Department

Natural Sciences

Document Type

Poster

Abstract

The gene CDT1 is believed to be important for cadmium tolerance in plants. Here, we describe the production of a reporter construct to study CDT1 gene expression in the model plant Arabidopsis thaliana. We used Gibson assembly to insert the CDT1 promoter sequence into a plasmid containing the GUS reporter gene. The Gibson Assembly procedure provides an efficient method to join multiple DNA fragments. The resulting plasmid was transformed into E. coli using a heat-shock protocol. We confirmed successful transformations using colony PCR. Further DNA sequence analysis indicated that the CDT1prom-GUS plasmid has successfully been built! Next the CDT1prom-GUS construct will be introduced into Agrobacterium for plant transformation. Ultimately, we will create transgenic plants in which we can visualize CDT1 expression using the GUS reporter.

Publication Date

Spring 4-9-2026

Comments

Spring 2026: Student Research Conference

Best Overall, 1st Place – Ebrima Den 

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