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Journal of Bacteriology, September 2004, p. 6316-6319, Vol. 186, No. 18
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.18.6316-6319.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Bacterial Thymidylate Synthase with Intein, Group II Intron, and Distinctive ThyX Motifs

Xiang-Qin Liu* and Jing Yang

Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia, Canada

Received 8 April 2004/ Accepted 25 May 2004


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ABSTRACT
 
The ThyX class of thymidylate synthases was previously characterized by a common ThyX motif, RHRX7S. We report bacterial ThyX sequences having distinctive ThyX motifs, suggesting a more general ThyX motif, R/THRX7-8S. One ThyX sequence has an intein in its ThyX motif that was shown to do protein splicing and a group II intron in its gene, suggesting a hot spot for these self-splicing mobile elements.


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TEXT
 
The recently discovered ThyX class of thymidylate synthases is not similar to ThyA in its structure (16) or in its reductive mechanism (10, 19), revealing complexity in the evolution of thymidine production in DNA synthesis. ThyX exists in organisms lacking ThyA and shows a sporadic phylogenetic distribution indicating lateral gene transfers (19). Its presence in many pathogenic bacteria and absence in humans make ThyX an attractive target for potential antibacterial drugs. To realize this potential, knowledge is needed regarding important structural elements including the common ThyX motif found in previously known ThyX sequences.

Inteins and introns are rare and have not been found previously with ThyX. An intein is a protein intervening sequence that can self-excise and concomitantly splice together its flanking extein sequences (21). Many inteins also harbor an endonuclease domain that initiates intein homing, which confers genetic mobility on the intein (3, 5) and explains its sporadic phylogenetic distribution (20). Group II introns are another type of self-splicing mobile element, and most bacterial group II introns encode a reverse transcriptase-like (RTL) protein (23) that assists intron splicing and mobility, including retrotransposition (2, 11, 12). Group II introns are believed to be evolutionary ancestors of nuclear spliceosomal introns (4), but they are strongly excluded from conserved protein-coding genes in bacteria (6-8), although some bacteriophage genes encode both inteins and group I introns (9, 13, 14). Surprisingly, a bacterial ribonucleotide reductase (RIR)-encoding gene was found recently to encode multiple inteins and group II introns (18). To explore and understand this new phenomenon, we searched for similar inteins and introns in related genes.

An intein- and intron-encoding thyX gene was found during a BLAST search (1) of the GenBank database. This gene is from the oceanic N2-fixing cyanobacterium Trichodesmium erythraeum. As illustrated in Fig. 1, the three exon and extein coding sequences are 196, 80, and 444 bp long, respectively, and they together predicted a 240-amino-acid ThyX sequence that is very similar to known ThyX sequences. The intron was identified by its strong sequence similarity to known group II introns in this organism, which included the T.er.I4 intron in an RIR-encoding gene (18) and the Tr.e.I1 intron in an intergenic sequence (6). It is more than 80% identical to the other introns in the ~680-nucleotide folded region (data not shown), although it lacks the RTL coding sequence present in domain IV of the other introns.



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  		FIG. 1. Illustration of the T. erythraeum thyX gene and predicted expression products. Black boxes represent the three exons and exteins. aa, amino acids; nt, nucleotides.

The intein was recognized by its intein sequence motifs (Fig. 2), and its boundaries were readily identified through comparisons with inteinless ThyX sequences. The intein clearly has sequence motifs (A, B, F, and G) for a splicing domain, but it either lacks or has incomplete sequence motifs (C, D, E, and H) for a homing endonuclease domain. It showed less than 15% sequence identity and no insertion site similarity to other known inteins. For example, it showed 14% sequence identity and 28% sequence similarity to the Synechocystis sp. strain PCC6803 DnaB intein. Nevertheless, it showed efficient protein splicing in a recombinant protein in Escherichia coli (Fig. 3).



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  		FIG. 2. Intein sequence comparison. The T. erythraeum ThyX intein sequence is aligned with the sequence of the previously identified Synechocystis sp. strain PCC6803 DnaB intein, and putative intein sequence motifs (A through H) are underlined. Dashes represent gaps introduced to optimize the alignment.



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  		FIG. 3. Protein splicing of T. erythraeum ThyX intein. (Top) Schematic illustration of the fusion protein construct consisting of the maltose binding protein sequence (M), the intein sequence (gray box), and the thioredoxin sequence (T). (Bottom) Observation of protein splicing. Protein production and splicing were carried out with E. coli, and the resulting products were visualized by Western blotting with anti-thioredoxin antibody as previously described (22). Lanes: 1, protein splicing of the Synechocystis sp. strain PCC6803 DnaB mini-intein as a known standard; 2, protein splicing of the T. erythraeum ThyX intein. The letter P marks the position of the precursor protein, which matches closely the predicted sizes of 74 and 91 kDa in lanes 1 and 2, respectively. The letter S marks the position of the spliced protein, which matches closely the predicted sizes of 57 and 56 kDa in lanes 1 and 2, respectively.

The T. erythraeum thyX gene is only the second bacterial gene (except for phage genes) known to encode inteins and introns, following an RIR-encoding gene (18). It is not certain why these two genes appear to be hot spots for intein and intron insertions, which most likely involve intein homing and group II intron retrotransposition. The ThyX intein likely had a homing endonuclease domain and later lost it, on the basis of observation of putative remnants of this domain in the intein. The ThyX intron and the T.er.I4 intron of the RIR-encoding gene, showing strong sequence identity, are likely related through recent retrotransposition, and it is tempting to speculate that the RTL-less ThyX intron is assisted in retrotransposition by the RTL protein encoded in the T.er.I4 intron. It is interesting that the thyX gene and the RIR-encoding gene both encode proteins involved in nucleic acid metabolism, because such genes have been recognized as favored homes of inteins and introns for various reasons (8, 17). We further noticed that the ThyX intein is inserted in the conserved ThyX motif, which prompted further analysis of ThyX motifs.

