Question
How can siRNAs that target the promoter region of a gene be made? Present evidence to support your hypothesis.
Step 1
Begin by selecting the gene of interest for which you want to design siRNAs. Use bioinformatics tools to locate the promoter region of the gene, which is typically found upstream of the transcription start site (TSS). Databases like Ensembl or UCSC Genome Show more…
Show all steps
Your feedback will help us improve your experience
Joanna Quigley and 64 other educators are ready to help you.
Ask a new question
Labs
Want to see this concept in action?
Explore this concept interactively to see how it behaves as you change inputs.
Key Concepts
Recommended Videos
How do siRNAs work?
During experimental RNAi, how does the researcher affect expression of a target gene? Inject custom, lab-made siRNAs complementary to the target gene's transcript. Inject custom, lab-made double-stranded RNA into the specimen that will be targeted by the cell's existing Dicer to create siRNA complementary to the target gene's transcript. Inject lab-made Dicer proteins into the specimen which will cut up the target gene's transcript.
Scientists have exploited the siRNA pathway to perform a technique called $R N A$ interference-a means to knock down the expression of a specific gene without having to make mutations in it. The idea is to introduce dsRNA corresponding to the target gene into an organism; the dsRNA is then processed into an siRNA that leads to the degradation of the target gene's mRNA. One clever method for delivery of the dsRNA to some organisms (the nematode C. elegans, for example) is to feed them bacteria transformed with a recombinant plasmid that expresses dsRNA.
Transcript
18,000,000+
Students on Numerade
Trusted by students at 8,000+ universities
Watch the video solution with this free unlock.
EMAIL
PASSWORD