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Systematics and Evolution |
Microbial Collection and Screening Laboratory, Institute of Molecular and Cell Biology, 30 Medical Drive, Singapore 1176091
Author for correspondence: Yue Wang. Tel: +65 7783207. Fax: +65 7791117. e-mail: mcbwangy{at}imcb.nus.edu.sg
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ABSTRACT |
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 TOP ABSTRACT INTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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Keywords: complexity hypothesis, lateral gene transfer, mosaic gene, phylogeny, evolution
Abbreviations: LGT; lateral gene transfer
The GenBank accession numbers for the 23S rRNA sequences determined in this study are AF192136–AF192150.
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INTRODUCTION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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, 1998 ). rRNA sequence comparisons led to the construction of a ‘universal tree of life’, dividing all life on Earth into three equidistant domains: Eukarya, Bacteria and Archaea (Woese et al., 1990 ). It is believed that this tree provides the basis for a natural classification system of organisms. Recently, the availability of complete genome sequences of organisms representing the three domains has allowed biologists to use many other gene sets to verify the topology of the universal tree. Such analyses have frequently produced trees with branching patterns rather different from that of the universal tree (Woese, 1998 ; Doolittle, 1999 ). Sometimes organisms representing different domains were found intermixed (Woese, 1998 ). Currently, the popular explanation for this confusion is that a considerable fraction of the genome of any organism is the products of lateral gene transfer (LGT) (Doolittle, 1999 ). Lawrence & Ochman (1997 ) calculated that approximately 18% of the genome of Escherichia coli was acquired via LGT during the 100 million years after its divergence from the Salmonella lineage. Nelson et al. (1999 ) also reported that 24% of the genome of the bacterium Thermotoga maritima was introduced from Archaea. These numbers do not yet include genes whose origins have been obscured in the long process of amelioration after transfer or those that are from relatively closely related organisms (Lawrence & Ochman, 1997 ). With such a high intensity of LGT, one has to ask whether there is any gene that may still record faithfully the entire or a significant part of the evolutionary history of life. Analyses of different gene sets also revealed that not all genes are equally susceptible to LGT (Rivera et al., 1998 ; Jain et al., 1999 ). When genes are grouped according to biological functions, those involved in transcription, translation and DNA replication are seldom identified as products of LGT (Jain et al., 1999 ; Koonin et al., 1999 ; Nelson et al., 1999 ). In contrast, a considerable fraction of metabolic genes are believed to be laterally transferred. In the Thermotoga maritima genome, only six out of 124 translation-related genes exhibit higher similarities to Archaea than to Bacteria, while 92 out of 181 genes involved in electron transport are more closely related with Archaea than with Bacteria (Nelson et al., 1999 ). The hypothesis interpreting the greatly unequal probability of lateral transfer of genes with different functions is that the chance of successful transfer of a gene is inversely correlated with the complexity of interactions its product makes with other cellular components (Woese, 1998 ; Rivera et al., 1998 ; Jain et al., 1999 ). Jain et al. (1999 ) called this the ‘complexity hypothesis’. The rRNA genes may be among those least likely to be laterally transferred, because rRNAs must interact in a highly coordinated manner with more than 100 other gene products to form the ribosomes and carry out protein synthesis.
Although the complexity hypothesis is largely correct, it overlooks one important aspect of LGT: the gene is not the smallest unit of transfer. Sawyer (1989 ) deduced that the average units of LGT are DNA patches of 100–200 bp, suggesting that transfer of parts of genes is common in nature. When a gene is broken down to small pieces, the complexity will be greatly simplified. For example, a gene fragment encoding a domain, such as a hairpin of an rRNA molecule, may replace a corresponding region of the host gene via a single recombinational event. A new hairpin in an rRNA molecule may not be detrimental to the organism as long as the local secondary structure remains identical or similar (Gutell et al., 1994 ; Van de Peer et al., 1996 ; Asai et al., 1999 ). This process may occur repeatedly, involving different parts of a gene, leading to gradual changes of the nucleotide sequence. This ‘simplified complexity hypothesis’ predicts a mosaic nature for rRNA genes (as well as for other genes). Unlike the replacement of an entire gene, the step-by-step segmental replacement gradually obscures the evolutionary history documented in the nucleotide sequence. Although there have been previous reports of mosaic genes arising from local gene exchange between related bacterial species (Smith et al., 1991 ; Groisman et al., 1992 ), it is not clear whether and how frequently rRNA genes are affected by the lateral transfer of gene segments.
