- Research article
- Open Access
Conservation of intron and intein insertion sites: implications for life histories of parasitic genetic elements
BMC Evolutionary Biology volume 9, Article number: 303 (2009)
Inteins and introns are genetic elements that are removed from proteins and RNA after translation or transcription, respectively. Previous studies have suggested that these genetic elements are found in conserved parts of the host protein. To our knowledge this type of analysis has not been done for group II introns residing within a gene. Here we provide quantitative statistical support from an analyses of proteins that host inteins, group I introns, group II introns and spliceosomal introns across all three domains of life.
To determine whether or not inteins, group I, group II, and spliceosomal introns are found preferentially in conserved regions of their respective host protein, conservation profiles were generated and intein and intron positions were mapped to the profiles. Fisher's combined probability test was used to determine the significance of the distribution of insertion sites across the conservation profile for each protein. For a subset of studied proteins, the conservation profile and insertion positions were mapped to protein structures to determine if the insertion sites correlate to regions of functional activity. All inteins and most group I introns were found to be preferentially located within conserved regions; in contrast, a bacterial intein-like protein, group II and spliceosomal introns did not show a preference for conserved sites.
These findings demonstrate that inteins and group I introns are found preferentially in conserved regions of their respective host proteins. Homing endonucleases are often located within inteins and group I introns and these may facilitate mobility to conserved regions. Insertion at these conserved positions decreases the chance of elimination, and slows deletion of the elements, since removal of the elements has to be precise as not to disrupt the function of the protein. Furthermore, functional constrains on the targeted site make it more difficult for hosts to evolve immunity to the homing endonuclease. Therefore, these elements will better survive and propagate as molecular parasites in conserved sites. In contrast, spliceosomal introns and group II introns do not show significant preference for conserved sites and appear to have adopted a different strategy to evade loss.
Inteins are intervening polypeptide sequences that are translated as part of a protein [1–4], and are removed in the maturation of the final protein product. Some inteins contain a homing endonuclease  that has a large specific recognition site (12-40 base pairs). The intein-encoding DNA is inserted in frame within a host gene; after translation the intein catalyzes its own excision resulting in removal of the intein (internal protein) and splicing of the extein (external protein, the mature active host protein) (see  for detailed review) [2, 7, 8]. Comparative analyses have shown that all inteins are homologs; however, their sequences are so divergent that phylogenetic analyses of inteins inserted into different host proteins remains largely unresolved [4, 9]. Inteins that are found in different insertion sites of the same host protein are not necessarily closely related to each other, and often highly divergent. However, inteins inserted into the same site in orthologous proteins are closely related to each other and share a common ancestor, but their molecular phylogeny does not always reflect the history of the host protein or of the host organism [4, 10, 11], indicating transfer of the intein between divergent hosts.
Introns are defined as non-coding regions of a gene that are excised during post-transcriptional processing. Since their discovery in 1977  three major groups of introns have been identified: group I, group II, and spliceosomal introns. Group I and group II introns have distinct structures that facilitate their self-splicing activity (see [13, 14] for detailed review), and they often encode an open reading frame (ORF) or contain an internal ORF [15–17]. The internal ORF of the group I introns encodes a homing endonuclease and the ORF of the group II introns encodes proteins with one to four of the following functionally defined domains: reverse transcriptase (RT), maturase, DNA-binding protein, and endonuclease [17, 18]. These proteins serve two functions for the intron: assisting in splicing and folding, and allowing the intron to act as a mobile element and invade intron-free alleles via retrohoming or retrotransposition [13, 17–19].
Endonucleases  provide mobility to some inteins and introns, through a process called "homing" [15, 16, 20]. These endonucleases are known as homing endonucleases (HE). The HEs initiate homing by cleaving the HE free allele. Similar to traditional restriction endonucleases, the HE makes a double strand break, and the HE containing element is copied during repair into the intein/intron free allele . The HE recognition site is accessible in the host gene when flanking regions of the intron or intein integration sites are joined. Presence of the HE containing element makes the allele resistant to HE digestion. Free-standing HE genes also function as molecular parasites/symbionts [21–24], and can provide mobility for neighbouring HE-less group I introns through a collaborative homing mechanism .
Previous work found inteins and group I introns in conserved parts of their host genes [4, 25–27], while group II introns were shown not to target conserved genes [28, 29]. Here we provide quantitative support and extend previous analyses to other proteins that host inteins, group I, group II and spliceosomal introns across all three domains of life.
Where are inteins and spliceosomal introns located in their host sequence and structure?
Our earlier analyses of three host proteins, ATPase catalytic subunit, replication factor C (RFC), and cell division control protein 21 (CDC21), confirmed the notion that inteins appear at highly conserved sites within their host proteins . Since publication of  the number of inteins discovered in these three proteins has increased substantially, including some found in new insertion sites.
