Genetics System Review

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Questions and Answers

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?

  • RY (correct)
  • ry
  • rY
  • RR

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?

<p>9:3:3:1 (C)</p> Signup and view all the answers

Which of the following is a phenotype resulting from the F2 generation Punnett square?

<p>Wrinkled and Green (B)</p> Signup and view all the answers

In the F2 generation, how many phenotypes are present based on the Punnett square?

<p>4 (D)</p> Signup and view all the answers

Which of these gamete combinations results in the genotype RrYY?

<p>RY from one parent and RY from another (C)</p> Signup and view all the answers

Which term refers to the visible traits expressed in an organism, as determined by genotype?

<p>Phenotype (B)</p> Signup and view all the answers

What is one major advantage of sexual reproduction?

<p>Ability to adapt to changing environments (A)</p> Signup and view all the answers

What occurs during Meiosis Prophase I?

<p>Homologous chromosomes pair and crossing over occurs (B)</p> Signup and view all the answers

How many chromosomes does each gamete contain after meiosis?

<p>23 (D)</p> Signup and view all the answers

What is the significance of crossing over during meiosis?

<p>It allows for genetic variation among offspring (D)</p> Signup and view all the answers

During which phase of meiosis do homologous chromosomes line up in pairs?

<p>Meiosis I Metaphase (C)</p> Signup and view all the answers

What happens to sister chromatids during Anaphase II?

<p>They separate and move to opposite poles (D)</p> Signup and view all the answers

What occurs during Meiosis Telophase I and Cytokinesis?

<p>Cells divide into two daughter cells with unique genetic material (C)</p> Signup and view all the answers

What is the result of meiosis at the end of Telophase II?

<p>Formation of four cells with 23 chromosomes each (C)</p> Signup and view all the answers

What does the phenotype represent in a genetic context?

<p>The physical traits of an organism (C)</p> Signup and view all the answers

Which of the following represents a heterozygous genotype?

<p>Rp (A)</p> Signup and view all the answers

According to Mendel's Second Law, what does the Law of Independent Assortment state?

<p>Genes located on separate chromosomes assort independently during gamete formation (A)</p> Signup and view all the answers

If two plants with the genotypes RRYY and rryy are crossed, what are the possible gametes from the first parent?

<p>RY only (D)</p> Signup and view all the answers

What percentage of offspring from a dihybrid cross between RRYY and rryy are expected to be homozygous recessive?

<p>0% (B)</p> Signup and view all the answers

In a genetic cross, which term describes an organism that has identical alleles for a gene?

<p>Homozygous (D)</p> Signup and view all the answers

Using the FOIL method, which combination describes the gametes produced from the genotype RrYy?

<p>RY, Ry, rY, ry (A)</p> Signup and view all the answers

When discussing genetic traits, what does the term 'dominant' refer to?

<p>An allele that can mask the presence of another allele (D)</p> Signup and view all the answers

What is the primary role of a dominant allele in inheritance?

<p>It determines the expression of recessive traits. (B)</p> Signup and view all the answers

What is a characteristic of incomplete dominance?

<p>Traits blend to form a new phenotype. (C)</p> Signup and view all the answers

Which of the following best describes codominance?

<p>Both alleles show their effects independently and equally. (D)</p> Signup and view all the answers

How are sex-linked traits inherited in males?

<p>Traits are inherited solely from the mother. (A)</p> Signup and view all the answers

What does a karyotype specifically help identify?

<p>The total count of chromosomes and structural abnormalities. (B)</p> Signup and view all the answers

What mutation is described as an abnormal number of chromosomes?

<p>Aneuploidy (B)</p> Signup and view all the answers

Which scenario correctly describes a female carrier for color-blindness?

<p>XBXb has normal vision but carries the gene. (B)</p> Signup and view all the answers

Which gene involved in color vision is located on the X chromosome?

<p>b for color-blindness (A)</p> Signup and view all the answers

Which genotype corresponds to blood type O?

<p>ii (B)</p> Signup and view all the answers

Which blood type can type O individuals receive blood from?

<p>O (D)</p> Signup and view all the answers

What does the Law of Dominance state?

<p>One allele may mask the expression of the other. (C)</p> Signup and view all the answers

If an individual has the genotype IAi, what is their blood type?

<p>Type A (D)</p> Signup and view all the answers

What happens during the process of incomplete dominance?

<p>Two alleles create a blend phenotype. (A)</p> Signup and view all the answers

Which of the following phenotypes shows complete dominance?

<p>Tall pea plants and short pea plants only showing tall offspring. (C)</p> Signup and view all the answers

Which blood types can type AB individuals receive from?

<p>A, B, AB, and O (D)</p> Signup and view all the answers

How does the Law of Segregation apply to genetics?