In this study, we investigated the distribution of nucleotide variations in the alignments of the 16S rDNA sequences of actinomycete species belonging to several well-defined genera. We frequently found the occurrence of two or three types of drastically different sequences in short and rather conserved regions of rRNA genes among species of the same genus. The nucleotide substitutions involve three to five base pairs of compensating covariations and are found within the stems of individual hairpins in the rRNA molecule. These observations strongly support our ‘simplified complexity hypothesis’ to explain how LGT may affect the highly conserved genes. We also demonstrate how this segmental gene transfer may lead to confusion in rDNA sequence-based phylogenetic analysis.
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METHODS |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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Preparation of genomic DNAs.
The genomic DNA of the actinomycetes was prepared as previously described (Wang et al., 1996 ).
PCR amplification, cloning and sequencing.
The 5' one-third of the 23S rRNA genes was amplified by PCR using a pair of primers, one targeting a conserved region at the end of the 16S rRNA gene and the other a conserved block within the 23S rRNA gene. The PCR product also includes the spacer region. The sequences of the two oligonucleotides are as follows: 5'-GGTTGGATCCACCTCCTT-3', corresponding to nt 1525–1542 of E. coli 16S rRNA (Brosius et al., 1978 ); and 5'-ACCAGTGAGCTATTAGCG-3' (nt 1090–1107). After the cloning of the PCR products, the M13 forward and reverse universal primers were used for sequencing the ends of each clone. The internal regions were sequenced in both orientations by using the following two sets of oligonucleotide primers targeting two conserved sequences within 23S rDNA. The first set of primers, targeting nt 45–60 of E. coli 23S rRNA gene, are 23S-40f (5'-CCGATGAAGGACGTGGGA-3') and 23S-40r (5'-TCCCACGTCCTTCATCGG-3'); and the second set of primers, targeting nt 456–472, are 23S-460f (5'-CCTTTCCCTCACGGTACT-3') and 23S-460r (5'-AGTACCGTGAGGGAAAGG-3').
Sequence alignment and phylogenetic analysis.
Multiple sequence alignment of the rRNA gene sequences was carried out by the CLUSTAL method of the DNASTAR program (DNASTAR, Inc.) and verified according to the consensus secondary structure model (Gutell et al., 1994 ). Phylogenetic trees were constructed by using both a distance method (Saitou & Nei, 1987 ) and a parsimony method (Swofford & Begle, 1993 ). The two methods generated very similar trees and only the neighbour-joining trees are shown in this paper. The confidence level of phylogenetic tree topology was evaluated by the bootstrap method (Felsenstein, 1985 ). The softwares for the tree construction and bootstrap analysis are contained in the CLUSTAL V (Higgins et al., 1992 ) and the PAUP (Swofford & Begle, 1993 ) phylogenetic analysis software packages.
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RESULTS |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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; Koch et al., 1996 ; Wang et al., 1996 ; Ward-Rainey et al., 1996 ; Rheims et al., 1998 ; Zhang et al., 1998 ). A 16S rDNA sequence alignment was generated for each genus for visual inspection. We focused our attention on regions that are normally quite conserved within a genus. In nearly all the sequence alignments short regions (20–70 bases) were found where the sequences could be divided into two or three distinct types differing at 6 to 10 positions (Fig. 1a). The pattern of base variations in these regions distinguished them from the random mutations occurring in the known highly variable regions. First, the base variations occurred in a short gene segment outside the known highly variable regions. Second, nearly all of the base variations are compensating covariations of paired bases corresponding to the stem of a hairpin in the 16S rRNA molecule (Fig. 1b). Third, besides the two or three distinct types of sequences, there are no other types of base changes in these regions that may represent the transitional states between the distinct types. For example, Actinomadura species have two types of sequences in an approximately 30 bp segment corresponding to nt 1301–1335 of E. coli rRNA (Fig. 1a). The two sequences differ at three pairs of positions, but no other sequence exists within the genus that has other base variations, indicating the insusceptibility of this region to random base changes. To determine whether sequences identical or highly similar to the different sequence variants are present in species of other taxa, we searched the database using the BLAST program and readily found such sequences (examples are shown below). In summary, the discovery of and all the properties displayed by the localized sequence variations in rRNA genes fulfil the predictions of the ‘simplified complexity hypothesis’.
