A single change or alteration in the nucleotide base of the genetic material of the cell is called a point mutation. It can be a deletion, addition or inversion of a single nucleotide base.
In the following, the mutations that occurred are 1. C and 2. B.
<h3>How the mutation can be explained?</h3>
- <u>Silent mutation</u> occurs in a single base of the triplet codons of the bases but the alterations do not cause an observable effect and they remain as a neutral alteration. They do not affect the function of the protein. Thus, the glycine to glycine is a silent mutation.
- <u>Non-sense mutations</u> are caused when the single change in the nucleotide base results in the formation of the stop codon. Thus, lysine to stop codon is a nonsense mutation.
Therefore, silent and nonsense mutations are the correct options.
Learn more about point mutation here:
brainly.com/question/10473763
Answer:
genomic imprinting
Explanation:
Genomic imprinting is a mechanism for regulating gene expression that allows expression of only one of the parental alleles, although both alleles are functional. Unlike most genes in which expression is biallelic, genes that are subjected to this mechanism (imprinted genes) have monoalelic expression; By definition, in an imprinted loci, only one allele is active (maternal or paternal), and the inactive is epigenetically marked by histonic modification and / or methylation of cytosines.
Genomic imprinting can cause some disturbances, among them Prader-Willi syndrome, which is a genetic disorder that involves a partial deletion of chromosome 15q on the paternal chromosome.
The evernimoentol mark of chris is the first of the
Answer:
The correct answer is A
Explanation:
Eukaryotic cells have a nucleus containing their DNA, whereas prokaryotic cells do not have a nucleus.
