This process is called as imprinting. It occurs at a particular stage of life and is, therefore, a phase-sensitive learning process. It can be of many types, including filial imprinting, where an offspring gains some of its behavioral characteristics from the parent, or sexual imprinting, through which desirable characteristics of a mate are recognized by a young animal.
The theme is the writer's view of or comment about the subject. The answer to your question is D. I hope this is the answer that you are looking for and it comes to your help.
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:
basically a gene is made up of a DNA. lets say a gene is a functional and physical system that creates habits in you or choices you make. might be difficult to understand but a gene gives you a lifestyle.
~batmans wife dun dun dun...aka ~serenitybella
