Replication Flashcards

(30 cards)

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

silent mutation

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

point mutation

A

mutations that alter a single nucleotide pair in the DNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

somatic cell

A

normal body cell; anything but a gamete

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

chromatids (chromatiddies)

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

replication

A

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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
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
okazaki fragment
short sequences of DNA nucleotides which are synthesized discontinuously and later linked together by the enzyme DNA ligase to create the lagging strand
26
DNA ligase
facilitates the joining of DNA strands together by catalyzing the formation of a phosphodiester bond - repairs single-strand breaks
27
telomere
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
telomerase
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
replication accuracy
DNA replication is extremely accurate due to DNA polymerases and mismatch repair - estimate is one error per billion base pairs
30
polymerase chain reaction
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