Inheritance and DNA Flashcards

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1
Q

Gene

A

a fundamental unit of heredity that is passed from parent to offspring. Genes are made up of DNA and are located on chromosomes in the nucleus of cells. They contain information for making proteins, which are responsible for specific traits or functions in the body

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2
Q

Allele

A

alternate forms of a gene that code for different proteins

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3
Q

Wild type

A

allele present in most of the population

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4
Q

Mutation

A

stable, inherited change in genetic material, where new alleles arise

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5
Q

True breeding

A

a term used in genetics and selective animal breeding to describe organisms or animals that pass on the same traits to their offspring

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6
Q

Phenotype vs genotype

A
  • Phenotype: physical appearance of an organism
  • Genotype: genetic constitution of an organism
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7
Q

Dominant vs recessive

A
  • Dominant alleles: are expressed; exert their effects whenever they’re present
  • Recessive alleles: effect is masked if dominant allele also present; may be mutated and no longer expressed, or encode non‐functional proteins
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8
Q

Homozygous vs heterozygous

A
  • Homozygous: two alleles are the same
  • Heterozygous: two different alleles; one may be dominant and the other recessive
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9
Q

P vs. F1 vs. F2

A

The parent or P generation refers to the individuals being crossed; the offspring are the filial or F generation. F₁ or the first filial represents the children of the parents; F₂ represents children of the F₁ or grandchildren of the parents

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10
Q

Gregor Mendel’s 1st law

A

Law of segregation: the two copies of a gene separate during gamete formation; each gamete receives only one copy

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11
Q

Mendel’s 2nd law

A

Law of independent assortment: copies of different genes assort independently

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12
Q

Who do offspring inherit alleles from

A

Offspring inherit alleles from both of their parents; each parent contributes one allele for every gene, meaning the offspring receives a pair of alleles for each trait, one from the mother and one from the father

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13
Q

Multiplication rule

A

probability of two independent events
happening together –multiply by probabilities of the individual events
– Tossing two coins: probability that both will come up heads = ½ x ½ = 1/4

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14
Q

Addition rule

A

the probability of an event that can occur in two different ways is the sum of the individual probabilities
– In F2, there are two ways to get Rr, thus ¼ + ¼ = ½

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15
Q

Codominant vs incomplete dominance

A

Codominance: more than one allele
encodes a functional protein
Incomplete dominance: alleles are neither dominant nor recessive – heterozygotes have an intermediate phenotype

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16
Q

Locus

A

specific position on a chromosome

17
Q

Linked genes

A

genes that are located close together on a chromosome and are often inherited together

18
Q

Pleiotropic vs. epistatic

A

Pleiotropic: one allele has multiple phenotypic effects
Epistasis: phenotypic expression of one gene influenced by another gene

19
Q

What environmental conditions can affect expression of genotype

A

Light, temperature, nutrition, etc., can affect expression of the genotype

20
Q

Coat patterns of Siamese cats and rabbits

A

Point restriction coat patterns in Siamese cats and rabbits
- Enzyme that produces dark fur inactive at higher temps.
- Nose, ears, etc., are cooler, thus darker in color

21
Q

How can prokaryotes exchange genes

A

horizontal gene transfer” which primarily occurs through three mechanisms: conjugation (direct cell-to-cell contact via a pilus), transformation (taking up free DNA from the environment), and transduction (transfer of DNA by a virus)

22
Q

Plasmid and what genes it contain

A

small, circular DNA molecules that can contain a variety of genes, including those that confer antibiotic resistance, virulence, and the ability to grow in adverse conditions

23
Q

Rosalind Franklin

A

Rosalind Franklin prepared crystallography from DNA samples
- Her images suggested a double helix with 10 nucleotides/turn
- 2 nm diameter suggested the sugar‐phosphate backbone must
be on outside

24
Q

Crick and Watson

A

used model building, plus physical and
chemical evidence, to solve DNA structure
– Published their results in 1953

25
Q

Structure of DNA

A

Biochemists knew DNA is a polymer of nucleotides
– Each nucleotide consists of deoxyribose, a phosphate group, and a nitrogen‐containing base

26
Q

Four different nucleotides differing only in the bases

A

Purines: adenine (A) and guanine (G)
Pyrimidines: cytosine (C) and thymine (T), holds DNA together

27
Q

DNA vs. RNA nucleotides

A

DNA: Pu. A -> Py. T, Pu. G -> Py. C
RNA: Pu. A -> U (Uracil), Pu. G -> Py. C

28
Q

DNA structure setup

A
  • Bases are on the inside of each strand
  • Sugar‐phosphate groups on outside
  • Chains are antiparallel: run in opposite direction
  • DNA can be found in the nucleus of the cell
29
Q

Chargaff’s rule

A

The amount of adenine is always equal to the amount of thymine found in a sample. The amount of cytosine is always equal to the amount of guanine found in a sample

30
Q

DNA strands held together by

A
  • hydrogen bonds between complementary base pairs
  • Van der Waals forces between adjacent bases on same strand
31
Q

DNA replication

A

the process by which cells create two identical copies of DNA from a single original DNA molecule

32
Q

Semi conservative

A

each parent strand is a template; new molecules have one old and one new strand

33
Q

2 step DNA replication

A
  • Double helix unwound, making two template strands
  • New nucleotides form complementary base pairs with the template DNA strand and are linked by phosphodiester bonds
34
Q

origin of replication and replication fork

A
  • Origin of replication (ori): specific region of DNA that indicates the starting point of replication
  • In E. coli, DNA is unwound, and replication proceeds in both directions, forming two replication forks
35
Q

Leading vs. lagging strand and Okazaki fragments

A
  • Leading strand: grows at the 3’ end as the fork opens
  • Lagging strand: the exposed 3’ end gets farther from the fork, and an unreplicated gap form
  • Okazaki fragments: small, discontinuous stretches of new DNA
36
Q

3 repair mechanisms

A
  • Proofreading: DNA polymerase recognizes mismatched pairs
    and removes incorrectly paired bases
  • Mismatch repair: newly replicated DNA is scanned for mistakes by other proteins, and mismatches can be corrected
  • Excision repair: enzymes scan DNA for damaged bases – they’re excised, and DNA polymerase I adds the correct ones
37
Q

PCR

A

Polymerase chain reaction (PCR): an automated process that makes multiple copies of short DNA sequences for genetic
manipulation and research