The vacuolar ATPase catalytic subunit hosts both inteins and spliceosomal introns in two intein insertion sites, "a" and "b". We find that these insertion sites are among the most conserved sites in the protein (p = 0.0099). The intein database InBase  lists 27 inteins in insertion site "a" and seven in insertion site "b" (Figure 1). Inteins in insertion site "a" are found in members of the Saccharomycetales and inteins in insertion site "b" are found in two orders of euryarchaeotes (Thermoplasmatales and Thermococcales) (Figure 1). The archaeal inteins are located 20 amino acids downstream of where the yeast inteins are located. The spliceosomal introns in this protein are not restricted to conserved sites (p = 0.3909). Inteins in positions "a" and "b" are mapped to the structure of the ATPase catalytic subunit of Pyrococcus horikoshii OT3 (Figure 1B). This mapping shows that both inteins are located in the conserved catalytic binding site of the subunit , suggesting that the presence of the intein prior to removal would disrupt catalytic activity of the subunit.
The replication factor C (RFC) is less than 300 amino acids long, but accommodates inteins in three different sites (a-c) and spliceosomal introns in 10 different sites (Figure 2). InBase  reports 10 inteins located in these insertion sites; six in insertion site "a", two in insertion site "b" and two in insertion site "c" (Figure 2). The three insertions sites are among the most conserved parts of the host protein (p = 0.0209); and mapping of these sites on the structure of a RFC confirms that these sites are in conserved and centrally located regions of the protein. The 10 spliceosomal introns are not found to be in conserved sites of the protein (p = 0.2404).
The intein database currently list 16 inteins located in the CDC21 protein from nine various archaeal species. These inteins are found in three different sites: six are found in location "a", five in location "b", and three in location "c". Similar to the inteins found in the ATPase catalytic subunit and RFC, these inteins are found in highly conserved sites of the CDC21 protein (p = 0.0022) (Figure 3).
In addition, we analyzed all proteins that were reported in InBase  as containing an intein for conservation of the insertion site. With one exception all of these additional 30 proteins harbor their inteins in conserved regions of the respective host protein. The fillamentous hemmagglutinin protein was annotated by InBase as being an allele for an intein; however, this element has been shown to be a bacterial intein-like protein domain (BIL) . BILs are found in non-conserved regions of hypervariable proteins and our analysis supports this notion as the BIL was not found to be in a conserved site. (See additional file 1 for profiles and p-values.) Using Fisher's combined probability method to calculate the overall significance level for inteins (omitting the BIL) inserting into conserved sites is p < 0.0001 (in calculating the combined probability, p-values for individual proteins p < 0.01 were considered as equal to 0.01).
Where are group I and group II introns located in their host sequence and structure?
We analyzed intron insertion positions for DNA polymerase I and cytochrome C oxidase subunit I. Analysis of group I introns containing HE ORFs indicated that, similar to inteins, these elements tend to target conserved sites of their host protein. The DNA polymerase I of Bacillus phage SPO1 contains a group I intron , which is found in a conserved site of the host protein (p = 0.022) (Figure 4).
The cytochrome C oxidase subunit I (cox1) gene found in the mitochondria of eukaryotes accommodates self-splicing group I and group II introns in more than forty different sites (See additional file 2 for intron insertion sites.). The number of introns found in different species varies. The cox1 gene of Podospora anserine, an ascomycete fungus, is more than 24 kb long and harbours 14 group I and two group II introns . In Saccharomyces cerevisiae different strains host a total of six group I and three group II introns [18, 35, 36]. Similar to inteins, group I introns appear to target more conserved sites (p = 0.0003), and similar to spliceosomal introns, group II introns were found not to have a significant preference for conserved sites (p = 0.4176).
A linear regression analysis was performed to determine if there is a correlation between the number of fungal species that harbour the introns in a particular site and the conservation of the intron insertion site. A weak negative correlation between site conservation and number of species with group I introns is found at each site (p = 0.0609), while there is no correlation between site conservation and number of species with group II introns at each site (p = 0.2907). These findings suggest that for fungi, either group I introns tend to target conserved DNA sites more frequently, or group I introns survive in conserved sites for longer periods of time, while group II intron targeting is not strongly influenced by site conservation.
An additional eight proteins which host group I and group II introns were analyzed. These represent all protein families reported in the comparative RNA web site database  as containing group I and group II introns. These proteins followed a similar pattern where the group I introns showed a strong preference for conserved sites and the group II introns did not. Two exceptions were Chlorophyll alpha apoprotein A2 and NADH dehydrogenase subunit 3 where neither intron type showed a preference for conserved sites (See additional file 1 for p-values and profiles.).
