You have been assigned a DNA stretch. What is the complementary strand when you replicate the template

The complementary strands of a DNA are read in the opposite direction to one another

Explanation:

A DNA strand/stretch can be represented with a number of bases. The bases in a DNA strand are Adenine (A), Thymine (T), Cytosine (C) and Guanine (G). The Adenine can bind to Thymine (and vice-versa) while the Guanine can bind to Cytosine (and vice versa). These bonded bases are called "base pairs".

Complementary DNA strands are read in opposite direction to one another. Each end of a DNA strand is either a 5' end or a 3' end. Hence, if one strand runs from the 5' to 3' end, the complementary strand will run from the 3' to 5'. Thus, they are represented "on paper" the way they run.

For example,

If the DNA strand assigned is AGTCTAG running 5' to 3', the complementary strand will be CTAGACT (starting from the 3' end) and NOT TCAGATC (which starts from the 5' end)

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.

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