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Bioinformation. 2010; 4(10): 452–455.
Published online 2010 April 30.
PMCID: PMC2951701

Low thymine content in PINK1 mRNAs and insights into Parkinson’s disease

Abstract

Thymine is the only nucleotide base which is changed to uracil upon transcription, leaving mRNA less hydrophobic compared to its DNA counterpart. All the 16 codons that contain uracil (or thymine in gene) as the second nucleotide code for the five large hydrophobic residues (LHRs), namely phenylalanine,v isoleucine, leucine, methionine and valine. Thymine content (i.e. the fraction of XTX codons, where X = A, C, G, or T) in PINK1 mRNA sequences and its relationship with protein stability and function are the focus of this work. This analysis will shed light on PINK1's stability, thus a clue can be provided to understand the mitochondrial dysfunction and the failure of oxidative stress control frequently observed in Parkinson’s disease. We obtained the complete PINK1 mRNA sequences of 8 different species. The distributions of XTX codons in different frames are calculated. We observed that the thymine content reached the highest level in the coding frame 1 of the PINK1 mRNA sequence of Bos Taurus (Bt), that is peaked at 27%. Coding frame 1 containing low thymine leads to the reduction in LHRs in the corresponding proteins. Therefore, we conjecture that proteins from the other organisms, including Homo sapiens, lost some of their hydrophobicity and became susceptible to dysfunction. Genes such as PINK1 have reduced thymine in the evolutionary process thereby making their protein products potentially being susceptible to instability and causing disease. Adding more hydrophobic residues (thymine) at appropriate places might help conserve important biological functions.

Keywords: thymine distribution, PINK1, sequence analysis, protein stability, frame analysis

Background

Parkinson’s disease (PD) is the most prevalent neurodegenerative movement disorder and affects about 1% of the elderly population. Cell death of midbrain dopaminergic neurons is the key pathological feature, and clinical symptoms include bradykinesia, tremor and rigidity among others [1]. The disease etiology remains largely unknown although aberrant protein degradation and mitochondrial dysfunction have been highlighted as probable causes. PD has a much higher proportion of sporadic cases as compared to familial or inherited cases. Yet “significant advances in our understanding of PD have stemmed directly from the study of [those] genes associated with a small proportion of familial cases” [2] and mitochondrial dysfunction has been implicated as a common pathogenic mechanism in both familial and sporadic PD. Mitochondrial dysfunction in PD can occur along three pathogenic pathways [3]. However for many PD genes the precise mechanism through which mitochondrial integrity remains still unknown.Six PD associated genes namely α­ synuclein, Parkin, PINK1 (PTEN­induced putative kinase 1), DJ-1, LRRK2 (Leucine­rich repeat kinase 2) and HTRA2 (high temperature requirement protein A2) have been identified to show involvement in mitochondrial dysfunction and oxidative stress. Intensive work on mutational studies demonstrated their importance for normal mitochondrial function [4]. Of these 6 genes we chose PINK1 for a study of thymine levels as ample evidence exists that this gene product is targeted to mitochondria and is located upstream of Parkin in the pathogenic pathways leading to mitochondrial dysfunction [5,6,7]. Recessive mutations of PINK1 have caused mitochondrial failure and an inability of the mitochondrion to cope with oxidative stress. Maguire Zeiss et al.,[8] & Pridgeon et al., [9] have conducted an analysis on an inherited form of early-onset PD which has been linked to mutations in both copies of PINK1. It was also reported that PINK1 phosphorylates tumor necrosis factor receptor-associated protein 1 (TRAP1), and in turn TRAP1 prevents oxidative stress by preventing mitochondria from releasing cytochrome c ­­­ a crucial step in cell death. Such mutational studies seek functional insights by implicating genes and proposing models of PD pathways. However it may also be useful to study those genes from a wider perspective by performing a comparison of sequence analysis across different organisms. PD gene studies have sought to identify possible loci of implicated genes, to understand gene function through deletions, knock­out mutations and other studies. However to the best of our knowledge no study on sequence analysis of PD genes comparing nucleotide differences across different organisms has been carried out. This is important as besides site specific or targeted gene mutations, naturally differing levels of certain nucleotides may affect hydrophobicity of proteins when compared across differing organisms. This provides a possible reason as to why certain proteins are more likely to be unstable despite the fact that no disease causing mutations or hereditary disease causes can be identified. Here we use a macro approach to PD mechanisms by focusing on PINK1 mRNA sequences to compare the differing distribution of thymine content across species in an attempt to identify protein instability due to the loss of hydrophobic residues.

Methodology

Dataset

PINK1 mRNA sequences in FASTA format for Homo sapiens (Hs), Pan troglodytes (Pt), Bos taurus (Bt), Mus musculus (Mm), Macaca mulatta (Mmu), Gallus gallus (Gg), Danio rerio (Dr) and Caenorhabditis elegans (Ce) are taken from NCBI Genbank [10]. The total number of bases in the mRNA sequence for each organism is listed in Table 1 (see supplementary material).

