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How dna works essay
How dna works essay
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All living things contain DNA. The molecule deoxyribonucleic acid or DNA is what contains an organism’s genetic information. The genetic information contained in DNA is what an organism requires to not only develop and reproduce but also survive. A DNA molecule is built up of nucleotides. Nucleotides are composed of several different things and what the nucleotides are composed of determines the name of it. Another job of DNA is to pass the genetic information through the process of protein synthesis. The DNA can show birth defects in the fetus using different testing. The knowledge of the birth defects of the fetus can be both positive and negative. DNA is a simple yet complex molecule that is used by all living things and makes us the way …show more content…
Protein synthesis consists of two main steps: transcription and translation. The DNA is found inside of the nucleus and there in the nucleus a copy of one side of the DNA strand is made, this is the messenger RNA or mRNA. After this the mRNA travels through the cytoplasm with the DNA copy and arrives at the ribosomes. The mRNA then goes through the ribosome three bases at a time. A transfer RNA molecule or tRNA then bring the correct amino acid to match the codon. The amino acids then link together to form a long chain of proteins, making amino acids the building blocks of …show more content…
Prenatal DNA testing for birth defects itself is very good and beneficial for the parents. What the parents decide to do with the knowledge though is where it can become negative and a bad thing. If you decide to have the prenatal DNA testing done and you find out that your child is going to be born with Down Syndrome you will then have decide to if you are going to continue the pregnancy or not. If the parents decide to have an abortion the moral ramifications of this are the parents might feel guilt or regret for killing an innocent unborn child or they might be relieved that they do not have to raise what they might consider a burden. This is one way prenatal DNA testing can be negative but there are also ways it can be positive because not everyone decides to have an abortion. If parents decided to keep the baby they can prepared for the baby and the lifestyle they will have. The parents could speak to other parents who have raised a child with Down Syndrome and the parents will feel prepared and happy with their choice to bring their beautiful child into the world. These test can go both ways, you can find out that you are going to have a healthy baby but waiting for your results can also bring unnecessary stress and worry which is also not good for the baby. In the end the moral ramifications of the tests are determined by what you do with
... to go through the DNA make-up child. When choosing prenatal DNA sequencing there are many positives that come along with it, such as being able to lessen the amount of genetic diseases within in the child. Although there can be many positives, there are many negatives that fall along with prenatal DNA sequencing, such as whether its right for the parent to alter their child’s genes. If a parent is still quite unsure of their decision they are able to go to genetic counselor, counselors in which are trained to help make an informed decision for the parent. Genetic counselors also are trained to provide information to the parent of a child with genetic diseases. A huge factor when choosing whether to undergo prenatal DNA sequencing is the cost of the procedure. Also if the family chooses to use a genetic counselor that adds on to the cost of prenatal DNA sequencing.
DNA is a molecule that is found in all living things. Almost
All cells contain a complex structure known as deoxyribonucleic acid (DNA). DNA is a chemical that determines how we are. The multiple combinations of its components are what makes a difference in each person. Long molecules of DNA are organized into chromosomes, which are grouped into 23 pairs. Then the chromosomes are broken down into short segments of DNA known as genes.
Genetic testing has potential benefits whether the results are positive or negative for a gene mutation. Test results can provide a sense of relief from uncertainty and help people make informed decisions about managing their health care. (What) Being able to see the genetic disorder that you baby may have while still in the womb, is really awesome how you don’t have to deliver the baby to see of they have a disorder. Even though you can find this out before the baby is born and it can be pretty scary you still have a higher chance that the baby
Proteins are the building blocks of muscle. Protein synthesis is the process of building new proteins. This process happens at a cellular level.
The first step in converting or copying genetic information is by the process called transcription. Transcription occurs in the nucleus of the eukaryotic cell and begins when the sigma is binded to the promoter of the start of the gene (Freeman). Next, the RNA polymerase unwinds part of the DNA and interprets the mRNA (which holds the encoded information) adding ribonucleotides complementary to the DNA strand (Freeman). Finally, transcription ends with a terminational signal ...
