- Open Access
Indications that "codon boundaries" are physico-chemically defined and that protein-folding information is contained in the redundant exon bases
© Biro; licensee BioMed Central Ltd. 2006
Received: 16 December 2005
Accepted: 07 August 2006
Published: 07 August 2006
All the information necessary for protein folding is supposed to be present in the amino acid sequence. It is still not possible to provide specific ab initio structure predictions by bioinformatical methods. It is suspected that additional folding information is present in protein coding nucleic acid sequences, but this is not represented by the known genetic code.
Nucleic acid subsequences comprising the 1st and/or 3rd codon residues in mRNAs express significantly higher free folding energy (FFE) than the subsequence containing only the 2nd residues (p < 0.0001, n = 81). This periodic FFE difference is not present in introns. It is therefore a specific physico-chemical characteristic of coding sequences and might contribute to unambiguous definition of codon boundaries during translation. The FFEs of the 1st and 3rd residues are additive, which suggests that these residues contain a significant number of complementary bases and that may contribute to selection for local RNA secondary structures in coding regions. This periodic, codon-related structure-formation of mRNAs indicates a connection between the structures of exons and the corresponding (translated) proteins. The folding energy dot plots of RNAs and the residue contact maps of the coded proteins are indeed similar. Residue contact statistics using 81 different protein structures confirmed that amino acids that are coded by partially reverse and complementary codons (Watson-Crick (WC) base pairs at the 1st and 3rd codon positions and translated in reverse orientation) are preferentially co-located in protein structures.
Exons are distinguished from introns, and codon boundaries are physico-chemically defined, by periodically distributed FFE differences between codon positions. There is a selection for local RNA secondary structures in coding regions and this nucleic acid structure resembles the folding profiles of the coded proteins. The preferentially (specifically) interacting amino acids are coded by partially complementary codons, which strongly supports the connection between mRNA and the corresponding protein structures and indicates that there is protein folding information in nucleic acids that is not present in the genetic code. This might suggest an additional explanation of codon redundancy.
The protein folding problem has been one of the grand challenges in computational molecular biology. The problem is to predict the native three-dimensional structure of a protein from its amino acid sequence. It is widely believed that the amino acid sequence contains all the information necessary to make up the correct three-dimensional structure, since protein folding is apparently thermodynamically determined; i.e., given a proper environment, a protein will fold up spontaneously. This is called Anfinsen's thermodynamic principle .
The thermodynamic principle has been confirmed many times on many different kinds of proteins in vitro. Critics says that the in vivo chemical conditions are different from those in vitro, the correct folding is determined by interactions with other molecules (chaperons, hormones, substrate, etc.) and protein folding is much more complex than re-naturation of denatured poly-amino acids. The fact that many naturally-occurring proteins fold reliably and quickly to their native state, despite the astronomical number of possible configurations, has come to be known as Levinthal's Paradox .
Anfinsen's principle was formulated in the 1960s using purely chemical experiments and a lot of intuition. Today, many sequences and structures are available to establish a logical and understandable link between sequence, structure and function. But it is still not possible to predict the structure (or a range of possible structures) correctly from the sequence alone, ab initio and in silico .
There are two potential, external sources of additional and specific protein folding information: (a) the chaperons (other proteins that assist in the folding of proteins and nucleic acids ; and (b) the protein-coding nucleic acid sequences themselves (which are templates for protein synthesis, but are not defined as chaperons).
The idea that the nucleotide sequence itself could modulate translation and hence affect co-translational folding and assembly of proteins has been investigated in a number of studies [5–7]. Studies on the relationships between synonymous codon usage and protein secondary structural units are especially popular [8–10]. The genetic code is redundant (61 codons code 20 amino acids) and as many as 6 synonymous codons can code the same amino acid (Arg, Leu, Ser). The "wobble" base has no effect on the meaning of most codons, but nevertheless codon usage (wobble usage) is not randomly defined [11, 12] and there are well-known, stable species-specific differences in codon usage. It seems logical to search for some meaning (biological purpose) for the wobble bases and try to associate them with protein folding.
Another observation concerning the code redundancy dilemma is that there is a widespread selection (preference) for local RNA secondary structure in protein coding regions . A given protein can be encoded by a large number of distinct mRNA species, potentially allowing mRNAs to optimize desirable RNA structural features simultaneously, in addition to their protein coding function. The immediate question is whether there is some logical connection between the possible optimal RNA structures and the possible optimal biologically active protein structures.
Single-stranded RNA molecules can form local secondary structures through the interactions of complementary segments. Watson-Crick (WC) base pair formation lowers the average free energy, dG, of the RNA and the magnitude of change is proportional to the number of base pair formations. Therefore the free folding energy (FFE) is used to characterize the local complementarity of nucleic acids . The free folding energy is defined as FFE = (dGshuffled - dGnative)/L × 100, where L is the length of the nucleic acid, i.e., free energy difference between native and shuffled (randomized) nucleic acids per 100 nucleotides. Higher positive values indicate stronger bias toward secondary structure in the native mRNA, and negative values indicate bias against secondary structure in the native mRNA.
We used a nucleic acid secondary structure predicting tool, the mfold  to obtain dG values and the lowest dG was used to calculate the FFE. The mfold also provided the folding energy dot plots, which are very useful for visualizing the energetically most favored structures in a 2D matrix.
A series of JAVA tools were used: SeqX to visualize the protein structures in 2D as amino acid residue contact maps ; SeqForm to select sequence residues in predefined phases (every third in our case) . Structural data were downloaded from PDB , NDB , and the Integrated Sequence-Structure Database (ISSD) .
Structures were generally randomly selected regarding species and biological function (a few exceptions are mentioned in the Results). Care was taken to avoid very similar structures in the selections. A propensity for alpha helices was monitored during selection and structures with very high and very low alpha helix contents were also selected to ensure a wide range of structural representations.
Linear regression analyses and Student's t-tests were used for statistical analysis of the results.
Higher FFEs in subsequences of 1st and 3rd codon residues than in the 2nd indicate the presence of a larger number of complementary bases at the right positions of these subsequences. However, this might be the case only because the first and last codon residues form simpler subsequences and contain longer repeats of the same nucleotide than the 2nd residues. This would not be surprising for the 3rd (wobble) base but would not be expected for the 1st residue, even though it is known that the central codon letters are the most important for distinguishing among amino acids (as shown in the in the Common Periodic Table of Codons and Amino Acids ). It is more significant that the FFEs for the 1st and 3rd residues are additive and together they represent the entire FFE of the intact mRNA (Figure 1D).
More direct statistical support might be obtained by analyzing and comparing residue co-locations in these structures. Assume that the structural unit of mRNA is a tri-nucleotide (codon) and the structural unit of the protein is the amino acid. The codon may form a secondary structure by interacting with other codons according to the WC base complementary rules, and contribute to the formation of a local double helix. The 5'-A1U2G3-3' sequence (Met, M codon) forms a perfect double string with the 3'-U3A2C1-5' sequence (His, H codon, reverse and complementary reading). Suboptimal complexes are 5'-A1X2G3-3' partially complemented by 3'-U3X2C1-5' (AAG, Lys; AUG, Met; AGG, Arg; ACG, Thr; and CAU, His; CUU, Leu; CGU, Arg; CCU, Pro, respectively).
These perfectly or partially complementary codon patterns, read in direct or opposite directions, defined 8 different ways in which amino acids can be paired on the basis of their codon complementarities: the 8 possible amino acid – amino acid (or protein-protein) interaction codes.
It is well known that coding and non-coding DNA sequences (exons/introns) are different and this difference is somehow related to the asymmetry of the codons, i.e. that the third codon letter (wobble) is less important in defining the meaning of the codon than the first and second letters. Many Markov models have been formulated to find this asymmetry and predict coding sequences (genes) de novo. These in silico methods work rather well but not perfectly and some scientists remain unconvinced that codon asymmetry explains the exon-intron differences satisfactorily.
Another codon-related problem is that the well-known, non-overlapping, triplet codon translation process is extremely phase-dependent and there is theoretically no tolerance for any phase shift. There are famous examples of single nucleotide deletions that destroy the meaningful translation of a sequence and are incompatible with life. However, considering the magnitude and complexity of the eukaryotic proteome, the precision of translation is astonishingly good. Such physical precision is not possible without a massive and consistent physico-chemical underpinning. Therefore, discovery of the existence of secondary structure bias (folding energy differences) in coding regions of many organisms  was very welcome because it clearly defined codon boundaries on a physico-chemical basis.
Our experiments with free folding energy (FFE) confirmed that this bias exists. In addition, there is a very consistent and very significant pattern of FFE distribution along the nucleotide sequence. Comparing the FFEs of phase-selected subsequences, those subsequences comprising only the 1st or only the 3rd codon letters showed significantly higher FFE than those consisting only of the 2nd letters. This FFE difference was not present in the intronic sequences preceding and following the exons, but it was present in exons from different species. This is an interesting observation because these phenomena might not only distinguish between exons and introns on a physico-chemical basis, but might also clearly define the tri-nucleotide codons and thus the phase of the translation. This codon-related phase-specific variation in FFE may explain why mRNAs have greater negative free folding energies than shuffled or codon choice randomized sequences .
Free folding energy in nucleic acids is always associated with WC base pair formation. A higher FFE indicates more WC pairs (presence of complementarity) and a lower FFE indicates fewer WC pairs (less complementarity). The FFEs in the 1st and 3rd codon positions were additive, while the 2nd letter did not contribute to the total FFE; the total FFE of the entire (intact) nucleic acid was the same as that of subsequences containing only the 1st and 3rd codon letters (2nd deleted). This indicates that local RNA secondary structure bias is caused by complementarity of the 1st and 3rd codon residues in local sequences. This partial, local complementarity is more optimal in reverse orientation of the local sequences, as expected with loop formations.
FFEs are obtained by considering free folding energies of substrings that do not represent the real molecule: forcing nucleotides to be consecutive is an extreme methodological approach to measuring the structure features of coding sequences. However, this bioinformatical method has been successfully used by others [13, 21]. In addition, the behaviors of the 1st, 2nd and 3rd codon bases separately are useful for showing that the 2nd codon position does not have the same significance in the codons as the other two positions . Intronic sequences do not contain codons and consequently thy show no position-related periodic-FFE variation.
It is known that single-stranded RNA molecules can form local secondary structures through the interactions of complementary segments. The novel observation here is that these interactions preferentially involve the 1st and 3rd codon residues. This connection between the RNA secondary structure and codons immediately directs attention toward the question of protein folding and its long-suspected connection to RNA folding [22, 23].
Only about one-third (20/64) of the genetic code is used for protein coding, i.e., there is a great excess of information in the mRNA. At the same time, the information carried by amino acids seems to be insufficient (as stated by some scientists) to complete unambiguous protein folding. Therefore, it is believed that the third codon residue (wobble base) contains information additional to that already present in the genetic code. A specialized database, the ISSD , was established in an effort to connect different features of protein structure to wobble bases  with more or less success.
We found a significant correlation between FFE ratios and the helix/sheet contents of protein structures. It was possible to make direct visual comparison of mRNA structures (as statistically predicted by mfold energy dot-plots) and protein structures (as 2D residue contact maps). This method suggests similarity between nucleic acid and protein structures.
It is known that some complex protein structures are very similar even if there is less than 30% sequence similarity. It was interesting to see whether the same principle might apply to nucleic acids, and structural similarity might exist even when the sequence similarity is low. Furthermore, significant similarity between nucleic acid and protein structures might exist even without translational connection. Structure seems to be more preserved, even in nucleic acids, than sequence. However, although the matrix comparisons are suggestive, they remain semi-quantitative. Better support was necessary.
A working hypotheses grew out of these observations, namely that (a) partial, local reverse-complementarity exists in nucleic acids that form the nucleic acid structure; (b) there is some degree of similarity between the folding of nucleic acids and proteins; (c) protein structure determines the amino acid co-locations; (4) in consequence, amino acids coded by interacting (partially reverse complementary) codons might show preferential co-locations in the protein structures. And it seems to be the case: codons that contain complementary bases at the 1st and 3rd positions and are translated in reverse orientation result in preferentially co-located (interacting) amino acids in the 3D protein structure. Other complementary residue combinations or translation in the same (not reverse) direction (as many as seven combinations in total) did not result in any preferentially co-locating subset of amino acid pairs.
Construction of residue contact maps for protein structures and statistical evaluation of residue co-locations is a frequently used method for visualization and analysis of spatial connections among amino acids [25–27]. The amino acid co-locations in real protein structures are clearly not random [28, 29] and therefore residue co-location matrices are often used to assist in the prediction of novel protein structures [30, 31]. We have carefully examined the physico-chemical properties of specifically interacting amino acids in and between protein structures, and concluded that these interactions follow the well-known physico-chemical rules of size, charge and hydrophobic compatibility (unpublished data), well in line with Anfinsen's prediction. The recent study supports the conclusion that there is a previously unknown connection between the codons of specifically interacting amino acids; those codons are complementary at the 1st and 3rd (but not the 2nd) codon positions.
The idea that sequence complementarity might explain the nature of specific protein-protein interactions is not new and was suggested as long ago as 1981 [32, 35, 36]. I was never able to confirm my own original theory experimentally, the suggestion of perfect complementarity between codons of interacting amino acids [32, 33], though others were more successful . The explanation is that codon complementarity is suboptimal and does not involve the 2nd codon residue. Experimental in vitro confirmation is required to validate this recent theoretical and in silico prediction.
Availability: http://www.janbiro.com/downloads: SeqX, SeqForm.
The author of this article (J.C.B.) believes that he was the first scientist suggesting the existence of a "proteomic code". The original idea was published in 1981 in the Medical Hypotheses [32, 35, 36] as well as some aspects of the recent concept of a "protein-protein interaction code"  that was further developed in this article.
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