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Questions and Answers
In a scenario where four offspring are produced from a cross, and both parents are heterozygous for a trait (Bb), what explains a deviation from the expected 3:1 phenotypic ratio?
In a scenario where four offspring are produced from a cross, and both parents are heterozygous for a trait (Bb), what explains a deviation from the expected 3:1 phenotypic ratio?
- The 3:1 ratio is a statistical expectation that is not guaranteed in small sample sizes. (correct)
- The parents are showing incomplete dominance leading to a different phenotypic ratio.
- The sample size is large enough to guarantee the expected phenotypic ratio.
- The alleles are showing complete dominance so the phenotypic ratio will always be 3:1.
What is the primary purpose of performing a test cross?
What is the primary purpose of performing a test cross?
- To create new genetic variations within a population.
- To identify if an organism with a dominant phenotype is homozygous or heterozygous. (correct)
- To determine the exact number of dominant alleles an organism possesses.
- To produce offspring with only recessive traits.
If a test cross between an organism with a dominant phenotype and a homozygous recessive organism yields only offspring with the dominant phenotype, what can be inferred about the genotype of the dominant parent?
If a test cross between an organism with a dominant phenotype and a homozygous recessive organism yields only offspring with the dominant phenotype, what can be inferred about the genotype of the dominant parent?
- The offspring inherited a new mutation causing them to express the dominant trait.
- The parent with the dominant phenotype is homozygous dominant. (correct)
- The parent with the dominant phenotype is heterozygous.
- The parent with the dominant phenotype carries two different dominant alleles.
In humans, what is the approximate probability of a conceived child being male?
In humans, what is the approximate probability of a conceived child being male?
Why is the phenotypic ratio of males to females approximately 1:1 in humans?
Why is the phenotypic ratio of males to females approximately 1:1 in humans?
In X-linked inheritance, why are males more likely to express recessive traits compared to females?
In X-linked inheritance, why are males more likely to express recessive traits compared to females?
In a cross between a healthy man ($X^HY$) and a woman carrier of hemophilia ($X^HX^h$), what is the probability that their son will have hemophilia?
In a cross between a healthy man ($X^HY$) and a woman carrier of hemophilia ($X^HX^h$), what is the probability that their son will have hemophilia?
A couple, where the male has hemophilia and the female is homozygous healthy, plan to have a child. What is the probability that their daughter will be a carrier of hemophilia?
A couple, where the male has hemophilia and the female is homozygous healthy, plan to have a child. What is the probability that their daughter will be a carrier of hemophilia?
A hemophilic man and a homozygous healthy woman have children. What is the probability that their son will inherit hemophilia?
A hemophilic man and a homozygous healthy woman have children. What is the probability that their son will inherit hemophilia?
What is the term for the observable characteristics or traits of an organism?
What is the term for the observable characteristics or traits of an organism?
What does a genetic diagram (Punnett square) primarily illustrate?
What does a genetic diagram (Punnett square) primarily illustrate?
What is the term for different versions of a gene at a specific locus?
What is the term for different versions of a gene at a specific locus?
What is meant by the term 'homozygous' for a specific trait?
What is meant by the term 'homozygous' for a specific trait?
Which of the following statements correctly describes the relationship between genotype and phenotype?
Which of the following statements correctly describes the relationship between genotype and phenotype?
Flashcards
What is a test cross?
What is a test cross?
A cross to determine if an individual with a dominant phenotype is homozygous or heterozygous. It involves crossing the individual with a homozygous recessive individual.
Test cross ratio (heterozygous)
Test cross ratio (heterozygous)
If the dominant phenotype individual is heterozygous, a 1:1 phenotypic ratio will be observed in the offspring.
Test cross ratio (homozygous)
Test cross ratio (homozygous)
If the dominant phenotype individual is homozygous, all offspring will have the dominant phenotype.
Sex chromosome distribution
Sex chromosome distribution
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Probability of sex
Probability of sex
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Sex inheritance
Sex inheritance
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Sex determination using diagrams
Sex determination using diagrams
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Gamete chromosome
Gamete chromosome
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Genetic diagrams (sex-linked)
Genetic diagrams (sex-linked)
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Hemophilia alleles
Hemophilia alleles
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Carrier mother, passing allele
Carrier mother, passing allele
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Hemophilic son chance
Hemophilic son chance
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Healthy Daughters
Healthy Daughters
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Hemophilic Sons Probability
Hemophilic Sons Probability
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Hemophilic father outcome
Hemophilic father outcome
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Study Notes
- More offspring from a single cross leads to the observed phenotypic ratio of the offspring matching the estimated phenotypic ratio.
- A large number of offspring (e.g., 100) should approach a phenotypic ratio of 3:1 in a cross between F1 offspring.
Test Cross
- A test cross determines if an individual with a dominant phenotype is homozygous or heterozygous for a trait.
- It involves crossing the individual with the dominant phenotype with an individual known to be homozygous recessive for the studied trait.
- A 1:1 phenotypic ratio suggests the individual with the dominant phenotype is heterozygous.
- All offspring having the dominant phenotype suggests the individual with the dominant phenotype is homozygous.
Sex Determination Using Genetic Diagrams
- Genetic diagrams can be used to study sex inheritance
- Normal eggs (female gametes) carry one X chromosome
- Females have two X chromosomes and no Y chromosomes
- The probability of an egg carrying an X chromosome is normally 1
- Sperm (male gametes) carry either a Y chromosome or an X chromosome.
- Approximately half of sperm carries a Y chromosome and the other half carries an X chromosome
- The probability that a sperm will contain an X chromosome is 0.5
- The probability that a sperm will contain a Y chromosome is 0.5.
- The phenotypic ratio of males to females is 1:1
- There is a probability of 0.5 (50% chance) that a zygote will be male
- There is a probability of 0.5 (50% chance) that a zygote will be female
Genetic Diagrams for Sex-Linked Inheritance and Codominance
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Hemophilia's X-linked inheritance involves the allele for a healthy clotting factor (XH) and the altered allele for hemophilia (Xh).
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In a cross between a healthy man (XHY) and a healthy woman carrier (XHXh):
- The probability of the man passing on the healthy X allele (XH) is 0.5, and the probability of passing on the Y chromosome is 0.5.
- The probability of the woman passing on the healthy allele (XH) is 0.5, and the probability of passing on the altered allele (Xh) is 0.5.
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The probability of a healthy daughter (either XHXH or XHXh) is 1 where:
- The healthy daughter with the XHXH genotype is 0.5
- The healthy carrier of the XHXh genotype is 0.5
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All female offspring will be healthy; none will have hemophilia, but half will be carriers.
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The probability of a healthy son (XHY) is 0.5 and of a hemophilic son (XhY) is also 0.5.
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A son of a woman carrier and a healthy man has a 50% chance of being hemophilic.
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The phenotypic ratio of healthy to hemophilic males in this cross is 1:1, where there is a 1 in 2 chance of receiving a mutated allele and a 1 in 2 chance of receiving a healthy allele
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The phenotypic ratio of healthy to hemophilic offspring for all children is 3:1, where there is a 3 in 4 chance the offspring will be healthy and a 1 in 4 chance the offspring will be hemophilic
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In a cross between a hemophilic man (XhY) and a homozygous healthy woman (XHXH):
- The woman will pass a healthy allele (XH) to her offspring is 1
- The man will contribute an X chromosome carrying the altered hemophilic allele, is 0.5, and the probability that he will contribute a Y chromosome, is 0.5
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The probability that this couple will have a healthy daughter carrier (XHXh) is 1
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The probability that this couple will give birth to a healthy son (XHY) is 1.
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None of the sons will receive a mutant hemophilia allele, and all of the daughters will receive only one mutant hemophilia allele
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None of the children of a hemophilic father and a homozygous healthy woman will exhibit hemophilia.
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