Science, discussed.

Synthetic biology made circular [preprint]

Clever use of group I permuted intron-exon sequences to obtain circular riboregulators that performs better than their linear counterparts.


For the whole story, read the preprint on @bioRxiv
Engineering a circular riboregulator in Escherichia coli
William Rostain, Shensi Shen, Teresa Cordero, Guillermo Rodrigo, Alfonso Jaramillo

Circular RNAs have recently been shown to be important gene expression regulators in mammalian cells. However, their role in prokaryotes remains elusive. Here, we engineered a synthetic riboregulator that self-splice to produce a circular molecule, exploiting group I permuted intron-exon (PIE) sequences. We demonstrated that the resulting circular riboregulator can activate gene expression, showing increased dynamic range compared to the linear form. We characterized the system with a fluorescent reporter and with an antibiotic resistance marker. Thanks to the increased regulatory activity by higher stability, isolation due to self-splicing, and modularity of PIE, we envisage engineered circular riboregulators in further synthetic biology applications.

About Pietro Gatti

Interested in discussing (good) Science Lover of coffee & good films. Ideas all & only my own.

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This entry was posted on 25/09/2014 by in preprintreview, Synthetic Biology.


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