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; Ward-Rainey et al., 1996 ; Zhang et al., 1998 ). The result of a partial 23S rDNA (
1200 bases, nt 1–1108 of E. coli numbering) sequence analysis conducted in this study largely confirms the phylogenetic integrity of each genus, but demonstrates significant discrepancy at the subgenus level. For example, Fig. 2 shows that the members of Nonomuraea form a very stable clade in both 16S and 23S rRNA trees. In the 16S rDNA tree, N. pusilla and N. ferruginea form one subclade with the deepest branch; and N. roseola, N. africana and N. recticatena form another subclade separated from the third containing the rest of the Nonomuraea species. However, drastically different species relationships are reconstructed in the 23S rRNA tree. To seek possible explanations for the observed discrepancy, we visually scanned the sequence alignments and found that the Nonomuraea species can be grouped by the sharing of covaried nucleotide substitutions involving 10 base pairs located in two stems within a short region (nt 587–753) in the 16S rRNA sequences. These base variations occur outside of the highly variable regions and their numbers are comparable to or even higher than those observed in these regions. The occurrence of a large number of non-random base variations in a rather stable region of the gene is most likely the consequence of lateral transfer of short segments of rRNA genes. Supporting this hypothesis, we found identical sequences matching each variation in species of other genera in the same family. These results are summarized in Fig. 3. Such a gene segment replacement is not expected to have much effect on the local and the overall secondary or tertiary structure of the rRNA and the function of ribosomes. According to the nucleotide variability map of 16S rRNA (Van de Peer et al., 1996 ), this region is highly conserved in secondary structure but variable in nucleotide sequences characterized largely by covariation of paired bases in the helices, indicating the importance of the secondary structure of this region for ribosomal function.
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. In the first tree (Fig. 4a), the 10 nucleotides nt 668–672 and 734–738 were excluded from all the sequences. The overall topology of this new tree is very similar to that of the tree shown in Fig. 2, except that the species cluster pattern within the Nonomuraea clade is significantly different. Although N. roseola, N. recticatena and N. africana still aggregate tightly, they are now placed among other Nonomuraea species. In the second tree (Fig. 4b), where nt 612–616 and 624–628 were excluded, the N. pusilla and N. ferruginea clade and the N. roseola, N. recticatena and N. africana clade switched positions in comparison with the tree shown in Fig. 2. The use of the maximum-parsimony method on the same sets of sequences also showed a similar change of cluster patterns of Nonomuraea species between different trees (trees not shown). Despite the fact that some species clusters are not supported by sufficiently high bootstrap values, this result nevertheless shows that the occurrence of such short stretches of varied nucleotide sequences will have a significant effect on the topology of the phylogenetic trees.
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). In addition, the approximately 1000 bp 16S rDNA fragments PCR-amplified by the pair of universal primers (PU5' and PU3'; Fig. 5) were cloned and five independent clones from each species picked for sequence analysis. Again, all the sequences from each species are identical except those from N. pusilla. Three sequences of N. pusilla were found differing between each pair at one or two positions (nt 1248 A or G, nt 1267 T or C, and nt 1296 G or C; E. coli numbering), which are outside of the regions of concern (alignment not shown).
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is the positions of two Streptosporangium species, S. corrugatum and S. claviforme. Independent of the outgroups used and whether the distance (neighbour-joining) or the parsimony (PAUP) method was employed for the tree construction, the two species have been consistently shown to aggregate with the Microtetraspora/Microbispora clade in the 16S rRNA tree and with Streptosporangium clade in the 23S rRNA tree. The phylogenetic associations of the two species shown in both trees are supported by high bootstrap values (877 and 878). Since multiple entries of nearly identical sequences from the same organisms are available in databases, the possibility of artefact sequences is excluded. Then, why do 16S and 23S rRNA genes, which are thought to be under the same level of functional constraints, give drastically contradictory organismal phylogenies? An inspection of the sequence alignments revealed that the 16S rDNA sequences of S. corrugatum and S. claviforme can be roughly divided into two halves, with the 5' half carrying nearly all the signatures characterizing Microbispora/Microtetraspora and the 3' half containing nucleotides specific to most Streptosporangium species (Fig. 6a). When two new trees were constructed by using the two halves of the 16S rRNA sequences separately, the two species were placed next to the Microbispora/Microtetraspora clade in the 5' tree, in contrast to a placement next to the Streptosporangium clade in the 3' tree (Fig. 6b). The position of the two Streptosporangium species in the 5' tree is supported by a high bootstrap value (990). The bootstrap value for the two species to cluster with Streptosporangium species in the 3' tree is lower (682), probably due to the presence of far fewer genus-specific nucleotides in this half of the sequence. Nevertheless, the relationship shown in the 3' tree is consistent with the result of the 23S rDNA analysis and also with the unifying morphological feature, namely the growth of sporangia by all Streptosporangium species. No species in other genera in the family Streptosporangiaceae grows sporangia. Why do the two halves of the 16S rRNA gene record conflicting evolutionary histories? The most plausible answer to this question is that the 16S rRNA genes of S. corrugatum and S. claviforme are mosaics of segments originating from different organisms. This could have happened to the two Streptosporangium species simply by replacing a region of the endogenous gene with a corresponding gene segment from a Microbispora species via a double crossover or gene conversion (Hillis et al., 1990 ; Syvanen, 1994 ). In fact, nearly all the signature nucleotides specific to Microbispora in the 16S rRNA genes of S. corrugatum and S. claviforme are localized in the region between nt 600 and 750 encoding two connected hairpins in the rRNA (see Figs 1b and 3 for location).
