between MODB and ZFIN.
MODB is a scalable, searchable and readily adaptable online MySQL database with a PHP interface. MODB includes storage and retrieval of results generated by our screens and public access of published and unpublished information on morpholinos MODB not only allows dissemination of target-specific information such as effect of knockdown, but also facilitates analysis of morpholino-specific data such as toxicity, dosage, mortality and design. MODB is a new, online, publicly accessible database for data-mining zebrafish morpholino knockdown effects and morpholino non-specific effects.
Construction and Content
NCBI BLAST 2.2.13  is invoked by PHP through system calls in the sequence search functions. The MODB BLAST target database is updated automatically when a new morpholino sequence is entered into the database. The ZFIN anatomy ontology  was downloaded (release date 08/16/2007) from the ZFIN web site in the OBO format  and transferred into the database. An anatomy browser was written in PHP and incorporated in MODB.
Early in 2007, MODB contained over 700 unique morpholino sequences generated from several screens, individual projects and control morpholinos. The first generation Secretome Screen  is the largest overall contributor of morpholino sequences. From 150 candidate genes sequences, 209 morpholinos were designed. Each morpholino was subjected to a variety of morphological and molecular assays to determine the effect of down-regulating a particular gene product during the first 5-days of zebrafish development . This Secretome Screen identified 26/150 gene targets that produced reproducible effects on specific aspects of early development in early morphology and a variety of organ systems including visual, renal, cardiovascular, cranio-facial, hematopoiesis, and pigment. The more focused Hematopoietic Stem Cells Screen identified 16/64 targets as being necessary for proper blood development . The bulk of the data entered into MODB (124/150 target gene morpholinos in the Secretome Screen and 48/64 in the Hematopoietic Stem Cell Screen) consists of morpholinos that had no observed developmentally specific effect in our screening tests, caused toxic effects such as a high amount of cell death and/or mortality, or produced pleiotropic effects we could not decipher. This information is of use to the scientific community for optimizing morpholino design and learning dosage data and overall effect of previously designed and tested morpholinos.
Since MODB is a living database, new data is regularly being submitted. In the coming year another 50 to 150 morpholinos will be added to the database for the continuing Hematopoietic Stem Cell and secretome screens. To allow the release of data in defined formats and quality, MODB has three data sharing quality control levels. Users are capable of accessing and modifying data related to their designated morpholinos. To facilitate collaborative efforts, a shared designation has been developed to allow members of consortium laboratories to access data related to morpholinos designed by any user within the laboratories that are connected by a relationship within MODB. The third designation ('public') allows morpholino data to be used to generate the summary reports available to the open scientific community via the MODB website. Nearly all morpholinos (779/784) in MODB, with the exception of non-zebrafish morpholinos, are designated as public in MODBv1.
A major function of MODB is data compilation of morpholino-specific information generated by primary research. There are two main ways to add data. Currently, administrators alone enter new listings that provide basic information on a morpholino. Authorized users can submit morpholino sequence and results from specific morphological or molecular experiments for a given observation point and dose. Researchers can apply for an authorized-user identification and password (see author contact information).
MODB v1 Public Interface
With advent of whole-genome sequencing technology, a greater emphasis on gene function is emerging. Functional genomic screening tools available in zebrafish such as ENU mutagenesis, GripNAs, RNAi, insertional mutagenesis and morpholinos allow for large functional gene screens that produce an enormous amount of biological information (reviewed in [2, 6, 7, 31–33]). Efficient data storage is critical to allow for retrieval of results in a meaningful fashion and to facilitate data mining. MODB is a non-proprietary, relational database with online accessibility that acts as a storehouse for critical information relating to sequence-specific morpholino knockdown screens. MODB is, to our knowledge, unique among the available databases in that it offers searchable morpholino-specific data and fixed-vocabulary defects ontological cataloging of morphants that allows for cross-species analysis using a common, PATO-derived ontology. Cross-linking to ZFIN provides additional value of MODB for the research community.
Continued screening efforts in zebrafish using morpholinos and other sequence-specific knockdown or knockout technologies will expand our knowledge of gene function. MODB provides a central repository for morpholino information. This schema is potentially applicable to any sequence-based screening approach in zebrafish or related systems. For example, MODB is currently being adapted to the creation of a transposon database that includes insertional mutagenesis and expression analysis data.
By offering public access to our schema and the data contained within MODB, we hope to aid in the advancement of functional genetic studies and gene annotation as well as improvements in morpholino analysis and design. The dissemination of valuable knowledge gained via large screens such as the Secretome  and Hematopoietic Stem Cell  screens goes beyond published gene target characterization and provides a foundation for future research.
Availability and requirements
MODB is accessible via the web http://www.secretomes.umn.edu/MODB/. To be added as an authorized user, contact the corresponding author M.K. or S.C.E. Morpholinos are readily available for purchase through Gene Tools  or Open Biosystems . The authors have no affiliation, financial or otherwise, with either corporate entity.
The authors would like to acknowledge the numerous collaborations that have contributed to the development of MODB such as the laboratories of Drs. Farber, Hammerschmidt, Pickart, Schimmenti, Sivasubbu, and Verfaillie. We would also like to acknowledge the bioinformaticians who have worked on this project including Dr. Eric Klee and Kyong Jin Shim. Funding for this project was obtained from the NIH to SCE (GM63904 and CA65493). This work was supported in part by the University of Minnesota Supercomputing Institute.
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