Difference between revisions of "Part:BBa K864440"
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<partinfo>BBa_K864440 short</partinfo> | <partinfo>BBa_K864440 short</partinfo> | ||
− | + | This part is a component of the Uppsala University iGEM 2012 modular small RNA screening system, together with the target construct <partinfo>K864444</partinfo>. | |
− | + | This is the small RNA spot42 from E coli MG1655 coupled to the strong promoter <partinfo>J23101</partinfo>. The spot42 regulates the galactose metabolism by binding to the mRNA and recruiting Hfq proteins [1], blocking initiation of translation. The spot42 has proven to be an especially suitable sRNA for engineering of silencing sRNA:s, by replacing its RNA-binding domain[2]. | |
− | + | To create a random sRNA library, the RNA-binding domain can be randomized by site-directed mutagenesis using the primers <partinfo>K864445</partinfo> and <partinfo>K864446</partinfo>. | |
− | + | ||
− | === | + | ===References=== |
− | Engineering Artificial Small RNAs for Conditional Gene Silencing in Escherichia coli | + | [http://www.ncbi.nlm.nih.gov/pubmed/12101127] Møller, T., Franch, T., Udesen, C., Gerdes, K., and Valentin-Hansen, P. ( 2002) Spot 42 RNA mediates discoordinate expression of the E. coli galactose operon Genes Dev. 16, 1696– 1706 |
− | + | ||
− | ACS Synthetic Biology 2012 1 (1), 6-13 | + | [http://pubs.acs.org/doi/full/10.1021/sb200001q] Sharma V., Yamamura A., and Yokobayashi, Y. (2002): Engineering Artificial Small RNAs for Conditional Gene Silencing in Escherichia coli. ACS Synthetic Biology 2012 1 (1), 6-13 |
Revision as of 16:21, 29 September 2012
Small RNA spot42
This part is a component of the Uppsala University iGEM 2012 modular small RNA screening system, together with the target construct BBa_K864444.
This is the small RNA spot42 from E coli MG1655 coupled to the strong promoter BBa_J23101. The spot42 regulates the galactose metabolism by binding to the mRNA and recruiting Hfq proteins [1], blocking initiation of translation. The spot42 has proven to be an especially suitable sRNA for engineering of silencing sRNA:s, by replacing its RNA-binding domain[2].
To create a random sRNA library, the RNA-binding domain can be randomized by site-directed mutagenesis using the primers BBa_K864445 and BBa_K864446.
References
[http://www.ncbi.nlm.nih.gov/pubmed/12101127] Møller, T., Franch, T., Udesen, C., Gerdes, K., and Valentin-Hansen, P. ( 2002) Spot 42 RNA mediates discoordinate expression of the E. coli galactose operon Genes Dev. 16, 1696– 1706
[http://pubs.acs.org/doi/full/10.1021/sb200001q] Sharma V., Yamamura A., and Yokobayashi, Y. (2002): Engineering Artificial Small RNAs for Conditional Gene Silencing in Escherichia coli. ACS Synthetic Biology 2012 1 (1), 6-13
Sequence and Features
- 10COMPATIBLE WITH RFC[10]
- 12INCOMPATIBLE WITH RFC[12]Illegal NheI site found at 7
Illegal NheI site found at 30 - 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]