Sheet 10-Test 4 Flashcards

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1
Q

How did Hammerling show that heredity information is probably stored in the nucleus?

A
  • -Used Acetobularia (unicellular marine algae; grows up to 5cm)
    • one cell differentiated into foot, stalk and cap
  • -could regenerate parts of nucleus was present
  • -nucleus determines cap shape
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2
Q

.How did Briggs, King, and Gurdon prove that hereditary information is stored in the nucleus?

A

.–removed nucleus from frog egg; no development until a nucleus from an embryo was added
– gurdon transplanted nuclei from tadpole cells

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3
Q

How did steward prove that (nearly) every cell in a plant is totipotent?

A

–threw carrots in a blender
–every cell gave rise to new individual
toti poten– each cell has full set of hereditary instructions; can generate adult individual

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4
Q

how did Ian Wilmut clone a sheep and what did cloning a sheep teach us about animal cells?

A
  • -close is genetically idnetical to DNA donor (dolly is the name of the clone)
    • Dolly was the first sucessful clone from a differentiated animal cell

Cloning Sheep showed that:
transplanted nucleus could direct the developent of a new individual (totipotent)

*paper

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5
Q

what are some practical problems and what are some ethical problems created by cloning humans?

A

Pratical

1) susceptibility to disease
2) low success rate
3) clone as old as donor of DNA

Ethica:

1) bad for child
2) low success rate
3) slows evoultionc

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6
Q

what are some alternatives to cloning humans for organ transplants?

A

Therapeutic Cloning– use DNA of patient needing transplant to produce stem cells in an embryo

  • -stem cells used to produce organ
    • less liklihood of rejection
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7
Q

what are stem cells, and why are they useful

A

Stem cells are undifferentiated, yet continue to divde (havent been told their job yet)
–cells can be isolated from cell mass of blastocyst ad gown in culture as embyronic stem cells

  • -stem cells may be:
    1) totipotent- can become any cell type
    2) pluripotent- can become multiple different cell types ex. bone marrow cells
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8
Q

what is genetic transformation

A

.a change in the genome of an indivdual

ex. making E. coli ampicillin resistant + able to glow green

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9
Q

how did griffith discover genetic transformation

A

mouse injected with non pathogen: lives
mouse injected with virulent bacterium: dies
mouse injectd with dead pathogenic bacerteria: lives
mouse injected with dead virulent and live non pathogenic: dies

pathogen is streptococcus pneumoniae virulent strain has polysaccharied coat

  • -virulent bacteria were recovered
  • -live bacteria had been transformed
  • -genetic information specifying polysaccharide coat had been passed from dead bacteria to living bacteria
  • -howeveer, griffith didnt know wht had transformed cells
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10
Q

why did Avery, MacLeod, and McCarty conclude that DNA is the transforming principle?

A

digested extract of dead coated bacteria with DNA ase, RNA ase, or protease

–activity was affected by DNA ase, not RNA ase or protease

–concluded DNA is transforming principle (hereditary material)

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11
Q

why did very few people believe in them

A

didnt provide a mechanism, believed protein was hereitary material

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12
Q

why did Hershey and chase decide that DNA is the hereditary material in T2 bacteriophage?

A

–used bacteriophase: T2
–bacteriophage is a virus that infects bacteria
t–they labeled viral DNA with radioactive phosphorus
–they labeled viral protein with readioacctive sulfur
–know that viruses inject genetic material into has cell
found infected cell contained 32^P

SO: DNA stores hereditary material

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13
Q

what is the primary structure of DNA?

A

Ladder

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14
Q

why do we say that nucleic acids run 5’ to 3’

A

any strand of DNA (or RNA) will have a free 5’ phosphase group at one end and a free 3- hydroxy group at the other end

-* write base sequences 5’ to 3’
5’ Aug 3’

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15
Q

what are chargaffs rules

A

Amount of A = Amount of T

Amount of C= G

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16
Q

how did Rosalind Franklin help to determine the structure of DNA?

A

X ray crystallographic analysis

diffraction patterns suggested DNA had the shape of a double helix

17
Q

what is the Watson/Crick Model of DNA tertiary structure

A

.ladder twists into a double helix

18
Q

what holds the two DNA strands together in the Watson/Crick model

A

hydrogen bonds

19
Q

why are the two strands of DNA anti-parallel in the watson/crick model?

A

this is the only way hydrogen bonds can form
one strand runs 5’ to 3’
other strand runs 3’ to 5’

20
Q

why do we say that each DNA strand is the reverse and complement of the other strand?

A

strands are antiparallel (reverse); one strand runs 3’ to 5’; the other runs 5’ to 3’

complementary A–T and C–G

21
Q

why was the watson/crick model such an important milestone in the histroy of biology?

A

.explained how DNA could store information and be copied

22
Q

what is PCR and why is it useful?

A
  • -polymerse chain reactions

- -used to make copies of a DNA sequence

23
Q

why did you use lysozyme?

A

lysozyme used to remove the cell wall so that DNA would be released when the plasma membrane was dissolved

24
Q

why does gel electrophoresis separate molecules?

A

separation is by size; smallest molecules go farthest; compare unknown to molecules of known molecular weight

25
Q

Why did you add ethanol to you DNA extract?

A

ethanol precipitates DNA

26
Q

What is undifferentiated?

A

Stem cells

27
Q

what is toti potent?

A

cell can become anything