Answer:
Deletion mutation usually takes place due to the errors in the process of DNA replication . DNA polymerase slips off on the template strand due to which that part of the DNA is not coded in the daughter strand.
It can skip from one nucleotide (point mutation) to an entire gene. Point deletion can result in frame-shift mutation if it takes place in the beginning or middle of the gene. However, if it takes place at the end of the gene then it may cause no harm.
For example, let us assume the original sequence of DNA as ATG-AGT-CGT-ATA-TAA. It will result in the formation of methionine, serine, arginine, isoleucine, and STOP codon.
Point deletion at the end of the gene results in ATG-AGC-GTA-TAT-AA sequence. Now it will code for methionine, serine, valine, and tyrosine as AA will not code for anything. Hence, the sequence of the protein remains the same.
Hence, if deletion mutation takes place at the last or stop codon of the gene then it will cause no harm or change in the protein sequence. However, if it takes place before that then it may result in frame-shift mutation and thus a mutated protein.
Answer:
Hello now,
The human body system that would be most affected in this scenario would be B, the Respiratory and circulatory system.
Answer:
A?
I think I'm wrong! please tell me what one it is if I'm wrong.
In the adults, the growth rate slows with age. The healing mechanism of the different cells if damaged is different than that of the younger ones. If a cartilage is damage in the adults, the chondrocytes which are still surviving secrete more extracellular matrix in order to heal the damaged cartilage. The chondrocytes cells are present in the cartilage, and they function to maintain the cellular matrix of the cartilage.
Answer:
Is this USA Test prep?
I believe that it is all except the 2nd one
Explanation:
