Chapter 3: Nucleic Acid Structure and Function Flashcards

1
Q

What is a genome?

A

The collection of genes in an organism

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2
Q

How condensed are chromosomes in interphase vs mitosis

A

Chromosomes are less condensed in interphase
Most condensed in mitosis for proper segregation

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3
Q

What is Euchromatin and heterochromatin and what are their functions

A

Euchromatin: Gene rich regions that need too be loose to allow access
Heterochromatin: regions of non coding DNA usually packed together

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4
Q

Describe the structure of a prokaryote gene

A

A promoter that binds a RNA polymerase through coding sequences resulting in RNA that can be used to make one(monocistronic) or many (polycistronic) proteins

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5
Q

Describe the structure of a eukaryote gene

A
  1. A promoter binds a RNA polymerase that starts at a 5’ UTR and goes toward the 3’ UTR and makes a transcript
  2. The transcript then has a 5’ cap and poly(A) tail added and the introns are removed
  3. The mature RNA then is translated by a ribosome making a protein
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6
Q

What is Alternative splicing and what is its purpose

A

When an RNA transcript is partially translated by different ribosomes meaning not all exons are included in the mRNA synthesis. This results in proteins that serve a similar function

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6
Q

What is HGPS?

A

A mutation resulting in rapid aging in children that is not inherited as the child dies too early to pass it on. 1 in 4 mil. is caused by a base change resulting in lamina build up on membrane which results in premature cell death

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7
Q

What is a plasmid?

A
  • A self replicating piece of circular DNA
  • Carry genetic info not found in chromosomal DNA
  • Found in prokaryotes and Eukaryotes
  • Can be cloned, conjugated, transformed, or transduced
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8
Q

What is cDNA and how is it made

A

DNA made complimentary to mRNA using reverse transcriptase
1. Primer added to mRNA poly A tail
2. Reverse transcriptase
3. Ribonuclease denatures mRNA
4. DNA poly used to make complimentary
5. DNA ligase fills in primers

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9
Q

What is the Sanger technique and how was it used

A

Uses fluorescent labeled ddNTPs, DNA primer, DNA poly, and DNA strand to sequence DNA. ddNTPs are added at the 3’ end and then detected by a laser that analyzes fluorescence

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10
Q

What is PCR? At what rate does it work? What are the Phases and what materials are needed?

A

-Polymerase Chain Reaction
- 2^n each cycle
- Denature, Anneal, Elongation
- Target DNA, Primers, NTP’s, DNA polymerase

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11
Q

What is CRSPR-Cas9? How does it work?

A

A form of adaptive immunity against bacteriophage viruses that targets specific DNA
- Cas9 introduced via plasmids
- Cas9 cleaves target DNA
- Non homologous end joining
- Gene knockout
- Homology directed repair causes gene knock-in

  • Can contain auto florescent protein to make identifying specific strand easier
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12
Q

Draw a deoxyribose and ribose sugar

A
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13
Q

What are the similarities and differences between DNA and RNA

A

DNA only:
- Double helix (antiparallel strands)
- Thymine
- Deoxyribose
- Stable
- Long lived

RNA only:
- Single stranded
- Uracil
- Ribose
- Ribozymes
- Unstable (due to cleaving)
- Short lived

Both:
- Adenine, Cytosine, Guanine
- Structure is nucleotides, phosphorus and sugar
- 5’ to 3’

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14
Q

What structural differences are there between A, B, and Z DNA

A

A:
- Right handed
- Helical structure
- Tightly packed

B:
- Right handed
- Helical structure
- Most stable

Z:
- Left Handed
- Zig-Zag arrangement

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15
Q

Why are G-C bonds stronger than A-T bond?

A

Because they can form 3 hydrogen bonds when they interact as opposed to A-T which can only form 2 h bonds

16
Q

What does Topoisomerases I and II do

A

Topoisomerase is used to relieve super coiled areas and return it to its natural state by cleaving strands
I:
- Breaks and nicks one strand

II:
- Breaks and nicks both strands

17
Q

Why does RNA autocleave?

A

RNA autocleaves and is unstable because of the presence of a 2’ hydroxyl group

18
Q

What is spontaneous deamination?

A

When a base is deaminated resulting for example a C to become a C* which pairs with an A and when replicated a T fills in creating a base change
- C-G -> A-T