Structure of Nucleotides and DNA Essay

A mutation is any type of alteration or change in DNA. There are many types of mutations that can occur. Depurination and deamination are common mutations that happen spontaneously. Depurination is a hydrolysis reaction that leads to the loss of purines in DNA. Deamination is also a hydrolysis reaction, and the cause of this reaction is an amino group gets detached. These types of mutations cause an alteration in the base sequence of amino acids and also effect the way a gene reads a protein. Another cause of DNA mutations may be environmental elements such as: chemicals or radiation. (pg. 567) A common chemical that is a mutagen is cigarettes and a example of

1. What type of mutation it is (loss of function, gain of function—look up ANY terms up in your book if you don’t know what they mean!

B. A frameshift mutation changes every base pair to follow it, resulting in multiple amino acids potentially being changed. A point mutation just changes a single amino acid, which may not even change the amino acid that codon pairs for.

In contrast missense mutation is where one DNA nucleotide is switched out with another one in a way that changes the amino acid specified. Whereas in silent mutation, there is no any change in the amino acid sequence of the protein product (Study 2017).

A mutation is a change made to the sequence of a base in the DNA. This change occurs mainly in the chromosomes or nucleotides; however, mutations that occur in a egg or sperm cell are the cause of generic variation. This mutation can be inherited by offspring.

Frameshift mutations are far more likely to lead to a defective protein than a point mutation because frameshift mutations cause change through inserting or deleting one or more nitrogen bases causing the rearrangement of triplets and them being read incorrectly causing problems. The point mutation, on the other hand, replaces, not inserts or deletes, a single nitrogen base with another, allowing for the amino acid to be or not to be affected causing the triplet to code as explained in the

Mutation is a change in the DNA of a cell, which may be passed on to offspring if it is a germ line cell. Mutation in bacteria reproduces faster than in human. When the mutation occurs the DNA will be different. Therefore, the medication that is used to treat bacteria may not work because the bacteria are different.

In order to descry the term mutation, it is crucial to grasp the definition of the word error. According the Merriam-Webster, error is “a deficiency or imperfection in structure or function.” Errors are mistakes; mistakes in nature occur in the formations of nucleotides, which is what makes up DNA. As stated by journalist, Rachel Rettner, nucleotides are composed of “four types of nitrogen bases,” which include: “adenine (A), thymine (T), guanine (G) and cytosine (C).” The sequence of the bases manipulates the instructions of DNA, and changes the genetic codes. When genetic codes are introduced to random influences an error occurs in the DNA formation and causes new recessive genes; these genes are called mutations. Mutation are a genetic error,

This process of natural selection can lead to significant changes in the appearance, behavior, or physiology of individuals in a population.Generally, mutation is reversed. DNA repair machines are constantly at work in our cells, fixing mismatched nucleotides and splicing broken DNA strands back together. Yet. some DNA changes remain. If a cell accumulates too many changes—if its DNA is so damaged that repair machinery cannot fix it—it either stops dividing or it self-destructs. If any of these processes go wrong, the cell could become cancerous. Environmental Factors

A mutation is when the structure of a gene is changed. It is caused by the alteration of single base units in DNA, or the deletion, insertion, or rearrangement of larger sections of genes. There are two types of mutations:

Mutations are errors that occur in DNA replication. A deletion mutation takes place when part of a DNA molecule is not copied during the replication of DNA. It can be a single nucleotide or even an entire chromosome. The deletion creates a frameshift in the sequence, which causes dramatic changes down the line. The loss of this DNA during replication can lead to a genetic disease such as William’s Syndrome.

Moreover, mutation is a result of the change in the nucleotide sequence of an organism's DNA. The cause of mutations is commonly attained in the somatic cells.

The DNA molecule is a double chain of nucleotides that can be divided into ¨bytes¨ of information, that we call genes, and each of these genes come together to create a specific protein. These proteins are those that

It provides a base triplet, a sequence of three bases on one of the strands of DNA, that code for one amino acid. The sequence of base triplets on DNA molecules determines the order of the amino acids on the protein chain. In the first phase of transcription, the first process of protein synthesis that occurs in the nucleolus, a portion of a DNA molecule unwinds and serves as a template. Free nucleotides floating in the nucleoplasm pair up with their complimentary bases on the DNA strand.

(Windows to the Universe. 2014). If sufficient damage to DNA is achieved, chromosome abnormalities may be noted, the damaged DNA can attempt to repair itself, sometimes forming patterns dissimilar to its prior layout. Karaman et al (2005) describes the removal of one or more nitrogenous bases within the DNA sequence as a deletion error. Substitution is explicated as an error which occurs when one base pair is replaced by another and insertion is defined as an error which arises as new base pairs are inserted into the DNA sequence. These mutations can result in either little or serious effect which can result in the loss of cell function.