Difference between revisions of "Part:BBa K4887001"
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Oligo 1 (GBSSI-sgRNA1): 5’-GTGGGGTTGGGTCAATTAGCCCTGAGGAGC-3'
 
Oligo 1 (GBSSI-sgRNA1): 5’-GTGGGGTTGGGTCAATTAGCCCTGAGGAGC-3'
 
Oligo 2 (GBSSI-sgRNA2): 5’-AACTGGTGGACTTGGAGATGTTCTTGGAGG-3’
 
Oligo 2 (GBSSI-sgRNA2): 5’-AACTGGTGGACTTGGAGATGTTCTTGGAGG-3’
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<b>Fig. 1 The target region of gene IbGBSSI and the location of the gRNA.</b> Exons are shown as square frames and surrounding introns appear as lines. sgRNA and PAM are highlighted in yellow and green, respectively.
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<i><b>Fig. 1 The target region of gene IbGBSSI and the location of the gRNA. </b>Exons are shown as square frames and surrounding introns appear as lines. sgRNA and PAM are highlighted in yellow and green, respectively.</i>
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<b>(2) The expression level of IbGBSSI in storage roots</b>
 
<b>(2) The expression level of IbGBSSI in storage roots</b>
 
The relative expression level of the gene IbGBSSI was determined with the method of Quantitative Real-time PCR with the root-tuber cDNA as templates. The result showed that the relative expression level of IbGBSSI in root tubers of the transgenic lines (0.1063 and 0.2407) was much lower than that of the wild type (1.0000) (Fig. 2). It revealed that the knock-out of IbGBSSI in the pathway of starch synthesis was successful.
 
The relative expression level of the gene IbGBSSI was determined with the method of Quantitative Real-time PCR with the root-tuber cDNA as templates. The result showed that the relative expression level of IbGBSSI in root tubers of the transgenic lines (0.1063 and 0.2407) was much lower than that of the wild type (1.0000) (Fig. 2). It revealed that the knock-out of IbGBSSI in the pathway of starch synthesis was successful.
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  <img class="bild" src="https://static.igem.wiki/teams/4887/wiki/images/images/part-q-pcr-result-of-the-relative-expression-level-of-ibgbssi-in-root-tubers.png">
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  <div class="unterschrift"><b>Fig. 2 Q-PCR result of the relative expression level of IbGBSSI in root tubers</b>
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===Usage and Biology===
 
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<span class='h3bb'>Sequence and Features</span>
 
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Revision as of 09:55, 6 October 2023


IbGBSSI

The encoding gene of granule-bound starch synthase I (GBSSI) in sweet potato (Ipomoea batatas). It is one of the starch biosynthetic pathway genes on the starch biosynthetic pathway.


(1) GBSSI-sgRNA design

The selected sgRNA is located 70 bp downstream of the start codon, with a total sequence length of 27 bp (Fig. 1). sgRNA oligos were obtained by annealing with the designed primers following: Oligo 1 (GBSSI-sgRNA1): 5’-GTGGGGTTGGGTCAATTAGCCCTGAGGAGC-3' Oligo 2 (GBSSI-sgRNA2): 5’-AACTGGTGGACTTGGAGATGTTCTTGGAGG-3’

Fig. 1 The target region of gene IbGBSSI and the location of the gRNA. Exons are shown as square frames and surrounding introns appear as lines. sgRNA and PAM are highlighted in yellow and green, respectively.



(2) The expression level of IbGBSSI in storage roots The relative expression level of the gene IbGBSSI was determined with the method of Quantitative Real-time PCR with the root-tuber cDNA as templates. The result showed that the relative expression level of IbGBSSI in root tubers of the transgenic lines (0.1063 and 0.2407) was much lower than that of the wild type (1.0000) (Fig. 2). It revealed that the knock-out of IbGBSSI in the pathway of starch synthesis was successful.

Fig. 2 Q-PCR result of the relative expression level of IbGBSSI in root tubers