Nucleic Acids Research Advance Access originally published online on October 24, 2006
Nucleic Acids Research 2007 35(Database issue):D874-D878; doi:10.1093/nar/gkl753
Nucleic Acids Research, 2007, Vol. 35, Database issue D874-D878
© 2006 The Author(s)
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
GABI-Kat SimpleSearch: an Arabidopsis thaliana T-DNA mutant database with detailed information for confirmed insertions
Yong Li1,2,
Mario G. Rosso1,2,
Prisca Viehoever1 and
Bernd Weisshaar1,*
1 Institute of Genome Research, Center for Biotechnology (CeBiTec), Bielefeld University, Universitaetsstrasse 25 D-33594 Bielefeld, Germany
2 Max Planck Institute for Plant Breeding Research, Carl-von-Linne-Weg 10 D-50829 Koeln, Germany
*To whom correspondence should be addressed. Tel: +49 521 106 6873; Fax: +49 521 106 6423; Email: bernd.weisshaar{at}uni-bielefeld.de
Received August 15, 2006. Accepted September 25, 2006.
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ABSTRACT
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Insertional mutagenesis approaches, especially by T-DNA, play
important roles in gene function studies of the model plant
Arabidopsis thaliana. GABI-Kat SimpleSearch (
http://www.GABI-Kat.de)
is a Flanking Sequence Tag (FST)-based database for T-DNA insertion
mutants generated by the GABI-Kat project. Currently, the database
contains >108 000 mapped FSTs from
64 000 lines which cover
64% of all annotated
A.thaliana protein-coding genes. The web
interface allows searching for relevant insertions by gene code,
keyword, line identifier, GenBank accession number of the FST,
and also by BLAST. A graphic display of the genome region around
the gene or the FST assists users to select insertion lines
of their interests. About 3500 insertions were confirmed in
the offspring of the plant from which the original FST was generated,
and the seeds of these lines are available from the Nottingham
Arabidopsis Stock Centre. The database now also contains additional
information such as segregation data, gene-specific primers
and confirmation sequences. This information not only helps
users to evaluate the usefulness of the mutant lines, but also
covers a big part of the molecular characterization of the insertion
alleles.
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INTRODUCTION
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Insertional mutagenesis approaches by using transposable elements
or Agrobacterium T-DNA, play important roles in plant functional
genomics (
1–
4). The use of T-DNA as an insertional mutagen
has several advantages (
3,
4). T-DNA integration results in stable
mutations in the genome, as opposed to transposons which often
excise after integration. Also, the low number of insertions
per transformant significantly reduces the additional work required
to remove unwanted mutations. The development of a simple
in planta Agrobacterium transformation method for
Arabidopsis thaliana allowed the high-throughput production of T-DNA insertion mutants
in this model plant (
5,
6). A number of large T-DNA mutagenized
A.thaliana populations have been generated that are intensively
used for gene function search studies and other reverse genetics
experiments (
7–
11). Initially, these populations were
screened for the desired insertion mutants in the gene of interest
by PCR. The PCR was performed with a gene-specific primer and
a T-DNA-specific primer on DNA templates from large pools of
mutant plants. The identification of a specific PCR product
indicated the existence of a T-DNA insertion in the gene of
interest, and the respective mutant was then identified by pool
deconvolution. An alternative strategy, which gained popularity
in recent years, was to amplify the DNA fragments flanking the
T-DNA insertion sites of individual plants with special PCR-based
methods, and to sequence-characterize the various insertion
alleles. When the whole genome sequence of the species is available,
the resulting Flanking Sequence Tags (FSTs) can be mapped to
the pseudo-chromosomes and indexed in databases. As a result,
the screening for a mutant insertion allele of a given gene
is simplified to a search for the corresponding FST in the database.
Obviously, the number of insertion mutants and FSTs in the database
should be large enough to allow most of the genes being covered
(
3).