The frames 1, 2 and 3 represent the 5'-3' mRNA sequences and frames 4, 6 and 5 are antisense strand. Each mRNA sequence is read in six different frames and the number of XTX occurrences in each frame is counted (i.e., Thymine nucleotide 2 in the second position of the codons is considered the beginning of frame 1.The next two immediate nucleotides 3 and 4 are considered the beginnings of frames 2 and 3 respectively. The antisense strand nucleotides of 2, 3 and 4 are considered frames 4, 6 and 5, respectively). The number of XTX occurrences for each frame is subsequently expressed as a fraction of the total number of codons for all six frames. This procedure is repeated for all 8 organisms and the results shown in Table 2. The proportion of XTX content thus obtained for each of the eight organisms for all six frames is plotted and shown in Figure 1.

Figure 1
The fraction of thymine (XTX) in the coding frames of PINK1 mRNA sequences in eight different species found in Table 2 (see supplementary material).

Discussion

It is observed that for frame 1 the thymine content is lower than 27% in all species studied here except for Bos taurus which has reached the expected genome wide thymine content level of 27% [11]. The coding frames of mRNA sequences contain a greater amount of thymine in frame 1 than frames 2, 3, 4, 5 and 6 (except for Caenorhabditis elegans). Frames 3 and 5 have similar fractions of XTX for Homo sapiens, Pan trogdolytes, Bos taurus and Mus musculus, except Macaca mulatta, Gallus gallus, Danio rerio and Caenorhabditis elegans. However, frames 2 and 6 show inconsistent fractions of thymine as seen in Figure 1.

As highlighted above, the thymine content in Frame 1 and Frame 4 of the PINK1 mRNA sequence in Homo sapiens is lesser than that of Bos taurus. Therefore, the coding frames of these mRNA sequences are more hydrophilic and may be more likely to contribute to impaired protein activity whereas the hydrophobicity is maintained in the corresponding coding frames of Bos taurus. From Figure 1, for Homo sapiens, Pan trogdolytes, Mus musculus, Macaca mulatta, Gallus gallus, Danio rerio and Caenorhabditis elegans, we also noticed that almost all frame 1 coding mRNA sequences code for more hydrophilic residues, which increases exposure to water and thus contributes to protein instability.

A recent study [12] has reported that hydrophobic interactions comprise the dominant force in most biochemical reactions which take place in water. Carbon is the main element which contributes to this interaction. This study also analyzed the carbon content at the protein functional sites of PINK1 which prefer to have 31.44% of total carbon along the chain. The PINK1 amino acid sequence in Homo sapiens seems to be less stable in comparison to that of Bos taurus. They suggested that the first 267 amino acids are hydrophilic and therefore do not contribute to protein stability as they lack the required carbon content. However in Bos taurus the hydrophobicity is maintained within this range of 267 amino acids. From our results and their findings, we suggest that the PINK1 protein loses large hydrophobic residues due to low thymine content in Homo sapiens rendering it more hydrophilic and thus susceptible to losing its stability and activity. This shows that mutations to the genetic sequence might have occurred suggesting evolutionary changes.

As a factor to balance the thymine content and distribution of LHR, more numbers of small hydrophobic residues (SHR) such as glycine, alanine, proline and cysteine are found in the PINK1 mRNA sequences. With the addition of these residues, the length of protein sequences also increases. This is the reason why the length of animal coding mRNA sequence increases and in turn protein length increases [12]. We expect that these genes and corresponding longer mRNA sequence of proteins contain low thymine content

The statistical distribution of hydrophobic residues along the protein chains and its implications to protein folding and evolution were reported by White and Jacobs in 1990[14]. They tested for randomness of hydrophobic residues in proteins but only on a limited number of sequences. They suggested that the folding of proteins into compact structures may be much more permissive with less sequence specificity than previously thought and that the clusters of hydrophobic residues along chains which are revealed by hydrophobicity plots are a natural consequence of a random distribution. Currently most of the protein sequences of several model organisms are available for a more thorough understanding which we have carried out here. White and Jacobs in 1993[15] further argued that the distribution of hydrophobic residues along a sequence cannot be distinguished from that expected for a random distribution and suggested that functional proteins may have originated from random sequences.

Conclusion

Our study strongly suggests that coding frames of mRNA sequences for Homo sapiens are closely associated with Pan troglodytes, Mus musculus, Macaca mulatta and Gallus gallus. The Homo sapiens coding frame 1 of the mRNA sequence in PINK1 has a thymine distribution of only 25% which is less than the random percentage of 27%. As introduced, the XTX thymine codons are responsible for coding LHRs in proteins. This thymine that has one extra methyl group compared to its RNA Globular proteins is expected to follow the 27% distribution profile. A protein’s stability, function and interaction with other proteins are primarily determined by LHRs. Thus, tracing a protein’s hydrophobicity via the thymine content levels can serve as a useful tool in identifying the coding frames of mRNA sequences that might contribute to diseases.

Large numbers of hydrophilic residues are found among seven of the eight organisms analyzed. This is especially true of Homo sapiens. Any reduction of hydrophilic amino acid residues or addition of hydrophobic residues can increase the functional activity of PINK1. Therefore, adding more thymine at appropriate places in mRNA or in the gene will improve the amount of hydrophobic residues which could contribute to better biological activity, and defects in the disease­causing sequence could be eradicated. Applying such a strategy for PINK1 might prevent mitochondrial dysfunction and oxidative stress.

Supplementary material

Data 1:

Footnotes

Citation:Anandagopu et al, Bioinformation 4(10): 452-455 (2010)

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