One of the group I introns in the cox1 gene is present in mitochondrial genomes of several vascular plants [38, 39]. This intron, which encodes a homing endonuclease, seems to have been recently acquired via horizontal transfer from a fungal donor . Our analyses showed that this intron is found in the most conserved site of the host protein (figure 5). The conservation of this site likely has played a crucial role in the successful transfer, allowing for HE target site recognition thereby facilitating the transfer of the intron between these distantly related organisms. In addition to vascular plants and fungi, many other eukaryotes host this intron, including the green algae Marchantia, Chara, and Prototheca, the liverworts Pellia, the soil-living amoeba Dictyostelium, and the single-celled protist Monosiga (see additional File 2).
The combined significance levels for group I and group II introns targeting conserved sites is p < 0.0001 and p = 0.49, respectively.
Introns have played a role in gene and genome evolution ; most or all of them may be later invaders of the genes in which they are currently located . Interesting questions remain regarding the origin and evolution of introns, including: (1) How often did they arise? (2) How are they transmitted between divergent species? (3) How has their activity been maintained by natural selection? [16, 17, 20, 42–44].
Regardless of their origin, many of the extant introns and inteins, especially the ones utilizing homing for survival, can be considered molecular parasites [20, 45, 46]. Some of these molecular parasites have acquired additional roles that are adaptive to the host [20, 45, 46]. While we discuss HE genes and self-splicing elements as molecular parasites that have their own life-cycles, this does not negate the fact that many of these elements adapted to play a beneficial or at least a necessary role for their host , and these roles may play a role in the long term survival of these elements .
In accordance with other studies [4, 25, 26], we find that inteins and group I introns are found in conserved regions of their respective host proteins. This same trend was also seen for 37 other protein families that host inteins and group I introns (see additional file 1). We also find that group I introns within highly conserved positions are more likely to be found in a broader range of species of fungi. Group II introns, BILs and spliceosomal introns do not reveal a significant bias toward conserved sites.
The splicing elements utilize a small portion of the flanking extein/exon region for splicing. Inteins are inserted before one of the following amino acids in the host protein: C, S, or T . The amino acid is required to complete the self-splicing reaction. For the group I intron an internal guide sequence binds to 6 - 12 nucleotides of the exon. This internal guide sequence is not conserved between different group I introns and exact base pairing between the guide sequence and exon is not required . Similarly, in the case of the group II introns two exon binding sites of the intron interact with six or more nucleotides each at the 5' and 3' flanking exon [13, 49]. For both group I and group II introns this base pairing between intron internal sequence and the flanking exon restricts the possible sites in which an individual intron can retain its splicing activity. However, this does not restrict the locations of the introns as a group, because most mutations in the exon binding sites change the site specificity without impacting catalytic activity. Therefore, the splicing mechanism can be ruled out as a reason group I introns are found in conserved sites at the amino acid level. Exon splicing enhancer and silencer nucleotide motifs have been characterized surrounding individual spliceosomal introns [50, 51]. In the case of spliceosomal introns these requirements for exon sequence motifs surrounding the intron have not led to a detectable preference of insertion sites that are conserved at the amino acid level.
Parasitic elements have likely evolved two different strategies to propagate and survive. Inteins and group I introns utilize homing endonucleases to target conserved sites. Conserved sites tend to be in functionally important; consequently, precise excision of the intein or group I intron is required to maintain functionality of the protein. Furthermore, the functional importance of the residues limits the range of substitutions that can modify the target sequence so that it no longer is recognized by the homing endonuclease. Although group I intron and intein insertions are targeted to a DNA sequence, this is merely a proxy for sequence conservation at the protein level, upon which purifying selection can act. Targeting conserved sites will also facilitate transfer of the intein or group I intron to new intron-less alleles, as they will likely contain near identical amino acid sequences in these regions. In contrast, group II introns use a more random and less specific retrohoming or retrotransposition mechanism (see  for review). This suggests an alternative strategy evolved by these elements, relying on frequent propagation to outpace more rapid loss. If group II introns are the ancestor of spliceosomal introns [28, 53], it would not be unexpected to find a similar site preference for group II and spliceosomal introns.
Both of these strategies have successfully ensured the survival and propagation of inteins, and group I and group II introns [15, 18, 20]. These genetic elements can be considered molecular parasites that have their own life cycle, only occasionally evolving functions that contribute to the fitness of the host organism, or that increase the complexity of the host in an irreversible manner, without necessarily increasing the host's fitness [47, 54].
In most eukaryotes the coxI gene (encoding cytochrome C oxidase subunit I) is found in the mitochondrion, and hosts many introns representing both group I and group II introns. Several studies provide evidence for horizontal gene transfer of this element between distantly related groups of eukaryotes, confirming an intron homing model of evolution [38, 55, 56].
