Simply put, a genetic mutation comes from a change in the DNA; this change can result from an extrachromosomal element, an alteration of the inherited nucleotide...
The basic building block of nucleic acids, such as DNA and RNA. It is an organic compound made up of nitrogenous, a sugar, and a phosphate group (http://www.biology-online.org/dictionary/Nucleotide)
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.
Assuming that the og cell is going through mitosis and not meiosis (sexual cell division) then the genetic code of the og cell and the daughter cells are the same. Thus, the genetic code of the daughter cells is AaSs.
Hello There!
Now, i'm not 100% sure on this but i think it is C.
Please let me know if it is correct..i'm sorry if it is wrong.
Hope This Helps You!
Good Luck :)
- Hannah ❤
