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An overview of mutations, their causes, different types including chromosomal mutations and point mutations, and their significance in living organisms. It also introduces the concept of 'sports' and mutation breeding.
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Review Questions Mutations
1. What is a mutation? A mutation is a change in the sequence of bases in a DNA molecule. A mutation can occur in any cell but the most important ones happen in the gamete-making cells because they are passed onto the next generation. 2. What causes mutations? Many mutations are caused by mutagens. Common mutagenic sources include radiation and DNA interacting-chemicals. Ultraviolet light has a shorter wavelength than visible light and has more energy. UV has enough energy to damage biological molecules like DNA. Ionizing radiation, such as x-rays, gamma rays, and the decay products of radioactive substances are even more damaging due to their shorter wavelengths and/or higher energies. All chemical carcinogens cause mutations: industrial compounds (e.g. benzene, formaldehyde, PCB’s), heavy metals, petroleum products, dyes, tobacco, asbestos, pesticides, base analogs. Many mutagens are products of the industrial revolution but there are also many that naturally occur. We are surrounded my mutagens. Another source of mutations is the replication machinery of a cell itself. Replication is not perfect. On average replication has an error rate of 1 out of every 10,000-100,000 base pairs. These mistakes are quickly fixed by special proofreading enzymes called exonucleases. For example, UV light damages DNA by making thymine-thymine dimers. UV causes adjoining thymine bases to bond together making a lump in the strand. Exonucleases recognize the error, remove the dimer, and replace it with correct DNA. Xeroderma pigmentosum is a genetic disorder in which a person is born without the exonuclease that repairs thymine-thymine dimers. The affected are highly susceptible to skin cancers if they are exposed to UV light. During the day they must remain indoors at all times and can only go outside at night.
The exonucleases are not perfect and do not catch every mistake. On average, for every 10 billion nucleotide pairs replicated there is one error. So every time a DNA molecule replicates there is a 33% chance of a mutation. Now add onto this the effects of everyday exposure to mutagens and the mutation rate rises. Mutations are fairly common.
downstream of the change to be different. We call this a change in the “reading frame”. A frameshift mutation is like taking a scantron test. If you accidentally get one question off every answer from then on will probably be wrong. Frameshift mutations radically change proteins. Most of the time they are quite deleterious. We can add to our classification of mutations. Anytime you have a deletion or insertion mutation you also have a frameshift. The only time an insertion or a deletion is not a frameshift is if a whole codon (or groups of codons) is inserted or deleted. Let’s say you have an insertion mutation that produces a premature stop. We would classify that as an insertion nonsense frameshift mutation. How about a deletion mutation? Deletion missense frameshift. You get the picture?
7. Why are mutations so important to living organisms? Most mutations are harmful to an organism. Random changes in the gene sequence may result in the malformation and subsequent loss of function of a protein. Humans suffer from over 3000 genetic diseases. Every one of these is caused by a mutation. Some mutations however are neutral. The protein may be identical or, if changed, works equally well. A very few mutations are beneficial to an organism. A different protein may alter or create a trait that better adapts an organism to its niche in life. In the big picture, all living organisms today are the result of the accumulation of beneficial mutations over the past 3.5 billion years.