A gonococcal homologue of meningococcal γ-glutamyl transpeptidase gene is a new type of bacterial pseudogene that is transcriptionally active but phenotypically silent
© Takahashi and Watanabe; licensee BioMed Central Ltd. 2005
Received: 13 June 2005
Accepted: 04 October 2005
Published: 04 October 2005
It has been speculated that the γ-glutamyl transpeptidase (ggt) gene is present only in Neisseria meningitidis and not among related species such as Neisseria gonorrhoeae and Neisseria lactamica, because N. meningitidis is the only bacterium with GGT activity. However, nucleotide sequences highly homologous to the meningococcal ggt gene were found in the genomes of N. gonorrhoeae isolates.
The gonococcal homologue (g gt g onococcal h omologue; g gh) was analyzed. The nucleotide sequence of the ggh gene was approximately 95 % identical to that of the meningococcal ggt gene. An open reading frame in the ggh gene was disrupted by an ochre mutation and frameshift mutations induced by a 7-base deletion, but the amino acid sequences deduced from the artificially corrected ggh nucleotide sequences were approximately 97 % identical to that of the meningococcal ggt gene. The analyses of the sequences flanking the ggt and ggh genes revealed that both genes were localized in a common DNA region containing the fbp-ggt (or ggh)-glyA-opcA-dedA-abcZ gene cluster. The expression of the ggh RNA could be detected by dot blot, RT-PCR and primer extension analyses. Moreover, the truncated form of ggh- translational product was also found in some of the gonococcal isolates.
This study has shown that the gonococcal ggh gene is a pseudogene of the meningococcal ggt gene, which can also be designated as Ψggt. The gonococcal ggh (Ψggt) gene is the first identified bacterial pseudogene that is transcriptionally active but phenotypically silent.
Two members of the gram-negative diplococci, Neisseria meningitidis and Neisseria gonorrhoeae, are particularly associated with pathological infections. N. meningitidis is specialized for the mucosa of the nasopharynx and causes meningitis and septicemia. N. gonorrhoeae is adapted for the mucosa of the urogenital tract and causes gonorrhoea and pelvic inflammatory diseases. Both species colonize only humans and share a great deal of relatedness at the nucleotide level . This high degree of relatedness is reflected in the many common genetic, biochemical and antigenic features of the two bacteria.
γ-Glutamyl transpeptidase (also called γ-glutamyl aminopeptidase) (EC18.104.22.168; GGT) catalyzes the hydrolysis of γ-glutamyl compounds, and is found in a variety of bacteria such as Escherichia coli  and Helicobacter pylori [3, 4]. To distinguish N. meningitidis from N. gonorrhoeae, GGT activity is used as one of the identification markers for N. meningitidis because N. meningitidis is positive for this activity but N. gonorrhoeae and related species, e.g., Neisseria lactamica, are not . In fact, the detection of GGT activity is applied for the identification of N. meningitidis in the Gonochek II enzymatic identification system (E-Y Laboratories Inc., U.S.A.) [6–9]. From these empirical facts, it was believed that the gene encoding for GGT should exist only in N. meningitidis, but this has not been proven yet .
Recent remarkable progress in the sequencing of various genomes has led to the detection of nucleotide sequences that appear to be phenotypically silent, termed pseudogenes. The pseudogenes are defined as DNA sequences of formerly functional genes rendered nonfunctional by mutations and usually identified by their disrupted open reading frames (ORFs). Pseudogenes have been identified in a variety of eukaryotes, including insects , plants , and particularly vertebrates [10, 12], but are relatively few in the bacterial genomes. Notable exceptions are intracellular bacterial parasites such as Rickettsia prowazekii and Mycobacterium leprae , which seem to have lost many genes due to obtaining nutritional supplies from the host cells. Cryptic genes such as the cel operon in E. coli [14–16] and the flagellar master operon in the genus Shigella [17–19] seem to be a kind of pseudogenes, but are different from pseudogenes because the cryptic genes completely retain intact ORFs, which can be occasionally activated by rare genetic events such as mutation, recombination, insertion of elements. As a whole, compared to the pseudogenes in eukaryotes, relatively few pseudogenes have been reported in bacterial genomes .
In this study, a gonococcal ggh gene, which is highly homologous to the meningococcal ggt gene, was found to be pseudogene. Sequence analyses of the flanking regions of both the ggt and ggh genes suggest that both genes were derived from a gene in a common ancestor, and subsequently diversified.
