Difference between revisions of "Part:BBa K5401004"
 
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===Characterization===
 
===Characterization===
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This part, together with our antisense oligonucleotide (ASO), and a lac promoter acts to regulate the expression of T7RNAP, thereby allowing a stable expression.
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This part, together with our antisense oligonucleotide (ASO), and a lac promoter acts to regulate the expression of T7RNAP, thereby allowing a stable expression. When the ASO system was cloned into the T7-expressing plasmid (plasmid 1c), the expression was T7RNAP was observed to be more stable, with lower frequency of insertions as compared to the predecessor plasmid (plasmid 1a).
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          <img src="https://static.igem.wiki/teams/5401/engine-page/engine3-4.png" style="display: inline-block; height: 300px; width: auto;">
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          <figcaption><i>Fig 1: Colony PCR results showed the presence of insertion sequences within the coding sequence of T7RNAP for E. coli reporter cells transformed with plasmid 1a. Band size corresponding to ~3000bp (different from expected band size of 1892bp) was observed for all 8 colonies picked from reporter cells transformed with plasmid 1a, thereby showing the unstable expression of T7RNAP. Band size corresponding to ~2000bp (expected band size of 2038) was observed for 7/8 colonies. for E. coli reporter cells transformed with plasmid 1c. The lower frequency of insertion observed shows a more stable expression of T7RNAP.</i></figcaption>
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Latest revision as of 19:26, 1 October 2024


Hfq scaffold sequence

Hfq is an RNA-binding protein that functions primarily as a riboregulator, facilitating the interaction between sRNAs and their target mRNAs. One of the key functions of the Hfq protein is RNA-RNA Interaction, through recognising its cognate Hfq scaffold sequence.

The DNA sequence provided contains a Hfq scaffold sequence to promote the binding of the Hfq protein.

Usage and Biology

One of the key functions of the Hfq protein is to enhance the base-pairing between sRNAs and mRNAs, which can lead to the regulation of translation.

In our design: the Hfq protein binds to sRNAs (an antisense oligonucleotide targeted against T7RNAP mRNA), thereby helping them to recognize and bind to complementary regions on mRNAs. This binding blocks ribosome access to the mRNA's start codon or Shine-Dalgarno sequence, thus inhibiting translation. This helps to knockdown the expression of T7RNAP, thereby regulating the expression of T7RNAP.

Characterization

This part, together with our antisense oligonucleotide (ASO), and a lac promoter acts to regulate the expression of T7RNAP, thereby allowing a stable expression. When the ASO system was cloned into the T7-expressing plasmid (plasmid 1c), the expression was T7RNAP was observed to be more stable, with lower frequency of insertions as compared to the predecessor plasmid (plasmid 1a).

Fig 1: Colony PCR results showed the presence of insertion sequences within the coding sequence of T7RNAP for E. coli reporter cells transformed with plasmid 1a. Band size corresponding to ~3000bp (different from expected band size of 1892bp) was observed for all 8 colonies picked from reporter cells transformed with plasmid 1a, thereby showing the unstable expression of T7RNAP. Band size corresponding to ~2000bp (expected band size of 2038) was observed for 7/8 colonies. for E. coli reporter cells transformed with plasmid 1c. The lower frequency of insertion observed shows a more stable expression of T7RNAP.


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 80
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]