The aim of the GABI-Kat project was to build a large T-DNA mutagenized A.thaliana population with sequence-indexed insertion sites (11). In June 2002, GABI-Kat SimpleSearch, the web interface of the database containing data about the GABI-Kat population, was opened (12). Since then, GABI-Kat lines have been ordered by many scientists from all around the world, and thousands of confirmed insertion mutants have been delivered to the scientific community. This shows that the GABI-Kat population became one of the major reverse genetics resources for A.thaliana functional genomics.
During the last few years and since we described the basic FST analysis pipeline (12), we have constantly improved the database as well as the interface, and incorporated several major updates. This took place in addition to the regular increase in the amount of FST data held in the database. Here, we summarize and describe the improvements, updates and new features of the SimpleSearch tool, including the recent addition of detailed information on insertion sites from allele-specific sequence data and genetic segregation data from 3509 (number as of June 2006) lines with confirmed insertions.
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DATABASE CONTENT
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FSTs and annotation
The FST production pipeline and the annotation procedure were
described in detail elsewhere (
12,
13). In brief, the genome
sequences flanking the T-DNA insertion site (FSTs) were obtained
by an adaptor-ligation PCR method which was adapted to high-throughput
conditions (
13). Each FST was mapped to the
A.thaliana genome
by BLAST (
14), and annotated with the information of the corresponding
BAC clone, and with the AGI gene code when the insertion qualifies
as a ‘gene hit’ (
12). We define ‘gene hit’
as the insertion site being located between 300 bp upstream
of the ATG and 300 bp downstream of stop codon of a gene, and
‘CDSi hit’ as the insertion site being located between
ATG and stop codon (CDS plus introns).
A.thaliana genome sequence
and annotation data from the TIGR version 5 dataset were used
as the basis for mapping and annotation (
15).
Table 1 gives
a summary of the data in the SimpleSearch database as of the
current release (GK release 21 of June 25, 2006). There are
>108 700 FSTs, and they were from >63 800 lines. Based
on the TIGR v5 annotation, >16 900 genes (64% of all annotated
A.thaliana protein-coding genes excluding pseudogenes) were
covered by at least one ‘gene hit’ and >12 200
genes (46%) were covered by at least one ‘CDSi hit’.
Data concerning confirmed insertions
One problem associated with the T-DNA mutagenized population
is that not all the insertions deduced from FSTs that were obtained
from T1 plants can be confirmed in the next (T2) generation.
The T1 generation refers to plants that were selected for resistance
conferred by the inserted T-DNA. Both SAIL (Syngenta population)
and GABI-Kat reported a confirmation rate of
76% (
9,
11). At
present, the confirmation rate at GABI-Kat is 78%. This number
is derived from
6000 lines for which confirmation was attempted
during the process of in-house confirmation to make sure that
only confirmed insertion lines were delivered to users. The
confirmation process consists of segregation analysis, genomic
DNA extraction from T2 plantlets, PCR using a T-DNA primer and
a gene-specific primer designed to fit the insertion site predicted
on the basis of the original FST annotation, and sequencing
of this allele-specific PCR product if the PCR was successful
(
11). For segregation analysis, we record the number of seeds
plated, the number of seeds germinated and the number of resistant
seedlings. This information is very useful as it gives an approximate
number of T-DNA loci of the specified line after statistical
evaluation according to Mendel's laws. In addition, distorted
segregation patterns often indicate that the line contains a
mutation in a gene important in pollen or female gametophyte
development (
16,
17). We have stored this information for lines
for which confirmation has been attempted in the database, and
in total there are 6000 lines for which segregation data are
available (
Table 1). The database also contains information
on
20% failed confirmation attempts (search for the FST with
GenBank accession No. ‘CR405437
[GenBank]
’ to see an example).
The products resulting from a successful allele-specific PCR
were sequenced from both directions, so usually two confirmation
sequences were obtained for a confirmed insertion. Currently,
there are 8840 confirmation sequences in the database, and they
were stored together with the primer information so that the
allele-specific PCR can be reproduced. Since July 2005, T3 seeds
(seeds produced by T2 plants) of confirmed GABI-Kat lines are
transferred to the Nottingham Arabidopsis Stock Centre (NASC).
