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Importance of dna in biology
The importance of DNA
Importance of dna in biology
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The identification of a substance/phenomenon/condition(s) is the first step toward a new discovery or invention of substantial application (human or otherwise). In the light of this fact, the knowledge of the discovery of DNA is vital to appreciate the beauty of evolution of the events that led to the discovery of DNA. Unlike the common belief that DNA was discovered by the American biologist James Watson and English physicist Francis Crick, the genetic material was first identified by the Swiss physiological chemist Friedrich Miescher in the 1860s. He named them “nuclein”. While having an intention of separating and identifying the proteins present in the white blood cells, he discovered a material inside the white blood cells that were similar to proteins but having high phosphorus content. Sensing the importance of his findings, Miesher wrote “It seems probable to me that a whole family of such slightly varying phosphorous-containing substances will appear, as a group of nucleins, equivalent to proteins”. It was only in 1953, that Watson and Crick put together pieces of experimental information by various investigators to bring forth the three dimensional structure of DNA. Although, various improvisations and extensions have been brought forth to the Watson Crick model, but the four major propositions still remain the same :
• DNA is a double-stranded helix, with the two strands connected by hydrogen bonds. A base are always paired with Ts, and Cs are always paired with Gs, which is consistent with and accounts for ...
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..., with which the redox moiety collides with the electrode and transfers electrons [24]
• The G-rich and C-rich DNAs individually form the parallel G-quadruplex and I-motif, respectively, in the molecular crowding condition, and the 1:1 mixture folds into the parallel G-quadruplex and I-motif but does not form a duplex. The ITC measurements indicated that the thermodynamic stability (ΔG°20) of the duplex formation between the G-rich and C-rich DNAs in the noncrowding condition was −10.2 kcal mol-1, while only a small heat change was observed in the ITC measurements in the molecular crowding condition. These ITC results also demonstrated that the molecular crowding condition prevents any duplex formation between G-rich and C-rich DNAs. These results indicate that a structural polymorphism of the telomere DNAs is induced by molecular crowding in vivo [25]
The following is a review of the book, The Double Helix, by James D. Watson that was published in 1968. Here the Norton Critical Edition will be used for page numbering and insights for this review, which was edited by Gunter S. Stent and published in 1980. The Double Helix is a personal recollection of the period of time when the structure of DNA was discovered. James D. Watson (Watson) along with Francis Crick (Crick) were the two scientists who published a paper in 1953 which purposed a structure for DNA. For the most part their structure has stood the test of time, and since that time period many people have wanted to know details of how they discovered DNA’s structure (pp. 3). Therefore Watson’s purpose in writing the book was to describe his personal view of the events that lead to discovery of DNA’s three-dimensional structure, when they happened in 1952-53. He is well qualified to give an account of these things, for he was there in the middle of everything; he was one of the main players. In order to describe the events, apart from his sharp memory, Watson used letters he wrote to his family to help him remember dates and details, as well as suggestions from his associates who reviewed his manuscript. In the following paragraphs I will summarize the text, and follow that with my own review of
The first and primary contribution to solving the DNA structure was the relationship of Crick and Watson. Without their teamwork and determination, another scientist would have discovered the structure before them. One of Crick’s bigger contributions was discovering the gene is self-replicating. After talking with John Griffith, Crick came up with the idea that the gene is self-replicating, meaning the gene has the ability “to be exactly copied when the chromosome number doubles during cell division”(126). With further discussion with Griffith, Francis believed that DNA replication involved specific attractive forces between the flat surfaces of the bases (128). One of Watson’s major contributions was after seeing the B form of DNA by Franklin, Watson knew that the structure of DNA was two-chained and that led to the building of the model of DNA (171). Also through research, Watson became aware that adenine and thymine pair together and are held by two hydrogen bonds that were identical in shape to the guanine and cytosine pair held together by at least two hydrogen bonds (194). This discovery showed that the two chains of DNA are complementary to each other. With these individual contributions coming together, Watson and Crick successfully were able to piece together the structure of DNA.