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DISCUSSION |
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TOPABSTRACTINTRODUCTIONMETHODSRESULTSDISCUSSIONREFERENCES |
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), is that genes are not equally susceptible to LGT; genes whose products must interact with multiple components in complex cellular systems are highly unlikely to be laterally transferred. The rRNA gene is perhaps the best example of this category of genes. Thus, a large part, if not the entire, evolutionary history of life may still be inferred by comparing these genes (Woese, 1998 ).
We initiated this study by hypothesizing that LGT might affect complex genes, such as rRNA genes, through gradual substitution of gene segments encoding individual domains. Though the overall structure and its interaction with other parts of the translation machinery are complex, an rRNA molecule consists of many hairpin structures, each of which may interact with only one or a few other components of the translation apparatus. In addition, it is well known that the secondary but not the primary structure of many hairpins in rRNA is essential for function (Gutell et al., 1994 ; Van de Peer et al., 1996 ). These two properties of rRNA molecules underscore the high possibility of the exchange of individual hairpins without damaging effect on the proper function of a ribosome. This view is supported by reports that an organism may have distinct types of rRNA genes with high levels of base variations throughout the entire gene (Gunderson et al., 1987 ; Mylvaganam & Dennis, 1992 ; Carranza et al., 1996 ; Wang et al., 1997 ; Yap et al., 1999 ). Niebel et al. (1987 ) demonstrated that the rRNA cistrons from Proteus vulgaris were expressed and the products correctly processed and assembled into ribosomes when transformed into E. coli. Recently, Asai et al. (1999 ) reported a complete exchange of rRNA genes between different bacterial species and replacement of a 23S rRNA gene segment of E. coli by the corresponding region of yeast. If a transgressed rRNA gene or gene segment brings to the recipient a beneficial property, such as antibiotic resistance (Green et al., 1997 ; Mankin, 1997 ), it will be kept and may eventually replace the endogenous gene(s) via gene conversion (Hillis et al., 1990 ). High levels of localized intergenic base variations corresponding to the stem of a hairpin have also been reported (Ueda et al., 1999 ; Yap & Wang, 1999 ). Ueda et al. (1999 ) found two types of base variations in the highly variable 
region of the 16S rRNA gene and suggested that both random mutation and LGT contribute to rRNA gene heterogeneity of a bacterium.
In this study, we found high levels of base variations localized to the stem of hairpins of rRNA molecules that seldom experience random mutations between species of the same genus or closely related genera. We propose that the LGT of gene segments is the most plausible explanation of this phenomenon. We observed this phenomenon in the 16S rRNA genes of almost all genera we examined, indicating that such events probably happen with considerable frequency in nature. Although it is difficult, if not impossible, to determine the donor of a transferred DNA fragment, identical or nearly identical sequences are always found in species often belonging to distantly related taxa. Introduction of a piece of foreign DNA will certainly corrupt the evolutionary history recorded in the affected gene, though the extent of damage will depend on the size and the number of changed bases of the region involved. In most cases we have investigated, the presence of sequence variations in one hairpin does not affect the stable aggregation in one clade of all the species of a genus, reflecting the overall evolutionary stability of 16S rRNA genes. At subgenus level, the pattern of species clustering may be affected by the presence of these localized sequence variations, as shown in the analysis of the 16S rDNA of Nonomuraea species. However, it is not clear whether the sharing of a short DNA sequence is a result of common ancestry, or whether the sequences were introduced in independent events. The cluster pattern of Nonomuraea species shown in the 16S rDNA trees, constructed by including or excluding the short regions of sequence variations, was not reproducible in the 23S rRNA tree. In the study of Streptosporangium species, we speculate that the lateral transfer of a larger DNA fragment encoding two adjacent hairpins was the likely cause of the confusion at genus level of the positions of S. corrugatum and S. claviforme in the 16S rRNA tree. Regardless of whether the 16S or the 23S tree is correct, the dramatically different positions of the two species in the two trees are unlikely to be the result of random mutational events.
