Podcast
Questions and Answers
What is the genotype of the F1 generation from the cross RRYY × rryy?
What is the genotype of the F1 generation from the cross RRYY × rryy?
- RrYyY
- rrYY
- RrYy (correct)
- RRYy
When using the FOIL method with the cross RrYy × RrYy, what is the 'Outside' component?
When using the FOIL method with the cross RrYy × RrYy, what is the 'Outside' component?
- RY (correct)
- ry
- rY
- RR
How many different gametes can be produced from a RrYy parent?
How many different gametes can be produced from a RrYy parent?
- 2
- 8
- 4 (correct)
- 16
What is the genotype ratio in the F2 generation from the cross RrYy × RrYy?
What is the genotype ratio in the F2 generation from the cross RrYy × RrYy?
Which of the following is a phenotype resulting from the F2 generation Punnett square?
Which of the following is a phenotype resulting from the F2 generation Punnett square?
In the F2 generation, how many phenotypes are present based on the Punnett square?
In the F2 generation, how many phenotypes are present based on the Punnett square?
Which of these gamete combinations results in the genotype RrYY?
Which of these gamete combinations results in the genotype RrYY?
Which term refers to the visible traits expressed in an organism, as determined by genotype?
Which term refers to the visible traits expressed in an organism, as determined by genotype?
What is one major advantage of sexual reproduction?
What is one major advantage of sexual reproduction?
What occurs during Meiosis Prophase I?
What occurs during Meiosis Prophase I?
How many chromosomes does each gamete contain after meiosis?
How many chromosomes does each gamete contain after meiosis?
What is the significance of crossing over during meiosis?
What is the significance of crossing over during meiosis?
During which phase of meiosis do homologous chromosomes line up in pairs?
During which phase of meiosis do homologous chromosomes line up in pairs?
What happens to sister chromatids during Anaphase II?
What happens to sister chromatids during Anaphase II?
What occurs during Meiosis Telophase I and Cytokinesis?
What occurs during Meiosis Telophase I and Cytokinesis?
What is the result of meiosis at the end of Telophase II?
What is the result of meiosis at the end of Telophase II?
What does the phenotype represent in a genetic context?
What does the phenotype represent in a genetic context?
Which of the following represents a heterozygous genotype?
Which of the following represents a heterozygous genotype?
According to Mendel's Second Law, what does the Law of Independent Assortment state?
According to Mendel's Second Law, what does the Law of Independent Assortment state?
If two plants with the genotypes RRYY and rryy are crossed, what are the possible gametes from the first parent?
If two plants with the genotypes RRYY and rryy are crossed, what are the possible gametes from the first parent?
What percentage of offspring from a dihybrid cross between RRYY and rryy are expected to be homozygous recessive?
What percentage of offspring from a dihybrid cross between RRYY and rryy are expected to be homozygous recessive?
In a genetic cross, which term describes an organism that has identical alleles for a gene?
In a genetic cross, which term describes an organism that has identical alleles for a gene?
Using the FOIL method, which combination describes the gametes produced from the genotype RrYy?
Using the FOIL method, which combination describes the gametes produced from the genotype RrYy?
When discussing genetic traits, what does the term 'dominant' refer to?
When discussing genetic traits, what does the term 'dominant' refer to?
What is the primary role of a dominant allele in inheritance?
What is the primary role of a dominant allele in inheritance?
What is a characteristic of incomplete dominance?
What is a characteristic of incomplete dominance?
Which of the following best describes codominance?
Which of the following best describes codominance?
How are sex-linked traits inherited in males?
How are sex-linked traits inherited in males?
What does a karyotype specifically help identify?
What does a karyotype specifically help identify?
What mutation is described as an abnormal number of chromosomes?
What mutation is described as an abnormal number of chromosomes?
Which scenario correctly describes a female carrier for color-blindness?
Which scenario correctly describes a female carrier for color-blindness?
Which gene involved in color vision is located on the X chromosome?
Which gene involved in color vision is located on the X chromosome?
Which genotype corresponds to blood type O?
Which genotype corresponds to blood type O?
Which blood type can type O individuals receive blood from?
Which blood type can type O individuals receive blood from?
