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Journal of Bacteriology, May 2002, p. 2837-2840, Vol. 184, No. 10
0021-9193/02/$04.00+0     DOI: 10.1128/JB.184.10.2837-2840.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

The secE Gene of Helicobacter pylori

Claudine Médigue,^1,2 Benjamin Chun-Yu Wong,³ Marie Chia-Mi Lin,⁴ Stéphanie Bocs,² and Antoine Danchin^5*

Génétique des Génomes Bactériens, Institut Pasteur, Paris,¹ Génomique Comparative des Micro-organismes Pathogènes, Génopole, Evry, France,² Department of Medicine,³ Institute of Molecular Biology, University of Hong Kong,⁴ HKU-Pasteur Research Center, Hong Kong, China⁵

Received 28 December 2001/ Accepted 6 February 2002

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Despite extensive annotation by two independent teams, the Helicobacter pylori genome appeared to lack a complete secretion machinery. The use of clinical isolates to substantiate in silico annotation is used here to identify the missing secE component of the major secretion machinery of Helicobacter pylori.

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Two independent sequences of the Helicobacter pylori genome, with many clinical isolates from hospital laboratories, have been annotated by two independent consortia. It is therefore expected that the identification errors have been kept to a minimum. Naturally, some genes of unknown function may have escaped attention while spurious sequences have been taken for bona fide genes. It is, however, important for the community to be sure that no essential gene has been missed or misannotated since most scientists now rely on data library searches to substantiate their experiments. How would the discovery of an important gene sequence stand in a much explored (and patented) sequence? By combining and chaining a series of independent tasks meant to identify coding sequences (CDSs) in bacterial genomes (2), we explored in silico the genome of H. pylori to see whether important genes have escaped notice. To predict CDSs, this strategy combined periodical Markov chain analysis (the original GeneMark program, which works by discrimination of relevant protein coding sequences from the background [5]) and now popular derivatives (such as Glimmer, which works by assimilation from previously known sequences [10]) together with BlastX computation and identification of tRNAs, terminators, and putative ribosome binding sites by using the platform Imagene (6). In contrast with the usual approaches, which mostly rest on one single method for gene identification, this allows one to discriminate with fair certainty between spurious genes and bona fide genes. The method is therefore particularly important for reannotating regions where genes have already been thought to be identified.

In the case of the H. pylori genomes, the situation presented downstream of the nusG gene was puzzling: GeneMark predicted a short CDS in the same orientation as nusG with a good upstream ribosome binding site, whereas Glimmer proposed a longer sequence in the opposite strand (and a poor indication of the former putative CDS) (Fig. 1). In many instances GeneMark is preferred over Glimmer because it discriminates between coding and noncoding regions while Glimmer assimilates putative coding regions to known ones. This results in the carrying over of features from one strand to its complement as soon as they are palindromic in nature (e.g., the RNY coding rule is true both in the coding strand and in its complement [9]). A Blast search revealed that the latter sequence did not display similarity with known sequences, whereas the former was similar to the secE gene present in a variety of organisms. The neighboring gene order was consistent with this, since secE is often part of an operon with genes involved in translation, as shown by Pohlschroder et al. at a time when the first genome sequences appeared (8).

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FIG. 1. The nusG region in H. pylori. Four frames with putative CDSs are displayed in the tufB nusG region. The upper line is the prediction by GeneMark, and the lower line is the prediction by Glimmer. While Glimmer predicts a long CDS in the opposite strand, GeneMark predicts an excellent CDS between rmpG and nusG. The present work shows that this corresponds to the secE gene.

The sequence of the two known H. pylori genomes (http://genolist.pasteur.fr/PyloriGene) suggested that secE was a bona fide gene, but the data were too scarce and contradictory to warrant this hypothesis. (Only eight codons differed in the two reference sequences, including one modified in its second base position, therefore arguing against the hypothesis. One expects that most sequences display synonymous mutations; therefore, mutations would appear in the third codon position.) To substantiate this interpretation, we sequenced the homologous region in seven H. pylori isolates collected at the University of Hong Kong. The new sequences differed from those of the model strains at 10 more significant positions. Twelve positions corresponded to synonymous replacements while six others yielded conservative replacements in the secE frame (Fig. 2). The only position which was not strictly conservative (AAA to GAA) is located immediately after the start of the protein at a nonconservative position (a gap in some SecE proteins). These same mutations would yield several nonconservative replacements in the complementary putative coding sequence (in particular an AAA (lysine) ATA (isoleucine) replacement). Interestingly, the sequences indicate that the Asian isolates are from a common group that differs from those of the rest of the world (1).

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FIG. 2. The H. pylori SecE gene and protein. The upper part is an alignment of the nucleotide sequences of several H. pylori isolates. Capital letters represent strains from the Hong Kong University Department of Medicine, and lowercase letters represent the sequences of the two model genomes, 26695 and J99 (http://genolist.pasteur.fr/PyloriGene). Boldface letters represent the codon specifying the most-conserved residues in SecE. Codons on a light grey background indicate the placement of mutations with conservation of the protein sequence, and codons in italics indicate mutations leading to conservative replacements. The lower part is an alignment of reference SecE protein sequences. The Escherichia coli sequence is truncated from its two amino-proximal transmembrane domains. Boldface letters represent highly conserved residues (in particular, residues making contact with SecY); letters in italics are conservative replacements (ASTPG, MLIV, DNEQ, RKH, FYW). In the sequence of SecE from H. pylori, conservative replacements are noted in parentheses. RBS, ribosome binding site; HP, H. pylori; CJ, Campylobacter jejuni; DR, Deinococcus radiodurans; EC, E. coli; BS, Bacillus subtilis.

The structure of the SecE protein is comprised of a cytoplasmic domain, a transmembrane helix, and a periplasmic domain. The bacterial translocase consists of the SecEYG membrane protein complex and the peripheral-membrane-associated SecA dimer (for a review, see reference 3). In the present sequence, residues in both the cytoplasm and the periplasm are conserved (in particular, the residues making contact with SecY) in comparison with other bacterial counterparts (this is in complete agreement with the identifications made by Hartmann et al. [4] and Murphy and Beckwith [7], thus further substantiating our identification of the secE gene) while the extremities of the transmembrane helix are also conserved, with the hydrophobic core preserving not the residue but its hydrophobic nature (11) (Fig. 3). SecE, which in most bacteria is comprised of a single transmembrane domain (as predicted by the present study), is an essential component of the highly conserved general secretion machinery. In addition to placing H. pylori in the normal class of secreting bacteria and providing a new example of the SecE structure, this work emphasizes the need for continuous reannotation of genome sequences, including those regions which have been previously annotated thoroughly, and the associated experimental substantiation.

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FIG. 3. The SecE protein in context. Phylogenetically conserved residues are in grey. Inverted colors correspond to the transmembrane segment of the protein. Stars correspond to residues encoded by synonymous codons in the various H. pylori isolates. The six variable residues are shown as indicated (e.g., K > E at the beginning of the protein).

ADDENDUM IN PROOF We have recently noted that Doig et al. (P. Doig, B. L. de Jonge, R. A. Alm, E. D. Brown, M. Uria-Nickelsen, B. Noonan, S. D. Mills, P. Tummino, G. Carmel, B. C. Guild, D. T. Moir, G. F. Vovis, and T. J. Trust, Microbiol. Mol. Biol. Rev. 63:675-707, 1999) in their in silico prediction of the H. pylori genes have suggested in passing the existence of a secE counterpart. However, this prediction has not been included in the corresponding databases, perhaps for want of experimental substantiation. This is now done in the present work.

 
* Corresponding author. Mailing address: HKU Pasteur Research Centre, Dexter HC Man Building, 8, Sassoon Road, Pokfulam, Hong Kong, China. Phone: 852 2816 8403. Fax: 852 2168 4427. E-mail: adanchin{at}hkucc.hku.hk.

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Journal of Bacteriology, May 2002, p. 2837-2840, Vol. 184, No. 10
0021-9193/02/$04.00+0     DOI: 10.1128/JB.184.10.2837-2840.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

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This Article Abstract Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Reprints and Permissions Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via HighWire Citing Articles via Google Scholar Google Scholar Articles by Médigue, C. Articles by Danchin, A. Search for Related Content PubMed PubMed Citation Articles by Médigue, C. Articles by Danchin, A.