Conclusion
Complementing the complexity hypothesis, the simplified complexity hypothesis suggests that due to the overall functional constraints, the lateral transfer of parts of genes is likely to be the main mode of LGT occurring to the genes encoding components of complex systems. This mode of LGT results in gradual corruption of the evolutionary history written in the nucleotide sequences. The rate of sequence corruption of a gene should be a function of the complexity of interactions with other cellular components by the gene product. Even highly conserved genes like rRNA genes may only roughly record part of the evolutionary history of life, though how far back is not known. There is probably an increasingly high restriction for successful transfer of gene segments with widening evolutionary distance, which may explain why the three-domain separation of life largely holds when proteins of the information-processing machinery are used to derive phylogeny (Woese, 1998 ; Jain et al., 1999 ). The results of this study caution that in bacterial taxonomy the effect of LGT on the result of sequence-based phylogenetic analysis should be considered. Analysis of more than one gene set together with the examination of major phenotypic characteristics should be practised in future. Given that LGT is well established, it is now important to identify the principles that govern gene distribution patterns across prokaryotic genomes to determine the values of genes of different functional groups in bacterial taxonomy.
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ACKNOWLEDGEMENTS |
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Received 8 February 2000;
revised 22 July 2000;
accepted 7 August 2000.
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P. van Berkum, Z. Terefework, L. Paulin, S. Suomalainen, K. Lindstrom, and B. D. Eardly Discordant Phylogenies within the rrn Loci of Rhizobia J. Bacteriol., May 15, 2003; 185(10): 2988 - 2998. [Abstract] [Full Text] [PDF]
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 J. P. Gogarten, W. F. Doolittle, and J. G. Lawrence Prokaryotic Evolution in Light of Gene Transfer Mol. Biol. Evol., December 1, 2002; 19(12): 2226 - 2238. [Abstract] [Full Text] [PDF]
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M. A. Parker, B. Lafay, J. J. Burdon, and P. van Berkum Conflicting phylogeographic patterns in rRNA and nifD indicate regionally restricted gene transfer in Bradyrhizobium Microbiology, August 1, 2002; 148(8): 2557 - 2565. [Abstract] [Full Text] [PDF]
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M. A. Parker Bradyrhizobia from Wild Phaseolus, Desmodium, and Macroptilium Species in Northern Mexico Appl. Envir. Microbiol., April 1, 2002; 68(4): 2044 - 2048. [Abstract] [Full Text] [PDF]
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C. Moreno, J. Romero, and R. T. Espejo Polymorphism in repeated 16S rRNA genes is a common property of type strains and environmental isolates of the genus Vibrio Microbiology, April 1, 2002; 148(4): 1233 - 1239. [Abstract] [Full Text] [PDF]
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M. W. Friedrich Phylogenetic Analysis Reveals Multiple Lateral Transfers of Adenosine-5'-Phosphosulfate Reductase Genes among Sulfate-Reducing Microorganisms J. Bacteriol., January 1, 2002; 184(1): 278 - 289. [Abstract] [Full Text] [PDF]
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P. J. Keeling and J. D. Palmer Lateral transfer at the gene and subgenic levels in the evolution of eukaryotic enolase PNAS, August 23, 2001; (2001) 191337098. [Abstract] [Full Text] [PDF]
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M. A. Parker Case of Localized Recombination in 23S rRNA Genes from Divergent Bradyrhizobium Lineages Associated with Neotropical Legumes Appl. Envir. Microbiol., May 1, 2001; 67(5): 2076 - 2082. [Abstract] [Full Text]
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P. J. Keeling and J. D. Palmer Lateral transfer at the gene and subgenic levels in the evolution of eukaryotic enolase PNAS, September 11, 2001; 98(19): 10745 - 10750. [Abstract] [Full Text] [P |
