The largest amount of dna in a plant cell is contained in

The largest amount of dna in a plant cell is contained in a nucleus.

Explanation:

The nucleus is like the "brain" of the cell, because it is from it that "decisions" depart. This is where the chromosomes composed of deoxyribonucleic acid molecules, DNA, are located, which carry all the information about the characteristics of the species and participate in the hereditary mechanisms.

Each region of DNA is made up of genes that encode the information for protein synthesis that occurs in ribosomes. According to the encoded gene, a type of protein will be synthesized which will be used for specific purposes.

Moreover, when the organism needs to grow or reproduce the cell goes through divisions that also happen in the nucleus.

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.