- Open Access
An Ambystoma mexicanumEST sequencing project: analysis of 17,352 expressed sequence tags from embryonic and regenerating blastema cDNA libraries
© Habermann et al.; licensee BioMed Central Ltd. 2004
- Received: 17 November 2003
- Accepted: 29 June 2004
- Published: 13 August 2004
The ambystomatid salamander, Ambystoma mexicanum (axolotl), is an important model organism in evolutionary and regeneration research but relatively little sequence information has so far been available. This is a major limitation for molecular studies on caudate development, regeneration and evolution. To address this lack of sequence information we have generated an expressed sequence tag (EST) database for A. mexicanum.
Two cDNA libraries, one made from stage 18-22 embryos and the other from day-6 regenerating tail blastemas, generated 17,352 sequences. From the sequenced ESTs, 6,377 contigs were assembled that probably represent 25% of the expressed genes in this organism. Sequence comparison revealed significant homology to entries in the NCBI non-redundant database. Further examination of this gene set revealed the presence of genes involved in important cell and developmental processes, including cell proliferation, cell differentiation and cell-cell communication. On the basis of these data, we have performed phylogenetic analysis of key cell-cycle regulators. Interestingly, while cell-cycle proteins such as the cyclin B family display expected evolutionary relationships, the cyclin-dependent kinase inhibitor 1 gene family shows an unusual evolutionary behavior among the amphibians.
Our analysis reveals the importance of a comprehensive sequence set from a representative of the Caudata and illustrates that the EST sequence database is a rich source of molecular, developmental and regeneration studies. To aid in data mining, the ESTs have been organized into an easily searchable database that is freely available online.
- Gene Ontology
- Neural Tube
- Annotate Contigs
- Perform BLASTN Search
The Caudata (tailed amphibians such as salamanders) are a major focus of work in vertebrate evolution and speciation [1, 2]. The salamander is also an important vertebrate model organism for understanding regeneration, being one of the few vertebrates that is able to regenerate entire body structures such as the limb, tail and jaw as an adult. Despite the pivotal role of this animal order in research, comparatively little sequence information is available. In contrast, 458,413 nucleotide sequences exist for the Anura (frogs and toads). This high number is primarily attributable to large EST sequencing efforts for the model organisms for embryology - Xenopus laevis and Silurana tropicalis.
A salamander EST project is particularly important as these organisms have extremely large genomes, making a genome project unwieldy and unlikely without specialized approaches such as methylation filtration . Genome sizes range from 8.5 billion base pairs for Desmognathus monticola (seal salamander) to nearly 70 billion base pairs for Plethodon vandykei (Van Dyke's salamander) . The ambystomatid Ambystoma mexicanum, a species important for studies in evolution, regeneration and development, has an estimated genome size between 21.9 billion and 48 billion base pairs [5, 6] and measurements of its genome in centimorgans (cM) has yielded the largest size reported for a living vertebrate so far (7,291 cM ). In maize, another organism with a large genome, 60,000 sequence reads were required before genome sequencing of methylation-filtered genomic libraries generated significantly more gene sequence information than the available maize EST sequences .
Molecular evolution studies of salamanders have relied primarily on mitochondrial genes such as those for ribosomal RNAs and cytochrome c . The lack of sequence information among the Caudata hinders the ability to perform sequence comparison with other important gene families. Furthermore, because of the lack of clones, the number of molecular markers available to study salamander embryology and regeneration is low. To address this gap in sequence availability we have generated a large gene sequence set for A. mexicanum. We chose this species because of its role in evolutionary, developmental and regeneration studies. A. mexicanum is easily bred in the laboratory, and animals can be obtained from a large, NSF-funded colony . We have sequenced inserts from two cDNA libraries, one produced from dorsal regions of stage 18-22 embryos, consisting primarily of neural tube, somite and notochord. The second library was constructed from day-6 regenerating tail blastema tissue. By sequencing from these two sources, our goal was to obtain sequences of transcripts involved in organizing and regenerating the primary body axis. Here we describe the EST gene set, provide an example of molecular phylogenetic analysis of one gene from this collection, and describe the database created for organizing the A. mexicanum EST information. This database is also being implemented for EST sequences from a full-length X. laevis cDNA library, and for sequences from a Canis familiaris EST project.
Assessment of library and EST sequence quality
Some characteristics of the A. mexicanum EST contigs
Number of sequences
Number of contigs (+ singlets)
Number of clones in contigs
Number of clones in singlets
St18-22 neural tube
6D tail blastema
The blastema and neural tube libraries were unnormalized and unamplified. We assessed library quality and diversity on the basis of the number of redundant clones in the library. Redundancy was estimated by performing BLASTN searches  against all clones sequenced. After sequencing 10,752 clones of the blastema library 42% of the sequences were still unique, and 50% of clones were still singlets after sequencing 7,680 clones from neural tube, indicating that both libraries display high diversity.
EST assembly into contigs
Gene definition of the most abundant contigs in the A. mexicanum EST libraries
Number of clones in contig
Cytochrome c oxidase subunit I
Nuclear factor 7
Keratin type II
Comparison to existing A. mexicanumgenes in NCBI: 6,000 new contig sequences
A total of 1,134 ESTs were available from A. mexicanum in the National Center for Biological Information (NCBI) EST databases prior to this work, most of which originate from a sequencing effort of the Voss laboratory ( and S.R. Voss, D. King, N. Maness, J.J. Smith, M. Rondet, S.V. Bryant, D.M. Gardiner, and D.M. Parichy, unpublished work (NCBI-accession numbers BI817205-BI818091); see also ). We examined to what extent our EST dataset overlapped with the sequences available to date. Only 600 of the ESTs in the public database identified one of our contigs in a BLASTN search as a homolog; in 85% of cases, the E-value was below 1E-50 and the sequences can be considered as potentially identical. Existing ESTs in the database largely originate from regenerating limb (S.R. Voss, D. King, N. Maness, J.J. Smith, M. Rondet, S.V. Bryant, D.M. Gardiner and D.M. Parichy, unpublished work). There was, however, only a slight bias of matching contigs to regenerating blastema (49%) as compared to neural tube (44%). Seven percent of identified contigs were found in both libraries. These results mean that our EST data enriches the existing sequence resource of A. mexicanum with approximately 6,000 new gene sequences.
BLAST analysis of A. mexicanumcontigs to assign homologies
To identify putative homologies to known proteins, we subjected the contigs to BLASTX searches against the non-redundant protein database (NR, NCBI) where a cutoff E-value of 1e-05 was used for parsing output files. In our annotation, we used an E-value of 1e-20 as an upper limit to assign significant homology. We note that this does not imply that such sequences are true orthologs. In addition, in cases where no significant homology was found, we used an E-value limit of 1e-05 to designate weak homology. We find this additional category of 'weak homology' useful for data mining. As most contigs do not represent full-length sequences, it is possible that only a highly divergent region of a gene sequence is available in our collection. The category of weak homology allows us to find potential homologs in such situations. For example, the BLAST search for contig Am_4671 yielded the GenBank entry NP_004055, cyclin-dependent kinase inhibitor 1B (Homo sapiens), as the top hit with an E-value of 4e-07. This assignment was based on the carboxy-terminal 120 amino acids of the protein, which represents the less conserved region. When we isolated a full-length clone for Am_4671 from our library, we could confirm that it is indeed the axolotl ortholog of cyclin-dependent kinase inhibitor 1B (p27Kip1), as discussed later.
To estimate how many of the clones are full length we examined the BLAST alignments for the position of the alignment in respect to the database sequence. Of the 3,718 sequences with homologs, 1,107 (29.8%) could be aligned in the amino terminus (with the alignment starting before position 10). As the library was poly(dT) primed, many of these clones are likely to represent full-length inserts. Of these 199 (5.4%) could be aligned from the amino terminus to the carboxy terminus and are potential full-length sequences.
Forty percent of our EST sequences did not generate a significant hit in the non-redundant protein database. The availability of additional sequence databases including complete genome sequences from several organisms allowed us to expand our BLAST searches to identify all possible homologs to the A. mexicanum contigs. With the remaining set of contigs, we first performed BLASTN searches against the nucleotide non-redundant (NT) database and BLASTX searches against the EST database. Finally, we performed BLASTX searches against the fugu and human proteomes. In all cases, an E-value of 1e-05 was used to assign potentially homologous sequences. Sequences in the NT database identified an additional 134 contigs and a further 220 contigs found a hit in the EST databases. A homolog was found for 3,340 (52%) contigs in the fugu proteome and 3,698 (58%) contigs shared homology with a protein from the human proteome. In total, an additional 468 contigs identified a homolog in the selected databases beyond the original assignment from the non-redundant protein database (Figure 2b).
