Difference between revisions of "Part:BBa K4169014"

 
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Based on the characteristics of secondary structure changes of RNA under different temperature conditions, the RNA thermometer element was introduced in this project. An RC sequence is present on this RNA thermometer, which recruits RNase E to degrade subsequent RNA fragments. At low temperatures,such as 27℃, RNA thermometers will maintain the secondary stem-loop structure, and RC sequences will complement and pair with other bases, unable to recruit RNase, so subsequent sequences will be expressed normally. However, at 37℃, the secondary structure opens, and the subsequent RNA fragments are cleaved and degraded by RNA enzymes.We want to change the temperature at which it functions by mutating its gene sequence.So we mutated its gene sequence, that is, the first A before RC was changed to T, and the eighth C after RC was changed to T
 
Based on the characteristics of secondary structure changes of RNA under different temperature conditions, the RNA thermometer element was introduced in this project. An RC sequence is present on this RNA thermometer, which recruits RNase E to degrade subsequent RNA fragments. At low temperatures,such as 27℃, RNA thermometers will maintain the secondary stem-loop structure, and RC sequences will complement and pair with other bases, unable to recruit RNase, so subsequent sequences will be expressed normally. However, at 37℃, the secondary structure opens, and the subsequent RNA fragments are cleaved and degraded by RNA enzymes.We want to change the temperature at which it functions by mutating its gene sequence.So we mutated its gene sequence, that is, the first A before RC was changed to T, and the eighth C after RC was changed to T
  
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===Usage and Biology===
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===Design and Mutation===
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<p>We designed the mutation primers <b>(Figure 1.)</b>and the expected mutation sequences<b>(Figure 2.)</b></p>
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<center><img src="https://static.igem.wiki/teams/4169/wiki///rna-t/rna-thermometer-mutation-5.png
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<center><b>Figure 1. </b> the mutation primers</center>
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<center><img src="https://static.igem.wiki/teams/4169/wiki///rna-t/rna-thermometer-mutation-5-2.png
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<center><b>Figure 2. </b> the expected mutation sequences are highlighted in red</center>
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<span class='h3bb'>Sequence and Features</span>
 
<span class='h3bb'>Sequence and Features</span>
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===Functional Parameters===
 
===Functional Parameters===
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<partinfo>BBa_K4169014 parameters</partinfo>
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<partinfo>BBa_K4169010 parameters</partinfo>
 
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Revision as of 11:23, 12 October 2022


A RNA thermometer mutation 5

Based on the characteristics of secondary structure changes of RNA under different temperature conditions, the RNA thermometer element was introduced in this project. An RC sequence is present on this RNA thermometer, which recruits RNase E to degrade subsequent RNA fragments. At low temperatures,such as 27℃, RNA thermometers will maintain the secondary stem-loop structure, and RC sequences will complement and pair with other bases, unable to recruit RNase, so subsequent sequences will be expressed normally. However, at 37℃, the secondary structure opens, and the subsequent RNA fragments are cleaved and degraded by RNA enzymes.We want to change the temperature at which it functions by mutating its gene sequence.So we mutated its gene sequence, that is, the first A before RC was changed to T, and the eighth C after RC was changed to T

Design and Mutation

We designed the mutation primers (Figure 1.)and the expected mutation sequences(Figure 2.)

无标题文档

Figure 1. the mutation primers
Figure 2. the expected mutation sequences are highlighted in red

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    INCOMPATIBLE WITH RFC[1000]
    Illegal SapI site found at 39