Functional annotation of 19,841 Populus nigra full-length enriched cDNA clones
- Tokihiko Nanjo†1Email author,
- Tetsuya Sakurai†2,
- Yasushi Totoki3,
- Atsushi Toyoda3,
- Mitsuru Nishiguchi1,
- Tomoyuki Kado4,
- Tomohiro Igasaki1,
- Norihiro Futamura1,
- Motoaki Seki2,
- Yoshiyuki Sakaki3,
- Kazuo Shinozaki2 and
- Kenji Shinohara1
© Nanjo et al; licensee BioMed Central Ltd. 2007
Received: 19 July 2007
Accepted: 03 December 2007
Published: 03 December 2007
Populus is one of favorable model plants because of its small genome. Structural genomics of Populus has reached a breakpoint as nucleotides of the entire genome have been determined. Reaching the post genome era, functional genomics of Populus is getting more important for well-comprehended plant science. Development of bioresorce serving functional genomics is making rapid progress. Huge efforts have achieved deposits of expressed sequence tags (ESTs) in various plant species consequently accelerating functional analysis of genes. ESTs from full-length cDNA clones are especially powerful for accurate molecular annotation. We promoted collection and annotation of the ESTs from Populus full-length enriched cDNA clones as part of functional genomics of tree species.
We have been collecting the full-length enriched cDNA of the female poplar (Populus nigra var. italica) for years. By sequencing P. nigra full-length (PnFL) cDNA libraries, we generated about 116,000 5'-end or 3'-end ESTs corresponding to 19,841 nonredundant PnFL clones. Population of PnFL cDNA clones represents 44% of the predicted genes in the Populus genome.
Our resource of P. nigra full-length enriched clones is expected to provide valuable tools to gain further insight into genome annotation and functional genomics in Populus.
The use of forest trees as a sustainable environmental resource has underscored the importance of genomics in aiding the genetic modification of trees for preferable performance and the development of DNA markers for selective breeding. In this context, the development of the genomic resources of Populus has gained increasing importance because these species have a small genome (~480 Mbp) when compared to other tree species. For example, international groups of researchers have determined the nucleotide sequence of the entire genome of the black cottonwood (Populus trichocarpa) [1, 2]. But because the sexual reproduction span of Populus is long, it has proven to be an unsuitable model for forward genetics like mutant-based studies. Reverse genetic approaches based on the functional genomics are therefore essential. As one of important tools, Populus ESTs have been collected [3–13]. The publicly available EST collections of Populus including poplar, aspen, cottonwood and their hybrids have already grown to 385,000 .
Full-length cDNA resources are very useful, not only for gene annotation and the determination of transcriptional start sites, but also for functional analyses , especially when analyzed within the context of genomic sequences. Various methods have been developed that allow preferential cloning of cDNA that corresponds to full-length mRNAs that have 5'-proximal cap structures . These methods have been applied to large-scale analyses of transcripts from human , mouse [17, 18], fruit fly , rice , Arabidopsis , and moss . Although population of Populus EST has grown steadily, the ESTs may appear not to be from full-length cDNAs to a large extent. Recently, Populus ETS has been tried to obtain from a full-length enriched cDNA library constructed by the method of the oligo-capping  or the biotinylated CAP trapper [2, 13]. In the study we report herein, we constructed a full-length enriched cDNA library from poplar (Populus nigra var. italica) by using the biotinylated CAP-trapper method.
Functional annotation of ESTs that uses integrated prediction tools and proper curation of the results is not only necessary to complete the annotation process but to find actual biological processes. We annotated our P. nigra ESTs primarily by using the BLAST program to search the databases of The Institute for Genomic Research (TIGR)  and The Universal Protein Resource (UniProt) . Although 90% of our PnFL clones were identified through these databases, the rest remained functionally unknown. To identify the remaining PnFL clones, we substituted the coding sequences (CDS) of P. trichocarpa for PnFL ESTs. 65% of the substituted CDS was able to be described using the BLAST against the public protein databases. We treated 35% rest with another computational work of a protein domain analysis. Resultant domains found in these sequences may provide a critical clue to understand molecules specific in trees and/or P. nigra, a series of such substitutive procedures is somewhat artificial though. Furthermore genome-wide analysis of poplar was done using comparative genomics with herbaceous model plants Arabidopsis and rice in the present study. We anticipate that the information we gathered in this comparative analysis will make possible global comparisons among plant species by using functional genomics.