"The discovery of the structure by Crick and Watson, with all its biological implications, has been one of the major scientific events of this century." (Bragg, The Double Helix, p1) In the story of The Double Helix, James Watson tells of the road that led to the discovery of life's basic building block-DNA. This autobiography gives insight into science and the workings within a professional research laboratory that few members of society will ever be able to experience. It also gives the reader an idea of the reality of life for one scientist and how he struggled with the problem of DNA. However, the author's style is marked by his lack of objectivity and inclusion of many biased opinions and personal prejudices.
By utilizing, and, if possible, modifying this special DNA structure, one may see a reduction of age related illness, diseases, and signs of aging. In this review of human telomeres, we will discuss the roles and functions of the telomere, its structure, and the relation of telomere length to aging and tumorigenesis. Role and Functions of The Telomeres Telomeres are special DNA structures that consist of repetitive nucleotide sequences, which serve as a “cap” to protect the ends of the chromosomes. These repetitive sequences can range from thousands of base pairs in Vertebrates to about a few hundreds of base pairs in yeast cells (Oeseburg, et al. 2009). The 'Secondary' of the 'Secondary' of the 'Secondary' of the 'Secondary' of the 'Secondary' of the 'Secondary' of the 'Secondary' of the 'Secondary' of the 'Secondary' of the 'S Located at the ends of the chromosomes, the telomeres serve as a biological life line for cells.
o At the end of the electron transport chain, oxygen accepts electrons and takes up protons to form water. 3. Explain the basic structure of DNA including base pairing. o DNA is made up of six smaller molecules – a five carbon sugar called deoxyribose, a phosphate molecule and four different nitrogenous bases (adenine, thymine, cytosine and
Crick discovered the structure of DNA in 1953 and others discovered the genetic code a few years after. The old idea of genes as beads on a string, chromosomes, seemed to gain its vindication from the Watson and Crick model. Each of the three nucleotides in the DNA codes for an amino acid , a string of amino acids makes a protein. Many genes are separated by DNA sequences of nucleotides that are not transcribed into RNA. Proteins are coded by partial sequences on two or more chromosomes. Only a small percentage of DNA codes for proteins are higher than the organisms. In humans DNA codes for proteins are only one percent but not higher than two percent. Many of the rest contain sequences that are repeated over and over again.
With the knowledge of J.M. Gulland and D. O. Jordan’s papers on acid base titrations of DNA, Watson knew that bases form hydrogen bonds to other hydrogens, and that these bonds were present in DNA (183). Watson then thought that DNA had 2 chains with identical base sequences held together with hydrogen bonds, but struggled with figuring out if replication would work perfectly indefinitely, as the wrong bases could bind together (184-188). However, this model was soon found to be incorrect, as thymine and guanine were in enol form in Watson’s model, but should have actually been in keto form (190). Then, with this error found, Watson began rearranging the bases within DNA to see if there were any formations that would not disrupt the structure of the polynucleotide chains as previous models had. After rearranging the bases, Watson discovered that A+T pairs with 2 hydrogen bonds and C+G pairs with at least 2 hydrogen bonds were the same shape, and thus did not bend the chains in a way that was not mathematically possible.
In his autobiography on the discovery of the double helix, James D. Watson describes the process that he and Francis Crick took on in order to make the revolutionary discovery of the basic building block of the natural world, DNA. After reading, my perspective has changed in the following ways: I now understand the research, competition, and exhaustion that went into the discovery, I understand how truly groundbreaking a discovery it was, and how it changed the sciences of biology and chemistry for the better. In the past, DNA was just a subject in my biology classes that we referred to when we were talking about seemingly more important topics, specifically genetics. However, I never fully understood the measures taken to achieve the knowledge
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.
She discovered phosphates are on the outside of the DNA strands. The phosphates are on the outside so that the phosphate-phosphate interhelical bonds are disrupted by water. Also, the hydrophilic phosphates caused the molecule to soak up water and lengthen causing the wet DNA to produce a sharp diffraction picture that resembled the pattern of a x; further proving phosphates are on the outside. Through Franklin’s research, phosphates were discovered to be on the outside of DNA strands which allowed other information to be put in place; such as nitrogenous bases and sugar. It helped show that each nucleotide includes one nitrogenous base, attached to the 1’ carbon of the sugar, then the sugar is attached to 5’ of the phosphate. Franklin opened a passageway for Watson and Crick to further more their own discovery. In addition to finding phosphates are placed on the outside of DNA strands; Franklin also discovered DNA is
The Double Helix tells a tale of fierce competition, perseverance, and scientific innovation as we follow James Watson and his cohort Francis Crick on their quest to discover the secret to life, the structure of deoxyribonucleic acid. Although already fascinated with DNA, Watson struggled with finding chemistry exciting enough to learn it in depth. He had studied birds in college and thereby managed to avoid any formal chemistry or physics courses. As he later pursued a PhD in biochemistry, he realized he could put it off no longer and attempted to learn organic chemistry at Indiana University. However, after a mishap in the lab, he was encouraged instead to study nucleic acid chemistry with Herman Kalckar in Copenhagen. There, his mind strayed from his work and he began doing unauthorized research in the lab of Ole Maaløe, studying phages. Herman stopped teaching Watson after going through a divorce with his wife, and sent Watson off to a scientific conference in Naples. Although he was bored by many of the lectures, Maurice Wilkins’s talk about X-ray diffraction fascinated Watson. He was struck by an X-ray diffraction picture of DNA that Maurice presented and was determined to study the acid. He later got to know more about Maurice’s colleague, Rosalind Franklin, who was proud, stubborn, and very difficult to work with. Watson greatly admired the lecture given by the renowned Linus Pauling, who had discovered the structure of the alpha-helix and was thought of as the leader in DNA research in the scientific world.
James Watson, had used most of the information from Franklin presentation and Photo 51 to attempt to build a 3D model of DNA with Francis Crick at Cambridge Cavendish Laboratory. As Petter Portin explains in his article, “The birth and development of the DNA theory of inheritance: Sixty years since the discovery of the structure of DNA,” Watson and Crick used Wilkins, Franklin and Gosling research to create the double helix model that proved accurate in structure to support DNA’s functions, code information on building proteins, auto replicate themselves through complimentary based pairing. The model also later helped to explain how mutation can happen within the nucleotides of DNA. This
Each base are paired up together in order to create DNA. For example, in the article Base pairs it states “Attached to each sugar ring is a nucleotide base, one of the four bases Adenine (A), Guanine (G), Cytosine (C), and Thymine (T). The first two (A, G) are examples of a purine which contains a six atom ring and five atom ring sharing two atoms. The second two (C, T) are examples of a pyrimidine which is composed of a single six atom ring…”
Correspondingly, DNA contains two nucleotides with purine bases and two nucleotides with pyrimidine bases. These nucleotides are labeled adenine (A), guanine (G), thymine (T), and cytosine(C). These parts come in pairs which forms the double helix shape of DNA. Adenine is always paired with guanine and thymine is always paired
How life arose is a question that is fundamental to both philosophy and science. Responses to it enable one, in turn, to answer such questions as, “Who am I?”, “Why am I here?”, and “How do I make sense of this world?” This secondary set of questions can be answered in a myriad of ways for a variety of reasons, but the answer to the first question has only two responses. As Douglas Futuyuma says, “Creation and evolution, between them, exhaust the possible explanations for the origin of living things” (197). Either we are the product of the chemical and physical laws of nature operating over time, or we have been formed, at least in part, by some supernatural Force or Deity. The acceptance of one of these options as a foundation will determine how one will establish a belief system to determine his place in the world. This is a matter of crucial importance, yet in most biology classes offered at U.C. Davis, we learn that life came from nonlife by strictly natural (as opposed to supernatural) processes. The possibility that perhaps the origin of life cannot be explained by a natural mechanism is ignored, and this is disturbing. For if we limit what explanations we are willing to accept for the origin of life, we could be closing our eyes to reality.