Gene sequences with no identifiable homology
Contig identities and GenBank identifiers of ESTs unique to A. mexicanum
Assignment of the A. mexicanumdataset to common Gene Ontology terms
From the homologous proteins found, contigs were assigned a biological process, molecular function and cellular component from the Gene Ontology (GO) database . The closest annotated homolog in the GO database was used, using an E-value of 1e-20 as a cutoff, for assigning these categories. A biological process could be assigned to 2,156 contigs (34% of all contigs and 58% of those sharing a homolog in the non-redundant database); 2,186 contigs (34% and 59%, respectively) were assigned a molecular function; and 2,198 contigs (34% and 59%, respectively) could be assigned a cellular component. The most abundant molecular function assigned was 'death receptor interacting protein', followed by 'peptidase', the highest-ranking biological process were 'biological process unknown' and 'proteolysis/peptidolysis' and the most abundant cellular components assigned were the 'actin cytoskeleton' and 'transcriptional repressor complex'.
The most abundant biological processes assigned to the A. mexicanum contigs
Total number of contigs
Fisher's exact (BL/NT)
Common SMART and PFAM domains in the A. mexicanumdataset
Common protein domains identified in the A. mexicanum contigs and comparison to domain occurrences in other vertebrate species
We assigned cellular functions to the identified domains and analyzed the output according to the functional distribution of contigs (Figure 3b). The most abundant domains were found in the category 'intracellular transport'; this is due to redundant annotations of small GTPases. The second largest fraction belonged to 'RNA-binding and metabolism', followed by 'DNA-binding and transcriptional control'.
In silico differential display of A. mexicanumcontigs in blastema and neural tube
Regeneration versus development
We were interested to see if there were strong differences in the sequence representation of the libraries that reflect the different biological processes taking place in each tissue. To this end, we compared the representation of ESTs in the two libraries. This type of in silico differential display has been performed for ESTs in the NCBI collection, and, as with the NCBI differential display data, we have assessed the statistical significance of the differences using Fisher's exact test. A total of 104 contigs met the cutoff value of 0.005 in Fisher's exact test and can therefore be considered differentially expressed.
Table 4 provides a detailed comparison of EST representation categorized according to their biological process annotation. Considering the biological properties of the blastema tissue versus the neural tube tissue, we were particularly interested in differential display results of gene sequences that had been assigned to the biological functions of RNA metabolism (as an indicator of an high proliferation index), cell cycle and proliferation and differentiation. The blastema library was produced from tail tissue that was in the process of forming the blastema progenitor cells for regeneration. Blastema formation involves dedifferentiation of mature cells, and entry into rapid cell cycles. In contrast, the neural tube library contains tissue undergoing cell specification and differentiation, such as neurogenesis and somitogenesis. Although these embryonic tissues are still proliferating, the proliferation index of the cells from neural tube should be lower than from blastema.
A total of 168 contigs annotated under RNA metabolism (127 when normalized to the ratio of sequenced ESTs from blastema and neural tube) were more frequently sequenced or uniquely sequenced in blastema (6% of assigned contigs, 2.6% of all contigs). This group included RNA metabolism, RNA processing, splicing, editing, nuclear export, binding, catabolism, cleavage, capping, rRNA modification, rRNA transcription and tRNA aminoacetylation. Forty-five contigs assigned a process in RNA metabolism were upregulated or unique in neural tube (2% of assigned and 0.7% of all contigs). After Fisher's exact test analysis, 24 of the clones were considered differentially regulated in the two libraries; 22 out of the 24 contigs were enriched or unique in blastema (Table 4).
