Part:BBa_K3154001
Second Generation Toehold Switch for hsa-miR-21-5p with GFPmut3b
Toehold switches are a class of de novo designed mRNA based riboregulators that possess unique properties such as low crosstalk, high orthogonality and high dynamic range. They are hence highly desirable as agents of translational regulation of reporter protein genes in abiotic situations for many synthetic biology applications. Toehold switches have free energy and sequence constraints amongst the various domains that determine their optimal conformation. The regions of the toehold switch are the unique toehold or switch domain to which the trigger RNA binds via base pairing, the bottom stem, the secondary loop that contains the start codon, the top stem containing a scar site in the descending portion, the primary loop that consists of a preRBS and RBS sequence, and a horizontal linker sequence that concatenates the toehold switch to the downstream reporter gene. In the OFF state, the RBS cannot come in contact with the ribosome, and therefore no translation occurs. In the ON state, the unfolding of the switch into a linear molecule allows for the ribosome- RBS interaction to take place and translation to occur. This part is a de novo engineered second generation toehold switch for detecting the microRNA sequence hsa-miR-21-5p, wherein we recommend this part for its utility in the regulation of the downstream reporter gene followed by subsequent quantification of the microRNA hsa-miR-21-5p. The second generation toehold switch design allows for higher programmability of the involved sequences, resulting in better performance of the toehold switch. The significance of the second generation design is necessitated by the presence of a stop codon in the open reading frame of the sequence of hsa-miR-21-5p. The toehold domain and the ascending segment of the bottom stem must be complementary to the trigger RNA in order to linearize the switch in its ON state. The descending segment of the bottom stem will thus be complementary to the ascending segment, resulting in a subsequence of the trigger itself. This allows for the stop codon to repeat itself in the reading frame after the start codon in the secondary loop. Therefore, translation stops at that point and no downstream gene can be expressed. The stop codon in the open reading frame of the switch sequence can be avoided by modifying the trigger sequence binding to it. An antisense RNA, or antimiR, is designed such that it is partially complementary to the microRNA. This creates a hybrid, T shaped trigger sequence where the base paired stem of 12 nt length sequesters the stop codon, and the free ends of 22 nt in total, hybridize with the toehold switch.
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000INCOMPATIBLE WITH RFC[1000]Illegal BsaI.rc site found at 79
Illegal BsaI.rc site found at 745
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