DNA Replication Flashcards

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1
Q

gregor mendel

A

worked with peas to develop preliminary ideas about genetics and inheritance

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2
Q

genotype

A

what the genes say (Rr, rr, RR)

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3
Q

phenotype

A

what the genes show (blue eyes, tall, etc.)

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4
Q

erwin & chagoff

A

demonstrated that DNA had equal masses of A/T and C/G, helping watson and crick with their theory

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5
Q

purines

A

A/G, because they have two C rings

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6
Q

pyrimidines

A

C/U/T, one ring

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7
Q

structure of DNA

A

phosphate-sugar-base-base-sugar-phosphate

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8
Q

antiparallel

A

dna strands go in opposite directions, on is 3’-5’, the other is 5’-3’

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9
Q

polymerase

A

enzymes that replicate DNA, works only in the 5’-3’ direction

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10
Q

leading strand

A

5’-3’ strand, synthesized continuously

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11
Q

lagging strand

A

3’-5’ strand, synthesized in chunks

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12
Q

polymerase 1

A

reads bases and corrects mistakes

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13
Q

polymerase 3

A

adds bases

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14
Q

single-strand binding proteins (SSBP)

A

stabilizes the DNA when it has been forked

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15
Q

helicase

A

splits H-bonds and creates a DNA fork

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16
Q

RNA primase

A

starts the new strand by adding a chunk of RNA to the old strand

17
Q

ligase

A

connects the Okazaki fragments

18
Q

Okazaki fragments

A

parts of the DNA that have been copied in the opposite direction of the replication direction (3’-5’ strand copied) but not connected to form a longer DNA strand

19
Q

Messelson & Stahl (M&S)

A

theorized the process of DNA replication through an experiment in which they used a radioactive marker to mark the original DNA strand. after several rounds of replication, they tested to see what the DNA looked like, finding that there was a small amount of marked DNA settled at the bottom of the test tube, showing that DNA is replicated in a semiconservative model.

20
Q

conservative model

A

original strand is kept intact and essentially copy/pasted to create the new one. the two strands at the end are one new, one old. the tube in M&S would show such a small amount of the original DNA that it wouldn’t even be observable.

21
Q

dispersive model

A

original strand replicated such that the two new strands have the old strand equally distributed throughout. the test tube in M&S would show the marker dispersed within it.

22
Q

semiconservative model

A

original strand is split in two and the daughter strands have one old side and one new side. M&S tube shows a small amount of marked DNA at the bottom, enough to be observable. (this is what they saw)

23
Q

deletion (chromosomal mutation)

A

section of chromosome is removed (ABCDE -> ADE)

24
Q

duplication (chromosomal mutation)

A

section of a chromosome is repeated (ABCDE -> ABCBCDE)

25
Q

inversion (chromosomal mutation)

A

reverses a sequence within a chromosome (ABCDE -> ADCBE)

26
Q

reciprocal translation (chromosomal mutation)

A

two different chromosomes cross over and trade (not 13/13, but 13/10; creates chromosome sections that code for genes not addressed on that chromosome)

27
Q

Rosalind Franklin

A

showed through an X-ray graph that DNA was a double helix

28
Q

Hershey & Chase

A

marked viral DNA and viral proteins to see which conveyed genetic information. results showed that it was DNA

29
Q

point mutation

A

a change made to a single base during DNA replication

30
Q

silent mutation (point mutations)

A

change in a single base that has no effect on the protein that is coded for

31
Q

nonsense mutation (point mutation)

A

change in a single base resulting in a strand that doesn’t code for anything

32
Q

conservative missense mutation (point mutation)

A

change in a single base that codes for a new protein with similar properties to the original, resulting in little change to the trait

33
Q

non-conservative missense mutation (point mutation)

A

change in a single base that codes for a new protein entirely, resulting in observable change to the trait

34
Q

frameshift mutation

A

changes the codons through insertion or deletion of bases

35
Q

deoxyribose (DNA) vs dideoxyribose (dDNA)

A

DNA has an OH group on the 3’ carbon, which means the sequence can continue. dDNA has simply an H on the 3’ carbon, so the sequence stops replicating.

36
Q

sanger sequencing steps

A
  1. split the DNA into four tubes, adding dDNA bases for one base in each tube (one has A, one has T, once has C, and one has G)
  2. let the DNA replicate in the tubes, creating strands of different lengths
  3. run this through a gel and sequence the genes (longest on top, so the last base would be the top mark)
  4. [optional] if the DNa was color-dyed, you can use a computer to sequence the DNA