Cell cycle and proliferation
126 contigs (95 when normalized to sequencing ratios) were assigned as cell-cycle genes (5% of assigned contigs and 1.5% of total contigs) and were more frequently sequenced or uniquely sequenced in the blastema library, compared with 52 in the neural tube library (2.5% and 0.8%, respectively). This category included regulation of mitosis, mitosis, cell-cycle regulation, regulation of cyclin-dependent kinase (CDK) activity, cell proliferation, DNA replication, M phase, mitotic spindle checkpoint, mitotic spindle assembly, chromosome segregation and cytokinesis. As an example, 10 different types of cyclins were found, from various stages of the cell cycle. Seven of the contigs found in cell-cycle regulation met the cutoff criteria of statistical significance in Fisher's exact test. Five out of the seven contigs were more highly represented or unique in blastema (Table 4).
Whereas proliferation-associated genes were found with a higher sequence representation in the blastema library, genes that had been electronically annotated as involved in 'cell differentiation' had a higher representation in the neural tube library. A total of 28 contigs were electronically assigned the biological process 'differentiation'. After Fisher's exact test, five contigs showed differential regulation in this group. Three out of the five contigs were found in neural tube (Table 4). Taken together, these results indicate that the two cDNA libraries have differences in sequence representation that appear to correlate with the physiological processes taking place in the two tissues.
Gene families involved in cell-cycle control and development in the A. mexicanumdataset
As mentioned earlier, the Mexican axolotl is an important model organism for a number of reasons. First, it is the premier vertebrate model for studying regeneration. Second some aspects of caudate development, for instance mesoderm involution and notochord formation, more closely resemble those found in higher vertebrates than do those in other amphibian embryological models such as X. laevis . Finally, the axolotl has interesting developmental features, particularly in relation to metamorphosis. The axolotl undergoes 'cryptic metamorphosis', which is defined by its existence in a perrenibranchiate state and retaining some larval features into adulthood (for instance gills, larval skin morphology, caudal fins). The animals become sexually mature in this state, and develop only small rudimentary lungs. So far, very few markers are available to study these processes in this organism.
Gene families identified that are either involved in cell-cycle control or developmental processes
Putative ID of contig
Activin receptor type II
Retinoblastoma binding protein 2
Phylogenetic analysis of the CDKN1 gene family in vertebrates: amphibians contain an unusual CDKN1 family member
In contrast, we obtained a quite different picture when we examined the CDKN1 family. In most vertebrates, this family consists of three members: p21 (CDKN1A), p27Kip1 (CDKN1B) and p57 (CDKN1C). In X. laevis, however, only a single family member called p28Kix1 (also called p27Xic1), which shows unusual sequence features compared to the p27 sequences from any other vertebrate species, had been described in the literature [24, 25]. We wondered whether A. mexicanum harbored the 'canonical' p27Kip1 or a p28Kix1 similar to that of Xenopus. We initially searched our A. mexicanum data for CDKN1 orthologs and, in contrast to Xenopus, we found a bona fide p27Kip1 sequence that clusters closer to vertebrate p27Kip1 sequences compared to the Xenopus p28Kix1 (Figure 4c,d). Considering this interesting finding, we then undertook a more complete analysis of the CDKN1 family in vertebrates by searching for CDKN1 family members in several databases: the sequenced genomes from human, mouse, rat, fugu or zebrafish, the recently released genome sequence of X. tropicalis, the X. laevis EST collection, the zebrafish and fugu genomes, and a complementary A. mexicanum and A. tigrinum EST set generated by Putta et al. .
Occurrence of CKI-family members in different vertebrate species
Second, CDKN1B (p27Kip1) and CDKN1C (p57) were present in the A. mexicanum databases but were not found in either X. laevis or X. tropicalis, which have far more EST and genome sequence information (Table 7, Figure 4c,d). While it is not possible to conclude definitively that Xenopus species lack these genes, the current data are highly suggestive of such a scenario.
We examined in depth the phylogenetic relationships of the CDKN1 family members among vertebrates by constructing unrooted phylogenetic trees, either using the most conserved, amino-terminal 88-amino-acid domain, which includes the functionally important Cdk2-interaction region, or the entire coding sequence. Analysis of the amino terminus showed that while A. mexicanum p27 and p57 clearly grouped with their respective orthologs from other vertebrates, the p28Kix1 proteins from axolotl and the two Xenopus species clustered as a group distinct from any of the other CDKN1 families (Figure 4c). The p28Kix1 family showed a closer relationship to p57 than to other CDKN1 members, branching off close to the p57 family. Phylogenetic analysis using the entire coding sequence of the CDKN1 genes, which includes the Cdk2- and PCNA-binding site, resulted in a closer grouping of p28 with the p27 branch (Figure 4d). In both cases, however, the p28 family clearly formed a separate group from the other CDKN1 families.
