Help:Tutorial:Step 6
From WikiPathways
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==== 1. Stack the mCry/mPer DataNodes ==== | ==== 1. Stack the mCry/mPer DataNodes ==== | ||
| - | To illustrate that the mCry/mPer genes are activated by the E-box element, we can stack them below the 'Gene' label. Place the mPer/mCry DataNodes below the 'Gene' label and stack them in two vertical pairs, using the | + | To illustrate that the mCry/mPer genes are activated by the E-box element, we can stack them below the 'Gene' label. Place the mPer/mCry DataNodes below the 'Gene' label and stack them in two vertical pairs, using the [[Image:stackverticalcenter.gif]] ''stack vertically'' button. Group each stacked pair. |
==== 2. Copy the gene-products ==== | ==== 2. Copy the gene-products ==== | ||
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As long as Per1 or Per2 is not dimerized with Cry1 or Cry2, it will be degraded. We can indicate degradation by using the ''degradation'' shape: | As long as Per1 or Per2 is not dimerized with Cry1 or Cry2, it will be degraded. We can indicate degradation by using the ''degradation'' shape: | ||
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You will notice that this shape is not on the toolbar, so to insert it, we have to insert another shape (e.g. a rectangle) and change it's ''Shape Type'' property. Insert a rectangle, select it and change the ''Shape Type'' property in the [[Help:Tutorial#Used terms and abbreviations|properties table]] to ''mim-degradation'': | You will notice that this shape is not on the toolbar, so to insert it, we have to insert another shape (e.g. a rectangle) and change it's ''Shape Type'' property. Insert a rectangle, select it and change the ''Shape Type'' property in the [[Help:Tutorial#Used terms and abbreviations|properties table]] to ''mim-degradation'': | ||
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Revision as of 00:00, 13 May 2010
Target genes are activated by the E-box element
After the Clock/Bmal1 dimer binds to the E-box element, transcription of several target genes are activated. This simplified version of the Circadian clock pathway, will restrict to the mPer/mCry genes, which will act as a negative feedback loop. As long as Per1 or Per2 exist as monomers, they will be phosphorylated by casein kinase 1 delta or epsilon, followed by degradation. In the pathway drawing we simplify it a bit by leaving out the phosphorylation event, resulting in the following representation:
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| Drawing the transcription of mPer/mCry and degradation of mPer |
1. Stack the mCry/mPer DataNodes
To illustrate that the mCry/mPer genes are activated by the E-box element, we can stack them below the 'Gene' label. Place the mPer/mCry DataNodes below the 'Gene' label and stack them in two vertical pairs, using the 
stack vertically button. Group each stacked pair.
2. Copy the gene-products
The genes will be translated into proteins, to show this on the pathway, copy the stacked genes and move them to the right of the stacked DataNodes.
3. Draw a line from the genes to the gene-products
To illustrate that the genes are translated into proteins, we draw a dashed arrow from each pair of genes to the copied pair. Connect the start and end points to the groups.
5. Create a degradation shape
As long as Per1 or Per2 is not dimerized with Cry1 or Cry2, it will be degraded. We can indicate degradation by using the degradation shape:
|
You will notice that this shape is not on the toolbar, so to insert it, we have to insert another shape (e.g. a rectangle) and change it's Shape Type property. Insert a rectangle, select it and change the Shape Type property in the properties table to mim-degradation:
|
When you selected mim-degradation as property, you will see the rectangle change into a degradation shape.
6. Draw an arrow from the mPer DataNodes to the degradation shape
To show that the mPer proteins are degraded, draw an dashed arrow from the two mPer DataNodes to the degradation shape. Connect the start of this line to group 2.1 to specify that only the mPer proteins are degraded.
