TEST 2 Flashcards
Which regions of the X chromosome can recombine during meiosis?
the pseudoautosomal regions
In mammals, dosage compensation for X linked genes is achieved by:
Inactivation of one X chromosome during early development
An X chromosome that has been inactivated becomes a ______ in female mammals.
Barr body
An organism that has only one copy of a gene is called a
Hemizygote
A white eyed Drosophila female (white/white) is crossed with a red eyed male. Assuming the trait for eye color is sex-linked. what are the possible phenotypes of the progeny?
Red-eyed females and white-eyed males
A color blind male marries a woman who has normal vision. The woman has no history of colorblindness in her family. What percentages of their sons are expected to be colorblind?
0%
Assume that a man who carries an X linked gene has children. Assuming normal meiosis and random combination of gametes the man would pass this gene to____
all of his daughters.
Sex linked conditions are more common in men than woman bc
men need to inherit only one copy of the recessive allele for the condition to be fully expressed
Which of the following is the part of the Y chromosome that is critical for normal male development?
SRY
An individuals with 2 kinds of gametes (X bearing and Y bearing) is referred to as
Heterogametic
Pedigree
Recessive, autosomal
Why is the Y chromosome able to pair with the x chromosome during meiosis?
The X and Y chromosomes share small gene segments that allow them to act like homologues during meiosis.
Female mammals that contain 2 types of cell lineages in which the parental X chromosome is inactivated in some cell and the maternal X chromosome is inactivated in others are known as:
Genetic mosaics
In some animal species, like humans, sex is determined by:
The presence of the Y chromosome
If an X linked disorder is lethal to the affected individual prior to the age at which one reaches reproductive maturation, the lethality will be expressed only in males. Why is this so?
The only sources of the lethal allele in the population are heterozygous females who are carriers and do not express the disorder