Which one of the following is least likely to cause mutations in dna?

Which one of the following is least likely to cause mutations in dna?

Which of the following is least likely to cause a mutation

Mutations in a single gene cause certain genetic disorders, such as cystic fibrosis. A gene is made up of DNA “letters” that contain the instructions for producing a particular protein. When a protein isn’t produced properly, it may cause a chain reaction of issues.
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A new dna strand elongates only in the 5′ to 3′ direction because

Somatic mutations are a type of mutation that occurs in the body. Somatic mutations only affect the current organism’s body, as the term comes from the Greek word soma, which means “body.” Somatic fundamental property of an individual—such as survival capacity—from an evolutionary perspective. Cancer, for example, is a powerful somatic mutation that threatens the survival of a single organism. Evolutionary theory, on the other hand, has a different emphasis.
While a single mutation may have a significant impact, evolutionary change is mostly based on the accumulation of several small mutations. Depending on the background or position, mutational effects may be beneficial, negative, or neutral. The majority of non-neutral mutations are harmful. In general, the larger the impact of a mutation and the greater the likelihood of the mutation becoming deleterious, the more base pairs affected by the mutation.
Researchers have begun to estimate distributions of mutational effects (DMEs), which measure how many mutations occur with what effect on a given property of a biological system, in order to better understand the influence of mutations. The property of interest in evolutionary studies is fitness, but other emerging properties may be of interest in molecular systems biology. Since the resulting effects range from lethal to neutral to advantageous, obtaining accurate information about DMEs is extremely difficult; in addition, many confounding factors often complicate these studies. To make it even more complex, several mutations interfere with one another, altering their effects; this is known as epistasis. Despite these uncertainties, recent research has consistently shown that the vast majority of mutations have very minor effects (Figure 1; Eyre-Walker & Keightley, 2007). Of course, much further research is needed to learn more about DMEs, which are a fundamental property that regulates the evolution of all biological systems.

Telomere shortening is a problem in which types of cells?

No, only a small percentage of variants cause genetic disorders, and the vast majority have no effect on health or growth. Some variations, for example, modify the DNA sequence of a gene but not the function of the protein produced by the gene.
Before a gene is expressed and an altered protein is formed, some enzymes repair gene variants that could cause a genetic disorder. Enzymes identify and repair DNA errors through a variety of pathways in each cell. DNA repair is an essential mechanism by which the body protects itself from disease because DNA can be modified or damaged in a variety of ways.
Only a small percentage of all variants have a beneficial effect. These mutations result in new protein versions that aid an individual’s ability to respond to changes in his or her environment. A beneficial variant, for example, might result in a protein that protects a person and future generations from a new bacterial strain.
When deciding whether a gene variant is linked to a genetic disorder, scientists look at the latest scientific evidence, such as how the variant affects the role or development of the protein produced by the gene, as well as previous variant classification results. The variant is then placed on a spectrum based on its likelihood of causing the disorder.

If a cell were unable to produce histone proteins, which of the following would be a likely effect

DNA is the recipe for all life on Earth, since it codes for the proteins that make up the whole body. Our bodies have intricate mechanisms in place to ensure that our DNA is properly arranged and that each new cell receives a complete and unaltered copy. A mistake in the sequence of DNA may occur if the complex system involved in copying DNA fails, or if bad things are present in the environment. These errors, known as mutations, can occur at any stage of life, from a developing baby’s first cells to an adult’s mature cells. Some mutations are linked to severe health issues. The aim of this article is to illustrate the many dangerous villains that cause mutations, known as mutagens, and how we can protect our bodies from harm by living a safe lifestyle and preventing needless exposure to the types of hazards that can cause mutations.
So, how many of these bases do you think there are? Human DNA comprises approximately 3 billion bases, with approximately 99 percent of these bases being the same in all humans [2]. The 1% difference applies to all of the special qualities and attributes that distinguish you from other people, such as eye color or health status. Your DNA sequences differ from those of your classmates, relatives, and siblings, which explains how you differ from them. Each of your parents contributes about half of your DNA. When an organism’s DNA differs by more than 1% from ours, it is classified as a separate species. Chimpanzee DNA is just 1% to 2% different from human DNA (meaning that chimpanzee DNA is 98–99 percent similar to human DNA), making them our nearest animal relatives [3].