This allows direct user access to potential homozygous mutant
materials, and the SimpleSearch database provides the molecular
and genetic background information for these lines.
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WEB INTERFACE
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In addition to the search for insertion alleles by the AGI gene
(or locus) code or keyword and the sequence-based search by
BLAST, we recently introduced the feature of searching by line
ID or GenBank accession number. This gives a more thorough access
to the data in database. Searching by line ID or GenBank accession
number will directly lead to the FST data display page (
Figure 1).
On top of the FST page is information for the line from which
the FST was generated. These include the vector used to transform
the line, with a link to the GenBank entry of the vector at
NCBI, information about line availability and when available
segregation data. The ‘line availability’ field
tells if a given line is dead (e.g. because no viable seeds
were produced by the T1 plant), or if it is available from GABI-Kat
or NASC. When a line is available from NASC, the NASC code is
given and linked to the NASC seeds stock detail page of the
line, so that the user can order it easily. The segregation
data are presented as three numbers: total number of seeds evaluated,
number of seeds germinated and number of resistant seedlings.
Since more than one FSTs were produced for many T1 plants in
the population, the line information page includes data for
one or more FST-derived (predicted) insertion sites or loci.
For each displayed insertion, the FASTA format sequence of the
original FST, the respective GenBank accession number (which
is linked to the GenBank entry at NCBI), a link to the graphic
locus view (
Figure 2), the information about the location of
the T-DNA border/plant DNA junction if detected, the BAC clone
code and the confirmation status are shown. If the insertion
site qualifies as a gene hit, links to the respective TIGR,
TAIR (
18), MIPS MAtDB (
19) and SIGnAL (
10) gene pages are provided.
For confirmed lines available in NASC, a link is provided to
a page showing all the allele-specific confirmation sequences
derived from the respective insertion site. Unlike the original
FST sequences, which are of varied quality, the confirmation
sequences are generally of high quality and length. The sequences
representing the T-DNA were not trimmed from the confirmation
sequences. Therefore, the user has access to the exact T-DNA
border/plant genome junction structures of the insertion sites.
View larger version (56K):
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Figure 1 Screenshot of the FST page that results from a search for GenBank accession number AL936383. The data are from line 048E04. The meaning of the three numbers describing the result of the genetic segregation data is found by following the link on the numbers. The upper part shows the line-specific information followed by the FST DNA sequence data in the lower part of the page. For the chosen line, data on additional insertions other than the one displayed are available. Therefore, a link to information about all the insertions from the line is given at the bottom.
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View larger version (17K):
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[in a new window]
[Download PowerPoint slide]
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Figure 2 Screenshot of the graphical view page of gene At4g23270. All annotated genes and FSTs in the genome region centered on the locus At4g23270 are presented in an image map. Mouse-over text on the FSTs and the genes tells the line ID and the gene annotation text, respectively. Clicking on the FST icon leads to the respective FST page.
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For all the different kind of searches, results are organized
around the FST page. When coming to the FST page from searching
GenBank accession number or from the BLAST search result page,
only the corresponding FST is displayed. If there are more than
one insertion from the same line, a link to showing all the
insertions of the line is given. When coming to the FST page
from searching line ID, all the insertions of the line are shown
and for each insertion the best FST is displayed.
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AVAILABILITY
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The GABI-Kat SimpleSearch database is freely available at
http://www.GABI-Kat.de and can be queried through the web interface described above.
The FST data were submitted to EMBL/GenBank/DDBJ as genomic
survey sequence, and can also be downloaded in a flat file format
from our web site. Finally, users can find our FST data at external
A.thaliana web sites such as MIPS MAtDB (
19), FLAGdb++(
20) and
SIGnAL (
10). However, it is worth noting that minor differences
do exist in the FST annotation on these sites when compared
with SimpleSearch as they do not necessarily use an identical
annotation procedure. Also, the external databases that rely
on the FST data in GenBank may indicate the existence of an
insertion in a given gene, but the respective line is dead which
in turn means that the insertion allele described by the FST
does not exist any more.
