Source:
Generated By: https://synbiohub.org/public/igem/igem2sbol/1
Created by: Angelina Munabi
Date created: 2014-10-09 11:00:00
Date modified: 2015-05-08 01:10:41
P_PiI6, marchantia promoter
| Types | DnaRegion |
| Roles | promoter Regulatory |
| Sequences | BBa_K1484344_sequence (Version 1) |
Description
This part is an untested potential promoter for Marchantia polymorpha. It is thought to initiate transcription under conditions of inorganic phosphate (Pi) starvation. We identified the promoter during a broader search for potential inputs to our genetic circuit, and we think it may be used as such, but testing will definitely be required to confirm this.We submit this part as a foundation for future marchantia work. We were able to physically obtain DNA from a PCR of a marchantia genome.
Notes
The removal of illegal restriction sites was considered but not completed due to direct interaction of the DNA with regulatory proteins. Also, it was ensured that the region selected for this part was directly upstream of the first ATG of the gene used to identify the promoter sequence. This was so that the 5' UTR, that is vital in plants, was maintained.Source
This part was found by screening the genome of the Marchantia polymorpha Cam strain maintained by the Haseloff lab for homologues to Phosphate Transporter and Purple Acid Phosphatase proteins in A. Thaliana, known respectively as AtPT2 and AtPAP10. Transcription is thought to be induced by re-supply of inorganic phosphate after starvation.Matches to the protein CDS sequence were found using Geneious to perform a tblastn search on the genome scaffolds. Predicted genes that contained hits graded above 30% and with at least 40% congruence to mRNA transcript sequences were shortlisted. The best gene candidates (judged according to number and distribution of hits along its length, and supporting mRNA sequence) formed the basis for our predicted promoters. This part was isolated from a 2kb region upstream of the first ATG of such a gene.