Difference between revisions of "Part:BBa K726012"
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This part contains YefM the antitoxin of the yefM-yoeB toxin-antitoxin system. It is behind a T7 Promoter with a , lac operator, ribosome binding site, and 6x his tag. The construct can be moved to any plasmid for expression. | This part contains YefM the antitoxin of the yefM-yoeB toxin-antitoxin system. It is behind a T7 Promoter with a , lac operator, ribosome binding site, and 6x his tag. The construct can be moved to any plasmid for expression. | ||
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===Usage and Biology=== | ===Usage and Biology=== | ||
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| + | Within the <i>E.coli</i> genome, there is the naturally occurring toxin-antitoxin system whose production is altered in response to various types of stress. In layman’s terms, a toxin-antitoxin system consists of two genes: one coding for the toxin, or “poison”, and one coding for the antitoxin, or “antidote”. | ||
| + | There are three different types of toxin/antitoxin systems, all with different products effectively committing apoptosis. A general overview of all types are listed below. | ||
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| + | <li> Type 1: Inhibition takes place when the antitoxin RNA binds to the complementary toxin mRNA. If there is not enough antitoxin RNA being transcribed, toxin proteins will be produced, inducing toxicity through cell membrane damage. Toxin RNA has a half life of ~20 minutes, while antitoxin RNA has a half life of ~30 seconds.</li> | ||
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| + | <li> Type 2: both genes code for separate proteins, which bind to each other in a normal, unstressed state. While undergoing stressful conditions, the production of antitoxins will drastically decrease, allowing the toxin protein to act as a pseudo-RNAase, cleaving mRNA.</li> | ||
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| + | <li> Type 3: The most recently discovered, inhibition of this toxin requires the interplay between a toxin protein and an antitoxin RNA gene. There is only one example of this system so far - the ToxIN system from the bacterial plant pathogen Erwinia carotovora. </li> | ||
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| + | <regulartext> <b>YefM is a Type 2 antitoxin. For the purposes of the 2012 UCSF iGEM team, (tuning population ratios of symbiotic strains), Type 2 systems were determined to be ideal, since they have the greatest chance of longevity/sustainability as proteins, rather than RNA strands.</b> | ||
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| + | <img align="center" style="margin-bottom:10px; width: 250px;height:100; margin-top:20px; padding:2; margin-left:200px;" src="https://dl.dropbox.com/u/24404809/iGEM%202012/igem%202012%20website%20photos/toxins/Toxin1.jpg"> | ||
| + | <regulartext> <br> In a Type 2 system (diagrammed above), the antitoxin gene is usually upstream of the toxin gene and its product is usually the more unstable of the two, degrading much more rapidly than the toxin. As this is the case, antitoxin proteins are produced in a much larger quantity in order to counteract the toxin. Antitoxin and toxin pairs are coded into proteins and bind to each other to prevent an accumulation of toxin. In stressful situations – when there is DNA damage, drastic change in temperature, or lack of nutrients – stress-induced proteases cleave antitoxins and leave the toxins to cleave the mRNA strands. <br> | ||
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| + | </html> | ||
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Revision as of 18:48, 3 October 2012
T7Prom+HisTag+YefM
This part contains YefM the antitoxin of the yefM-yoeB toxin-antitoxin system. It is behind a T7 Promoter with a , lac operator, ribosome binding site, and 6x his tag. The construct can be moved to any plasmid for expression.
Usage and Biology
Sequence and Features
Within the E.coli genome, there is the naturally occurring toxin-antitoxin system whose production is altered in response to various types of stress. In layman’s terms, a toxin-antitoxin system consists of two genes: one coding for the toxin, or “poison”, and one coding for the antitoxin, or “antidote”.
There are three different types of toxin/antitoxin systems, all with different products effectively committing apoptosis. A general overview of all types are listed below.
In a Type 2 system (diagrammed above), the antitoxin gene is usually upstream of the toxin gene and its product is usually the more unstable of the two, degrading much more rapidly than the toxin. As this is the case, antitoxin proteins are produced in a much larger quantity in order to counteract the toxin. Antitoxin and toxin pairs are coded into proteins and bind to each other to prevent an accumulation of toxin. In stressful situations – when there is DNA damage, drastic change in temperature, or lack of nutrients – stress-induced proteases cleave antitoxins and leave the toxins to cleave the mRNA strands.