New ThyX sequences having distinctive ThyX motifs were found through BLAST searches of the GenBank database. Although not having inteins or introns, they showed ThyX motifs that are similar to but distinct from the previously defined ThyX motif RHRX7S (Table 1 and Fig. 4). Most of the new ThyX sequences (T. erythraeum, Nostoc punctiforme, Nostoc sp. strain PCC7120, Synechococcus sp. strain WH8102, mycobacteriophage Bxz1, Streptomyces coelicolor, and Streptomyces avermitilis MA-4680) are readily identified because they are more than 20% identical and 30% similar to the functionally identified Helicobacter pylori J99 ThyX protein and to the structurally determined Thermotoga maritima ThyX protein. ThyX sequences from the two thermophilic sources (Thermosynechococcus elongatus and thermophilic bacteriophage RM378), however, were less easy to identify because of their striking differences from other ThyX sequences at the N and C termini (Fig. 4B). Nevertheless, they are approximately 18% identical and 34% similar to T. erythraeum ThyX over four-fifths of the T. erythraeum ThyX sequence, which is quite significant in light of the generally low levels of sequence conservation among ThyX proteins. For example, the ThyX sequences of two cyanobacterial species (T. erythraeum and Synechocystis sp. strain PCC6803) are only 17% identical and 33% similar. The shortened N-terminal sequence of the T. elongatus and thermophilic bacteriophage RM378 ThyX proteins, relative to that of other ThyX proteins, may be compensated for by the extended C-terminal sequence, although the extended C-terminal sequence does not show similarity to that of other ThyX sequences. T. elongatus ThyX is also the only recognizable thymidylate synthase (which is functionally essential) that could be predicted from the complete genome sequence of this organism.


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  		TABLE 1. Distinctive ThyX motifs in ThyX sequences of various organisms



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  		FIG. 4. ThyX protein sequence comparisons. In panel A, sequences are grouped according to ThyX motifs including THRX8S (T. erythraeum [Ter], N. punctiforme [Npu], Nostoc sp. strain PCC7120 [Nsp], and Synechococcus sp. strain WH8102 [SWH]), RHRX8S (Nostoc sp. strain PCC7120 [Nsp], S. coelicolor [Sco], and S. avermitilis MA-4680 [Sav]), and RHRX7S (Synechocystis sp. strain PCC6803 [Ssp], H. pylori J99 [Hpy], and T. maritima [Tma]). Positions conserved within each group are highlighted in gray. In panel B, positions conserved between the T. erythraeum sequence and the T. elongatus or thermophilic bacteriophage RM378 sequences are highlighted in gray. The intein insertion site in the T. erythraeum sequence is indicated by underlining of the two flanking residues (CS). The ThyX motif is also underlined, with the conserved R/THR and S residues in bold.

These ThyX sequences, when grouped by their ThyX motifs as in Table 1, showed higher sequence identities within a group than between groups. In particular, the ThyX sequences of four cyanobacteria (T. erythraeum, N. punctiforme, Nostoc sp. strain PCC7120, and Synechococcus sp. strain WH8102), having the same ThyX motif, THRX8S, have more than 60% sequence identity with each other. But they show less than 20% sequence identity with the ThyX sequences of other cyanobacteria (e.g., Synechocystis sp. strain PCC6803) that have a different ThyX motif. The previously identified ThyX motif RHRX7S has the widest distribution, encompassing bacteria, archaea, and eucarya; therefore, it likely is the original ThyX motif present in the common ancestor of ThyX proteins. The new ThyX motifs THRX8S and THRX7S, found in some cyanobacterial species, likely represent later divergence from the presumed original ThyX motif, and they could also have been acquired through lateral gene transfer. Interestingly, three of the four distinctive ThyX motifs have been found with bacteriophage, which could have facilitated lateral transfer of thyX genes.

We suggest a more general ThyX motif, R/THRX7-8S, in order to accommodate all four of the distinctive ThyX motifs (Table 1). While this report was under review, others reported the functional characterization of two residues of the ThyX motif RHRX7-8S located at the catalytic site (15). The absolutely conserved S residue (S84) was shown to function as a nucleophile, and the first R residue (R74) was shown to participate in flavin adenine dinucleotide and dUMP binding. But our findings show that the first R residue is not absolutely conserved. However, when a ThyX motif begins with T instead of an R, it either has an R immediately before a T (in T. erythraeum, N. punctiforme, Nostoc sp. strain PCC7120, and Synechococcus sp. strain WH8102) or has a second R internally (in T. erythraeum and thermophilic bacteriophage RM378), and this could suggest functional replacement of alternative R residues.


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ACKNOWLEDGMENTS
 
This work was supported by research grants from the National Science and Engineering Research Council of Canada.


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FOOTNOTES
 
* Corresponding author. Mailing address: Department of Biochemistry and Molecular Biology, Dalhousie University, Halifax, Nova Scotia B3H 4H7, Canada. Phone: (902) 494-1208. Fax: (902) 494-1355. E-mail: pxqliu{at}dal.ca. Back


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Journal of Bacteriology, September 2004, p. 6316-6319, Vol. 186, No. 18
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.18.6316-6319.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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