What does the Law of Dominance state?
What does the Law of Dominance state?
If an individual has the genotype IAi, what is their blood type?
If an individual has the genotype IAi, what is their blood type?
What happens during the process of incomplete dominance?
What happens during the process of incomplete dominance?
Which of the following phenotypes shows complete dominance?
Which of the following phenotypes shows complete dominance?
Which blood types can type AB individuals receive from?
Which blood types can type AB individuals receive from?
How does the Law of Segregation apply to genetics?
How does the Law of Segregation apply to genetics?
What type of sample is commonly used in blood tests for genetic testing?
What type of sample is commonly used in blood tests for genetic testing?
What is a potential risk associated with amniocentesis or CVS?
What is a potential risk associated with amniocentesis or CVS?
How would you describe a heterozygous trait?
How would you describe a heterozygous trait?
Which method requires you to drink water beforehand?
Which method requires you to drink water beforehand?
What does a normal result indicate in genetic testing?
What does a normal result indicate in genetic testing?
What erroneous misconception might someone have about phenotype?
What erroneous misconception might someone have about phenotype?
What is a significant characteristic of a homozygous trait?
What is a significant characteristic of a homozygous trait?
Which of the following best describes a bone marrow test?
Which of the following best describes a bone marrow test?
Flashcards
Homozygous Trait
Homozygous Trait
Both genes for a trait are the same.
Heterozygous Trait
Heterozygous Trait
Both genes for a trait are different.
Genotype
Genotype
The genetic makeup of an organism (what's in the DNA).
Phenotype
Phenotype
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Dihybrid Cross
Dihybrid Cross
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Homozygous
Homozygous
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Heterozygous
Heterozygous
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Dominant Allele
Dominant Allele
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Recessive Allele
Recessive Allele
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FOIL Method
FOIL Method
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F1 Generation
F1 Generation
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F1 Generation Cross
F1 Generation Cross
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F2 Generation Cross
F2 Generation Cross
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Punnett Square
Punnett Square
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Genotype Ratio
Genotype Ratio
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Phenotype Ratio
Phenotype Ratio
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9:3:3:1 Phenotype Ratio
9:3:3:1 Phenotype Ratio
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Crossing Over in Meiosis I
Crossing Over in Meiosis I
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Random Assortment in Meiosis I
Random Assortment in Meiosis I
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Cytokinesis
Cytokinesis
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Meiosis
Meiosis
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Anaphase I in Meiosis
Anaphase I in Meiosis
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Metaphase I in Meiosis
Metaphase I in Meiosis
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Prophase II in Meiosis
Prophase II in Meiosis
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Prophase I in Meiosis
Prophase I in Meiosis
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Law of Dominance
Law of Dominance
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Incomplete Dominance
Incomplete Dominance
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Codominance
Codominance
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Sex Chromosomes
Sex Chromosomes
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X Chromosome
X Chromosome
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Y Chromosome
Y Chromosome
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Karyotype
Karyotype
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Aneuploidy
Aneuploidy
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Blood type
Blood type
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Rh factor
Rh factor
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Law of Segregation
Law of Segregation
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Law of Independent Assortment
Law of Independent Assortment
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Study Notes
Genetics System Review
- DNA structure is a double helix composed of nucleotides.
- Nucleotides consist of a sugar, phosphate group, and a nitrogenous base (adenine, thymine, guanine, or cytosine).
- Cytosine bonds with guanine via two hydrogen bonds, and adenine bonds with thymine via three hydrogen bonds.
- Chargaff's rule: A=T and G=C, meaning the amount of adenine equals thymine, and the amount of guanine equals cytosine.
DNA Study Facts & Review
- Genes in DNA determine organism characteristics.
- Mutations are alterations in DNA caused by chemicals, natural processes, or radiation.
- Mutations can happen during DNA replication.
- A chromosome has telomeres (chromosome ends), a centromere (chromosome middle), and chromatids (chromosome halves).
DNA Replication Notes
- DNA has a structure that allows for easy copying.
- The DNA molecule unzips and each side becomes a template for a new complementary half.
- The resulting two DNA molecules are identical.
Cell Division Review
- DNA must replicate for new cells to receive complete genetic information.
