Answer:
(A). Result in different amino acids to be read due to frame shifts
Explanation:
Insertion or deletion mutations (or Indel mutations) can be defined as mutations in DNA due to insertion (addition) or deletion of nucleotide bases in DNA.
These mutations lead to change in reading frames (sequence of codons), which leads to formation of protein having completely different amino acid sequence. Hence, these mutations are also cause frameshift mutations.
This is due due to triplet nature of genetic codes as insertion or deletion of one or more bases (but not three) would change change in codon sequence and mutated sequence can form a non-functional or truncated protein.
Thus, the correct answer is option (A).
Answer:
cold with high salt content
Answer:
Explanation:
DNA contains the instructions needed for an organism to develop, survive and reproduce. To carry out these functions, DNA sequences must be converted into messages that can be used to produce proteins, which are the complex molecules that do most of the work in our bodies.
Neural control of GFR is mediated by Sympathetic neurons that innervate alpha receptors on vascular smooth muscle causing Vasoconstriction.
<h3>How is GFR regulated?</h3>
- The sympathetic division of the nervous system regulates the GFR or Glomerular Filtration Rate.
- GFR is the sum total of filtration rates of all the working nephrons in the kidney.
- Sympathetic division comes into action when the mean arterial pressure is very low (below 80mmHg).
- In response to low blood pressure, the medulla releases norepinephrine through sympathetic nerves.
- Norepinephrine leads to activation of alpha receptors on arteries which cause vasoconstriction.
- Alpha receptors are more abundant on afferent arterioles.
- This leads to vasoconstriction (narrowing) of arteries supplying to the glomerulus.
- This decreases blood flow to glomerulus, leading to decrease in GFR.
Learn more about Glomerular Filtration Rate here:
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