Transcription activity
For this activity, we will be using the “3-D Molecular Designs Flow of Genetic Information Kit”.
In your kit, please find the following items (put the rest back in the box)
- Transcription of DNA into RNA placemat
- Sequence I Replication & Transcription DNA strip
- 4 bags of DNA nucleotides (yellow = Thymine, green = Guanine, red = Adenine, blue = Cytosine)
- 4 bags of RNA nucleotides (these have a square shape; the colors are the same as for DNA except Uracil is white).
- Begin by fully assembling the double-stranded DNA sequence as it is shown on the paper strip.
- Notice the 3’ and 5’ directionality of the DNA
- Notice that one molecule (strand) is the reverse complement of the other. They are not identical.
- Which is the 3’ end and which is the 5’ end of each nucleotide?
- Place your assembled DNA on the right of the placemat. Slide it toward the left.
- The RNA polymerase will separate the two strands of DNA.
- The top strand will be the template strand. It serves as a template for creating the mRNA.
- The bottom strand will be the non-template strand. It serves no purpose in transcription.
- The bottom strand is also called the “coding” strand because it has the same code as the mRNA.
- Push your DNA through the RNA polymerase so that about 8 nucleotides have been separated from the other strand.
- At the active site shown, add an RNA nucleotide (they are relatively square) that is complementary to the DNA nucleotide that is in the active site.
- Push the DNA sequence one base further in.
- Add another RNA nucleotide that is complementary to the DNA. Connect this second RNA nucleotide to the first.
- Continue to push the DNA further into the polymerase and adding mRNA nucleotides to the growing mRNA strand. Notice that, as with DNA, RNA is synthesized at the 3’ end.
- As the DNA exits from the polymerase, re-join the hydrogen bonds to re-create the double helix of DNA.
- The mRNA that has been growing will remain single-stranded.