Unit 10 part 2 Flashcards

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1
Q

Synthesizing a new DNA Strand

A
  • The initial nucleotide strand is a short RNA primer
  • The RNA primer is synthesized by the enzyme
    primase
  • Primase can start an RNA chain from scratch:
  • Adds RNA nucleotides one at a time
  • Uses parental DNA as a template
  • The primer is short (5–10 nucleotides long) and the 3′ end of primer serves as the starting point for the new DNA strand
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2
Q

primase

A
  • start RNA chain from scratch
  • adds the rna nucleotides one at a time
  • 3’ end of primer serves as the starting point for the new dna strand
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3
Q

Building nucleic acid polymers

A
  • Each nucleotide that is added to a growing DNA strand is a nucleoside triphosphate (dNTP)
  • Each monomer joins the DNA strand, viaa dehydration reaction
  • two phosphate groups are lost as a molecule of pyrophosphate
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4
Q

dATP

A

supplies adenine to dna and is similar to the ATP of energy metabolism
- deoxyribose… atp has reibose as sugar

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5
Q

Antiparallel Elongation

A
  • The antiparallel structure of the double helix affects replication
  • DNA polymerases add nucleotides only to the free 3′ end of a growing strand
  • Therefore, a new DNA strand can elongate only in the 5′ -> 3′ direction
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6
Q

When the replication bubble opens, replication occurs

A

in two directions
* Replication bubbles use leading and lagging strand synthesis

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7
Q

Leading Strand Synthesis

A
  • Along one template strand of DNA, the DNA polymerase synthesizes a leading strand continuously, moving toward the replication fork (5’ –> 3’)
  • Requires:
  • RNA primer, primase, DNA Pol III, template DNA, helicase, ssBPs
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8
Q

leading strand requires

A

rna primer, primase, DNA pol III, template DNA, helicase, ssBPs

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9
Q

Lagging Strand Synthesis

A
  • To elongate the other new strand (the lagging strand):
  • DNA polymerase works in the direction away from the replication fork
  • The lagging strand is synthesized as a series of segments called Okazaki fragments, which are joined together by DNA ligase
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10
Q

DNA POL III

A
  • using parental DNA as a template, synthesis new DNA strand by adding nucleotides to an RNA primer or a pre-exsisting DNA strand
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11
Q

DNA pol I

A

removes RNA nucleotides of primer from 5’ end and replaces them with DNA nucleotides added to 3’ end of adjacent fragment

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12
Q

ligase

A

joins okazaki fragments of lagging strand
- joins the 3’ end of dna

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12
Q

Proofreading and Repairing DNA

A
  • DNA polymerases proofread newly made DNA, replacing any incorrect nucleotides
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13
Q
  • DNA can be damaged by:
A
  • exposure to harmful chemicals or physcial agents such as cigs, xray, UV rays
  • spontaneous chnages
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14
Q

mismatch repair

A

repair enzymes correct errors in base pairing

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15
Q

nucleotide excision repair

A

nuclease cuts out adn replaces damaged stretches of DNA

15
Q

If errors are not repaired

A
  • The error rate after proofreading and repair is low but not zero
  • Sequence changes may become permanent and can be passed on to the next generation
16
Q

mutations are

A

0 source of genetic variation upon which natural selection operates
- ultimately responsible for the appearance of new species
- some mutations can be deleterious (disease causing)

17
Q

Limitations of DNA polymerase create

A

problems for the linear DNA of eukaryotic chromosomes
* Only adds nucleotides at 3’ end of polymer
* Not an issue for prokaryotes: circular
chromosomes
Replication machinery provides no way to complete the 5′ ends
- repeated rounds of replication produce shorter DNA molecules with uneven ends

18
Q

Telomeres

A

Eukaryotic chromosomal DNA molecules have special nucleotide sequences at their ends
* Telomeres do not prevent the shortening of DNA molecules
* Telomeres postpone the erosion of genes near the ends of DNA molecules
- repeates of sequence at end of chromosomes
- similar to shoelace caps

  • shortening of telomers is linked to aging
19
Q

telomerase

A

catalyzes the lengthening of telomeres in germ cells
- if not, essential genes would be mussing in the gametes they produce (germ cells)

There is evidence of telomerase activity in cancer cells, which may allow cancer cells to persist

20
Q

Chromosomal Packaging

A
  • DNA is combined with proteins in a complex known as chromatin
  • Double helix
  • DNA sequence
  • Histones:
  • Proteins that help with first level of DNA packing
  • Histone tails involved in gene expression regulation
  • Nucleosome:
  • DNA wrapped around histones
  • Beads on a string, 10 nm fiber
21
Q
  • Metaphase chromosome:
A
  • Compacted chromatin we see as metaphase chromosome
21
Q

Chromosome location in cells

A
  • Interphase chromosomes occupy specific restricted regions in the nucleus
  • The fibers of different chromosomes do not become entangled
  • Homologous chromosomes are not next to each other
22
Q

Euchromatin

A
  • loosely packed chromatin, more accessible for gene expression
23
Q

heterochromatin

A
  • highly condense chromatin, less accessible for gene expression