As shown in figure 5, the cox1 gene introns were found in both conserved and variable regions of the host; however, introns that are found in numerous species are more often found in highly conserved sites. The only group I intron found in the cox1 gene of several vascular plants  is inserted in the most conserved site of the host protein. The intron present in plants was reportedly acquired from a fungal donor . As the conservation of the insertion site is the key for homing process, the observed preference for conserved sites may reflect the mode of propagation of the group I introns.
It is possible that inteins and group I introns target all sites but only the ones that end up in a conserved site are retained. The two exceptional proteins in this study, NADH dehydrogenase subunit 3 and Chlorophyll alpha apoprotein A2, may be an example of this. This mechanism would result in a preference for conserved sites even in the absence of a site specific homing mechanism. Such independent preference for conserved sites may have caused splicing elements (introns and inteins) and homing endonucleases to target the same sites, resulting in the fusion of these elements . Free-standing HE genes are found in intergenic regions, their survival is dependent on the homing cycle [23, 24] and they might be more easily eliminated as compared to HE associated with self-splicing elements since their removal does not need to be precise. Upon fixation of the HE in the population, homing is no longer possible, because the HE is already present in all target sites. If the HE has not acquired another function that can create a selection pressure to maintain the HE gene, it is likely to decay and be lost .
The fact that BILs do not show a conserved site preference  suggests that the conserved site preference is associated with the life-cycle of the homing endonuclease containing molecular parasite. This life cycle was first formulated as a homing cycle involving movement of the molecular parasite across population or species boundaries [4, 59], but it has been suggested that this life cycle, with its succession of empty target sites, sites invaded by a molecular parasite with functioning homing endonuclease, sites containing a dysfunctional homing endonuclease, can operate within in spatially distributed population , and for some values of fitness reduction of individuals carrying molecular parasites may also operate continuously in homogenous well mixed populations . As discussed above, both the invasion phase and the deletion phase of life cycle may cause a conserved site preference. The targeting of a conserved site will make it more difficult for the host protein to evolve immunity towards the homing endonuclease, and it will make deletion of the molecular parasite more difficult.
The rate and tendencies to gain and lose introns vary considerably between lineages of eukaryotes [42, 43], with the number of spliceosomal introns per gene and the degree of sequence conservation at spliceosomal intron boundaries also varying greatly . Spliceosomal introns can be gained via homologous recombination with intron-containing genes unrelated to the conservation of the site, and through retrohoming [42, 62, 63]. The intron removal processes also appears to be unrelated to the sequence conservation at the insertion sites. The best characterized model for intron loss in multicellular eukaryotes is via homologous recombination between intron containing genes and spliced cDNAs produced by reverse transcription [42, 62, 63].
We have provided statistical support for the notion that inteins and group I introns target conserved protein sites for survival. This may also provide evidence for the homing cycle that describes the life cycle of these two molecular parasites. Furthermore, our findings suggest that group II and spliceosomal introns persist in their host genes using a different evolutionary strategy.
Construction of the Conservation Profiles
To calculate conservation profiles along a protein sequence, BLASTP  was used to detect homologous protein sequences from the NCBI protein database. Each dataset was aligned using the CLUSTALW program version 1.83 , and inspected for alignment accuracy.
To construct archaeal/vacuolar-type ATPase catalytic subunit A protein sequence alignments sequences from 29 Eukaryotic species, 13 Archaeal species, and four Bacterial species were aligned. Ten Archaeal species and fifteen Eukaryotic species were aligned to construct the Replication factor C protein sequence alignments. Nine Archaeal species and 21 Eukaryotic species were aligned to construct the cell division control protein 21 protein sequence alignment. Sequences from two Eukaryotic species, 18 Bacterial species and four phage sequences were used to construct the DNA polymerase I protein sequence alignments. 21 Eukaryotic species and nine Archaeal species were use for the Cytochrome C Oxidase Subunit I protein alignment. All other proteins found in the InBase database  (data retrieved November 2009) that host inteins were also analyzed. And all other proteins found in the comparative RNA web site database  (data retrieved November 2009) were analyzed for group I introns and group II introns positions. (See additional file 3 for accession numbers.)
The conservation profiles were calculated from the protein alignments using an in house PERL script (Olga Zhaxybayeva, Dalhousie University, see additional file 4). This program calculates the number of substitutions over a sliding window of 11 aligned positions and the window is moved through the alignment one position at a time. Inteins, introns, and sites where more than 50% of the sequences had a gap inserted into the alignment are omitted in the calculations. The lower the conservation score the more conserved the position is and the higher the conservation score the less conserved the positions is. These conservation scores for each protein were mapped on the protein structures using MacPyMOL .