Results and Discussion
Quality of the cDNA Library
We constructed a full-length enriched cDNA library (PnFL2) from P. nigra buds, roots, twigs, and stress-treated leaves by using the biotinylated CAP-trapper method, together with trehalose-thermoactivated reverse transcriptase . This library was named PnFL2 after P. n igra f ull-l ength cDNA library version 2. The quality of the cDNA library was evaluated before large-scale sequencing by examining 96 randomly selected but representative clones. The mean size of the insert DNA was estimated to be about 1.4 kb (range, 0.8 kb to 3.5 kb) by measuring the length of the Pvu II fragments of 86 independent clones from among the 96 sample clones.
By comparing the transcripts longer than 3.0 kbp with the ESTs contained in the PnFL2 library, we found 631 corresponding substituted CDS. This computational estimation was partially reconfirmed by subjecting 96 of the extracted 3.0-kbp or greater sized clones to electrophoresis (data not shown). We found that the PnFL population would provide useful resources for Populus researchers with well intact molecules.
To analyze the cDNA population, on the other hand, 96 selected clones were sequenced from their 5'-ends and blastn-searched in the GenBank nucleotide database, resulting that 92.7% of clones contained an insert. Clones whose query start position was greater than the hit start position in the aligned region were defined as being full-length. The ratio of full-length clones was calculated as A/(A+B), wherein A is the number of full-length clones and B the number of those that are shorter. This calculation yielded a ratio of 0.75. Overall, the duplication rate of the genes in the PnFL2 library was substantially lower than that of the PnFL1 library , most likely because of the normalization process used in the construction of the PnFL2 library.
One-pass sequencing of PnFL2 clones and integrated clustering of PnFL ESTs
We randomly selected 39,936 clones (PnFL2-001_A01 through PnFL2-104_P24) from the PnFL2 cDNA library and sequenced them from the 5'-end and the 3' end by using a high-throughput DNA sequencing process. We identified 39,183 clones that had 5'-end-based and/or 3'-end-based ESTs (phred quality value of ≥ 20). The nucleotide sequences of the PnFL2 ESTs have been submitted to the DDBJ/EMBL/GenBank [DB874873 through DB910976] and are provided in Additional file 1. These ESTs were first clustered by using the phrap program, and the phrap-assembled sequences were then subjected to a round-robin blastn search within their own population. Through these clustering processes, we obtained 15,581 tentative contigs and 17,412 singletons that did not have a partner with pairwise homology either within the total pool of sequences or within a given cluster, representing 18,578 nonredundant PnFL2 clones. We also found that the consensus sequences of 2,387 tentative contigs and of 3,421 singletons each covered a whole transcript. For better annotation of Populus genes and comparative studies among plant species, complete reading of full-length clones should be important. Although our present work did not focus only on completely read cDNAs, we obtained those of 5,808. Other group also collected 4,664 Populus cDNAs whose sequences were completely read . Altogether, this information should be valuable in the functional annotation of the Populus genome.
When the 4,522 PnFL1 ESTs  were filtered out, 4,316 PnFL2 ESTs remained. These remaining ESTs were integrated and assembled into clusters as described in the Methods section. For each cluster, we considered the clone that had the longest 5' read among other cluster members to be a cluster representative. This procedure allowed us to eliminate diverse variations in the length of the 5'-untranslated region within each cluster. The resulting population of nonredundant PnFL clones was comprised of cluster representatives and singletons. In total, 19,841 nonredundant PnFL clones were obtained; 17,153 were PnFL2-specific, 1,263 were PnFL1-specific, and 1,425 were common to both the PnFL2 and PnFL1 libraries (PnFL2/PnFL1-common). This population of nonredundant clones corresponds to 44% of the entire Populus CDS .
