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An essay on the biological role of DNA
Importance of dna in biology
Importance of dna in biology
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Many people have wondered what it is exactly that makes us...human. What is it that separates us from one another that makes us unique? DNA and Genes is what makes every person up. Everyone is different because of it. Humans are different from each other by their skin color, their facial features, and it’s all due to Deoxyribonucleic Acid. DNA or Deoxyribonucleic Acid is a molecule that contains the genetic instructions that are used in the functioning, the development, and the reproduction that is a necessity to humans and other living organisms.
Deoxyribonucleic Acid (DNA) was first discovered in the year the year 1869 by Swiss physiological chemist, Friedrich Miescher. Back then they didn’t have the technology that we have today, so it
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Each of the nucleotides accommodate a phosphate group, sugar group, and a nitrogen base. There is four nitrogen bases in DNA. The four nitrogen bases are; Adenine (A), Thymine (T), Guanine (G), and Cytosine (C). Each of the bases are connected to a sugar molecule and a phosphate molecule. They are then positioned into two long strands that form a spiral called a double helix (DNA). The nitrogen bases are paired up with one another. Adenine and Thymine will always be paired with each other because of the bonds between them. Between A and T, there are two hydrogen bonds. The same goes with Guanine always being paired with Cytosine due. Between both G and C there is three hydrogen bonds. The nitrogen bases Adenine and Guanine won’t pair up with each other because, of their size. Both the nitrogen bases Adenine and Guanine are a purine base. Thymine and Cytosine are both a pyrimidine base. Adenine pairs with Thymine, and Guanine pairs with Cytosine, because they are of opposite …show more content…
Genes more specifically, are passed down from the parents down to the child. A child is a combination of both its parents. The child receives half of his mother’s genes and half of his father’s genes. Genes act like instructions, giving you certain features. According to the Human Genome Project, it is estimated that humans have 20,000 to 25,000 genes.
There is also genetic mutations which is a conversion in DNA. Mutations can affect chromosomes, which have multiple genes. Gene mutations are known to cause more medical conditions. Genetic mutations are able to mess with the normal development of a child. There is truly no way to prevent genetic mutations, because they are passed from the parent down to the child. Mutations aren’t always passed down to a child. They can sometimes skip a generation or more, it all just depends.
Along with genetic mutations, there is also genetic diseases. Genetic diseases are an abnormality in the DNA. One of the most known and common genetic disease is “Chromosome 21” or formally known as Down syndrome. It is where a child is born with three sets of the Chromosome 21 instead of being born with only two. How it happens is when a part of a chromosome 21 becomes attached to another one during the stage of reproduction. You are able to tell if a person has Down syndrome or not. Most of the physical features are obvious. By looking at a person’s face you are able to tell, because
DNA Timeline: DNA Science from Mendel to Today. (2014). Retrieved May 29, 2014, from http://www.dnai.org/timeline/
On a normal person, you have 23 pairs of chromosomes. In each pair, 1 gene comes from the mother, and 1 gene comes from the father. This is how things get passed down from parents to children (like eye color, height, skin tone etc...).
The molecule consisted of a double helix with phosphates, deoxyribose sugar molecules, and nitrogenous bases. If the spirals were split, the DNA could replicate, which explained why genes were transferred from parents to their children. Additionally, the order of compounds on the DNA indicated that there was a unique ‘code’ on each strand. Watson and Crick believed that this ‘code’ was translated into specific proteins. , ,
Mutation results in the changes in physical or physiology of an organism. Like in the movie, Mystique who can change someone else physically. Mutation could be beneficial, neutral or harm the organisms as mutation occur randomly. In the movie, the mutation that occur in their X genes led to super ability which is beneficial. However, mutation in the movie is not possible in real life. This is because mutation in human in chromosomal mutation only harm and will not give any superpower like in the movie. Chromosomal mutation in human are as a result of deletion, duplication, inversion and translocation of chromosomes. All these will results in either excess chromosomal numbers or less chromosomal numbers, Aneuploidy such as Down syndrome. Mutation is one of the reasons which is one of the factor that led to
... have been doing a phenomenal job of figuring this out. DNA is the chemical in each cell that carries our genes. DNA is the source of just about everything. It not only determines what we look like, but also many other things. Instructions are on some of our genes to let them know when they need to multiply and divide. Cancers can be caused by DNA defects.
