Genetics Flashcards

1
Q

What is the definition of phenotype?

A

The physical expression or characteristics of an organism, influenced by genotype and environmental factors

Examples include eye color, height, and hair color.

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2
Q

What is the definition of genotype?

A

The genetic makeup of an organism; the combination of alleles for a particular gene

Examples include AA, Aa, aa.

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3
Q

What does homozygous mean?

A

Both alleles for a given trait are the same

Examples include AA or aa.

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4
Q

What does heterozygous mean?

A

The two alleles for a given trait are different

Example: Aa.

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5
Q

What is the Law of Segregation?

A

Each organism has two alleles for each trait, which separate during gamete formation

Each gamete carries only one allele for each gene.

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6
Q

What is the Law of Independent Assortment?

A

Genes located on different chromosomes are inherited independently of each other

This leads to genetic variation in offspring.

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7
Q

What is the classic ratio for a monohybrid cross?

A

3:1 (dominant: recessive phenotype)

This occurs in a cross between two heterozygous organisms.

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8
Q

What is the typical ratio for a dihybrid cross?

A

9:3:3:1

This ratio represents the phenotypes for two traits in a cross between two heterozygous organisms.

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9
Q

What is a dominant allele?

A

An allele that is expressed in the phenotype when present

Example: A.

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10
Q

What is a recessive allele?

A

An allele that is only expressed in the phenotype when two copies are present

Example: aa.

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11
Q

What is incomplete dominance?

A

Neither allele is completely dominant, resulting in a blend of traits

Example: red flower crossed with white flower produces pink flowers.

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12
Q

What is co-dominance?

A

Both alleles are fully expressed in the phenotype

Example: AB blood type where both A and B alleles are visible.

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13
Q

What are autosomal traits?

A

Traits found on non-sex chromosomes

Examples include eye color and hair color.

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14
Q

What are sex-linked traits?

A

Traits found on sex chromosomes, often affecting males more than females

Examples include color blindness and hemophilia.

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15
Q

What is a carrier in genetics?

A

An individual with one recessive allele for a genetic trait and one dominant allele

Example: A carrier for cystic fibrosis is heterozygous (Ff) but does not show symptoms.

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16
Q

What are multiple alleles?

A

More than two alleles exist for a given gene

Example: The human ABO blood system has three possible alleles: A, B, and O.

17
Q

What are the possible genotypes for the ABO blood system?

A
  • AA
  • AO
  • AB
  • BB
  • BO
  • OO

A and B are dominant, while O is recessive.

18
Q

What is a monohybrid cross?

A

A cross between two individuals focusing on one trait

Example: Aa × Aa.

19
Q

What is a dihybrid cross?

A

A cross between two individuals focusing on two traits

Example: AaBb × AaBb.

20
Q

What is a pedigree?

A

A diagram used to track traits through generations

Squares represent males, circles represent females.

21
Q

What is the structure of DNA?

A

A double-helix made up of nucleotides

Each nucleotide contains a sugar (deoxyribose), a phosphate group, and a nitrogenous base.

22
Q

What are the base pairing rules in DNA?

A

A pairs with T, and C pairs with G

Strands are anti-parallel.

23
Q

What is DNA replication?

A

The process by which DNA makes a copy of itself

Involves helicase, DNA polymerase, and ligase.

24
Q

What is transcription in protein synthesis?

A

DNA is used as a template to make mRNA

RNA polymerase binds to DNA to synthesize mRNA.

25
Q

What is translation in protein synthesis?

A

mRNA is translated into an amino acid sequence at the ribosome

tRNA brings amino acids that match mRNA codons.

26
Q

What is a point mutation?

A

A single nucleotide is altered

Example: sickle cell anemia.

27
Q

What is a substitution mutation?

A

One base is replaced by another

28
Q

What is an insertion mutation?

A

An extra base is added

29
Q

What is a deletion mutation?

A

A base is removed

30
Q

What is a frameshift mutation?

A

Insertion or deletion of nucleotides shifts the reading frame

Often results in a nonfunctional protein.

31
Q

What are chromosomal mutations?

A

Deletions, duplications, inversions, or translocations of large portions of chromosomes

32
Q

What is amniocentesis?

A

A procedure where a sample of amniotic fluid is taken to test for genetic disorders

Example: Down syndrome.

33
Q

What is a karyotype?

A

A visual representation of an individual’s chromosomes

Used to detect chromosomal abnormalities.

34
Q

What is mitosis?

A

The process by which somatic cells divide, resulting in two identical daughter cells

Phases include Prophase, Metaphase, Anaphase, Telophase, and Cytokinesis.

35
Q

What is meiosis?

A

The process by which gametes are formed, involving two rounds of division

Results in four non-identical daughter cells.

36
Q

What is the genetic significance of mitosis?

A

Essential for growth, repair, and asexual reproduction

Produces genetically identical cells.

37
Q

What is the genetic significance of meiosis?

A

Essential for sexual reproduction, producing gametes with genetic variation

Ensures genetic diversity and maintains chromosome number across generations.