Difference between revisions of "Part:BBa K1875010"
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<partinfo>BBa_K1875010 short</partinfo> | <partinfo>BBa_K1875010 short</partinfo> | ||
− | + | Target sequence g13 is expressed by a guide RNA (gRNA) expression vector from the [http://2016.igem.org/Team:BostonU 2016 BostonU] Gemini Library. The gRNA binds to dCas9-VPR and targets a paired gRNA operator reporter to activate a downstream gene of interest (figure 1). One way to decrease expression of the gRNA operator reporters is to mutate the guide target sequence of the guide operator (the guide target sequence followed directly by the PAM). The 2016 BostonU iGEM team made single point mutations on each base of the guide target sequence to test the binding affinity of dCas9. The point mutation was determined by whether the base was a purine or a pyrimidine and the complement of the base. If the base was a purine, it was mutated to be a pyrimidine and of the opposite coupled nucleotide (i.e: A <-->C, G<-->T). Results concluded that the expression dramatically decreased at base 10 of the target sequence (figure 2). Due to its significantly lower expression when placed in their operator reporters, the BostonU team submitted chose to submit [https://parts.igem.org/Part:BBa_K1875019 BBa_K1875019] which contains gRNA 13. Part [https://parts.igem.org/Part:BBa_K1875016 BBa_K1875016], an operator reporter with one binding site, also contains the same target sequence. | |
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+ | [[File:T--BostonU--ProjectDescription.png|400px|thumb|left|Figure 1: [http://2016.igem.org/Team:BostonU BostonU 2016] Project description]][[File:T--BostonU--single_mutations.png|400px|thumb|center|Figure 2: Screen of GFP expression in an operator reporter (containing g13) with sequentially mutated base.]] | ||
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Latest revision as of 16:54, 19 October 2016
Base 10 target mutation to make mutated guide operator 13
Target sequence g13 is expressed by a guide RNA (gRNA) expression vector from the [http://2016.igem.org/Team:BostonU 2016 BostonU] Gemini Library. The gRNA binds to dCas9-VPR and targets a paired gRNA operator reporter to activate a downstream gene of interest (figure 1). One way to decrease expression of the gRNA operator reporters is to mutate the guide target sequence of the guide operator (the guide target sequence followed directly by the PAM). The 2016 BostonU iGEM team made single point mutations on each base of the guide target sequence to test the binding affinity of dCas9. The point mutation was determined by whether the base was a purine or a pyrimidine and the complement of the base. If the base was a purine, it was mutated to be a pyrimidine and of the opposite coupled nucleotide (i.e: A <-->C, G<-->T). Results concluded that the expression dramatically decreased at base 10 of the target sequence (figure 2). Due to its significantly lower expression when placed in their operator reporters, the BostonU team submitted chose to submit BBa_K1875019 which contains gRNA 13. Part BBa_K1875016, an operator reporter with one binding site, also contains the same target sequence.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]