Functional annotation and classification of PnFL ESTs
Domain detection by InterProScan for characterizing of no-hit clones a
Clone name b
Ribosomal protein L41
Pistil-specific extensin-like protein
Heavy metal transport/detoxification protein
Ricin B lectin
Ricin B-related lectin
IQ calmodulin-binding region
Wilm's tumour protein
Ricin B lectin
Ricin B-related lectin
IQ calmodulin-binding region
Pistil-specific extensin-like protein
Protein of unknown function DUF1070
Zinc finger, CCHC-type
Peptidylprolyl isomerase, FKBP-type
IQ calmodulin-binding region
Complex 1 LYR protein
Pistil-specific extensin-like protein
Comparative genomic analysis of PnFL ESTs
Putative physical mapping of PnFL ESTs
Full-length cDNAs are essential for the correct annotation of genomic sequences and for the functional analysis of genes and their products. Collections of full-length cDNAs are available in some plant species such as Arabidopsis, rice, moss and poplar . In poplar, our collection of PnFL cDNAs was updated with 19,841 nonredundant clones. This population represented 44% of the predicted genes in the Populus genome. To improve the curation and distribution of this bioresource, all the PnFL cDNA clones and their applicable information will be released through RIKEN .
Plant materials and stress treatments
Leaf buds, flower buds, and portions of wooden twigs were sampled from a mature stand of female poplar (P. nigra var. italica). The samples were briefly washed with distilled water and then stored at -80°C until the RNA preparation procedure.
Explanted shoots of female poplar were axenically grown in Biopots (Watanabe TAI Co., Ltd, Osaka, Japan) that were 90 mm in diameter × 130 mm in height. The explants were covered with 100 mL of medium (pH 5.7) that contained 1× McCown's woody plant basal salt mixture (Sigma-Aldrich Corp., St. Louis, MO), 2% (w/v) sucrose, and 2% (w/v) activated charcoal that was solidified with 0.3% (w/v) gellan gum (Gelrite, Wako Pure Chemicals, Osaka, Japan). The temperature of the cleanroom was maintained at 25 ± 1°C, and cool-white fluorescent bulbs supplied 40–60 μmol m-2 s-1 of light alternated with 8 h of darkness.
After the plants had grown in the Biopots for ~2 months, the roots were sampled and washed with distilled water. Leaflets were then cut off at a petiole and subjected to a series of stress treatments that included dehydration, chilling, heating and exposure to NaCl, abscisic acid, salicylic acid, jasmonate, and H2O2 for varying periods (1, 2, 5, 10, and 24 h; except, 6 h for the salicylic acid and jasmonate exposure). For the dehydration treatment, the leaves were desiccated in 90 mm × 20 mm Petri dishes under dim light at 25°C and in an atmosphere of 50% to 60% humidity. For the chilling and heating treatments, the leaves were placed in Petri dishes with a wet paper towel and then exposed respectively to temperatures of 4°C and 34°C in the dark. For all other treatments, the leaves were soaked in 50-mL aqueous solutions of 400 mm NaCl, 100 μm abscisic acid, 100 μm salicylic acid, 100 μm jasmonate, and 200 mm H2O2, under dim light at 25°C. For the wounding treatment, leaflets were wounded by boring with a prick. All the samples were then frozen in liquid nitrogen for RNA extraction.
RNA isolation and construction of full-length enriched cDNA library
Total RNA was extracted in a solution of phenol-guanidine isothiocyanate (TRIzol® Reagent, Invitrogen™ Life Technologies, Carlsbad, CA). A total RNA mixture derived from all the samples described above was further purified using a MACS mRNA Isolation Kit (Miltenyi Biotec, Gladbach, Germany), and resultant poly(A)+ RNA served the following construction of a cDNA library. A full length-enriched cDNA library (PnFL2 library) was constructed with a normalization step according to the method of biotinylated CAP trapper using trehalose-thermoactivated reverse transcriptase .
EST sequencing and clustering
The appropriate aliquots of library solution in storage tubes were spread on Luria-Bertani (LB) agar plates containing 100 μg/mL of ampicillin and incubated at 37°C overnight.
The colonies that grew were randomly picked and inoculated into 384-well microtiter plates, the wells of which were filled with 40 μL of LB medium that contained 100 μg/mL of ampicillin. Sequencing templates were prepared from these arrayed clones by using the TempliPhi DNA Sequencing Template Amplification Kit (Amersham Biosciences, Uppsala, Sweden). The sequencing reactions were performed according to the protocol of the BigDye Terminator v3.1 Cycle Sequencing Kit (Applied Biosystems, Foster City, CA). The sequence primer used for 5' sequencing was 5'-TGT AAA ACG ACG GCC AGT-3' ; and the primers used for 3' sequencing were 5'-AGC GGA TAA CAA TTT CAC ACA GGA-3' for 16 plates that correspond to PnFL2 clones 1–16 and 5'-AAT ACG ACT CAC TAT AGG G-3' for 88 plates that correspond to clones PnFL2 17–104. The products of the sequencing reaction were purified by precipitation with ethyl alcohol and then loaded onto an Applied Biosystems ABI3700 DNA sequencer.
