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Importance of dna in biology
The importance of DNA
Cell Reproduction
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Biology Key Skills
Poodles make more poodles. Sheep make more sheep. Replication is a
basic fact of life. All living things make other living things that
are to one degree or another duplicates of themselves. What is the
mechanism behind all this? The answer lies in a molecule called DNA.
In 1869, Friedrich Miescher extracted a substance, which he called
nuclein from the nuclei of white blood cells. Nuclein later became
known as nucleic acid. Living cells contain two kinds of nucleic
acids-ribonucleic acid (RNA) which contains the sugar, ribose and
deoxyribonucleic (DNA) which contains the sugar, deoxyribose. Nucleic
acids are found in all living things, from the simplest protozoan to
the most complex forms of animal and plant life
.
Two young scientists-James Watson and Francis Crick-finally pieced
together the precise structure of DNA. The model proposed by Watson
and Crick for the structure of DNA is shaped like a twisted ladder.
This type of figure is known as a double helix. The sides of the
twisted ladder are made up of alternating units of deoxyribose and
phosphate. The rungs of the ladder are composed of paired nitrogen
bases. Adenine always pairs with thymine, and guanine always pairs
cytosine. The bases are held together by hydrogen bonds.
Watson and Crick's model also suggested a way in which DNA could make
copies of itself. First, the ladder untwists. Then the bases break
apart. Since and adenine nucleotide can only bond with thymine, and
guanine can only bond with cytosine, new units are assembled in
precisely the same order as old. When the splitting and pairing
processes are competed, two identical DNA molecules stand in the place
of one. The process by which DNA makes copies of itself is called
replication.
DNA replication
DNA replication begins with a partial unwinding of the double helix at
an area known as the replication fork. This unwinding is accomplished
by an enzyme known as DNA helicase. This unwound section appears under
electron microscopes as a "bubble" and is thus known as a replication
DNA is made up of nucleotides, and a strand of DNA is known as a polynucleotide. A nucleotide is made up of three parts: A phosphate (phosphoric acid), a sugar (Deoxyribose in the case of DNA), and an organic nitrogenous base2 of which there are four. The four bases are as followed: Adenine (A), Cytosine
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. , ,
In April of 1953, James Watson and Francis Crick published a game changing paper. It would blow the mind of the scientific community and reshape the entire landscape of science. DNA, fully knows as Deoxyribonucleic Acid is the molecule that all genes are made of. Though it is a relatively new term with regard to the age of science, the story of DNA and the path to its discovery covers a much broader timeframe and had many more contributors than James Watson and Francis Crick. After reading the paper the audience should have a better understanding of what DNA is, the most important experiments that contributed to its ultimate discovery and the names and contributions of the lesser-known scientists that helped Watson and Crick turn their idea
Examine 3 different natural selections using brine shrimp and salt solutions. It will test the hatching viability of roughly 20 brine shrimp eggs in three different NaCl solutions over the course of 48 hours.
The Double Helix by James Watson is his personal reflection on discovering the structure of the DNA molecule. With contributions of other scientists, James Watson and Francis Crick were able to solve the structure of DNA. Through contributions and integral relationships of Watson and Crick to Maurice Wilkins, Rosalind Franklin, Linus Pauling, and other smaller contributors the DNA structure was finally solved.
"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.
The Double Helix was written by James D. Watson. James Dewey Watson was born on April 6th, 1928, in Chicago Illinois. He was a precocious student, and entered the University of Chicago when he was only 15. He received his Bachelor of Science degree in zoology four years later, and then went on to earn a Ph.D. in the same subject at Indiana University. Watson Joined Francis Crick at Cambridge in 1951, in an attempt to determine the chemical structure of living matter. They continued their work until February 28, 1954 when they made a historic discovery. They had determined the structure of DNA. In June they published their findings in the British science journal Nature. In acknowledgment, Francis Crick and James Watson shared the 1962 Nobel Prize for Physiology and Medicine. The discovery of the structure of the molecule deoxyribonucleic acid led James Watson to write the personal account of how the structure of DNA was discovered. He wrote the book to give people an honest, accurate account that would include the bad along with the good aspects of how science is done and to give people a sense of how competitive it is in the world of science.
Precise chromosomal DNA replication during S phase of the cell cycle is a crucial factor in the proper maintenance of the genome from generation to generation. The current “once-per-cell-cycle” model of eukaryotic chromosome duplication describes a highly coordinated process by which temporally regulated replicon clusters are sequentially activated and subsequently united to form two semi-conserved copies of the genome. Replicon clusters, or replication domains, are comprised of individual replication units that are synchronously activated at predetermined points during S phase. Bi-directional replication within each replicon is initiated at periodic AT-rich origins along each chromosome. Origins are not characterized by any specific nucleotide sequence, but rather the spatial arrangement of origin replication complexes (ORCs). Given the duration of the S phase and replication fork rate, adjacent origins must be appropriately spaced to ensure the complete replication of each replicon. Chromatin arrangement by the nuclear matrix may be the underpinning factor responsible for ORC positioning. The six subunit ORC binds to origins of replication in an ATP-dependent manner during late telophase and early G1. In yeast, each replication domain simply contains a single ORC binding site. However, more complex origins are characterized by an initiation zone where DNA synthesis may begin at numerous locations. A single round of DNA synthesis at each activated origin is achieved by “lic...
A chromosome is made up of two identical structures called chromatids. The process of nuclear division is called interphase; each DNA molecule in a nucleus makes an identical copy of itself. Each copy is contained in the chromatid and a characteristic narrow region called the centromere holds the two chromatids together. The centromere can be found anywhere along a chromosome but the position is the characteristic for a particular chromosome. Each Chromatid contains one DNA molecule. DNA is the molecule of inheritance and is made up of a series of genes. The fact that the two DNA molecules in the sister chromatids, and hence their genes, are identical is the key to precise nuclear division.
The biggest challenge I ever faced personally is when I decided to taken AP Biology during my senior year of high school. One of the reasons I took this class, was that I wanted to gain a few credits before I started college. The other was that, my original plan was to take a class that have me a step into my future major, Biology. Technically the major I wanted to take was Zoology, but very few colleges, especially Farmingdale, don't have it.
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.
Inside the cells that produce sperm and eggs, chromosomes become paired. While they are pressed together, the chromosomes may break, and each may swap a portion of its genetic material for the matching portion from its mate. This form of recombination is called crossing-over. When the chromosomes glue themselves back together and separate, each has picked up new genetic material from the other. The constellation of physical characteristics it determines is now different than before crossing-over.
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.
...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).
During this phase the DNA aka “deoxyribose nucleic acid” clone then forms chromatin. Chromatin is the mass of genetic material that forms into chromosomes. Interphase is divided into smaller parts: G1 Phase, S phase and G2 Phase. Throughout all the phases, the cells continuously develop by producing mitochondria, endoplasmic reticulum, and proteins. The actual division occurs during the S phase bur the G phases are mainly for the purpose of growing. Starting with the G1 phase the cell grows in preparation for certain intracellular components and DNA replication. This phase makes sure the cell is prepared for the process of DNA replication. It reviews the size and environment to ensure that is it ready to go, and cannot leave the G1 until it is complete. But what happens to a cell when it is not complete and cannot exit out of the phase? It will pause and transfer to phase G0. There’s no certain time to be in this phase but it will remain until it reaches the fitting size and is in a supportive surroundings for DNA replication. It will exit either G1 or G0 and there is no other way besides these. Then the cell will advance to the next phase which is the S phase. Synthesis, or more known as S phase is the section of the cell cycle when the DNA is wrapped into chromosomes then duplicated. This is a very important part of the cycle because it grants each of them that is created, to have the exact same genetic