<p>Each organism carries two alleles for each trait that segregate during gamete formation. (D)</p> Signup and view all the answers

What type of sample is commonly used in blood tests for genetic testing?

<p>Small blood sample from the arm vein (C)</p> Signup and view all the answers

What is a potential risk associated with amniocentesis or CVS?

<p>Mild stinging or cramping (D)</p> Signup and view all the answers

How would you describe a heterozygous trait?

<p>Both genes for a trait are different (C)</p> Signup and view all the answers

Which method requires you to drink water beforehand?

<p>Amniocentesis/CVS (C)</p> Signup and view all the answers

What does a normal result indicate in genetic testing?

<p>46 chromosomes without abnormalities (C)</p> Signup and view all the answers

What erroneous misconception might someone have about phenotype?

<p>It is the same as the genotype (B)</p> Signup and view all the answers

What is a significant characteristic of a homozygous trait?

<p>Both alleles for a trait are identical (B)</p> Signup and view all the answers

Which of the following best describes a bone marrow test?

<p>It takes marrow from the hip bone for testing (D)</p> Signup and view all the answers

Flashcards

Homozygous Trait

Both genes for a trait are the same.

Heterozygous Trait

Both genes for a trait are different.

Genotype

The genetic makeup of an organism (what's in the DNA).

Phenotype

The physical appearance or traits that you can see.

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Dihybrid Cross

A genetic cross involving two traits, each with two different alleles.

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Homozygous

The situation where both alleles for a trait are the same (e.g., RR or pp).

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Heterozygous

The situation where the alleles for a trait are different (e.g., Rr).

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Dominant Allele

The allele that masks the expression of the recessive allele when present.

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Recessive Allele

The allele that is masked by the dominant allele when present.

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FOIL Method

A method used to determine the possible gametes (sperm or egg cells) produced by an individual.

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F1 Generation

The first generation of offspring produced from a cross between two homozygous parents.

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F1 Generation Cross

A cross between two homozygous parents, one dominant (RRYY) and one recessive (rryy), resulting in all heterozygous offspring.

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F2 Generation Cross

A cross between two heterozygous individuals from the F1 generation.

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Punnett Square

A visual representation of all possible genotype combinations from a cross using gametes from two parents.

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Genotype Ratio

The ratio of different genotypes in a population.

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Phenotype Ratio

The ratio of different phenotypes in a population (physical traits).

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9:3:3:1 Phenotype Ratio

A phenotypic ratio observed in dihybrid crosses with two genes, each with two alleles. For example, in a cross between RrYy and RrYy, the phenotype ratio is 9:3:3:1.

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Crossing Over in Meiosis I

The process where homologous chromosomes (one from the mother and one from the father) exchange segments of DNA.

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Random Assortment in Meiosis I

Chromosomes line up randomly at the center of the cell, creating a unique arrangement of genes.

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Cytokinesis

The division of a cell into two identical daughter cells.

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Meiosis

The process of cell division that results in four daughter cells, each with half the number of chromosomes as the original parent cell.

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Anaphase I in Meiosis

The stage where homologous pairs of chromosomes separate and move towards opposite poles of the cell.

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Metaphase I in Meiosis

The stage where homologous chromosome pairs align at the center of the cell, ready to be pulled apart.

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Prophase II in Meiosis

The stage where the nuclear membrane breaks down and the spindle fibers form.

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Prophase I in Meiosis

The process where duplicated chromosomes condense and become visible, and homologous pairs of chromosomes pair up.

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Law of Dominance

A dominant allele masks the effect of a recessive allele, similar to a lead actor overshadowing a supporting role.

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Incomplete Dominance

Neither allele completely masks the other, resulting in a blended or intermediate phenotype. Imagine mixing red and white paint to get pink.

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Codominance

Both alleles are expressed equally, creating a phenotype where both traits are clearly visible. Think of two singers in a duet, each voice distinct.

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Sex Chromosomes

Chromosomes that determine an individual's sex.

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X Chromosome

The larger chromosome, carrying genes for various traits including some non-sexual ones. Females have two X chromosomes, while males have one X and one Y.

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Y Chromosome

The smaller chromosome, primarily responsible for male sex characteristics. Males have one Y chromosome.

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Karyotype

A picture of an individual's chromosomes, used to identify chromosomal abnormalities. Number, size, and structure are examined.

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Aneuploidy

A condition where a cell has an abnormal number of chromosomes, often caused by errors during cell division. Can lead to genetic disorders.

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Blood type

A person's blood type, determined by the presence or absence of specific antigens on red blood cells.

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Rh factor

A specific protein found on the surface of red blood cells, inherited from parents. It can be either positive (+) or negative (-)

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Law of Segregation

The principle that each organism inherits two alleles for each trait, which separate during gamete formation.

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Law of Independent Assortment

The principle that genes for different traits are inherited independently of each other, assuming they are on different chromosomes.

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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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