Gene Predictor(ChemGenome 2.0)
From DrugPedia: A Wikipedia for Drug discovery
(→ChemGenome - A Physico-chemical Model for Genome Analysis) |
(→ChemGenome - A Physico-chemical Model for Genome Analysis) |
||
(4 intermediate revisions not shown.) | |||
Line 9: | Line 9: | ||
*The second component was constructed by finding the Stacking energy(sum of electrostatic, hydrophobic and other forces which the trinucleotides are exposed to when it is stacked with other nucleotides in the B-DNA form). | *The second component was constructed by finding the Stacking energy(sum of electrostatic, hydrophobic and other forces which the trinucleotides are exposed to when it is stacked with other nucleotides in the B-DNA form). | ||
*The third component of the vector reflects the DNA protein interactions. It's assignment follows the “Conjugate” rule which is derived from the Wobble Hypothesis (For more on conjugate rule, refer to [Jayaram, B. Beyond the wobble: the rule of conjugates. J. Mol. Evol. 1997, 45, 704-705]. | *The third component of the vector reflects the DNA protein interactions. It's assignment follows the “Conjugate” rule which is derived from the Wobble Hypothesis (For more on conjugate rule, refer to [Jayaram, B. Beyond the wobble: the rule of conjugates. J. Mol. Evol. 1997, 45, 704-705]. | ||
- | [[Image: | + | [[Image:Picture2.JPG]] |
Every sequence is broken down into trinucleotides, the three components for each trinucleotide are added up. The values assigned to all the trinucleotides are normalized to lie in the range [-1,1]. These unit vectors are then plotted on unit spheres. | Every sequence is broken down into trinucleotides, the three components for each trinucleotide are added up. The values assigned to all the trinucleotides are normalized to lie in the range [-1,1]. These unit vectors are then plotted on unit spheres. | ||
A physical separation of the vectors corresponding to coding DNA sequences and the non-coding DNA sequences was observed by plotting them as dots on a 3D plane. All the coding DNA sequences are represented as red dots while the non-coding DNA sequences are represented as blue dots. | A physical separation of the vectors corresponding to coding DNA sequences and the non-coding DNA sequences was observed by plotting them as dots on a 3D plane. All the coding DNA sequences are represented as red dots while the non-coding DNA sequences are represented as blue dots. | ||
- | + | [[Image:A.gif|thumb]] [[Image:B.gif|thumb]] [[Image:C.gif|thumb]] | |
This physical separation of the vectors corresponding to genes and non-genes is the basis of the physico-chemical model of Gene Evaluation. Once the best separating plane is obtained, we only need to check if the new DNA sequence lies on the Gene side of the plane or the other side. | This physical separation of the vectors corresponding to genes and non-genes is the basis of the physico-chemical model of Gene Evaluation. Once the best separating plane is obtained, we only need to check if the new DNA sequence lies on the Gene side of the plane or the other side. | ||
Physico-chemical evaluation has proven accurate for Prokaryotes to an accuracy of >95% and forms the basis of Chemgenome 1.1. | Physico-chemical evaluation has proven accurate for Prokaryotes to an accuracy of >95% and forms the basis of Chemgenome 1.1. |
Current revision
[edit] ChemGenome - A Physico-chemical Model for Genome Analysis
Chemgenome is based on the hypothesis that both the structure of the DNA and its interactions with regulatory proteins and polymerases decide the function of a DNA sequence. It uses a simple three-parameter model based on Watson-Crick hydrogen-bonding energy, base-pair stacking energy, and a third parameter which is related to Protein-Nucleic Acid interactions. Each of these parameters acts as a dimension for a three-dimensional unit vector, whose orientation differs for each trinucleotide.
DNA sequence is made up of set of four bases (A, T, G, C) which combine in different possible manner to give 64 unique codons. Each of the 64 codons(trinucleotides) are assigned a X(Hydrogen Bonding Energy), Y(Stacking Energy) and Z(protein-Nucleic acid interaction).
- The first component was constructed by finding the Hydrogen bonding energy of trinucleotides(codons).
- The second component was constructed by finding the Stacking energy(sum of electrostatic, hydrophobic and other forces which the trinucleotides are exposed to when it is stacked with other nucleotides in the B-DNA form).
- The third component of the vector reflects the DNA protein interactions. It's assignment follows the “Conjugate” rule which is derived from the Wobble Hypothesis (For more on conjugate rule, refer to [Jayaram, B. Beyond the wobble: the rule of conjugates. J. Mol. Evol. 1997, 45, 704-705].
Every sequence is broken down into trinucleotides, the three components for each trinucleotide are added up. The values assigned to all the trinucleotides are normalized to lie in the range [-1,1]. These unit vectors are then plotted on unit spheres.
A physical separation of the vectors corresponding to coding DNA sequences and the non-coding DNA sequences was observed by plotting them as dots on a 3D plane. All the coding DNA sequences are represented as red dots while the non-coding DNA sequences are represented as blue dots.
This physical separation of the vectors corresponding to genes and non-genes is the basis of the physico-chemical model of Gene Evaluation. Once the best separating plane is obtained, we only need to check if the new DNA sequence lies on the Gene side of the plane or the other side. Physico-chemical evaluation has proven accurate for Prokaryotes to an accuracy of >95% and forms the basis of Chemgenome 1.1.