The gonococcal ggh gene was highly homologous to the meningococcal ggt gene
Variations of the nucleotide sequences of ggh genes among clinical isolates
Mutation types found in the ggh genes of 11 N. gonorrhoeae strains
I (+6 bp)
III (Δ7 bp)
IV (+46 bp)
NIID109 (48th A to G)
NIID105 (213th G to A)
Putative amino acid sequences in hypothetical coding region of the ggh genes
The genetic organization of the ggt- and ggh-flanking regions in the genomes of N. meningitidis and N. gonorrhoeae
The expression of the ggh gene in N. gonorrhoeae
In this study, it was shown that the gonococcal ggh gene is a member of bacterial pseudogenes, and is transcribed but not properly translated so that active ggh protein product is not produced. 11Fh-mtTFA , OsMu4-2 , NA88-A , Makorin1-p1 , Dnm3a2  and pseudoNOS  genes are known to be transcriptionally active eukaryotic pseudogenes. In neisseriae, the gonococcal porA and ΨopcB genes have been reported as neisserial pseudogenes [1, 32, 33]. The porA pseudogene contains mutations in the promoter and the coding regions, and is not translated . While some hypothetical bacterial pseudogenes with repetitive runs of A and T are speculated to be potentially expressed by transcriptional slippage , the expression, including the transcription, has not been proven yet. To our knowledge, the gonococcal ggh gene is the first identified bacterial pseudogene that is transcriptionally active.
The 15-kDa derivative of the putative ggh protein product is detected in the NIID103 and NIID106 N. gonorrhoeae strains but not in the ATCC49226 and NIID54 N. gonorrhoeae strains (Figure 6A). Since the predicted amino acid sequences of the putative 15-kDa proteins seem to be similar among the 4 gonococcal strains, the reason why the 15-kDa protein was not detected in ATCC49226 and NIID54 is not clear. The 15-kDa protein might be degraded in ATCC49226 and NIID54 backgrounds but not in NIID103 and NIID106 backgrounds. It seems unlikely that the 15-kDa protein encoded by the ggh gene has an essential function for N. gonorrhoeae because the 15-kDa protein is not always detected in any of gonococcal strains (Figure 6A).
Why does the gonococcal ggh gene still retain the transcriptional activity? There are some examples in which RNAs transcribed from pseudogenes have some biological functions: antisense RNA expressed from the pseudoNOS gene hybridizes with nNOS (nitric oxide synthase) mRNA, resulting in the suppression of the nNOS gene expression in the neurons of the snail Lymnaea stagnalis . RNA of Makorin1-1p, a pseudogene of Makorin1, regulates the Makorin1 mRNA stability, which is important for the correct formation of the kidneys and bone in mice . Some eukaryotic genes may be duplicated and one of the plural genes may be subsequently reconstructed due to its redundancy, resulting in a pseudogene. However, since a bacterial pseudogene generally does not have a functional counterpart (wild-type gene) in a single organism, the ggh RNA does not seem to have the same kind of biological function as the pseudoNOS and Makorin1-1p genes. In fact, we could not find any prominent phenotype for a Δggh gonococcal mutant (unpublished data). However, we cannot exclude the possibility that the ggh RNA has some biological function(s) in other milieus such as the urogenital tract and further analyses will be required to address this possibility.
The ggt and ggh genes are located in the fbp-ggt (ggh)-glyA-opcA-dedA-abcZ common gene cluster in the genomes of both N. meningitidis and N. gonorrhoeae (Figure 4) . The genome of N. lactamica lacks ggt and opcA homologues in the fbp-glyA-dedA-abcZ locus (Figure 4 and ). It would not be the result of chance that the two ggt (or ggh) and opcA genes are located in the same respective sites of the fbp-glyA-dedA-abcZ gene locus of both N. meningitidis and N. gonorrhoeae but not in that of N. lactamica. Moreover, it is also unlikely that a nonfunctional ggh gene was horizontally transferred into the gonococcal fbp-glyA-opcA-dedA-abcZ gene cluster since such a pseudogene could not have been sustained due to the lack of selection . Therefore, it seems more probable that the fbp-ggt-glyA-opcA-dedA-abcZ gene cluster was present in an ancestor of the three neisserial species, and has been subsequently diversified independently among the three species, as shown for the opcA gene . During the diversification, the meningococcal ggt gene has been maintained in an active state while the gonococcal ggh gene has been reconstructed by insertion, deletion and substitutions, resulting in the translational inactivation. In N. lactamica, the ggt and opcA homologues might have been lost because of their dispensability for N. lactamica (see below).
