Difference between revisions of "Part:BBa K2908444"
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===Usage and Biology=== | ===Usage and Biology=== | ||
- √ miRNA-BD (microRNA binding sites) Design<br/> | - √ miRNA-BD (microRNA binding sites) Design<br/> | ||
We designed, constructed, and sequence validated a miRNA sensor library containing all 620 sequences of mature human miRNAs designated as high confidence in miRBase 2124. Our library enables high-information-content screening of miRNA activity in cells and also serves as a source for sequence-validated templates of miRNA targets when building multi-input sensors. We synthesized miRNA target site sets bearing four repeats of the sequence perfectly complementary to the miRNA and inserted them into the 3′ UTR of a reporter construct.<br/> | We designed, constructed, and sequence validated a miRNA sensor library containing all 620 sequences of mature human miRNAs designated as high confidence in miRBase 2124. Our library enables high-information-content screening of miRNA activity in cells and also serves as a source for sequence-validated templates of miRNA targets when building multi-input sensors. We synthesized miRNA target site sets bearing four repeats of the sequence perfectly complementary to the miRNA and inserted them into the 3′ UTR of a reporter construct.<br/> | ||
It’s worth mentioning that, the design of this part is instructed by the 2019 team SYSU_CHINA (Detailed information of collaboration can be seen in the Team/Collaboration page in our wiki. Address: http://2019.igem.org/Team:CSU_CHINA/Collaborations)<br/> | It’s worth mentioning that, the design of this part is instructed by the 2019 team SYSU_CHINA (Detailed information of collaboration can be seen in the Team/Collaboration page in our wiki. Address: http://2019.igem.org/Team:CSU_CHINA/Collaborations)<br/> | ||
| − | - Construction: miRNA-BDs were constructed bearing four repeats of miR-21-5p in the 3’ UTR, or 5’ UTR. Since these miRNA-BDs do not have ATGs, several ATGs were added between the miRNA target sites in some sensors. Extra bases were added to separate the ATGs by a number of bases divisible by three. The distance between the last ATG and the true reporter start codon was either divisible by three or not . | + | - Construction: <br/> |
| + | miRNA-BDs were constructed bearing four repeats of miR-21-5p in the 3’ UTR, or 5’ UTR. Since these miRNA-BDs do not have ATGs, several ATGs were added between the miRNA target sites in some sensors. Extra bases were added to separate the ATGs by a number of bases divisible by three. The distance between the last ATG and the true reporter start codon was either divisible by three or not . | ||
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Revision as of 20:49, 17 October 2019
miR148b-BD
When binding with miR148b, it can inhibit the translation of mRNA which include the same sequence.This part is designed by assembling several complemental sequence with miR148b together and synthesized by company.It is used as a target aimed by miR148b to block the gene circuit in normal cells.
Usage and Biology
- √ miRNA-BD (microRNA binding sites) Design
We designed, constructed, and sequence validated a miRNA sensor library containing all 620 sequences of mature human miRNAs designated as high confidence in miRBase 2124. Our library enables high-information-content screening of miRNA activity in cells and also serves as a source for sequence-validated templates of miRNA targets when building multi-input sensors. We synthesized miRNA target site sets bearing four repeats of the sequence perfectly complementary to the miRNA and inserted them into the 3′ UTR of a reporter construct.
It’s worth mentioning that, the design of this part is instructed by the 2019 team SYSU_CHINA (Detailed information of collaboration can be seen in the Team/Collaboration page in our wiki. Address: http://2019.igem.org/Team:CSU_CHINA/Collaborations)
- Construction:
miRNA-BDs were constructed bearing four repeats of miR-21-5p in the 3’ UTR, or 5’ UTR. Since these miRNA-BDs do not have ATGs, several ATGs were added between the miRNA target sites in some sensors. Extra bases were added to separate the ATGs by a number of bases divisible by three. The distance between the last ATG and the true reporter start codon was either divisible by three or not .
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]