Genetics Flashcards

1
Q

Gene

A

A segment of DNA containing enough codons to produce all amino acids for one protein.
Example: ATTGACTACCGGTACGAATCG

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2
Q

Beadle and Tatum’s One Gene-One Polypeptide Hypothesis:

A

Concluded that genes direct the production of only one enzyme.

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3
Q

Vernon Ingram, One Gene-One Polypeptide Hypothesis:

A

Demonstrated the one gene-one polypeptide hypothesis by studying hemoglobin in individuals with sickle cell anemia. He concluded that a gene specifies the type and location of each amino acid in a polypeptide chain.

Examples: Hemophilia, cystic fibrosis.

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4
Q

Codon

A

A sequence of three mRNA bases (e.g., AUG) that codes for a specific amino acid.

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5
Q

Start Codon

A

AUG (signals translation start).

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6
Q

Stop Codons

A

Signal translation stop.

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7
Q

Triplet

A

A group of three nucleotides in DNA/RNA coding for an amino acid.

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8
Q

Anticodon

A

A complementary trinucleotide sequence on tRNA corresponding to an mRNA codon.

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9
Q

Amino Acid

A

Molecules that combine to form proteins.

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10
Q

DNA

A

A double-stranded helix held together by hydrogen bonds between base pairs.

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11
Q

Base Pairing (what pairs with what, and how?)

A

Adenine (A) pairs with Thymine (T) via 2 hydrogen bonds.

Cytosine (C) pairs with Guanine (G) via 3 hydrogen bonds.

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12
Q

Nucleotides (3 components)

A

5-carbon sugar (deoxyribose).

Phosphate group (C5).

Nitrogenous bases: Pyrimidines (C, T) and Purines (A, G).

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13
Q

Directionality

A

DNA is read 3’ → 5’ and synthesized 5’ → 3’.

3’ end: Hydroxyl group (-OH).

5’ end: Phosphate group.

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14
Q

Frederick Griffith (1928)

A

Discovered bacterial transformation.

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15
Q

Avery, MacLeod, McCarty (1944)

A

Identified DNA as the transforming principle.

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16
Q

Hershey-Chase (1952)

A

Proved DNA is the hereditary material using bacteriophages.

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17
Q

Erwin Chargaff (1950)

A

Developed Chargaff’s rules (A=T, C=G).

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18
Q

Rosalind Franklin (1952)

A

X-ray diffraction revealed DNA’s double helix.

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19
Q

Watson and Crick (1953)

A

Built the DNA double-helix model.

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20
Q

Meselson-Stahl (1958)

A

Demonstrated semiconservative DNA replication

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21
Q

DNA Replication: Key Steps

A
  1. Unwinding the DNA
  2. Priming
  3. Elongation
  4. Joining Fragments
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22
Q
  1. Unwinding the DNA
    Helicase -
A

Unzips the DNA.

23
Q

1.Unwinding the DNA
Topoisomerase -

A

Prevents overwinding.

24
Q
  1. Unwinding the DNA
    SSBs -
A

Stabilize separated strands.

25
Q
  1. Priming
A

RNA Primase: Lays down RNA primers.

26
Q
  1. Elongation
    DNA Polymerase III
A

Synthesizes new strands (5’ → 3’).

27
Q
  1. Elongation
    Leading Strand
A

Continuous synthesis.

28
Q
  1. Elongation
    Lagging Strand
A

Discontinuous synthesis with Okazaki fragments.

29
Q
  1. Joining Fragments
    DNA Ligase
A

Seals gaps

30
Q

Key Enzymes

A

Helicase, Topoisomerase, SSBs, RNA Primase, DNA Polymerase I/III, DNA Ligase.

31
Q

Protein Synthesis: 2 main steps

A

Transcription & Translation

32
Q

Where does transcription take place?

33
Q

Transcription steps

A
  1. Initiation
  2. Elongation
  3. Termination
34
Q

Initiation

A

RNA polymerase binds to promoter regions (e.g., TATA box).

35
Q

Elongation

A

RNA polymerase synthesizes mRNA complementary to the template strand.

36
Q

Termination

A

RNA polymerase releases the mRNA transcript.

37
Q

Post-Transcriptional Modifications:

A

5’ Cap, 3’ Poly-A Tail: Stabilize mRNA.

Splicing: Removes introns, joins exons.

38
Q

Where does translation occur?

39
Q

Steps of Translation?

A
  1. Ribosomes bind mRNA at the start codon (AUG).
  2. tRNA matches anticodons to mRNA codons, carrying amino acids.
  3. Ribosome links amino acids with peptide bonds.
  4. Process ends at stop codon.
40
Q

2 Main Types of Mutations?

A
  1. Point Mutations
  2. Frameshift Mutations.
41
Q

Types of Point Mutations

A

Silent, Missense, Nonsense

42
Q

Silent Mutation

A

No change in protein.

43
Q

Missense Mutation

A

Changes one amino acid.

44
Q

Nonsense Mutation

A

Introduces a stop codon.

45
Q

Framseshift Mutation:

A

Insertions/deletions alter the reading frame.

46
Q

What are Restriction Enzymes

A

Cut DNA at specific sites (sticky/blunt ends).

47
Q

What is Recombinant DNA?

A

Combines DNA from different sources.

48
Q

What are plasmids?

A

Circular DNA for gene insertion.

49
Q

What is Gel Electrophoresis?

A

Separates DNA by size

50
Q

What is PCR?

A

Amplifies DNA

51
Q

What is CRISPR-Cas9?

A

Precise gene editing

52
Q

Gene Control In Prokaryotes

A

Lac Operon: Induced by lactose to digest the sugar.

Trp Operon: Repressed by tryptophan to stop its production.

53
Q

Gene control is eukaryotes

A

mRNA Processing: Introns removed, exons joined.

Alternative Splicing: Produces multiple proteins from one gene.