- Cells divide for asexual reproduction, growth, and repair.
- Mitosis creates identical daughter cells.
- Mitosis involves division of the nuclear material (cytokinesis) and cytoplasm.
- Interphase is the main stage of cell cycle with three stages first being G1 which is cell growth, S phase which is DNA replication, and G2 which is cell preparation for mitosis.
- Prophase: Centrioles move to opposite cell poles, chromatin condenses into chromosomes, dissolution of nuclear membrane and spindle fibers.
- Metaphase: Chromosomes line up across cell equator, spindle fibers attach to the centromeres.
- Anaphase: Sister chromatids separate and move to opposite poles.
- Telophase: Chromosomes decondense, nuclear envelopes reform, cytokinesis occurs – cell membrane pinches inward.
Asexual vs Sexual Reproduction
- Mitosis maintains chromosome numbers and is for asexual reproduction and growth.
- Meiosis produces gametes with half the chromosome count for sexual reproduction.
- Asexual reproduction involves single parent, creating identical offspring (clones).
Meiosis & Mitosis Reproduction
- Meiosis involves two divisions (meiosis I and meiosis II) to reduce chromosome number.
- Meiosis produces four daughter cells.
- Meiosis includes prophase I, metaphase I, anaphase I, and telophase I/cytokinesis.
- Mitosis produces two identical daughter cells to maintain the number of the chromosomes.
- Meiosis involves interphase and meiosis I and II each following the PMAT stages.
Karyotype Practice Study Questions
- A karyotype is a genetic test examining chromosome structure, size, and number.
- A normal human has 46 chromosomes (23 pairs).
- Karyotypes assess for missing, extra, or structurally altered chromosomes.
- Karyotypes are used to detect genetic disorders or birth defects.
How to Remember It All
- Homozygous: "same" as matching pairs
- Heterozygous: "different" with unmatching pairs
- Genotype: Genetic makeup (letters, e.g., TT)
- Phenotype: Physical traits (appearance, e.g., tall)
Punnett Squares: Predicting Traits Like a Pro!
- Punnett squares are a tool to predict genetic outcomes.
- It involves mixing parental genes to calculate possible offspring genotypes and phenotypes.
Dihybrid Crosses: In-Depth Study Notes
- Dihybrid cross involves two traits.
- Mendel's second law (independent assortment) states genes for different traits are inherited independently. This explains how combinations of traits emerge in offspring
Blood Cells Genetics Review
- Blood types (A, B, AB, O) are determined by alleles (IA, IB, i).
- IA and IB are co-dominant, and i is recessive.
- Blood type compatibility is determined by the antigens on red blood cells.
- Rh factor is another protein on red blood cells.
Mendelian Genetics: The Blueprint of Heredity
- Law of Segregation: Each organism carries two alleles for each trait, that segregate during gamete formation.
- Law of Independent Assortment: Genes for different traits are inherited independently ,assuming they're located on different chromosomes.
- Law of Dominance: In a pair of alleles, one may mask the expression of the other (dominant allele).
Non-Mendelian Genetics: The Rainbow Beyond Dominance
- Incomplete dominance: A blended phenotype; neither allele is completely dominant (e.g., red x white snapdragon = pink).
- Codominance: Both alleles are fully expressed in the phenotype (e.g., speckled chickens show both black and white feathers without blending).
Sex Linked Inheritance Notes
- Sex chromosomes (X and Y) differ in size and carry different information.
- X-linked traits are more common in males because they have only one X chromosome.
- Sex-linked traits are carried on the X chromosome.
Chromosomal Mutations Notes
- Karyotype: A visual display of an organism's chromosomes, used to detect abnormalities.
- Mistakes in meiosis (nondisjunction), or failure of homologous chromosomes or sister chromatids to separate, can result in an abnormal chromosome number.
- Errors in crossing over can cause chromosomal mutations like duplication, deletion, inversion, or translocation.
X-Linked / Sex Linked Disorders
- X-linked disorders are genetic conditions caused by mutations in genes located on the X-chromosome.
- Males are more commonly affected because they have only one X-chromosome, so the affected allele on the X-chromosome expresses itself.
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