Mutations are a result of changes in the DNA sequences. These changes can happen as a point mutation, which is a change in one base pair of codons, or the can happen to an entire sequence of pairs or the breaking of pairs. Point mutations are substitution, insertion, and deletion. Another type of mutation is translocation, and this can occur in a chromosome or between different chromosomes. With a substitution mutation it can be one of 3 types. These types are nonsense, misssence, or silent. Some mutations are caused by exposure to radiation and due to certain medications and chemicals. If these mutations are within reproductive cells, they will be passed down to the next generation. They can inherit is as a recessive trait, a dominate trait, or get the recessive trait from both parents. If the mutation is dominate, the offspring will have the disease. This is also true if they inherit it from both parents. If it is only inherited as a recessive trait from one parent, then they will be a carrier and will pass it to their offspring. This mutation will pass through generations the same as a gene for eye color or height. The same is true for a helpful mutation, like the mutation for resistance to diseases, for stronger bones, or better color vision.
Everybody are born with genes. Genes are basic physical and functional unit of hereditary. It’s made up of DNA. DNA are like instructions that make molecules called proteins. Genes have different sizes depending on the DNA. You have two copies of genes, each coming from your mother and father. We also have something called chromosomes which most of our cells contain. Altogether we have 46 chromosomes and this is all where it starts. Sperm and egg cells contain 23 chromosomes . Two of the 46 chromosomes determine the sex of a person. Girls inherit two X- chromosomes from their mother and father. Boys get one small X chromosomes from their mother and small Y chromosomes from their father.
Mutation happens when the DNA gene gets changed, moves, or is damaged. When this happens it causes the genetic message to be carried by that gene to be different. This process can occur in somatic cells. The somatic cells are all the cells that are a living organism except the reproductive cells, meaning the body. For example, the skin cells on your legs are and will not be passed on to ones offsprings. In addition those leg cells will not effect the evolution. Another occurrence is called gametic mutations, which is in a woman's eggs and or in a man's sperm. These are cells that are and can be passed on to ones offsprings, and they are the essentials for the evolution. There are three effects mutation causes to a species. Species can only takes on one of the three. The three effects are bad, neutral, and good. Having a bad mutation can cause one to have a harder time being able to survive. Having a neutral mutation will not change or help one to survive. Having a good mutation will help one to survive and have a better chance of survival. However, mutation is random in the evolution, and provides raw material for natural selection, genetic drift, and gene flow...
Discoveries in DNA, cell biology, evolution, and biotechnology have been among the major achievements in biology over the past 200 years, with accelerated discoveries and insight’s over the last 50 years. Consider the progress we have made in these areas of human knowledge. Present at least three of the discoveries you find to be the most important and describe their significance to society, health, and the culture of modern life. 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.
“A mutation is a sudden and unpredictable change in the genetic structure of an organism” (Mind Action Series: Life Science Textbook and Workbook Grade 12 FET, 2010). Mutations can be somatic, which means they occur in the somatic cells which have a full set of chromosomes but they are not used to carry hereditary information to future generations. Mutations can also be germ line, which occurs in the germ cells which come together to form the embryo and are therefore passed on to offspring. Mutations can be caused by chro...
A genetic mutation is a permanent change in the sequence of the DNA that makes up a gene. A mutation of these sorts can be caused by either inheritance from the parent or caused sometime during the life of someone. The mutation that has been inherited is called a germline mutation. Germline mutations affect virtually the entire body, and they seem to be present in every cell. A somatic mutation, or one that is caused in the DNA of a single cell sometime during the life, can be caused by an environmental factor or a wrong bonding in the DNA molecule. These cannot be passed down to the next generation of children because they occur in a specific cell as opposed to in a reproductive cell. Some mutations occur in the embryo as it is growing. These may occur during cell division, and some of the cells may or may not inherit this mutation. Some mutations are extremely rare, and others are incredibly common. Those that occur in more than one percent across a population are considered polymorphisms. Polymorphisms are considered normal variations in DNA, and they are known to cause simple changes such as variations in blood types and hair color. Although these are not typically fatal, they can influence the creation of some disorders (Lister Hill National Center for Biomedical Communications, U.S. National Library of Medicine, National Institutes of Health, Department of Health and Human Services, USA.gov, 2013).
Also how all these subjects relate to me. Mutation is a change in the DNA code of an organism. Mutations can either affect the person in a negative or positive way. These changes are considered as alterations and can create new characteristics that can be inherited.
Genetics is the passing of characteristics from parents to offspring through genes. Genes are information
...f the structure of DNA by James Watson and Francis Crick in 1953 that was extremely influential for future researchers. They determined that DNA was a double helix structure composed of base pairings, with a sugar phosphate backbone. This model explained how “genes can duplicate themselves [and] would eventually lead to our current understanding of many things, from genetic disease to genetic engineering” (Salem).
Whats a gene mutation? Well, a gene mutation is when there is a change in a gene or chromosome.