It is also interesting that the ggh gene has not been fully deleted from the gonococcal genome. The kinds and sites of mutations in the ggh genes are relatively few and highly conserved, respectively, among the gonococcal isolates (Figure 2B, Table 2 and additional file). It is also noted that, while in general the RNA polymerase-binding sites and SD regions of pseudogenes are highly degraded, there are also a few exceptions in species such as Y. pestis that could have emerged in recent evolutionary times . Since the ribosome-binding sites (Shine-Dalgarno regions) of the gonococcal ggh gene are identical to those of the meningococcal ggt gene and the RNA polymerase-binding sites are almost completely conserved (with a one-nucleotide difference) (Figure 5D), it is speculated that the reconstruction of the ggh gene may have occurred in relatively recent evolutionary times. From the evolutional viewpoint, the drastic deletion of the approximately 2-kb DNA region containing the ggh gene in N. gonorrhoeae may not have been likely to occur in such a short period. Alternatively, deletion of the 2-kb DNA region may not be more advantageous for gonococcal evolution than reconstruction involving short deletions, insertions and substitutions.
The maintenance of a functional ggt gene in N. meningitidis would have some advantages for its survival. N. meningitidis causes meningitis, which is due to the meningococcal invasion into the human central nervous system, including cerebrospinal fluid (CSF) [36–38]. It has been shown that meningococcal GGT has a physiological function of acquiring cysteine from environmental γ-glutamyl-cysteinyl peptides under cysteine-limited environments such as the CSF . Almost all (98.8 %) meningococcal isolates from humans are positive for GGT activity . All of these results suggest that the GGT activity is important for N. meningitidis but not for N. gonorrhoeae. The dispensability of GGT activity for N. gonorrhoeae seems to be consistent with the fact that a cysteine-limited milieu such as the CSF in humans is not a natural gonococcal habitat. However, it is not very likely that the milieu of CSF exerts selective pressure for an active ggt gene because human CSF is not a relevant milieu for human-to-human spread of meningococcus . We believe that the meningococcal GGT must have some unknown essential function(s) for N. meningitidis and further studies will elucidate the function(s).
Our data on the ggh gene indicate that the ggh gene in N. gonorrhoeae is a pseudogene of the functional ggt gene in N. meningitidis. To our knowledge, the ggh gene is the first reported bacterial pseudogene that is transcriptionally active but phenotypically silent. Our findings may also contribute to understanding the speciation of N. meningitidis and N. gonorrhoeae.
Bacterial strains and growth conditions
Seven N. meningitidis strains (H44/76, H114/90, 2996, NIID68, NIID76, NIID413 and NIID414) were described in our previous reports [42, 43]. Ten N. gonorrhoeae strains (NIID54, NIID102, NIID103, NIID104, NIID105, NIID106, NIID107, NIID108, NIID109 and NIID111), one N. mucosa strain (NIID16) and one N. sicca strain (NIID17) were clinical isolates donated by T. Kuroki and Y. Watanabe. All of the clinical strains were mutually independent: they were isolated in different periods and from different persons who lived in different areas of Japan. The following 7 neisserial strains were obtained from ATCC (species / ATCC no.): N. gonorrhoeae / ATCC49226; N. lactamica / ATCC23970; N. flavescence / ATCC13120; N. denitrificans / ATCC14686; N. elongata / ATCC25295; N. canis / ATCC14687; N. cinerea / ATCC14685. All of the strains were stored by the gelatin disc method  and cultivated on GC agar (Becton-Dickinson) supplemented with 1 % IsovitaleX enrichment (Becton-Dickinson) at 37°C in 5 % CO2, or in GC broth (1.5 % proteose-peptone, 0.5 % NaCl, 0.05 % soluble starch, 0.1 % K2HPO4, 0.4 % KH2PO4, 1 % IsoVitaleX, 5 mM NaHCO3 10 mM MgCl2) at 37°C with shaking.
