Option C:
B. wild-type 5-AUGCAUACAUUGGAGUGA-3 mutant 5'-AUGCAUACAUCUGGAGUGA- 3'
Explanation:
A frameshift mutation is a genetic mutation such that the triplet nature of gene expression by codons, the insertion or deletion occurs in such as way that it alters the complete sequence of 3 codon sets and can change the reading frame, resulting in a completely different translation from the original.
As it is pertinent to understanding that all genes are normally translated in sets of 3 codons, which typically describes and explain a unique amino acid sequence. Thus, if a frame shift mutation occurs, it can affect many amino acid sequences and finally the entire protein.
If we look at option B:
wild-type 5-AUG CAU ACA UUG GAG UGA-3
mutant 5’- AUG CAU ACA UCU GGA GUG A-3’
An insertion of a base Uracil showed at the end of 3rd codon which affected and altered the whole sequence of codon triplets. This changed all next codons and finally all next amino acids will be altered.
The eggs of the fluke are passed into water supplies from feces and urine of infected people. After hatching the parasite actively swims and invades the body of a snail, usually by penetrating through the snail's foot. The parasite requires the presence of certain species of snails (e.g., Oncomelania, Biomphalaria, Bulinus) to transform (and multiply) itself into an infective stage, called cercaria.
Right when there is not that a lot of water within the body, pituitary organ releases additional vasoconstrictor to resorb more water in the circulatory framework therefore the pee are targeted..but once there is additional water in body, less ADH can be discharged to resorb less water within the blood therefore it leads to a weaken pee.
So the answer you are looking for is B. <span>It prompts the kidneys to reabsorb more water into the bloodstream to dilute the salts.
I hope this helps!</span>
Answer:
Tyrosine.
Explanation:
Tyrosine is a non-essential amino acid, it is part of proteins and is considered an aromatic amino acid. Its synthesis occurs from the hydroxylation of phenylalanine as long as it contains an adequate supply of this amino acid.Phenylketonuria is a hereditary disease whose main treatment is dietary restriction of the amino acid phenylalanine. People with phenylketonuria may have low levels of the amino acid tyrosine in their blood.Phenylalanine hydroxylase is an enzyme that converts phenylalanine to tyrosine. Deficiency of the enzyme phenylalanine hydroxylase is a congenital error of metabolism.
Answer:
A
Explanation:
Cancer is genetic; not working hard, having a bad attitude, and getting into accidents are not.
