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: Parietal lobe
Explanation:
The parietal lobes are one of the four main lobes of the cerebral cortex. It is positioned above the temporal lobes and behind the frontal lobes.
These lobes serves many important functions such as functioning and processing of the sensory information, body's awareness and spatial orientation.
This lobe processes the information about eye, head and body position.
Hence, the correct answer is parietal lobe.
Polar ice caps would melt and increase the sea level. The ozone layer would be depleted. And hurricanes are also related.
Hope it helped!
The answer is A because c doesn’t make sense if it’s vibrating wouldn’t we feel or see it?
Answer:
When helicase mutations occur, problems in DNA replication are found. The helicases are proteins that open the 2 strands of DNA to initiate the duplication, they are responsible for breaking the hydrogen bonds between the two DNA chains, thus separating the chains, also they have the function of repairing DNA mutations, if there is mutation in the gene that encodes them, various functions will be absent in the cell.
