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Questions

Question 1

In organisms with chromosomal sex determination, what term describes the sex that has two different sex chromosomes, such as XY in humans or ZW in birds?

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Question 2

In birds, which chromosomal system determines sex, and which sex is heterogametic?

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Question 3

What is the primary function of the SRY gene in human embryonic development?

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Question 4

How is sex determined in the fruit fly, Drosophila melanogaster?

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Question 5

What is the key mechanism of dosage compensation in mammals?

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Question 6

What is a Barr body?

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Question 7

What is the genetic basis for the patchwork of orange and black fur in female calico and tortoiseshell cats?

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Question 8

Red-green colorblindness is an X-linked recessive trait. Why is this condition significantly more common in chromosomal males (XY) than in chromosomal females (XX)?

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Question 9

What are the pseudoautosomal regions (PAR) on the human X and Y chromosomes?

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Question 10

In Complete Androgen Insensitivity Syndrome (CAIS), an individual with an XY genotype has a female phenotype. What is the underlying molecular cause?

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Question 11

What is the key distinction between a sex-linked gene and a sex-influenced gene?

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Question 12

Approximately how many genes does the human X chromosome carry?

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Question 13

What is the expected outcome in a reciprocal cross involving an X-linked trait that is not seen with an autosomal trait?

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Question 14

Why are germline mutations in proto-oncogenes considered to be typically embryonic lethal?

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Question 15

In the case of 5-alpha-reductase deficiency, individuals with an XY genotype may appear to have female or ambiguous genitalia at birth but develop male secondary sex characteristics at puberty. What causes this change?

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Question 16

Which condition is a sex chromosome aneuploidy where an individual has only one X chromosome (XO)?

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Question 17

What is the primary reason that sex chromosome aneuploidies are more common and generally less severe than autosomal aneuploidies?

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Question 18

According to the text, what is the definition of a person's gender?

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Question 19

In the human sex determination pathway, what is the role of anti-Müllerian hormone (AMH)?

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Question 20

How can the study of reciprocal crosses in fruit flies, like those performed by Thomas Hunt Morgan, demonstrate that a gene is X-linked?

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Question 21

In birds, which use a ZZ/ZW system, the DMRT1 gene on the Z chromosome is critical for maleness. Why does a ZW individual develop as a female?

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Question 22

What is the term for a gene that is located on an autosome but is expressed differently in males and females, such as male pattern baldness?

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Question 23

What is the genetic karyotype of the vast majority of rare male tortoiseshell or calico cats?

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Question 24

Why do heterozygous females for X-linked hemophilia A typically not have the disease, despite half of their liver cells not producing Factor VIII?

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Question 25

What is meant by the term 'hemizygous' in the context of X-linked genes?

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Question 26

What is the primary factor that triggers the development of ovaries in a human embryo with an XX genotype?

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Question 27

According to the text, approximately what percentage of the human population is estimated to have a Difference of Sex Development (DSD) when atypical sex chromosome ploidy is included?

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Question 28

An individual with Klinefelter syndrome has which sex chromosome genotype?

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Question 29

What does 'skewed X-inactivation' refer to, and what can be its consequence?

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Question 30

In the human sex determination pathway, genes like WNT4 and RSPO1 are essential for which process?

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Question 31

What is the key difference between a sex-limited trait and a sex-influenced trait?

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Question 32

In Congenital Adrenal Hyperplasia (CAH), a mutation in the 21-hydroxylase enzyme leads to what hormonal imbalance and resulting phenotype in XX individuals?

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Question 33

Why do chromosomal males (XY) always express the phenotype determined by their single allele for an X-linked gene?

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Question 34

A rare condition in humans is caused by a translocation of the SRY gene onto an X chromosome. What would be the expected chromosomal sex and phenotypic sex of an individual who inherits this X chromosome and a normal X chromosome from their other parent?

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Question 35

How many rows and columns would a Punnett square for a three-gene cross have, and how does this relate to the challenge of using them for multigene problems?

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Question 36

Which dosage compensation mechanism is employed by the roundworm C. elegans?

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Question 37

In the developmental cascade leading to a male phenotype in humans, which gene is directly activated by the SRY transcription factor?

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Question 38

Why are true Y-linked traits considered very rare in humans?

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Question 39

What is the developmental fate of the Müllerian ducts in a typical XY human embryo?

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Question 40

What happens to the Wolffian ducts in a typical XX human embryo?

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Question 41

What is the typical cause of Swyer syndrome, which results in an XY individual with a female phenotype?

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Question 42

According to Thomas Hunt Morgan's work, what did the results of reciprocal crosses for the 'white' eye color trait in Drosophila demonstrate?

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Question 43

If a female cat is homozygous for the black allele (O_B O_B) of the X-linked fur color gene, what will her phenotype be?

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Question 44

In the absence of a Y chromosome, what is the default phenotypic outcome for a human embryo regarding sex development?

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Question 45

What causes the different forms of red-green color blindness, such as protanopia and deuteranopia?

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Question 46

Why do individuals with an XYY genotype have a male phenotype?

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Question 47

A female is heterozygous for an X-linked recessive trait. Under what circumstances might she display the recessive phenotype?

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Question 48

How can X-inactivation in mammals be considered a form of epigenetic modification?

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Question 49

Why do true Y-linked traits have no dominant or recessive forms?

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Question 50

What is the consequence of a loss of function mutation in the 'white' gene in Drosophila melanogaster?

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