– This was a 2 day project that we did to refresh ourselves on the basis of DNA and Protein Synthesis.
Replication
1.Explain the structure of DNA – use the terms nucleotide, anti parallel strands, and complimentary base pairing.
The structure of DNA is a polymer comprised of nucleotides which is a compound of a nitrogen base (Usually referred to as Adenine, Thymine, Cytosine, and Guanine for DNA), and a five-carbon sugar which is bonded to one or more phosphate groups. The nitrogenous bases are always hydrogen bonded through their complementary base pairing which, in terms of DNA is Adenine-Thymine and Cytosine-Guanine. Similarly, through the complementary bases, an antiparallel strand of DNA gets bonded to the template DNA creating a double helix shape.
2.When does DNA replication occur?
DNA replication is the process of which the DNA makes identical copies of itself, as its structure is a mechanism for reproducing itself. DNA Replication occurs when the cell divides, more specifically before the mitosis phase of cell division.
3.Name and describe 3 steps involved in DNA replication. Why does the process occur differently on the “leading” and “lagging” strands?
In DNA replication, each strand of DNA can be a template to force a new stand of DNA through complementary base pairing. The steps in DNA replication are as follows: 1) The unzipping phase where the DNA double helix unwinds and the hydrogen bonds that hold the two strands together separate (break). 2) Complimentary base pairing is crucial, as new nucleotide move into the separated DNA strand to form a new and complete DNA. These nucleotide are always floating within the nucleoplasm. 3) Adjacent nucleotide bonding, where sugar-phosphate bonds form between the adjacent nucleotide of the new strand to compete the molecule. Afterwards, the new molecule winds into the double helix. Thus completing the replication.The lagging strand is organized continuously, by which is synthesized by adding nucleotides to the 5′ end. The leading strand is organized in short fragments that are ultimately stitched together. The leading strand is organized particularly by adding nucleotides to the 3′ end of the strand, which continues to grow.
4. Today’s modeling activity was intended to show the steps involved in DNA replication. What did you do to model the complementary base pairing and joining of adjacent nucleotide steps? In what ways was this activity well suited to showing this process? In what ways was it inaccurate?
In the replication modelling activity, to show the complementary base pairing we first formed the template DNA strand with paper cut-outs of the nucleotides, phosphate group, and sugar group while showing covalent bonds by solid lines and hydrogen bonds through dotted lines. Afterward, we had drawn the complementary bases of the template strand bonded through H-bonds (dotted lines) the comp bases are also accompanied by a sugar group and phosphorous group to form an antiparallel strand of DNA to the template DNA. Afterward, we used paper cut-outs of scissors to represent the helicase used in unzipping the DNA. Then, we showed two strands of DNA that start forming adjacent nucleotide bonds with a pointy circle to represent the polymerase and stars to represent the ligase. Doing this is an excellent way to visualize the idea of a single template DNA being replicated and turning into two new identical strands of DNA. Though this method can’t express aspects such as the double helix structure of the DNA
Transcription
1. How is mRNA different than DNA?
In its essence, mRNA is a copy of a DNA template strand that carries genetic information (code), from the nucleus into the cytoplasm and to the Ribosome. mRNA is a single strand molecule that is is structurally distinctive, as well as the fact that it has Uracil in replacement of Adenine. mRNA carries the genetic code for amino acids to create proteins. On the other hand, DNA is double stranded molecules of deoxyribose sugars and phosphate molecules, while RNA has ribose sugar. Furthermore, DNA is distinctive in its “double helix” shape before transcription is initiated, in which it “unwinds and “unzips” the double stranded molecules for transcription.
2. Describe the process of transcription
The process of transcription is the production of RNA from DNA. Transcription follows a sequence of steps that allow for a successful “mirror” replication following complimentary base pairs (with the exception of adenine replaced with Uracil). First, a section of DNA “unwinds” and “unzips,” exposing a set of bases for the second step: complementary base pairing along one of the two strands of DNA. Thirdly, adjacent RNA nucleotide forms sugar phosphate bonds. Fourthly, the RNA strand is released from DNA and follows the fifth step, which DNA molecule “rewinds,” and returns to its original shape of a double helix. Finally, once RNA is produced, mRNA strand is often processed, by which certain sections called introns are cut out and a “poly A” tail is added to the 3′ end, and a cap is added to the 5′ end. From there, the RNA leaves the nucleus and goes into the cytoplasm.
3. How did today’s activity do a good job of modelling the process of RNA transcription? In what ways was our model inaccurate?
In the paper model of RNA transcription, it had effectively shown how the mRNA is created based on the template DNA, though a few downsides to this method is that as the nitrogenous bases were just written on paper, it is impossible to show the differences between adenine, uracil, cytosine, and guanine. Furthermore, through the methods we used in the RNA transcription model, we weren’t able to show the effects of genetic mutations.
Translation
1. Describe the process of translation
Translation is the process that converts mRNA to actual proteins, which occurs outside of the nucleus, within the cytoplasm and on the surface of the ribosome. It is known that the order of bases in DNA, which is processed into RNA, determines the amino acid sequence necessary to produce the polypeptide chain that creates the protein. The process of translation can be categorized in three sub processes. Translation begins with initiation, where the mRNA and its start codon of AUG attaches to the ribosome, specifically at the R site. The AUG codon always initiates translation and it is the code for producing amino acid Methionine, or (MET) for short. The sequence of producing amino acids relies on 3 bases called the anti-codon that is complementary to the mRNA codon. Next, Elongation occurs where more and more amino acids are added to create a chain of amino acids (polypeptide). As Elongation occurs to lengthen the polypeptide chain, the final step of translation occurs: Termination. Termination ends translation, where a special codon called the “stop” codon is read. These stop codons can be UAA, UAG, or UGA. The stop codon does not produce an amino acid, but rather signals to stop the translation. In Termination, a protein called release factor binds directly to the stop codon in the A site, thus separating the chain from the last tRNA.
2. How did today’s activity do a good job modelling the process of translation? In what ways was our model inaccurate?
The modelling of the translation was a good way to show how the mRNA goes through the rRNA and how tRNA with its anticodons pairs with the codons on the mRNA and form a polypeptide chain. Some parts of the model that are inaccurate is that it couldn’t properly express that the rRNA are two subunits formed into one.