The Ambystoma mexicanumEST database
Some of the main advantages of this database are: first, the direct links to source databases such as the NCBI sequence database, GO database, CDD, and the Smart and Pfam databases for identified domains; second, direct visualization of source data such as sequence alignments of contigs to homologs and domains, as well as alignments of EST assemblies; third, easy retrieval of sequences for further analysis like BLAST-searching; fourth, user-specific annotation of contigs; and fifth, easy manipulation and editing of contig annotations. The database will be available from .
The salamander, and in particular the species A. mexicanum, represents an important vertebrate organism for evolutionary, developmental and regeneration studies. The salamanders provide an essential amphibian counterpoint to the anurans such as X. laevis, displaying distinct embryology and other physiological features. For example, mesoderm involution during gastrulation and subsequent notochord formation is distinctive between A. mexicanum and X. laevis. The characteristics of mesoderm involution in A. mexicanum more closely resemble those found in other vertebrates . This and other evidence indicates that A. mexicanum and other urodele amphibians are likely to have retained more ancestral features in common with the 'primitive' tetrapod compared to X. laevis, which appears to be more derived. It is interesting that we observed such segregation on the sequence level of the CDKN1 family. X. laevis appears to have a highly unusual make-up of CDKN1 family members. So far, CDKN1A (p21) and the highly derived p28Kix1 are the only CDKN1 family members found in both X. laevis and X. tropicalis. In contrast, the ambystomatids appear to have all the members of the CDKN1-family - including p28Kix1 - assuming that the p21 gene is missing purely as a result of lack of sequence information. In addition, our data suggest that p28 is an amphibian-specific variant of the CDKN1 family. Two major questions arise from these data: first, does the amphibian-specific p28 fulfill a cellular function that is unique to this phylogenetic lineage; and second, does the genotypic difference in the gene set of the CDKN1 family in the two amphibian species account for the macroscopic differences observed in developmental mechanisms. The fact that the CDKN1 family is an essential regulator of the cell cycle opens new possibilities for experimental research along these lines.
Given the estimates in the number of genes present in the human genome (20,000-50,000) , we estimate that our EST contig set (6,377) contains between 10 to 25% of the total number of genes in the axolotl. While the database is not yet complete, it represents a significant proportion of the axolotl transcriptome. Further sequencing efforts, including an NIH-funded EST sequencing project for the axolotl , will enlarge the current dataset to provide a comprehensive gene sequence resource for this organism. Our analysis indicates that the majority of A. mexicanum genes are homologous to genes present in other vertebrates. Sixty-six percent of contigs gave a significant match in either the non-redundant protein or nucleotide databases, the EST databases or the human and fugu protein databases. Thirty-four percent of contigs could not be assigned a homolog in any of the searched databases, and 44% of those could not be assigned a coding sequence and are therefore considered to be part of the UTR. Nineteen percent of the contigs seem to represent novel genes that have not been found in any other organism so far.
The expressed sequence tags generated in this study also provide a large source of sequence information for developmental and regeneration studies. For example, an examination of the database yielded 194 genes involved in cell proliferation, including pivotal cell-cycle genes such as those for Cdc2, 10 different cyclin family members, Cdk4 and p27. A search for developmental molecules involved in intercellular communication yielded Wnt8, Wnt5B, FGF receptor 4a (FGFR4a), Sonic hedgehog, BMP receptor (BMPR) and BMP-1, while a search for homeodomain-containing proteins yielded 11 members, including Cdx1, Cdx2, HoxA2, HoxC8 and HoxB13.
The ESTs were derived from two cDNA libraries, stage 18-22 embryonic neural tube/notochord/somite tissue, and day-6 regenerating tail tissue. The embryonic library represents a developmental stage where tissue specification is occurring, whereas the blastema library represents a tissue that is undergoing dedifferentiation, rapid proliferation and cell respecification. Accordingly, we find differences in transcript representation in the two libraries. The blastema library is particularly enriched in cell-cycle genes and RNA metabolism genes, presumably reflecting the high proliferative index of the early regenerating blastema.
This set of 17,352 ESTs from A. mexicanum was generated to provide a comprehensive sequence dataset for the community of biologists. Forty percent of genes could still be found in singlets, which reflects a high diversity of sequences in our cDNA set. Annotation of the assembled contigs revealed a substantial difference in gene representation in the two sequence libraries, reflecting their biological source - regenerating blastema being in a highly proliferative state and embryonic neural tube being a tissue undergoing differentiation. Sequence analysis of assembled contigs revealed that 64% of genes had a putative homolog in other species; 19.4% of the contigs contained a putative coding sequence and can be considered novel genes. From this, we conclude that A. mexicanum does not contain an unusually high number of organism-specific genes. The CDK inhibitor family CDKN1 was selected for comparative phylogenetic analysis. Unlike the frogs X. laevis and X. tropicalis, ambystomatids most probably contain all members of the CDKN1 family, including the amphibian-specific protein p28Kix1/p27Xic1, which shows unusual sequence divergence compared to CDKN1 members in other vertebrate species. Such data would support the contention that A. mexicanum is closer to a basal tetrapod compared to X. laevis. The EST sequences and annotated contigs presented in this paper will be a publicly available and useful resource for research in various fields.
Plasmid cDNA library construction
Total RNA was purified using Trizol (Invitrogen) from 6-day regenerating tail blastemas and from neural tube-somite-notochord-containing tissue dissected from stage 18-22 A. mexicanum embryos. Total RNA quality was assessed by determining the relative brightness of the 28S:18S rRNA bands (2:1). For library construction mRNA was purified and size fractionated, then poly(dT)-primed cDNA was synthesized and directionally cloned into the NotI-SalI sites of the pCMVSport6 vector. DNA was transformed by electroporation into EMDH10B-TONA bacteria (library construction performed by Invitrogen). Two separate, unnormalized libraries were produced. The blastema library contained an average insert size of 1.67 kb and 2.67 × 107 independent transformants and the neural tube library had an average insert size of 1.5 kb and 1.9 × 107 transformants. From each library 100,000 clones were arrayed into 384-well plates (Resource Zentrum/Primary Database, Berlin, Germany).
For sequencing, single-pass reads from the 5' end of the library inserts were performed using a custom-designed SP6 primer: GCACATTAGGCCTATTTAGGTGACA. DNA from bacterial library clones was amplified using the Templiphi reaction, based on φ29 rolling-circle replication of DNA (AP Biotech). Briefly, approximately 0.5 μl of bacterial glycerol stocks were picked up using 96-pin plastic replicators (Genetix) and centrifuged into 96-well PCR plates. Five microliters of denaturing buffer was added, and samples heated to 95°C for 3 min. After cooling, 5 μl Templiphi enzyme was added and samples incubated overnight in a 30°C incubator. The Templiphi reaction provides two advantages for large-scale sequencing projects on capillary sequencers. First, the reaction proceeds to an endpoint where all nucleotide is incorporated, yielding uniform quantities of DNA from varying amounts of starting bacteria (or DNA). Second, the rolling-circle reaction results in large pieces of DNA that, in contrast to plasmid DNA, do not enter the capillary and interfere with the sequencing run.
For sequencing reactions, the DNA preparation was diluted fivefold with distilled water. Sequencing reactions were performed using the DYEnamic ET Dye terminator kit diluted twofold with DYEnamic ET dilution buffer (AP Biotech). Five microliters of DNA was added to 5 μl of sequencing reaction mix with primer and cycled 30 times under the following conditions: 95°C 20 sec, 60°C 1 min. Sequencing was performed on a MegaBACE 1000 (AP Biotech). Runs were either performed at injection: 3 kV 60 sec, run: 8 kV 120 min, or injection: 3 kV 60 sec injection, run: 3 kV 360 min.
Analysis of library quality
The redundancy of the arrayed libraries was tested by performing BLASTN searches  against all sequenced ESTs from the two libraries. Hits against clones other than the query with an E-value lower than 1e-50 were considered for clustering.
Submission of ESTs to NCBI GenBank
The sequences were submitted to GenBank. After quality control, individual ESTs were used to search the non-redundant protein database (release of July 2004) using the program BLASTX from the standalone NCBI-BLAST package . For annotation of sequenced ESTs, the top hit of the BLAST output was used, whereby an E-value of 1e-20 was used for significant similarity and an E-value of 1e-05 was used as a cutoff value for weak similarity.
Analysis and assembly of sequence data
Quality control of sequenced ESTs was performed using the program Phred  using a cutoff of 20 for trimming low-quality regions, and vector trimming was performed using the program cross-match . (We note here that the arbitrary Phred score reflects the likelihood of a false base. A Phred score of 20 indicates that in 1 out of 100 trials (102), the base would be false, 30 would reflect a wrongly sequenced base in 1 of 1,000 trials (103), and so forth.) Sequence and contig files can be downloaded at . The resulting high-quality sequences were assembled into sequence contigs with the program TIGR-Assembler version 2 . Alignment of contigs was performed with the program ClustalW with the settings Gap Opening 5 and Gap Extension 85  or Cap3 , when ClustalW could not correctly assemble the sequences. Assembled contigs were used to perform BLAST searches (BLASTX, BLASTN from NCBI-BLAST ) against the non-redundant protein sequence database (release of November 2003), human and fugu protein databases and the NCBI EST database, all downloaded from the NCBI. Domain searches were done with RPS-BLAST against the conserved domain database (CDD ) from the NCBI. BLAST and domain-search output files were parsed for homologous sequences, whereby an E-value of 1e-05 was used as a cutoff for BLASTN and BLASTX searches against the sequence databases and the default cut-off of 0.01 was considered to yield significant homology to conserved domains from CDD. A gene identifier was assigned to those contigs that showed reliable homology to a sequence in the non-redundant database (E-value cutoff of 1e-20 for significant similarity and 1e-05 for weak similarity). Potential untranslated regions were identified using the program ESTScan .
Electronic annotation of contigs
Based on the GO annotation of the closest annotated homolog, contigs were assigned a molecular function, biological process and cellular component from the GO database . To this end, the GenBank annotation files from the GO database were downloaded and parsed for the gene identifier (gi) numbers of previously identified homologs. The cutoff for annotating an A. mexicanum contig was an E-value of 1e-20.
Isolation of the full-length p27Kip1gene from the EST sequence
Two EST sequences of the p27Kip1 gene were sequenced in the EST collection but neither were full-length sequences. To isolate the full-length sequence, 200,000 clones of our arrayed blastema and neural tube libraries were screened by PCR. Briefly, the bacterial library clones in each 384-well plate were pooled, mini-prepped and arrayed into 96-well plates (RZPD, Berlin), resulting in 576 DNA pools. These DNA pools were screened by PCR using the custom SP6 primer (GCACATTAGGCCTATTTAGGTGACA) as a forward primer and a gene-specific p27 reverse primer (TGATTTCCAATGGCTGGTTT). Fifty nanograms of DNA from each pool was used for PCR reactions and PCR cycling was performed at the following conditions: 94°C 2 min, 30 cycles of 94°C 15 sec, 65.5°C 30 sec, 72°C 90 sec, followed by 72°C 7 min). The largest positive band (1.1 kb) was gel purified and sequenced on an ABI377 machine using the SP6 primer.
Multiple sequence alignments were done with the program ClustalX  using standard parameters. Phylogenetic analysis of mitochondrial 12S rRNA was done using the programs dnadist, phylogenetic analysis of the cyclin B family and the CDK inhibitor family (CKI family) was done using protdist, both from the Phylip package . Trees were calculated with the program fitch from the same software package, using 100 iterations. For the CKI family, only the amino-terminal, CDK-inhibitory domain or the full-length sequences were used for construction of a phylogenetic tree. For the cyclin-B family, only the region overlapping in A. mexicanum contigs was used for tree construction. Trees were displayed using the program nj-plot  for the mitochondrial 12S rRNA tree and unrooted  for the CKI- and cyclin B families.
A relational database was created using the open source software MySQL as the database server to store and navigate through resulting sequence contigs and annotations. Scripts connecting the web-based front end to the database were written in the programming language Python.
We thank Wolfgang Zachariae, Ralf Kittler and S Randal Voss for critical reading of the manuscript. We are grateful to Tony Hyman, Albert Poustka and David Drechsel for advice and support. This work was funded by the Max Planck Institute of Molecular Cell Biology and Genetics, and the MeDDrive program of the Medical Faculty, Technical University of Dresden.
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