For each protein, n individual intron/intein insertions were given a probability score (p) based on the probability of a random position within the conservation profile containing an equal or greater conservation score than that at the position of the intron/intein insertion. If the protein contained more than one of each parasitic element these probabilities were then combined for each protein using Fisher's combined probability test , resulting in an overall probability (p*) of intron/intein insertions being randomly distributed within each conservation profile. To show that no one kingdom overwhelmingly contributed to the significance of p* each kingdom was removed from the alignment and a new conservation profile was made and the Fisher's combined probability test was performed (see Table 1). To test the applicability of Fisher's combined probability test we calculated the combined probability for the insertion of the two inteins in VMA intein dataset by calculating the sum of the conservation scores for all possible window pairs. The probability of the sum of two randomly chosen windows having a sum conservation score greater than the two intein sites was p = 0.0063, compared to p = 0.0099 as determined by the Fisher's combined test statistic. This shows that the Fisher's combined test provides a conservative measure of significance for these analyses.
Simple linear regression was used to correlate site conservation with intron/intein penetrance (the number of species infected with a specific element). Significance was then calculated using standard methods based upon the resulting correlation coefficient (r), and the degrees of freedom in the sample (n-1).
Pietrokovski S: Intein spread and extinction in evolution. Trends Genet. 2001, 17 (8): 465-472. 10.1016/S0168-9525(01)02365-4.
Perler FB, Davis EO, Dean GE, Gimble FS, Jack WE, Neff N, Noren CJ, Thorner J, Belfort M: Protein splicing elements: inteins and exteins--a definition of terms and recommended nomenclature. Nucleic Acids Res. 1994, 22: 1125-1127. 10.1093/nar/22.7.1125.
Liu XQ: Protein-splicing intein: Genetic mobility, origin, and evolution. Annual review of genetics. 2000, 34: 61-76. 10.1146/annurev.genet.34.1.61.
Gogarten JP, Senejani AG, Zhaxybayeva O, Olendzenski L, Hilario E: Inteins: structure, function, and evolution. Annu Rev Microbiol. 2002, 56: 263-287. 10.1146/annurev.micro.56.012302.160741.
Chevalier BS, Stoddard BL: Homing endonucleases: structural and functional insight into the catalysts of intron/intein mobility. Nucleic acids research. 2001, 29: 3757-3774. 10.1093/nar/29.18.3757.
Saleh L, Perler FB: Protein splicing in cis and in trans. Chem Rec. 2006, 6 (4): 183-193. 10.1002/tcr.20082.
Hirata R, Ohsumk Y, Nakano A, Kawasaki H, Suzuki K, Anraku Y: Molecular structure of a gene, VMA1, encoding the catalytic subunit of H(+)-translocating adenosine triphosphatase from vacuolar membranes of Saccharomyces cerevisiae. The Journal of biological chemistry. 1990, 265 (12): 6726-6733.
Kane PM, Yamashiro CT, Wolczyk DF, Neff N, Goebl M, Stevens TH: Protein splicing converts the yeast TFP1 gene product to the 69-kD subunit of the vacuolar H(+)-adenosine triphosphatase. Science. 1990, 250 (4981): 651-657. 10.1126/science.2146742.
Perler FB, Olsen GJ, Adam E: Compilation and analysis of intein sequences. Nucleic Acids Res. 1997, 25 (6): 1087-1093. 10.1093/nar/25.6.1087.
Koufopanou V, Goddard MR, Burt A: Adaptation for Horizontal Transfer in a Homing Endonuclease. Mol Biol Evol. 2002, 19 (3): 239-246.
Senejani AG, Hilario E, Gogarten JP: The intein of the Thermoplasma A-ATPase A subunit: Structure, evolution and expression in E. coli. BMC Biochem. 2001, 2 (1): 13-10.1186/1471-2091-2-13.
Sambrook J: Adenovirus amazes at Cold Spring Harbor. Nature. 1977, 268 (5616): 101-104. 10.1038/268101a0.
Lambowitz AM, Zimmerly S: Mobile group II introns. Annu Rev Genet. 2004, 38: 1-35. 10.1146/annurev.genet.38.072902.091600.
Haugen P, Simon DM, Bhattacharya D: The natural history of group I introns. Trends Genet. 2005, 21 (2): 111-119. 10.1016/j.tig.2004.12.007.
Chevalier BS, Stoddard BL: Homing endonucleases: structural and functional insight into the catalysts of intron/intein mobility. Nucleic acids research. 2001, 29 (18): 3757-3774. 10.1093/nar/29.18.3757.
Dujon B: Group I introns as mobile genetic elements: facts and mechanistic speculations--a review. Gene. 1989, 82 (1): 91-114. 10.1016/0378-1119(89)90034-6.
Robart AR, Zimmerly S: Group II intron retroelements: function and diversity. Cytogenetic and genome research. 2005, 110 (1-4): 589-597. 10.1159/000084992.
