Answer:
Epistasis
Explanation:
In epistasis, the interaction between genes is inimical, such that one gene masks or interferes with the expression of another. “Epistasis” is a word coined of Greek roots that mean “standing upon.” The alleles that are being masked or silenced are said to be hypostatic to the epistatic alleles that are doing the masking. The cause of the biochemical basis of epistasis is a genetic pathway in which the expression of one gene is dependent on the function of a gene that precedes or follows it in the pathway.
The example of epistasis given is the pigmentation of mice. we were told that "if a mouse has two recessive alleles for coat color, it is always albino no matter what the genotype of other genes involved in coat color"
Let say recessive allele (rr), it is always albino irrespective of other type of other genes, this is true in the stance that epistasis can be reciprocal such that either gene, when present in the dominant (or recessive) form, expresses the same genotype.
Im going to have to go with C. they pass through channels in the cell membrane
Mendelian disorder is the known disorder of a single gene
Answer:
The answer is C
Explanation:
Proteins that were sinthesized in the endoplasmic reticulum are able to leave this organelle inside vesicles that are formed through evagination of the reticulum membrane. These vesicles can merge with the golgi membrane, spreading its contents inside the golgi apparatus. This process can be repeated through all of Golgi's cisternaes, and when the last cisternae is reached, these vesicles can be directed towards the plasma membrane. Once the vesicles and the plasma membrane are merged, all the molecules that were contained inside the vesicle are exported from the cell into the extracellular space.
