Chapter 14 Flashcards

1
Q

A-T G-C

A

Chargaffs rule

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2
Q

Nucleotides

A

Are the monomers that build DNA

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3
Q

A nucleotide is made up of 1,2,3

A

1 Penrose sugar, 2 phosphate group, 3 nitrogenous base

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4
Q

RNA ONLY

A

No T (thymine) only U (uracil)

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5
Q

RNA is for

A

Complementary base pairing

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6
Q

Nucleotides combine with each other via

A

Phosphodiester bonds

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7
Q

Directionality

A

Opposite direction
3-5
5-3

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8
Q

Chromatin

A

Interphase

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9
Q

When the phosphate bond holding the third phosphate to the nucleoside is broken the energy released is used to form the

A

Phosphodiester bonds
Between the incoming nucleotides of the growing chain

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10
Q

DNA pol I is an

A

Accessory protein important is DNA polymerization

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11
Q

DNA pol II is required for

A

DNA repair

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12
Q

DNA pol III is the enzyme necessary for

A

Adding new nucleotides on to the growing chain

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13
Q

Helicase is an

A

Enzyme that unwinds the DNA by breaking down the hydrogen bonds between the nitrogenous base pairs using ATP

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14
Q

DNA pol II can only add new nucleotides to the

A

3’ end

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15
Q

DNA pol I pieces them together later away from the replication fork this,

A

Form fragments called Okazaki fragments

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16
Q

The strand with Okazaki fragments is called the

A

Lagging strand

17
Q

A protein called the sliding clamp holds the

A

DNA pol III in place

18
Q

DNA polymerase III

A

Bacteria
Starts adding nucleotides to the 3’ -OH end of the primers

19
Q

The gap between the two DNA fragments are sealed by DNA Ligase which helps in the formation of

A

Phosphodiester bonds

20
Q

Strand elongation (adding new nucleotides to the two new strands) is done by

A

Pol a, pol b, and pol e, in eukaryotes

21
Q

A sliding clamp protein called proliferating cell nuclear antigen (PCNA) holds the

A

DNA pol complex in place is eukaryotes

22
Q

Point mutations

A

Affect a single base pair usually substitutions

23
Q

Missense mutation

A

Result in the wrong amino acid being translated

24
Q

Frame shift mutation

A

Result from insertions or deletions of nucleotides which shift the reading frame and the production of a nonfunctional protein