History of DNA Flashcards

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1
Q

Who discovered substance in nuclei

A

miescher

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2
Q

Who identified components on nucleotides

A

levene

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3
Q

suggested a transforming factor existed to change bacteria from one strain to another

A

griffith

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4
Q

Who found that dna is genetic material

A

Avery-MacLeod-McCarty

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5
Q

Who Confirmed DNA as

genetic material

A

Hershey-Chase

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6
Q

Who discovered DNA Double helix

model

A

Franklin, Watson and

Crick

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7
Q

Who discovered
Semi-conservative
DNA replication

A

Meselson-Stahl

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8
Q

Who Deciphered the Genetic Code

A

Khorana, Holley, and

Nirenberg

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9
Q

Chromatin

A

DNA and its associated proteins

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10
Q

Replication origin

A

site where DNA duplication begins.

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11
Q

Centromere

A

Holds 2 chromosomes together to make sure each cell will get one copy during cell division

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12
Q

Telomere

A

Contains repeated nucleotide sequences required for proper replication and protects the ends of the chromosomes

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13
Q

Interphase vs. Mitotic Chromosomes

A

Mitotic: Two condensed chromosomes.

Interphase: Decondensed DNA

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14
Q

Function of histones

A

Associate with DNA, forming chromatin and promote chromosomes packing via nucleosomes

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15
Q

What are nucleosomes

A

composed of histones and DNA held together by noncovalent interactions.

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16
Q

how does histone acetylation affect packing

A

more acetylation causes less packing, more deacetylation causes more packing.

17
Q

Heterochromatin vs. Euchromatin

A

• Heterochromatin: Highly condensed DNA, enriched at
centromeres and telomeres. Contains very few genes,
and those genes contained within heterochromatin are
usually turned off.
• Euchromatin: Less condensed DNA

18
Q

function of dna helicase

A

unwinds the double helix, using energy from ATP

19
Q

Single-strand DNA-binding proteins

A

stabilize single-stranded DNA

20
Q

DNA Topoisomerases

A

Enzymes that allow rotation of the helix to relieve strain during DNA replication. • Prevents tangling of the DNA.

21
Q

DNA Primase

A

synthesizes RNA primers for initiation of DNA replication.

• RNA Primers serve as a red flag to ensure extra proofreading of these fragments, provides 3’OH site for DNA synthesis.

22
Q

Clamp loader

A

helps load the sliding clamp onto the DNA
DNA Polymerase associates with the clamp
Sliding clamp keeps DNA Polymerase on the DNA until it runs into double stranded DNA and falls off.

23
Q

Lagging Strand Synthesis

A
• Synthesis of lagging strand stops
when it runs into the 5’ end of
another fragment.
• RNA primer is degraded.
• Sequence filled in by DNA
Polymerase.
24
Q

DNA Ligase

A

• Enzyme that joins the 3’ end of one fragment to the 5’ end of another Okazaki fragment. • Uses one molecule of ATP to catalyze this otherwise unfavorable sealing reaction.

25
Q

describe 3 to 5 exonuclease proofreading activity

A

Incorrect nucleotide pair is cut out by DNA polymerase

26
Q

Why can’t dna synthesis occur in opposite direction?

A

If synthesis occurs in the 3 to 5 direction, polymerization can’t proceed due to there being no high energy bond to drive the reaction.

In the 5 to 3 direction, the open 3’ OH allows for the high energy bond to be cleaved, providing energy for polymerization.

27
Q

What is the function of telomerase?

A

Replenishes end sequences of chromosomes, contains bound RNA template.
Telomerase binds to template strand and adds additional telomere repeats to it. Then DNA polymerase completes the lagging strand.