Belfort M, Roberts RJ: Homing endonucleases: keeping the house in order. Nucleic Acids Res. 1997, 25 (17): 3379-3388. 10.1093/nar/25.17.3379.
Coros CJ, Landthaler M, Piazza CL, Beauregard A, Esposito D, Perutka J, Lambowitz AM, Belfort M: Retrotransposition strategies of the Lactococcus lactis Ll.LtrB group II intron are dictated by host identity and cellular environment. Mol Microbiol. 2005, 56 (2): 509-524. 10.1111/j.1365-2958.2005.04554.x.
Gogarten JP, Hilario E: Inteins, introns, and homing endonucleases: recent revelations about the life cycle of parasitic genetic elements. BMC Evol Biol. 2006, 6: 94-10.1186/1471-2148-6-94.
Liu Q, Belle A, Shub DA, Belfort M, Edgell DR: SegG endonuclease promotes marker exclusion and mediates co-conversion from a distant cleavage site. J Mol Biol. 2003, 334 (1): 13-23. 10.1016/j.jmb.2003.09.027.
Friedrich NC, Torrents E, Gibb EA, Sahlin M, Sjoberg BM, Edgell DR: Insertion of a homing endonuclease creates a genes-in-pieces ribonucleotide reductase that retains function. Proc Natl Acad Sci USA. 2007, 104 (15): 6176-6181. 10.1073/pnas.0609915104.
Bonocora RP, Shub DA: A likely pathway for formation of mobile group I introns. Curr Biol. 2009, 19 (3): 223-228. 10.1016/j.cub.2009.01.033.
Zeng Q, Bonocora RP, Shub DA: A free-standing homing endonuclease targets an intron insertion site in the psbA gene of cyanophages. Curr Biol. 2009, 19 (3): 218-222. 10.1016/j.cub.2008.11.069.
Goodwin TJ, Butler MI, Poulter RT: Multiple, non-allelic, intein-coding sequences in eukaryotic RNA polymerase genes. BMC Biol. 2006, 4: 38-10.1186/1741-7007-4-38.
Lazarevic V: Ribonucleotide reductase genes of Bacillus prophages: a refuge to introns and intein coding sequences. Nucleic Acids Res. 2001, 29 (15): 3212-3218. 10.1093/nar/29.15.3212.
Sandegren L, Sjoberg BM: Distribution, sequence homology, and homing of group I introns among T-even-like bacteriophages: evidence for recent transfer of old introns. J Biol Chem. 2004, 279 (21): 22218-22227. 10.1074/jbc.M400929200.
Dai L, Zimmerly S: Compilation and analysis of group II intron insertions in bacterial genomes: evidence for retroelement behavior. Nucleic Acids Res. 2002, 30 (5): 1091-1102. 10.1093/nar/30.5.1091.
Toro N: Bacteria and Archaea Group II introns: additional mobile genetic elements in the environment. Environ Microbiol. 2003, 5 (3): 143-151. 10.1046/j.1462-2920.2003.00398.x.
Perler FB: InBase: the Intein Database. Nucleic acids research. 2002, 30 (1): 383-384. 10.1093/nar/30.1.383.
Abrahams JP, Leslie AG, Lutter R, Walker JE: Structure at 2.8 A resolution of F1-ATPase from bovine heart mitochondria. Nature. 1994, 370 (6491): 621-628. 10.1038/370621a0.
Amitai G, Belenkiy O, Dassa B, Shainskaya A, Pietrokovski S: Distribution and function of new bacterial intein-like protein domains. Mol Microbiol. 2003, 47 (1): 61-73. 10.1046/j.1365-2958.2003.03283.x.
Goodrich-Blair H, Scarlato V, Gott JM, Xu MQ, Shub DA: A self-splicing group I intron in the DNA polymerase gene of Bacillus subtilis bacteriophage SPO1. Cell. 1990, 63 (2): 417-424. 10.1016/0092-8674(90)90174-D.
Cummings DJ, Michel F, McNally KL: DNA sequence analysis of the 24.5 kilobase pair cytochrome oxidase subunit I mitochondrial gene from Podospora anserina: a gene with sixteen introns. Curr Genet. 1989, 16 (5-6): 381-406. 10.1007/BF00340719.
Bonitz SG, Coruzzi G, Thalenfeld BE, Tzagoloff A, Macino G: Assembly of the mitochondrial membrane system. Structure and nucleotide sequence of the gene coding for subunit 1 of yeast cytochrme oxidase. J Biol Chem. 1980, 255 (24): 11927-11941.
Wenzlau JM, Saldanha RJ, Butow RA, Perlman PS: A latent intron-encoded maturase is also an endonuclease needed for intron mobility. Cell. 1989, 56 (3): 421-430. 10.1016/0092-8674(89)90245-6.
