Answer:
C) An extra chromosome is added, causing mismatching of the chromosome pairs.
Explanation:
Mutation is any change, whether big or small, that occurs in the nucleotide sequence of a gene. Mutation can be of different types depending on how it occurs.
According to the question, frameshift mutation is a mutation that causes the normal reading frame of the nucleotide sequence to be altered. It is caused when an extra chromosome is added (insertion) or when one chromosome is removed (deletion). In either way, there will be a mismatch or alteration in the chromosome pair, hence affecting the reading of the nucleotide sequence.
In frameshift mutation, the insertion or deletion causes the
normal CODONS (triplet nucleotide) to be missing or incomplete, hence, disrupts the manner at which the reading takes place (reading frame). Note, frameshift mutation only occurs as a result of insertion or deletion of chromosomes/bases that are not multiples of three that can maintain the normal reading pattern/frame.
Answer:
D
Explanation:
to find out how biological molecules could have first formed
1 one is correct.....he never think about linkage......later after chromosome mapping it was found that Mendel was lucky that they don't show much linkage !
The amount of stuff that an ecosystem
Answer:
Eukaryotic cells are generally larger and more complex than prokaryotic cells. They also contain a variety of cellular bodies called organelles. The organelles function in the activities of the cell and are compartments for localizing metabolic function.
Explanation:
