Answer: mother: XX^aa, father: X^YAa, son: X^YAa, daughter: X^X^aa.
Explanation:
Color blindness is a genetic disorder that affects the ability to distinguish colors. It is hereditary and is transmitted by an X-linked recessive allele. If a male inherits an X chromosome with the altered allele he will be color blind. In contrast, females, who have two X chromosomes, will only be colorblind if both of their X chromosomes have the altered allele. This is because <u>males have one X chromosome and one Y chromosome, while females have two X chromosomes</u>.
If the woman has normal vision, that means she cannot have both chromosomes affected. She can only have one affected chromosome (be a carrier) or none at all. Also, if she has blue eyes, which is a recessive trait, then both alleles are recessive. But the eye color is not on the X chromosome. For example, her eye color genotype can only be aa, because if she had at least one dominant allele she would have brown eye color. As for the other trait, she can be XX^, with X^ being an affected (carrier) allele or XX, i.e. both normal. So in summary, her genotype can be XXaa or XX^aa
If she has a brown-eyed male child who is also colour blind, he has inherited the allele for colour blindness from his mother, since the father does not pass on an X chromosome to the male children, only the Y. With this we can now rule out the mother's XXaa genotype since she had to have passed on her affected X^ chromosome. Then the genotype of the mother is XX^aa. And since her mother can only pass on one allele to (recessive) because she does not have allele A, the dominant that determines her brown eye color can only come from the father. So the genotype of this son is X^YAa. The female daughter has color blindness and blue eyes. So she had to inherit the affected X^ chromosome from the mother (which we already know she has) and an affected X^ chromosome from the father, because the daughter needs to inherit both affected X^ chromosomes to develop the disease. And if she also has blue eyes, she had to have inherited a recessive allele from the mother and another from the father. So with this information we can say that the father's genotype can only be X^YAa. Because the father must have both A and A alleles of the same eye color, because he passed the dominant one to the son and the recessive one to the daughter. At last, the genotype of the daughter is X^X^aa.
Structure- a bilipid membraneous layer composed of proteins and carbohydrates. It is fluid like.
Function - the cell membrane separates the cell from its external environment, and is selectively permeable (controls what gets in and out). It protects the cell and provides stability.
Proteins are found embedded within the plasma membrane, with some extending all the way through in order to transport materials.
Carbohydrates are attached to proteins and lipids on the outer lipid layer.
--CYTOPLASM
Structure - The jelly-like substance composed of mainly water and found between the cell membrane and nucleus. The cytoplasm makes up most of the "body" of a cell and is constantly streaming.
Function - Organelles are found here and substances like salts may be dissolved in the cytoplasm.
-- NUCLEUS
Structure - The largest organelle in the cell. It is dark and round, and is surrounded by a double membrane called the nuclear envelope/membrane. In spots the nuclear envelope fuses to form pores which are selectively permeable. The nucleus contains genetic information (DNA) on special strands called chromosomes.
Function - The nucleus is the "control center" of the cell, for cell metabolism and reproduction.
Answer: A
Explanation:
It can't be B or D because to get the polypeptide chain, we need the mNRA first to go through the ribosome. It's not C because after the mRNA is generated in the nucleus, it undergoes some modifications like splicing and the addition of the 5' cap and 3' tail.