Cannone JJ, Subramanian S, Schnare MN, Collett JR, D'Souza LM, Du Y, Feng B, Lin N, Madabusi LV, Muller KM, et al: The comparative RNA web (CRW) site: an online database of comparative sequence and structure information for ribosomal, intron, and other RNAs. BMC Bioinformatics. 2002, 3: 2-10.1186/1471-2105-3-2.
Cho Y, Qiu YL, Kuhlman P, Palmer JD: Explosive invasion of plant mitochondria by a group I intron. Proc Natl Acad Sci USA. 1998, 95 (24): 14244-14249. 10.1073/pnas.95.24.14244.
Sanchez-Puerta MV, Cho Y, Mower JP, Alverson AJ, Palmer JD: Frequent, phylogenetically local horizontal transfer of the cox1 group I Intron in flowering plant mitochondria. Mol Biol Evol. 2008, 25 (8): 1762-1777. 10.1093/molbev/msn129.
Rodriguez-Trelles F, Tarrio R, Ayala FJ: Origins and evolution of spliceosomal introns. Annu Rev Genet. 2006, 40: 47-76. 10.1146/annurev.genet.40.110405.090625.
Qiu WG, Schisler N, Stoltzfus A: The evolutionary gain of spliceosomal introns: sequence and phase preferences. Mol Biol Evol. 2004, 21 (7): 1252-1263. 10.1093/molbev/msh120.
Jeffares DC, Mourier T, Penny D: The biology of intron gain and loss. Trends Genet. 2006, 22 (1): 16-22. 10.1016/j.tig.2005.10.006.
Roy SW, Gilbert W: The evolution of spliceosomal introns: patterns, puzzles and progress. Nat Rev Genet. 2006, 7 (3): 211-221.
Zhaxybayeva O, Gogarten JP: Spliceosomal introns: new insights into their evolution. Curr Biol. 2003, 13 (19): R764-766. 10.1016/j.cub.2003.09.017.
Cavalier-Smith T: Selfish DNA and the origin of introns. Nature. 1985, 315 (6017): 283-284. 10.1038/315283b0.
Koonin EV: The origin of introns and their role in eukaryogenesis: a compromise solution to the introns-early versus introns-late debate?. Biol Direct. 2006, 1: 22-10.1186/1745-6150-1-22.
Stoltzfus A: On the possibility of constructive neutral evolution. J Mol Evol. 1999, 49 (2): 169-181. 10.1007/PL00006540.
Davies RW, Waring RB, Ray JA, Brown TA, Scazzocchio C: Making ends meet: a model for RNA splicing in fungal mitochondria. Nature. 1982, 300 (5894): 719-724. 10.1038/300719a0.
Michel F, Ferat JL: Structure and activities of group II introns. Annu Rev Biochem. 1995, 64: 435-461. 10.1146/annurev.bi.64.070195.002251.
Cartegni L, Chew SL, Krainer AR: Listening to silence and understanding nonsense: exonic mutations that affect splicing. Nat Rev Genet. 2002, 3 (4): 285-298. 10.1038/nrg775.
Long JC, Caceres JF: The SR protein family of splicing factors: master regulators of gene expression. Biochem J. 2009, 417 (1): 15-27. 10.1042/BJ20081501.
Toro N, Jimenez-Zurdo JI, Garcia-Rodriguez FM: Bacterial group II introns: not just splicing. FEMS Microbiol Rev. 2007, 31 (3): 342-358. 10.1111/j.1574-6976.2007.00068.x.
Ichiyanagi K, Beauregard A, Belfort M: A bacterial group II intron favors retrotransposition into plasmid targets. Proc Natl Acad Sci USA. 2003, 100 (26): 15742-15747. 10.1073/pnas.2536659100.
Wu H, Hu Z, Liu XQ: Protein trans-splicing by a split intein encoded in a split DnaE gene of Synechocystis sp. PCC6803. Proceedings of the National Academy of Sciences of the United States of America. 1998, 95 (16): 9226-9231. 10.1073/pnas.95.16.9226.
Goddard MR, Leigh J, Roger AJ, Pemberton AJ: Invasion and persistence of a selfish gene in the cnidaria. PLoS ONE. 2006, 1: e3-10.1371/journal.pone.0000003.
Rot C, Goldfarb I, Ilan M, Huchon D: Putative cross-kingdom horizontal gene transfer in sponge (Porifera) mitochondria. BMC Evol Biol. 2006, 6: 71-10.1186/1471-2148-6-71.
Derbyshire V, Belfort M: Lightning strikes twice: intron-intein coincidence [comment]. Proceedings of the National Academy of Sciences of the United States of America. 1998, 95 (4): 1356-1357. 10.1073/pnas.95.4.1356.
