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Genetic Changes Chapter 11.3
Any change in the DNA sequence is called a mutation.
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Genetic changes Mutations affect the reproductive cells of an organism by changing the sequence of nucleotides within a gene in a sperm or an egg cell.
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If Fertilization occurs
If fertilization occurs, the mutated gene would be duplicated in the new individual. This mutation could result in several different things: it could produce a new trait it could produce a defective protein it could cause structural or functional problems in cells and organism. it could be so severe that the embryo does not survive.
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All living creatures have genes, made up of DNA
All living creatures have genes, made up of DNA. Without DNA mutations, life on Earth could not have evolved. Mutations can affect the way a gene works, which may in turn cause changes in an animal's appearance, or behavior . Sometimes, a new gene variant may mean the animal is better adapted to its surroundings, improving its chances of survival. So this animal is more likely to have offspring, which will inherit the beneficial gene variant. This process is called natural selection.
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Positive mutations Some rare mutations have positive effects like increasing or decreasing the speed of certain reactions in the body. mutations that benefit a species plays an important role is the evolution of that species.
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Tortoises have evolved protective shells to retract into when faced by predators.
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Non reproductive cell mutation
If a mutation occurs in a non-reproductive cell, like a body cell, the mutation will not be passed on to the offspring. It will affect or cause damage to the organism. It may impair the function of the cell. Some mutations affect cell division, like cancerous cells They result in rapid cell division.
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DNA Muscles (AP) Somewhere in Germany is an extremely strong toddler: born in Berlin with bulging arm and leg muscles. Not yet 5, he can hold seven-pound weights with arms extended, something many adults cannot do. The boy - whose name is being withheld to protect his privacy - is reported to have muscles twice the size of other kids his age and half their body fat. Medical researches say DNA tests show the reason: he has a genetic mutation that boosts muscle growth. The discovery, reported in Thursday's New England Journal of Medicine, represents the first documented human case of such a mutation. Many scientists believe the find could eventually lead to drugs for treating people with muscular dystrophy and other muscle-destroying conditions. And athletes would almost surely want to get their hands on such a drug and use it like steroids to bulk up.
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Types of DNA mutations There are three major types:
1. Point mutation 2. Frameshift mutation 3. Chromosomal mutations
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Point mutation This is a result of an incorrect base being inserted into the DNA sequence. ex: TACCTC could change to TACCTT resulting in a new amino acid.
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point mutation A point mutation is a simple change in one base of the gene sequence. This is equivalent to changing one letter in a sentence, such as this example, where we change the 'c' in cat to an 'h': Original The fat cat ate the wee rat. Point Mutation The fat hat ate the wee rat.
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Point mutation 2. This can cause the wrong amino acid to be produced, resulting in the wrong protein, which could have various affects on the cell or organism.
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Point mutation and Sickle Cell
There is a certain genetic disorder known as Sickle Cell Anemia. It causes a warping of the blood cells, so you get cells like the one in the bottom left: This genetic trait will cause less oxygen to be delivered thought the blood, causing weakness and pain. It differs from a normal blood cell gene by one, single point mutation.
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Frameshift mutation When a base is added or deleted from the DNA sequence: ex: TACCTC could mutate into TACACTC or TACTC
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An example of a frame-shift mutation using our sample sentence is when the 't' from cat is removed, but we keep the original letter spacing: Original The fat cat ate the wee rat. Frame Shift The fat caa tet hew eer at.
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Frameshift mutation 2. This will shift the reading of the codons. Therefore, resulting in an incorrect amino acid chain.
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Chromosomal mutations
These are mutations in the formation of the chromosome where: parts of the chromosome may break off and become lost in the cell during mitosis or meiosis chromosomes may rejoin incorrectly
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Chromosomal mutations 2.
These types of mutations are more common in plants. Few of these mutations are passed on to offspring because more than likely the zygote does not survive.
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Causes of Mutations Mistakes in base pairing can occur during DNA transcription or replication Mutations are also caused by environmental factors. A mutagen is any agent that can cause a change in DNA. They include things such as chemicals, high energy radiation and high temperatures.
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Mutations 2 Mutations in cells are sometimes fixed by the body’s own self-check system. There are proof-reading enzymes inside the cell that check the DNA after replication or transcription that insert or delete incorrect base pairs.
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Mutations 3 Like most living things, it is not a perfect process, but works extremely well… just like a spell check on your computer fixes most things, it still skips over things that seem to make sense, but don’t. Ex: if you meant to write the word dye, but put die instead… spell check probably won’t catch it. how Do Mutations Occur? Copying errors are introduced when DNA replicates itself.Everyone acquires some changes to their DNA during the course of their lives. These changes occur in a number of ways. Sometimes there are simple copying errors that are introduced when DNA replicates itself. (Every time a cell divides, all of its DNA is duplicated so that the each of the two resulting cells have a full set of DNA.) Other changes are introduced as a result of DNA damage through environmental agents including sunlight, cigarette smoke, and radiation. Our cells have built in mechanisms that catch and repair most of the changes that occur during DNA replication or from environmental damage. As we age, however, our DNA repair does not work as effectively and we accumulate changes in our DNA.Germline mutations are what cause diseases to run in families.Some of these changes occur in cells of the body — such as in skin cells as a result of sun exposure — but are not passed on to children. But other errors can occur in the DNA of cells that produce the eggs and sperm. These are called germline mutations and can be passed from parent to child. If a child inherits a germline mutation from their parents, every cell in their body will have this error in their DNA. Germline mutations are what cause diseases to run in families, and are responsible for the kind of hereditary diseases covered by Genetic Health.
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Aging is said to be a possible genetic mutation
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