Replication Flashcards

1
Q

gene regulation

A

the process of turning genes on and off
- ensures that the appropriate genes are expressed at the proper times and helps an organism respond to its environment
- gene –(transcription)-> mRNA –(translation)-> protein

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2
Q

mutations

A

permanent changes in the DNA sequences of organisms are referred to as mutations
- mutations happen during DNA replication
and are induced by environmental factors

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3
Q

silent mutation

A

change in nucleotide sequence that does not change the amino acid specified by a codon
- no change; neutral

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4
Q

missence mutation

A

change in nucleotide sequence that changes the amino acid specified by codon
- change in primary structure of protein; may be beneficial, neutral, or deleterious

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5
Q

nonsense mutation

A

change in nucleotide sequence that results in an early stop codon
- leads to a shortened protein; almost always deleterious
- negatively impact protein function

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6
Q

frameshift mutation

A

addition or deletion of a nucleotide
- reading frame is shifted, altering the meaning of all subsequent codons; almost always deleterious
- negatively impact protein function

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7
Q

mutagens

A

chemicals or radiation that react with and alter DNA, such as arsenic, asbestos, and ultravlet radiation
- these changes make the molecule difficult for DNA polymerase to accurately read

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8
Q

point mutation

A

mutations that alter a single nucleotide pair in the DNA

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9
Q

chromatin

A

DNA and protein complex found in a eukaryotic cell
- the DNA is packaged into nucleosomes that have histone proteins as cores
- prokaryotes do not have chromatin

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10
Q

chromosome

A

a single strand of chromatin or a replicated set of chromatin pieces are attached to each other at the cenromere
- chromosome is just as much DNA as it is protein

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11
Q

somatic cell

A

normal body cell; anything but a gamete

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12
Q

chromatids (chromatiddies)

A

one of the two identical halves of a chromosome that has been replicated in preparation for cell division

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13
Q

replication

A

complementary base pairs provide a replication for DNA
- conservative, semiconservative, dispersive
- cannot be replicated heavier than before

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14
Q

conservative replication

A

produces two double helices in which one helix contains entirely old parental DNA and the other helix contains entirely new DNA

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15
Q

semiconservative replication

A

produces double helices in which each strand of the two double helices formed would have one old and one new strand

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16
Q

dispersive replication

A

the original DNA chain breaks and recombines in a random fashion before the double helix structure unwinds and separates to act as a template for messenger RNA synthesis

17
Q

replication bubbles

A

form in chromosomes, which allow enzymes to replicate DNA
- Only happens in prokaryotes (maybe)
- most of the action go in the replication fork

18
Q

DNA polymerase

A

DNA polymerases are enzymes that catalyze the polymerization of nucleotides into DNA
- can only add a nucleotide to the 3’ end of a nucleic acid
- always building in the 5’ -> 3’ direction

19
Q

helicase

A

enzymes that break hydrogen bonds to separate the two strands of DNA

20
Q

single-strand binding proteins

A

prevent the strands from reforming a double helix

21
Q

topoisomerares

A

enzymes that alleviate the twisting as DNA strands are separated
- as helicases separate the strands of DNA, twisting tension occurs in the double helix

22
Q

primase

A

enzymes that synthesize short sections of RNA (known as primers), which allow DNA polymerases to start replication

23
Q

leading strand

A

follows the replication fork

24
Q

lagging strand

A

produced in fragments
- exonucleases remove all RNA primers, DNA polymerases replace the missing nucleotides, and DNA ligases then catalyze the last bonds

25
Q

okazaki fragment

A

short sequences of DNA nucleotides which are synthesized discontinuously and later linked together by the enzyme DNA ligase to create the lagging strand

26
Q

DNA ligase

A

facilitates the joining of DNA strands together by catalyzing the formation of a phosphodiester bond
- repairs single-strand breaks

27
Q

telomere

A

regions at the ends of linear chromosomes in eukaryotes are referred to as telomeres
- an issue for lagging strands; chromosomes of most cells get shorter during each division due to this issue with replication
- DNA polymerases cannot finish replicating lagging strands due to the need for primers
- do not contain needed information but instead consist of repeating nonsense (our chromosomes end with repeats of TTAGGG)
- telomere shortening eventually causes cells to
stop dividing (usually around 40-60 divisions)

28
Q

telomerase

A

enzymes that counter the shortening of telomeres by using their own RNA templates to insert DNA nucleotides
- usually only active in germ cells (produce gametes) and some stem cells

29
Q

replication accuracy

A

DNA replication is extremely accurate due to DNA polymerases and mismatch repair
- estimate is one error per billion base pairs

30
Q

polymerase chain reaction

A

Polymerase Chain Reaction (PCR) is a lab technique that is used to replicate a specific region of DNA many times (amplification)
- DNA sample
- thermal cycler
- nucleotides
- DNA primers
- taq polymerase
- buffer solution
1. denaturing: separate strands with heat
2. annealing: anneal/attach primers to DNA
3. extension
- takes about 30 rounds of all 3