Answer:
In a diploid organism there are two copies of most genes.
The versions of the genes are called alleles.
Explanation:
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The genetic servants of a population are all variants of each of the genes present. These variables are possible thanks to the mutations that occur in the formation of the zygote (before or after fertilization).
When part of the DNA of an organism undergoes a point mutation (on one or a few nitrogenous bases) the body activates a series of responses to reverse it, however sometimes the mutation is maintained and can give rise to a change in a protein.
Sometimes and under certain circumstances (the change should not cause death or significant disadvantages in the body that is born) the mutation is maintained in the population giving rise to different alleles of the same gene.
In an organism there are two copies of each gene (genotype) but only one of them (phenotype) is expressed.
The allele of the gene that is expressed may depend on various factors but the dominant allele is usually expressed.
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Answer:
8,324,608 chromosome combinations
Explanation:
During meiosis, chromosomes separate independently so that only one chromosome came from the father and the other homologous chromosome came from the mother. This process of independent assortment produces a huge amount of possible combinations in the diploid zygote cell. In humans, the haploid number of chromosomes is n = 23, thereby there are 2²³ = 8,324,608 chromosome combinations. Thus, the independent assortment of chromosomes during meiosis is a key factor that contributes to genetic variation in the offspring.
In the matrix of mitochondria the reactions known as the citric acid or Krebs cycle produce a chemical called NADH. NADH is then used by enzymes embedded in the mitochondrial inner membrane to generate adenosine triphosphate (ATP). In ATP the energy is stored in the form of chemical bonds.