<span>The P-site of the ribosomes is the site of polypeptide elongation during translation of mRNA. Therefore, a drug that binds to this site ensures that there is no elongation hence, basically, the translation process is inhibited. The <span>growing bacteria cell will stop growing and die due to lack of structural and functional proteins to grow and perform its cellular processes respectively..</span></span>
They changed things up because its mixed or from up further in the family line. like your parents could have green eyes and you could get blue. it shoukd of came from your grandparents or other blood related relatives.
Proteins have many important roles in cell function like structural support, biocatalysts, receptors.
Answer and Explanation:
The Huntington disease is caused by a mutation in the gene that codifies for the Huntingtin protein (Htt). The mutation produces an altered form of the protein leading to the neuron´s death in certain areas of the brain.
The Huntington disease characterizes for being,
- Hereditary, passing from generation to generation. To express the disease, a person must have been born with an altered gene.
- Autosomal, affecting men and women equally, because the mutated gene is located on an autosomal chromosome.
- Dominant, which means that by getting only one copy of the altered gene coming from any of the parents, the receiving person will express the disease. The mutation in the gene dominates over the normal gene copy.
- Expressed by heterozygosis. Most people affected by the disease are heterozygous, with a normal copy and a mutated copy.
There are just a few cases all around the world (3% approximately) in which the disease is expressed with no family history. The progenitors are not affected by the mutation. These cases are very rare and are called <u>"de-novo" mutations.</u> A new mutation is spontaneously produced and it is not inherited from any of the parentals. It consists of an increase in the number of CAG repetitions. In a normal person, the number of CAG repetitions is less than 35. When there are 40 or more repetitions it occurs the disease. But when there are between 35 and 39 repetitions, the penetrance of the disease is incomplete. This is a "gray zone". Those alleles that fall in the gray zone are unstable and might produce the HD. Individuals with these unstable alleles have a tendency to increase the number of repetitions from generation to generation until the number reaches 40 repetitions and the person expresses the disease. This <u>usually occurs in the paternal germinal line</u>, as it is particularly unstable in sperm and probably meiosis greatly affects their instability, causing an increase in the number of CAG repeats.
In biopsychology, there is a system in the brain which is called the limbic system. The limbic system is responsible for one's memory, emotions and instincts -drives.
Many researchers suggest that the existence of emotions helped the animal kingdom to respond to sociality and survive better, emotion can also be translated into care and love. These traits also aid why infants, babies and other offsprings of animals are cared for which has a great influence on the survival of the species.
Amygdala, responsible for pain, aggression and grief which is anterior to the hippocampus factors why our memories have incorporated and is strengthened with emotions at that specific circumstance.
