The structure of the DNA double helix is likened to a spiral staircase in the notes, where the spiral steps represent nitrogen bases, and the spiral staircase consists of phosphate groups and deoxyribose sugar molecules.
The steps of DNA replication involve the splitting of nitrogen bases, transportation of new nucleotides into place, linking them together to form a complementary strand based on the rule of base pairing, and the formation of two new double helices.
DNA replication ensures the faithful transmission of genetic information by accurately copying the sequence of nitrogen bases, following the rule of base pairing.
DNA mutations can occur through deletion, where a nitrogen base is neglected during replication, leading to a change in the sequence, or substitution, where a nitrogen base is not copied properly, and a different base is substituted.
The sequence of nitrogen bases in DNA serves as a code for constructing protein molecules, and sets of three nitrogen bases form a triplet code, each coding for specific amino acids.
Dominant alleles, represented by capital letters (e.g., C, T), only require one copy for an organism to exhibit the trait, while recessive alleles, represented by lowercase letters, require two copies for the trait to be expressed.
Environmental features that can influence an organism's survival include the availability of food and water, infectious diseases, and factors like latitude and sunlight.
DNA replication involves DNA helicase breaking hydrogen bonds between strands, unzipping the double helix, and DNA polymerase helping bind free nucleotides to exposed strands, producing an identical copy.
Meiosis and independent assortment contribute to genetic variation by randomly arranging homologous chromosomes and segregating chromatids, resulting in the formation of daughter cells with a random set of chromosomes.
Crossing over during meiosis involves the swapping of sections between homologous chromosomes, producing new gene combinations and contributing to genetic variation.