The rungs of the double helix in DNA are made up of nitrogenous base pairs: Adenine, Thymine, Guanine, and Cytosine. The correct answer is C.
Answer:
There are two types of cell division: mitosis and meiosis. Most of the time when people refer to “cell division,” they mean mitosis, the process of making new body cells. Meiosis is the type of cell division that creates egg and sperm cells. Mitosis is a fundamental process for life. Mitosis is the division of a cell into two daughter cells that are genetically identical to the parent cell. Meiosis is the division of a germ cell into four sex cells (e.g. egg or sperm), each with half the number of chromosomes of the parent cell. Meiosis is a type of cell division that reduces the number of chromosomes in the parent cell by half and produces four gamete cells. This process is required to produce egg and sperm cells for sexual reproduction. Meiosis begins with a parent cell that is diploid, meaning it has two copies of each chromosome. Mitosis gives two nuclei, and hence two cells, while meiosis gives four. Mitosis gives identical cells to each other and to the mother cell, while meiosis leads to genetic variation due to crossing over and independent assortment. Mitosis includes one division, while meiosis includes two.
A gene mutation is a permanent alteration in the DNA sequence that makes up a gene, such that the sequence differs from what is found in most people. Mutations range in size; they can affect anywhere from a single DNA building block (base pair) to a large segment of a chromosome that includes multiple genes.
Gene mutations can be classified in two major ways:
<span>Hereditary mutations are inherited from a parent and are present throughout a person’s life in virtually every cell in the body. These mutations are also called germline mutations because they are present in the parent’s egg or sperm cells, which are also called germ cells. When an egg and a sperm cell unite, the resulting fertilized egg cell receives DNA from both parents. If this DNA has a mutation, the child that grows from the fertilized egg will have the mutation in each of his or her cells.Acquired (or somatic) mutations occur at some time during a person’s life and are present only in certain cells, not in every cell in the body. These changes can be caused by environmental factors such as ultraviolet radiation from the sun, or can occur if a mistake is made as DNA copies itself during cell division. Acquired mutations in somatic cells (cells other than sperm and egg cells) cannot be passed on to the next generation.</span>
Genetic changes that are described as de novo (new) mutations can be either hereditary or somatic. In some cases, the mutation occurs in a person’s egg or sperm cell but is not present in any of the person’s other cells. In other cases, the mutation occurs in the fertilized egg shortly after the egg and sperm cells unite. (It is often impossible to tell exactly when a de novo mutation happened.) As the fertilized egg divides, each resulting cell in the growing embryo will have the mutation. De novo mutations may explain genetic disorders in which an affected child has a mutation in every cell in the body but the parents do not, and there is no family history of the disorder.
Somatic mutations that happen in a single cell early in embryonic development can lead to a situation called mosaicism. These genetic changes are not present in a parent’s egg or sperm cells, or in the fertilized egg, but happen a bit later when the embryo includes several cells. As all the cells divide during growth and development, cells that arise from the cell with the altered gene will have the mutation, while other cells will not. Depending on the mutation and how many cells are affected, mosaicism may or may not cause health problems.
Most disease-causing gene mutations are uncommon in the general population. However, other genetic changes occur more frequently. Genetic alterations that occur in more than 1 percent of the population are called polymorphisms. They are common enough to be considered a normal variation in the DNA. Polymorphisms are responsible for many of the normal differences between people such as eye color, hair color, and blood type. Although many polymorphisms have no negative effects on a person’s health, some of these variations may influence the risk of developing certain disorders.
<span>haemoglobin. hope this helps!
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Answer:
25
Explanation:
In DNA, Guanine pairs with Cytosine, and Thymine pairs with Adenine. This tells us that there are equal numbers for each Guanine and Cytosine, and Thymine and Adenine. When there's 35 Guanine, there should be 35 Cytosine that goes with it. 120 - 2(35) = 50. The remaining 50 nucleotides are Thymine and Adenine, and since they are the same number, divide 50 by 2. 50 ÷ 2 = 25. There are 25 thymine in the sample of DNA.
