You are breeding a new variety of apple, the Omega Pippin. In the wild, Apple trees reproduce sexually, through pollination of flowers. Apple trees grown for agriculture are usually propagated asexually by grafting of buds or shoots. i. You are studying two loci in a new variety of apple: T and R. TT or Tt apples tend to be sweet and tart, whereas tt apples taste sour. RR or Rr apples rot quickly (a bad thing for you!) whereas rr apples can be kept in storage for a long time without losing their flavor. You survey several dozen trees and find the following haplotype abundances:TR = 0.3tR = 0.2Tr = 0.1tr = 0.4 Calculate the coefficient of linkage disequilibrium D for these loci.

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.

answer; (a) medicalized;

answerreferred pain;

what is the question?