Isolation of chromosomal DNA, PCR, Southern blotting and dot blotting
Isolation of chromosomal DNA, PCR, Southern blotting and dot blotting were performed as described in our previous report .
Nucleotide sequence determination and analyses
Oligonucleotides used in this study
Primers for the sequencing of ggt and ggh genes, and RT-PCR (for ggt-9 and ggt-10)
Position in sequence
Primers for RT-PCR
Primer for primer extension
GTATTAACCTTACCTTGATTGGCATG (Biotin-labeled at the 5'-terminus)
Construction of Δggh::spc N. gonorrhoeae mutants
HT1195 (NIID103 Δggh::spc) and HT1196 (NIID106 Δggh::spc), in which a spectinomycin resistance gene (spc) was inserted into the ggh gene, were constructed as follows: A 2-kb fragment containing the ggh gene of NIID103 or NIID106 was amplified by PCR and cloned in the Sma I site of pUC18 (Takara Bio) to construct pHT412 or pHT413, respectively. A blunted 1-kb fragment containing the spc gene  was inserted into the Eco RV sites of pHT412 and pHT413, respectively. The Eco RV sites are located at 277 bp and 1642 bp (NIID103 [DDBJ:AB175025]) and at 271 bp and 1590 bp (NIID106 [DDBJ:AB175027]) downstream from the transcriptional start point of each ggh gene, respectively (see Figure 5D). The resulting plasmids were named pHT414 and pHT415, respectively. Five hundred nanograms of the plasmids linearized by digestion with Eco RI were transformed into NIID103 and NIID106, respectively, as described previously . Spectinomycin-resistant clones were selected on GC agar plates containing 75 μg/ml spectinomycin. The resulting mutants were isolated as Δggh::spc NIID103 (HT1195), and Δggh::spc NIID106 (HT1196), respectively. The allelic exchange was confirmed by PCR and Southern blotting.
Bacteria grown on GC agar plates were suspended in 20 ml of GC broth to an OD600 of 0.1 and continuously cultured to mid-log phase (OD600 of ~ 0.6) at 37°C with shaking. The total RNA was isolated from the harvested bacteria as previously described  with an additional treatment with DNase I. RT-PCR was performed using one step RT-PCR Kit Ver. 1.1 (Takara Bio, Japan) with approximately 2 μg of total RNA according to the manufacturer's instructions. The products were visualized by electrophoresis in a 2 % agarose gel followed by ethidium bromide staining.
Primer extension analysis
Fifty micrograms of total RNA and 5 pmol of biotin-labeled primer (ggt-ext-2) were hybridized in 20 μl of buffer (10 mM Tris-HCl, pH 8.0, 1 mM EDTA, 250 mM KCl). The hybridized RNA-DNA probe was treated with 35 units of AMV reverse transcriptase (RTase) XL (Takara Bio) in a reaction mixture (250 μM dNTPs, 1 × AMV reverse transcriptase XL buffer) at 37°C for 30 min. The ethanol-precipitated DNA product was dissolved in 20 μl of formamide dye (80 % formamide, 10 mM NaOH, 1 mM EDTA, 0.025 % bromophenol blue, 0.025 % xylene cyanol). Sequencing of the ggt and ggh genes with the ggt-ext-2 primer was performed by using ΔTh polymerase sequencing high -cycle- (TOYOBO, Japan). Aliquots of the reaction products were analyzed by electrophoresis on 8 % acrylamide-7 M urea gel followed by capillary blotting to Hybond-N+ (Amersham). The bands were visualized with Imaging high (TOYOBO) according to the manufacturer's protocol.
SDS-PAGE and Western blotting
SDS-PAGE and Western blotting were performed as described previously  using 1 × 103-fold diluted anti-GGT polyclonal rabbit antiserum  and 2 × 103-fold diluted horseradish peroxidase-conjugated secondary antibody (Amersham)
open reading frame
We thank T. Kuroki and Y. Watanabe for donating neisserial clinical isolates. The data from the gonococcal genome sequencing project at the University of Oklahoma  and the genome sequence of Neisseria lactamica at the Sanger Institute are gratefully acknowledged. The N. lactamica genome sequence was generated by the Sanger Institute Pathogen Sequencing Unit . This work was supported by grants from the Ministry of Health, Labor and Welfare of Japan and from the Ministry of Education, Culture, Sports, Science and Technology of Japan (Grant no. 13770142 and 16790265).
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