QUESTION 16

4 points

Skin pigment in frogs is controlled by one gene with three alleles (SGSY and SW). The S allele makes

green pigment and is completely dominant over the SY and SW alleles. The s allele makes yellow pigment

and is completely dominant over the Wallele. The sWallele makes white pigment. The SG allele frequency

is 0.35 and the allele frequency is 0.45. What is the allele frequency of the SW allele?

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.

they have identical fossils of organisms that have evolved over time.

both have animal fossils preserved in them due to weathering and erosion.

they contain different fossils because life on earth has changed through time.

the fossils in them were formed on the surface of earth due to exposure to sunlight.