Gene optimization
Visual Gene Developer provides several algorithms to
optimize gene constructs and find the best candidates.
Here is a summary of
the implemented algorithms.
Module name |
Module category |
Description |
Monte-Carlo Codon Optimization |
Sequence
optimization |
Predefined
probability (defined in w-table file) based random mutation
(=Monte-Carlo simulation). Target codons will be replaced by new
codons that have a different probability.
It checks
following functions to screen out candidate gene constructs
(Check CAI, Check
restriction enzyme site, Check repeated sequence, Check
excluded sequence) |
Local mRNA Optimization |
mRNA structure optimization |
Adjust mRNA Gibbs energy to be in
the specified range given by lowest Gibbs Energy (AvgBaseGibbs_Low)
and highest Gibbs Energy (AvgBaseGibbs_High). It modified
sequence performing Codon optimization or synonymous
substitution. A user can set the target range given by Start and
End locations in a sequence. |
mRNA Profile Optimization |
mRNA structure optimization |
Improved from
Do_mRNAOpt_ProbabilityRandom. It optimizes an mRNA Gibbs energy
profile along a long sequence. A moving window method was
adopted. |
Local mRNA Profile
Optimization |
mRNA structure optimization |
Modification of Do_mRNAProfileOpt.
A user can set the target range given by Start and End locations
in a sequence. |
Silent removal v1 |
Gene manipulation |
Remove undesired sequences.
It can specify up to 10 sequences. |
Silent removal v2 |
Gene manipulation |
Remove undesired sequences.
Can process multiple query sequences. |
Silent removal of potential
polyadenylation sites |
Gene manipulation |
Remove predefined sequences
of potential polyadenylation signal sequences |
Silent removal of potential
intron cryptic splice sites |
Gene manipulation |
Remove predefined sequences
of potential intron cryptic donor and receptor signal sequences |
Check CAI |
Constraint |
Return 'Not pass' if CAI value is lower than setpoint |
Check
restriction enzyme site |
Constraint |
Return 'Not pass' if
the sequence contains a certain restriction enzyme sequence |
Check repeated
sequence |
Constraint |
Return 'Not pass' if
the sequence contains a certain number of repeated sequence |
Check excluded
sequence |
Constraint |
Return 'Not pass' if
the sequence contains a certain excluded sequence |
Check stable mRNA structure |
Constraint |
Return 'Not pass' if
the sequence
contains stable mRNA secondary structures
The
module retrieves sequence information and then generates lots of
sequence segments specified by 'Window size'. The moving window
scans along the sequence with a given 'Step size'. The
Visual Gene Developer predicts mRNA secondary structure and calculates
Gibbs free energy for each segment. If Gibbs energy is lower
than a specified value ('Threshold value'), it returns 'Not
pass' which means the gene includes stable mRNA secondary
structure. If all sequence segments of the target gene are more
unstable than the expected value ('Threshold value'), the module
returns 'Pass'. |
For more details about
the 'Module category', check
the 'Module development' section on the left menu. At the same time, all
predefined modules were summarized in the 'Class & module' section
on the
left menu.
Important!
Method 1 (Working on 'Workspace'):
Paste sequence to 'Workspace' window and then click on the 'Function > Codon
optimization'. You will see the 'Codon optimization' window. Adjust
parameters and then click on the 'Perform' button. For mRNA
structure optimization, click on the 'Function > mRNA optimization'. You
will see the 'mRNA optimization' window. Adjust parameters and then click on
the 'Analyze' button and then 'Optimize' button
Method 2 (Working on Gene construct): Firstly, configure optimization condition in the 'Configuration of gene
optimization' window and then do optimize a gene construct in the 'Gene
optimization' window.
o
Method 1
o Simply way to optimize
codon on 'Codon optimization' window
1. Paste any sequence
to the 'Workspace' window
2. Click on the menu
item (Menu: Function > Codon optimization)
3. A window titled 'Codon
optimization' will be shown.
4. Click on the
'Perform' button
5. Click on the 'Apply
and Close' button
o Simply way to optimize
codon on 'mRNA optimization' window
1. Paste any sequence
to the 'Workspace' window
2. Click on the menu
item (Menu: Function > mRNA optimization)
3. A window titled 'mRNA
optimization' will be shown.
4. Click on the
'Perform' button
5. Click on the 'Optimize'
button
6. Check results and
click on the 'Apply' button.
7. You can check the mRNA
profile clicking on the 'Draw' button
o
Method 2
o
How to configure optimization condition
1. Click on the 'Configuration' item in the 'Project Explorer'
window.
2. A window titled 'Configuration of gene
optimization' will be shown.
3. Click on one of the items.
4. Choose one of the algorithms.
5. In addition, you may click on the 'Constraint'
6. Choose one of the algorithms
7. Adjust parameters. For example, when you click
on the 'On' checkbox, it will deactivate a selected module and
an optimization
algorithm will neglect inactivated items.
o More details about gene optimization
procedure
There are 4 different categories of optimization conditions such as
'Sequence optimization', 'mRNA structure', 'Manipulation', and
'Constraint'.
It's up to you to classify the module to one of them. However, internal
algorithms orderly proceed from 'Sequence optimization' to 'Constraint'.
Therefore, 'Sequence optimization' has the highest priority than other
conditions and 'Constraint' is the lowest priority. For more details,
check the 'Module development' section on the left menu.
o How to optimize gene construct
1. Click on the 'Configuration' item in the 'Project Explorer'
window.
2. A window titled 'Configuration of gene
optimization' will be shown. Choose an algorithm and click on the 'Run' button. If
you want to stop the optimization, click on the 'Stop' button.
As shown in the figure, the 'Automated conditional search' algorithm produces
a lot of candidates that fit for the condition defined in 'Constraint'
in the 'Gene optimization condition' window.
3. Because the optimization algorithm initially starts from a selected gene
construct (=there are a parent gene construct and lots of child gene
constructs), simply choose a gene construct clicking in the table and then
start a new optimization cycle.
4. If you want to re-define the table, click on the 'Viewer setting' button in
the 'Gene
optimization' window.
5. Add/Delete functions in the 'Viewer setting' window.
o How to develop
a custom gene optimization
module?
The software supports developing
user-defined new algorithms for gene optimization. The module development
section on the left menu will be much helpful. Basically, users can
access the gene construct memory array using a class (class name:
GeneConstruct) to modify sequence.
Check the following example.
1. Click on the 'Module Library' in the 'Tool' menu
2. Choose 'GeneConstruct.ParameterValue' in
the 'Module Library' window
3. Click on the 'Edit Module' button
4. You can see the 'Module Editor' window. Click
on the 'Test
run' button
5. Check the result and source code.
Source code
VBScript
Function Main()
GeneComponentName=GeneConstruct.ComponentName(1,3)
'<--- Get 3rd gene component name
of the first gene construct
GeneSequence=GeneConstruct.ParameterValue(1,3,"Modified
DNA") '<---
Get parameter value of modified DNA
Msgbox GeneComponentName + " = " +
GeneSequence '<---
Show result consisting component name and its sequence
End Function |
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