Ahuman gene can possibly correct a defective gene in a yeast cell because

a. the common core set of genes is very similar between all organisms
b. humans can get yeast infections
c. that's impossible. humans have nothing in common with yeast
d. all organisms have completely identical genes

     This is a very good question and the answer to it is option A. The common core set of genes is very similar between all organisms.

      This is true because several facts, for example, all living beings on earth share the same gene code: DNA, all of them are based on DNA or RNA, which humans have it too. This was explained by Darwin's evolution theory, we are all descendants of just one single species, and because of that, all species have something in common between them.

       That's why there's a possibility that a human gene can correct a defective gene in a yeast cell. Although this could really happen, we are not sure about it, it's a possibility, don't always be sure of something in biology, there's always more to understand and to learn.

it would be rhyolitic hope this

an individual’s sex (i.e., whether they are a male or female) is determined by the sex chromosomes. most people have two sex chromosomes, one that is inherited from their mother and one that is inherited from their father. typically, females have two x chromosomes (xx) and males have one x chromosome and one y chromosome (xy). conditions caused by changes (“mutations”) in genes located on the x chromosome are considered x-linked.

x-linked recessive inheritance

most x-linked conditions are recessive. this means that in a person with two x chromosomes (most females), both copies of a gene (i.e., one on each x chromosome) must have a change or mutation whereas in a person with one x chromosome (most males), only one copy of a gene must have a mutation. a female with a mutation in one copy of a gene on the x chromosome is said to be a “carrier” for an x-linked condition. a male with a mutation in a gene on the x chromosome is typically affected with the condition. because females have two copies of the x chromosome and males have only one x chromosome, x-linked recessive diseases are more common among males than females. however, x-linked recessive diseases can occur in both males and females.

for x-linked recessive disorders, an unaffected carrier mother who has a mutation in a gene on the x chromosome can transmit either the x chromosome with this mutation or a “normal” x chromosome to her children. if the father is unaffected, none of her daughters will be affected and all of her daughters will be unaffected—since they will inherit at least one normal x chromosome from their father. however, each daughter will have a 50% chance of being an unaffected carrier like her mother and a 50% chance of both x chromosomes being normal.