In chromatin, substitution mutations are most common in linker regions. Option d is the correct answer.
Mutation by substitution When one nucleotide base is replaced by another, this occurs. Mismatch mutation A type of substitution mutation in which a single nucleotide is replaced, resulting in the coding of an incorrect amino acid, which usually results in a malfunctioning protein. Silent mutations are the result of genetic code redundancy (degeneracy): This is false, as silent mutations are the result of a base substitution that has no discernible effect on a protein's amino acid sequence.
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If the liver begins to release glycogen because the pancreas releases glucagon, the amount of <u>the concentration of insulin</u> in the bloodstream must be too low.
<u>Explanation:</u>
Glucagon is considered to be the primary catabolic hormone of the body and is produced by the pancreas.
When insulin in the bloodstream falls low, then the pancreas causes the liver to convert stored glycogen into glucose. Insulin allows glucose to be used by insulin-dependent tissue.
The body releases insulin and glucagon to keep the blood glucose level stable in the body. Under stress, the level of glucagon increases in the body.
Answer:
The acidic environment in the stomach stops the action of the amylase enzyme.
The stomach will secrete digestive juice that contain hydrochloric acid and digestive enzyme such as pepsin to digest protein.
The HCL create an acidic environment that will deform the ionic and hydrogen bond of the amylase which cause the enzyme to be denatured.
C) Folded mountain with waves, twists, and turns