Difference between revisions of "Part:BBa K1017404"

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<partinfo>BBa_K1017404 short</partinfo>
 
<partinfo>BBa_K1017404 short</partinfo>
  
We all know that sRNA is an important role on gene regulation. It will interact with the targeted mRNA by imperfect base pairing, reducing the translation efficiency and recruiting chaperones such as Hfq for translation termination. Since we choose sRNA to be part of our regulated-system, we need to prevent the sRNA from effecting undesired genes, so it is necessarily to design artificial sRNA that targets specifically to the desired genes.  
+
===Description of function===
 +
Small RNA is an important role on gene regulation.
 +
It will interact with the targeted mRNA by imperfect basepairing,
 +
reducing the translational efficiency and recruiting chaperones such as
 +
Hfq for translational termination.
  
 +
===How we design===
 
We first picked the sRNA from a library of artificial sRNA that was constructed by fusing a randomized antisense domain of Spot42, the scaffold that is known to recruit the RNA chaperons. As we want the sRNA we picked can specifically complementary to the SD sequence which in our designed RBS(BBa_K1017202[https://parts.igem.org/wiki/index.php?title=Part:BBa_K1017202]), we picked the one which contains a consensus sequence, 5’-CCCUC-3’. Our artificial sRNA also has three stem-loop double stranded RNA structures, and the loop closest to the 3’ terminus is complementary to a sequence preceding the initiation codon of mRNA, so that it can prevent the ribosome from binding to the initiation condon, so the translation would be repressed.
 
We first picked the sRNA from a library of artificial sRNA that was constructed by fusing a randomized antisense domain of Spot42, the scaffold that is known to recruit the RNA chaperons. As we want the sRNA we picked can specifically complementary to the SD sequence which in our designed RBS(BBa_K1017202[https://parts.igem.org/wiki/index.php?title=Part:BBa_K1017202]), we picked the one which contains a consensus sequence, 5’-CCCUC-3’. Our artificial sRNA also has three stem-loop double stranded RNA structures, and the loop closest to the 3’ terminus is complementary to a sequence preceding the initiation codon of mRNA, so that it can prevent the ribosome from binding to the initiation condon, so the translation would be repressed.
  
 
[[File:NCTU sRNA-2 structure predict.png|center]]
 
[[File:NCTU sRNA-2 structure predict.png|center]]
===Description of function===
+
 
 +
Since we choose sRNA to be part of our regulated-system, we need to prevent
 +
the sRNA from effecting undesired genes, so it is necessarily to design
 +
artificial sRNA that targets specifically to the desired genes.
 
===Quantitative data showing the Part or Device function===
 
===Quantitative data showing the Part or Device function===
 
===Acknowedgment of sources and references===
 
===Acknowedgment of sources and references===

Revision as of 13:32, 26 September 2013

sRNA-2

Description of function

Small RNA is an important role on gene regulation. It will interact with the targeted mRNA by imperfect basepairing, reducing the translational efficiency and recruiting chaperones such as Hfq for translational termination.

How we design

We first picked the sRNA from a library of artificial sRNA that was constructed by fusing a randomized antisense domain of Spot42, the scaffold that is known to recruit the RNA chaperons. As we want the sRNA we picked can specifically complementary to the SD sequence which in our designed RBS(BBa_K1017202[1]), we picked the one which contains a consensus sequence, 5’-CCCUC-3’. Our artificial sRNA also has three stem-loop double stranded RNA structures, and the loop closest to the 3’ terminus is complementary to a sequence preceding the initiation codon of mRNA, so that it can prevent the ribosome from binding to the initiation condon, so the translation would be repressed.

NCTU sRNA-2 structure predict.png

Since we choose sRNA to be part of our regulated-system, we need to prevent the sRNA from effecting undesired genes, so it is necessarily to design artificial sRNA that targets specifically to the desired genes.

Quantitative data showing the Part or Device function

Acknowedgment of sources and references

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal XhoI site found at 3
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]