DNA Replication and Protein Synthesis Modelling

Replication:

DNA strand                                             Unzipped DNA Strand

1. DNA, or deoxyribonucleic acid, is a double-stranded molecule that stores genetic information in all living organisms. Its structure consists of repeating units called nucleotides, which are composed of a sugar molecule, a phosphate group, and a nitrogenous base.

The sugar molecule in DNA is called deoxyribose. The phosphate group is attached to the 5′ carbon of the sugar molecule, while the nitrogenous base is attached to the 1′ carbon.

The four nitrogenous bases in DNA are adenine (A), guanine (G), cytosine (C), and thymine (T). The bases pair up in a specific pattern through hydrogen bonds to form the “rungs” of the DNA ladder. Adenine pairs with thymine, and guanine pairs with cytosine, known as complementary base pairing.

The two nucleotide strands in DNA are antiparallel or run in opposite directions. One strand runs from 5′ to 3′, while the other runs from 3′ to 5′. The direction of the strands is determined by the orientation of the sugar molecule, which has a free 3′ hydroxyl group on one end and a free 5′ phosphate group on the other end.

The double helix structure of DNA is formed when the two nucleotide strands twist around each other. The nitrogenous bases form the rungs of the helix, while the sugar-phosphate backbone forms the sides. The hydrogen bonds between the complementary base pairs hold the two strands together, providing stability for the double helix structure.

2. The DNA process is when the cells synthesize a copy of DNA is the cell’s nucleus. Before the cell divides it must copy or “replicate” its genome so that each daughter cell ends up with its own complete genome. DNA replication occurs during the “S Phase” and is the period in which the cell replicates its genetic content during the cell cycle before mitosis or meiosis and is the product of synthesis or replication.

3. Firstly, the DNA will unzip, which is when the unwinding of the double helix takes place. Additionally, the two strands of DNA will separate from one another while the hydrogen bonds that were formed between bases are broken. Secondly, complementary base pairing occurs where new nucleotides come into place to pair with the bases of the appropriate template strand of DNA. These new nucleotides are constantly roaming around the nucleoplasm. Finally, adjacent nucleotide bonding occurs where sugar-phosphate bonds are formed between adjacent nucleotides. These nucleotides come from the new strand which is required in order to complete the molecule. Each new strand of DNA has one old strand and one new strand which is called semi-conservative replication. This makes sure that there will be an accurate replication of the parent molecule. In the end, the product of replication by one DNA molecule is two complete double-stranded DNA molecules. Each molecule has one new strand and one old or original strand which had the role of being a template for replication.

The reason that the process occurs differently on the “leading” and “lagging” strands is because of the antiparallel orientation the two chromosomal DNA strands have. The leading strand is replicated in a processive way for the most part while the lagging strand is synthesized in short fragments.

4. We were given a Strand of DNA and we had to replicate the strand. Once we got to a certain point, we “unzipped” the strand of DNA. Once the DNA was unzipped, we could model the complementary base pairing and attach nucleotide where it belonged creating two strands. The model we made showed a simple understanding of how DNA replicated. This model could be accurate as sometimes incorrectly pairing one nucleotide with another.

 

Transcription:

Transcription from DNA strand to RNA strand

1. Describe the process of transcription

The process of transcription takes place in the nucleus. It uses the DNA to make a template for RNA also known as mRNA molecule. During the transcription process, an RNA stand is made to complement a DNA strand. Transcription starts when an RNA polymerase binds to a promoter sequence near the beginning of a gene through helper proteins. Transcription occurs when there is a need for a gene at a certain time or at a certain tissue. When transcription occurs it usually only copies 1 strand of DNA and is called a template strand. When in transcription the RNA molecules come together and produce a single-stranded messenger RNA (mRNA).

2. How did today’s activity do a good job of modelling the process of RNA transcription? In what ways was our model inaccurate?

It shows how the RNA strand is created from a template strand and how RNA is its own copy of a gene’s DNA sequence. Our model did a great job depicting the accuracy of the process of RNA transcription as the model shows how the ribosomal subunit goes across the template strand making complimentary base parings one by one until 3 of the nucleotides create a stop codon, where the m-RNA creation is stopped. Our model stops the process when we hit the stop codon.

Translation:

Translation from mRNA to Amino Acids 

1. The process of translation is when a cell uses the genetic information in m-RNA to make proteins. The information m-RNA carries tells cells how to link amino acids together to make proteins. Translation occurs in three steps, initiation, elongation, and termination. During initiation, a ribosome attaches itself to t-RNA which carries methionine they then bind to m-RNA at the start codon AUG. During elongation, the RNA strand gets longer as new nucleotides get added. The final step of translation is termination, where one of the three stop codons will arrive at the A site of the ribosome. No molecules from t-RNA bind to the stop codons so the peptide chain is released into the cytoplasm.

2. It was a good model because it showed the fundamental steps of how the process of translation occurs and how each amino acid is created based on the mRNA strand that was transcribed from the strand of DNA.  The way this was inaccurate was because mRNA translation occurs fast about 40 amino acids per second whereas we were doing one amino acid per 10 seconds.