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DISCUSSION
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FST-based insertion mutant databases exist for various species
for which insertional mutagenesis could be carried out in large
scale. For
A.thaliana, most of the insertion mutant databases
were initially developed for holding the data generated in their
own projects. While they are quite similar in the FST annotation
and query interface, each database has its own unique features.
Like GABI-Kat SimpleSearch, FLAGdb initially was a project database
of mapped FSTs from the Versailles T-DNA population (
8). Currently,
the FST data of FLAGdb has been integrated into FLAGdb++ (
http://urgv.evry.inra.fr/projects/FLAGdb++/HTML/index.shtml),
a database with JAVA front-end integrating different high-throughput
functional genomics data for
A.thaliana (
20). ATIDB (Arabidopsis
thaliana insertion database;
http://atidb.org) is a federated
database for archiving FSTs of transposon or T-DNA insertions
for
A.thaliana from different sources including SIGnAL, SAIL,
GABI-Kat, FLAGdb and the John Innes Centre (
21). Besides the
various search options, ATIDB provides analysis tools to study
the insertion distribution at a genome scale. The T-DNA Express
at SIGnAL (
http://signal.salk.edu/cgi-bin/tdnaexpress) is currently
the most comprehensive database of mapped FSTs for
A.thaliana (
10). It integrates not only FSTs from sources collected by
ATIDB mentioned above, but also include FST data from the Wisconsin
T-DNA population (
7) and the RIKEN transposon population (
22).
So far, >360 000 insertion sites have been stored in T-DNA
Express, and cover
90% of all
A.thaliana genes. The search interface
at T-DNA Express provide different ways to access the insertion
data. A useful tool at this site is ‘iSect toolbox’.
Among the many functions this tool offers, a very important
one is to design genomic primers to confirm the T-DNA insertions.
Although the GABI-Kat SimpleSearch database concentrates on
data generated from GABI-Kat, it allows searches and result
presentations comparable to these large and complex databases.
What distinguishes SimpleSearch from other databases is that it includes detailed information on single GABI-Kat lines like segregation data, line availability information, insertion site-specific primers and confirmation sequences for >3500 confirmed insertion sites. These data show the exact T-DNA border/plant genome junction structures. This detailed information not only helps users to evaluate the usefulness of the mutant lines, but also covers a big part of the molecular characterization of the insertions. The transfer of confirmed lines to NASC is an ongoing process at GABI-Kat. In addition to confirming lines that are requested by users, we have started to confirm a number of key GABI-Kat lines. These key lines were identified by analysing the results from the SIGnAL, SAIL, Wisconsin and GABI-Kat FST datasets for unique T-DNA insertion sites in the A.thaliana accession Columbia at the level of insertion alleles predicted to cause a knock-out of the respective gene. The seeds of these confirmed lines will also become available from NASC and this will contribute significantly to the goal of finding at least one mutant for every A.thaliana gene. Results from the genetic and molecular insertion confirmation pipeline will constantly be added to SimpleSearch.
A few further developments to further strengthen the SimpleSearch database were planned for the future. We are tracking published papers which made use of GABI-Kat mutant lines, and these references are currently listed on our web site on a HTML page. In most of these publications, it was clearly mentioned which GABI-Kat line was used. We plan to store the reference to these publications in the database and link them to the respective lines for display on the FST page. While GABI-Kat SimpleSearch will continue to function as a project database, we are also exploring the possibility for better interoperability with other A.thaliana database by ways such as a BioMOBY service (23).
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ACKNOWLEDGEMENTS
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We thank Nicolai Strizhov, Christa Höricke-Grandpierre
and Heike Hagemeyer for PCR, members of the GABI-Kat team for
greenhouse and seed handling work, members of the DNA core facility
at MPI for Plant Breeding Research and the Chair of Genome Research
at Bielefeld University for sequencing. This work was supported
by the German Federal Ministry of Education and Research (BMBF)
in the context of the German plant genomics program GABI (Förderkennzeichen
0312273). Funding to pay the Open Access publication charges
for this article was provided by BMBF/PTJ grant ‘GABI-Kat’
(0312273) to BW.
Conflict of interest statement. None declared.
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