Genes are segments of DNA located on chromosomes. A gene mutation is defined as an alteration in the sequence of nucleotides in DNA. This change can affect a single nucleotide pair or larger gene segments of a chromosome. DNA consists of a polymer of nucleotides joined together. During protein synthesis, DNA is transcribed into RNA and then translated to produce proteins. Altering nucleotide sequences most often results in nonfunctioning proteins. Mutations cause changes in the genetic code that lead to genetic variation and the potential to develop the disease. Gene mutations can be generally categorized into two types: point mutations and base-pair insertions or deletions.
Because evolution itself is a very slow process. Having said that, the chance of having a continuum of various animals would mean that evolution would have progressed very fast. Because evolution is slow, different species establish themselves for different ecological niches and environments, this enables them to become better through time at a certain environment which then leads to eventual diversification in the number of species.
There children will have type AB blood because both A and B are both dominant alleles so they will both be inherited.
Answer:
Breaks them into their simplest form. Glucose, amino acids, and fatty acids.
Explanation:
They have to be broken down into these forms to be absorbed into the bloodstream.