DNA (deoxyribonucleic acid) is a self-replicating molecule or material present in nearly all living organisms as the main constituent in chromosomes. It encodes the genetic instructions used in the development and functioning of all known living organisms and many viruses. Simply put, DNA contains the instructions needed for an organism to develop, survive and reproduce. The discovery and use of DNA has seen many changes and made great progress over many years. James Watson was a pioneer molecular biologist who is credited, along with Francis Crick and Maurice Wilkins, with discovering the double helix structure of the DNA molecule. The three won the Nobel Prize in Medicine in 1962 for their work (Bagley, 2013). Scientist use the term “double helix” to describe DNA’s winding, two-stranded chemical structure. This shape looks much like a twisted ladder and gives the DNA the power to pass along biological instructions with great precision.
First of all, I want to start by saying that I 'm not discriminating the disabled community, but this is a very large number that could possibly be diminished with the help of genetic testing. (1) I believe that there is nothing wrong with testing the genes of an unborn child to possibly determine if it could develop a genetic disorder in the future. One of the advantages that genetic testing provides is that the parents could now be informed of the situation, and keep track of their unborn child 's health. I 'm sure those parents are pleased with this technology, and the chances to be able to keep track of their baby. This a baby, and is something very precious, and valuable, and I believe that parents want to keep track of anything that may happen with the unborn child. I 'm sure that a large amount of people would agree would agree that they don 't want to suddenly take the hard hit. When the news is presented in the delivery room. This serves more as an advantage than a disadvantage, due to the fact parents. Pull be more prepared, or possibly have the option to abort it. This is a right that the parents should have regardless of the opposing side arguments towards it. Im a hundred percent sure that the opposing side has very strong arguments towards genetics testing, and one of the main ones is "playing God." The opposing side believed that some things in
Protein synthesis is one of the most fundamental biological processes. To start off, a protein is made in a ribosome. There are many cellular mechanisms involved with protein synthesis. Before the process of protein synthesis can be described, a person must know what proteins are made out of. There are four basic levels of protein organization. The first is primary structure, followed by secondary structure, then tertiary structure, and the last level is quaternary structure. Once someone understands the makeup of a protein, they can then begin to learn how elements can combine and go from genes to protein. There are two main processes that occur during protein synthesis, or peptide formation. One is transcription and the other is translation. Although these biological processes slightly differ for eukaryotes and prokaryotes, they are the basic mechanisms for which proteins are formed in all living organisms.
The first part of the process of protein synthesis is transcription - the creation of RNA based on the DNA template. First the enzyme RNA polymerase helps to unwind the DNA helix. Then the DNA is elongated. RNA polymerase binds to one strand of the DNA at the promoter sequence (a specific sequence of nucleotides on the DNA chain) and when it reaches the start signal, the formation of mRNA begins. Transcription stops when it reaches the termination signal.
Deoxyribonucleic acid (DNA) is a molecule, a material rather, that is present in almost all living organisms. It is self-replicating and is the main constituent of chromosomes. DNA contains genetic/hereditary information. The transmission of traits from one generation to the next is called
DNA- A nucleic acid that carries the genetic information in the cell and is capable of self-replication and synthesis of RNA. DNA consists of two long chains of nucleotides twisted into a double helix and joined by hydrogen bonds between the complementary bases adenine and thymine or cytosine and guanine. The sequence of nucleotides determines individual hereditary characteristics.
Translation is also a process that contains the RNA copy of DNA to make a protein. i.e the mRNA sequence is translated into a sequence of amino acids as a result protein is formed. During translation, RNA molecule is responsible
Protein synthesis is involved in gene expression. Gene expression is the process of DNA that controls protein synthesis. Genes code for certain proteins that are created by DNA transcription and translation (Reece, et al. 334). This happens by using an mRNA template to specify the order of amino acids. Protein synthesis starts on the free ribosomes within the cytosol. The signal sequence that initiates the process is located at the N-terminal end of the polypeptide chain. Different codons along the mRNA are translated into amino acids as a ribosome moves along it. Then, tRNAs act as adapters to control the movement of amino acids to the ribosome. This occurs through the base pairings of the codons of the mRNA and and anti-codon of the tRNA. The ribosome then forms the peptide bonds between the amino acids of the polypeptide chain (Erster Lect. 21). Creation of the polypeptide chain can be divided into three stages of initiation, elongation, and termination. Each stage requires the aid of protein factors. For certain parts initiation and elongation, energy may also be needed.
All living things are united by DNA. Small changes within the DNA create the vast variety that we see in the living creatures on earth. Each difference in humans makes the characteristics different and lead to different ways of thinking and new discoveries. DNA function in genes to create proteins that each have a specific and different purpose. These proteins carry out the vast different functions that keep a body functioning properly. Proteins