Dori-Bachash M, Dassa B, Peleg O, Pineiro SA, Jurkevitch E, Pietrokovski S: Bacterial intein-like domains of predatory bacteria: a new domain type characterized in Bdellovibrio bacteriovorus. Funct Integr Genomics. 2009, 9 (2): 153-166. 10.1007/s10142-008-0106-7.
Goddard MR, Burt A: Recurrent invasion and extinction of a selfish gene. Proc Natl Acad Sci USA. 1999, 96 (24): 13880-13885. 10.1073/pnas.96.24.13880.
Yahara K, Fukuyo M, Sasaki A, Kobayashi I: Evolutionary maintenance of selfish homing endonuclease genes in the absence of horizontal transfer. Proc Natl Acad Sci USA. 2009, 106 (44): 18861-18866. 10.1073/pnas.0908404106.
Irimia M, Maeso I, Penny D, Garcia-Fernandez J, Roy SW: Rare coding sequence changes are consistent with Ecdysozoa, not Coelomata. Mol Biol Evol. 2007, 24 (8): 1604-1607. 10.1093/molbev/msm105.
Mourier T, Jeffares DC: Eukaryotic intron loss. Science. 2003, 300 (5624): 1393-10.1126/science.1080559.
Derr LK, Strathern JN: A role for reverse transcripts in gene conversion. Nature. 1993, 361 (6408): 170-173. 10.1038/361170a0.
Altschul SF, Madden TL, Schaffer AA, Zhang J, Zhang Z, Miller W, Lipman DJ: Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucleic Acids Res. 1997, 25 (17): 3389-3402. 10.1093/nar/25.17.3389.
Thompson JD, Gibson TJ, Plewniak F, Jeanmougin F, Higgins DG: The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acids Res. 1997, 25 (24): 4876-4882. 10.1093/nar/25.24.4876.
DeLano WL: The PyMOL Molecular Graphics System. 2008, [http://www.pymol.org]
Whitlock MC: Combining probability from independent tests: the weighted Z-method is superior to Fisher's approach. J Evol Biol. 2005, 18 (5): 1368-1373. 10.1111/j.1420-9101.2005.00917.x.
Maegawa Y, Morita H, Yao M, Watanabe N, Tanaka I: Crystallization and preliminary X-ray diffraction study of the catalytic subunit of archaeal H+ -transporting ATP synthase from Pyrococcus horikoshii OT3. Acta Crystallogr D Biol Crystallogr. 2004, 60 (Pt 8): 1484-1486. 10.1107/S0907444904014222.
Seybert A, Singleton MR, Cook N, Hall DR, Wigley DB: Communication between subunits within an archaeal clamp-loader complex. Embo J. 2006, 25 (10): 2209-2218. 10.1038/sj.emboj.7601093.
Beese LS, Derbyshire V, Steitz TA: Structure of DNA polymerase I Klenow fragment bound to duplex DNA. Science. 1993, 260 (5106): 352-355. 10.1126/science.8469987.
Harrenga A, Michel H: The cytochrome c oxidase from Paracoccus denitrificans does not change the metal center ligation upon reduction. J Biol Chem. 1999, 274 (47): 33296-33299. 10.1074/jbc.274.47.33296.
The authors thank Olga Zhaxybayeva for providing perl scripts. This work was supported in part by grants from the UConn Research Foundation and NASA Exobiology Program (NNX08AQ10G, NNX07AK15G, NNG05GN41G).
JPG conceived and supervised the study. KSS and AGS generated the conservation profiles and wrote the manuscript. KSS generated the protein mapping and performed all analyses reported in additional file 4. GPF performed the statistical analyses and wrote the methods for the analyses. All authors read and approved the final manuscript.
Electronic supplementary material
Additional file 1: Table of p-values and alignment profiles for additional 37 intein, group I or group II host proteins. Arrows point to intron or intein positions. Blue dots indicate intein positions, green dots group I intron positions, and orange dots group II intron positions. (PDF 2 MB)
Additional file 2: List of Introns found in Cytochrome C oxidase subunit I. The list contains all introns from species for which at least one of their cox1 gene introns were BLAST hits when introns from Podospora anserina (X55026) and Saccharomyces cerevisiae (V00694) cox1 genes were used as query sequences. (PDF 103 KB)
Additional file 3: Accession numbers for sequences used in protein alignment. Lists of accession numbers for each protein used for each conservation profile. (DOC 212 KB)
Additional file 4: Perl scripts used to calculate the conservation profiles. Perl scripts used to calculate conservation profiles. (ZIP 3 KB)
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Swithers, K.S., Senejani, A.G., Fournier, G.P. et al. Conservation of intron and intein insertion sites: implications for life histories of parasitic genetic elements. BMC Evol Biol 9, 303 (2009). https://doi.org/10.1186/1471-2148-9-303
- Insertion Site
- Host Protein
- Conservation Score
- NADH Dehydrogenase Subunit
- Homing Endonuclease