Gilead Theme Park – The Handmaid’s Tale

 

https://create.piktochart.com/output/56985744-handmaid-s-tale-brochure

Our theme park is based off the novel The Handmaid’s Tale by Margaret Atwood. The book is about the republic of Gilead and their dangerously low reproduction rates. The handmaids are the only women that are able to have children for the elite couples. For my role I was given the responsibility of the character sketches. To prepare for my role i made sure that I spent more time focusing on the behaviors of the characters throughout the novel and when we completed the novel, I read the character analysis of my three selected characters, Offred, Aunt Lydia, and Nick. Then i went back and revised the book to find key quotes to support my descriptions and highlighted them with sticky notes. When we completed the project i feel that i gained a deeper understanding to the meaning of the novel and Margaret Atwood’s reasoning for writing it. Though trying to finish it in time was a bit stressful, doing this project was very informative about how Margaret Atwood came to writing this book and the journey along with it. It also gave me the opportunity to expand on my analyzing skills for English Literature.

What Darwin never knew

How did the discovery of DNA prove that Darwin’s theory of evolution was correct and how does it change the way we view evolution today and into the future?

 

Darwin’s went on a voyage in the southern hemisphere in 1835 on the HMS beagle, but primary he went to the Galapagos islands. During the five weeks he had spent there, he observed the animals from island to island, taking notes. When he returned to London after his 5-year trip on the HMS Beagle he realized that the finches had very slight variations between the finches on each island; specifically, that their beak shapes were different because of the available diet, but he didn’t know how the changes had happened. The missing pieces to his work would be found in DNA but since DNA hadn’t been identified until 1953.

Darwin’s research was the foundation of our knowledge of evolution. His book, On the Origin of Species, gave us the ability to discover DNA and genetics. Darwin had found that the tortoise’s shell and neck shape had changed from island to island. The herbivore tortoises that ate plants closer to the ground had shorter necks. That information could be used to compare the tortoises from the 1800s and now.

In the future we can see how the species of the past changed since Darwin had discovered them or in the pas 60 years due to natural selection. We will have more technology and knowledge to take our current knowledge about natural selection further.

 

“Evolution: Library: Adaptive Radiation: Darwin’s Finches”. Pbs.Org, 2021, https://www.pbs.org/wgbh/evolution/library/01/6/l_016_02.html.

“Origin of the Species: Where Did Darwin’s Finches Come from?” The Guardian, Guardian News and Media, 30 July 2018, https://www.theguardian.com/science/2018/jul/30/origin-of-the-species-where-did-darwins-finches-come-from.

Frazier, Jack. “Chapter 1 – the Galapagos: Island Home of Giant Tortoises.” ScienceDirect, edited by James P. Gibbs et al., Academic Press, 1 Jan. 2021, pp. 3–21, www.sciencedirect.com/science/article/pii/B9780128175545000046.

The science of metagenomics

Introduction

 Metagenomics was only introduced a few years ago, in 1998. It was introduced as an alternate form of microbiology about how genetics and microbes in a community interact with each other without studying one particular organism in particular. Since organisms typically don’t live completely isolated for their whole life, they need to be studied in a controlled environment amongst other organisms they would live and grow with.

 

 The greatest advancements in metagenomics

 One of the larger advancements in metagenomics took place in a study in the Baltic sea in Europe. The scientists who performed this study targeted bacterioplankton in the deepest area of the sea, at 459m. While conducting the study they compared their findings to a similar study done in 1991 that stated that the salinity in the water might be influencing the bacterial growth in the water. As they compared their findings, they found that the degree of the growth was much larger than they had anticipated it was in 1991, in point of fact they have concluded that the Baltic sea contains a higher amount of variation of bacteria than most other marine environments.

 

 How is the form of metagenomics being used?

 Metagenomics is a tool used to analyze DNA from samples of environments to review the community of microorganisms. Metagenomic scientists isolate the DNA and RNA from the received sample without identifying a particular organism. The DNA and RNA are then put through different procedures such as DNA sequencing to identify common genes.

 How metagenomics changes the future

 Metagenomics has been used in food production in recent years to diagnose pathogens. In the future scientists are hoping that it will be routine to do diagnostics and they will be able to recognize and extract or remove the foodborne pathogen if necessary. If this is possible to do, there will be less or even possibly no illness outbreaks in produce. 

Citations:

Wooley, John C, and Yuzhen Ye. Metagenomics: Facts and Artifacts, and Computational Challenges*. Jan. 2009, www.ncbi.nlm.nih.gov/pmc/articles/PMC2905821/.

10. Alneberg, BS. Bjarnason, et al. “Microbial Metagenomics in the Baltic Sea: Recent Advancements and Prospects for Environmental Monitoring.” Ambio, Springer Netherlands, 1 Jan. 1970, link.springer.com/article/10.1007/s13280-015-0663-7#Sec6.

National Research Council (US) Committee on Metagenomics: Challenges and Functional Applications. “Why Metagenomics?” The New Science of Metagenomics: Revealing the Secrets of Our Microbial Planet., U.S. National Library of Medicine, 1 Jan. 1970, www.ncbi.nlm.nih.gov/books/NBK54011/.

Forbes, Jessica D., et al. “Metagenomics: The Next Culture-Independent Game Changer.” Frontiers, Frontiers, 29 May 2017, www.frontiersin.org/articles/10.3389/fmicb.2017.01069/full.