How are gene mutations involved in evolution?
Evolution is the process by which populations of organisms change over generations. Genetic variations underlie these changes. Genetic variations can arise from gene mutations or from genetic recombination (a normal process in which genetic material is rearranged as a cell is getting ready to divide). These variations often alter gene activity or protein function, which can introduce different traits in an organism. If a trait is advantageous and helps the individual survive and reproduce, the genetic variation is more likely to be passed to the next generation (a process known as natural selection). Over time, as generations of individuals with the trait continue to reproduce, the advantageous trait becomes increasingly common in a population, making the population different than an ancestral one. Sometimes the population becomes so different that it is considered a new species.
Not all mutations lead to evolution. Only hereditary mutations, which occur in egg or sperm cells, can be passed to future generations and potentially contribute to evolution. Some mutations occur during a person’s lifetime in only some of the body’s cells and are not hereditary, so natural selection cannot play a role. Also, many genetic changes have no impact on the function of a gene or protein and are not helpful or harmful. In addition, the environment in which a population of organisms lives is integral to the selection of traits. Some differences introduced by mutations may help an organism survive in one setting but not in another—for example, resistance to a certain bacteria is only advantageous if that bacteria is found in a particular location and harms those who live there.
So why do some harmful traits, like genetic diseases, persist in populations instead of being removed by natural selection? There are several possible explanations, but in many cases, the answer is not clear. For some conditions, such as the neurological condition Huntington disease, signs and symptoms do not occur until after a person has children, so the gene mutation can be passed on despite being harmful. For other harmful traits, a phenomenon called reduced penetrance, in which some individuals with a disease-associated mutation do not show signs and symptoms of the condition, can also allow harmful genetic variations to be passed to future generations. For some conditions, having one mutated copy of a gene in each cell is advantageous, while having two mutated copies causes disease. The best-studied example of this phenomenon is sickle cell disease: Having two mutated copies of the HBB gene in each cell results in the disease, but having only one copy provides some resistance to malaria. This disease resistance helps explain why the mutations that cause sickle cell disease are still found in many populations, especially in areas where malaria is prevalent.
Topics in the Mutations and Health chapter
- What is a gene mutation and how do mutations occur?
- How can gene mutations affect health and development?
- Do all gene mutations affect health and development?
- What kinds of gene mutations are possible?
- Can a change in the number of genes affect health and development?
- Can changes in the number of chromosomes affect health and development?
- Can changes in the structure of chromosomes affect health and development?
- Can changes in noncoding DNA affect health and development?
- Can changes in mitochondrial DNA affect health and development?
- What are complex or multifactorial disorders?
- What does it mean to have a genetic predisposition to a disease?
- How are gene mutations involved in evolution?
- What information about a genetic condition can statistics provide?
- How are genetic conditions and genes named?
No hay comentarios:
Publicar un comentario