Raw sequence data were processed and base-called by using phred (CodonCode Corp., Dedham, MA), a base-calling program. The PnFL2 EST sequences were uploaded into a filtering program to remove vector, adaptor, and low-quality bases. These processed PnFL2 sequences were assembled with the phrap program (Laboratory of Phil Green, Genome Sciences Department, University of Washington)  under default conditions, except for the following criteria: -minmatch 400, -minscore 400, -repeat stringency .999, -trim quality 20. phrap-treated sequences, including tentative contigs and singletons, were sequentially processed as follows: a base with a quality value < 20 was temporarily converted into an "n"; sequences were sequentially deleted from both ends until there were at least 30 successive non-"n") bases (A, T, G or C); clones with sequences < 200 bp in length were discarded; an "n" conversion was undone and converted into the original base (A, T, G or C); and poly A/T sequences were deleted. These representative sequences were then subjected to a round-robin blastn search within their own population. In this process, sequences sharing not less than 99% identity over 200 or more contiguous bases were grouped into clusters. All the clusters were rearranged by taking the clone ID into account, that is, sequences that shared an identical clone ID were placed into the same cluster. Clones that had only one usable sequence out of the 5' and the 3' reads but had any hit were also placed into clusters.
Meanwhile, the base-called 5' and/or 3' sequences of the 4,522 nonredundant PnFL1 clones  were also processed as described above. The 2,489 sequences that resulted from the processing of the PnFL1 ESTs were integrated into the PnFL2 clusters by performing a blastn search under the same conditions as the round-robin blastn search for the PnFL2 clustering. The PnFL1 clones that were not integrated into the PnFL2 clusters were clustered within the remaining PnFL1 population by performing a blastn search under the conditions described above. Other removed sequences were determined on the basis of a blastn homology search against the integrated ESTs (E < 1.0e-50) with ribosomal RNA and organelle DNA query sequences (DDBJ/EMBL/GenBank accession: AF174629, AF206999, AF479118, AJ006440, AP000423, X52322, Y08501, Y08502, AF162215, AF168884, AF274652).
Tentative genome assignment of PnFL clones
The 5' and 3' sequences of 19,841 nonredundant PnFL clones were aligned with the P. trichocarpa genome sequence by using the blastn program. The maximum and minimum hit positions that came from queries of each PnFL clone were considered to show, respectively, the southernmost and the northernmost point of each locus on a P. trichocarpa chromosome. The northernmost (minimum) point was assigned to the chromosome as a corresponding locus. The information derived from the 5' ESTs was adopted only in the following cases: 1) the hit chromosome numbers differed between the 5' and 3' ESTs of each PnFL clone; and 2) the difference between the maximum and minimum hit positions was over 50,000. The lengths of the intergenic regions were then calculated by using the positional information of these tentative assignments. Variance in the lengths of the intergenic regions can be used as an indicator of gene distribution within the Populus genome. Consequently, we used a ratio of actual variance data to data that assumed the uniform distribution of genes on chromosome: I = Var Data /Var Uni , wherein I is the distribution index. To obtain an estimate of Var Uni , we repeated the simulation 10,000 times and calculated an average. The intergenic regions that were < 1000 bp in length were discarded before the distribution was calculated.
List of abbreviations
P. nigra full-length
expressed sequence tag
orthologous groups of proteins
The Institute for Genome Research
The Universal Protein Resource
We thank Dr. G. Tuskan at the Oak Ridge National Laboratory and the United States Department of Energy Joint Genome Institute for providing information on the P. trichocarpa genome, and Dr. H. Saito at Hokkaido University for kindly distributing P. nigra samples. We also appreciate the helpful suggestions of Dr. B. Ellis at the University of British Columbia and Dr. S. Jansson at Umeå Plant Science Centre. This work was supported by Research Grant #200607 of the Forestry and Forest Products Research Institute and in part by a Grant-in-Aid from the New Energy and Industrial Technology Development Organization.
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