The Hereditary Material - MT3 - Part 1 Flashcards

1
Q

What is the only molecule recognizable from its shape?

A

DNA

- double helix

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2
Q

What lead to the discovery of the structure of DNA?

A

History of the study of the hereditary material

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3
Q

What 2 streams consisted from the DNA?

A
  1. Genetic function

2. Structure of macromolecules

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4
Q

What was the DNA structure very suggestive for?

A

Function

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5
Q

What was the function they proposed from the structure of DNA?

A

Replication

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6
Q

Who discovered DNA?

A

Friedrich Miescher

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7
Q

How did Miescher discover DNA?

A

He isolated nuclei from pus and found a new kinda of molecule called nuclein

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8
Q

Who discovered the shape of DNA?

A

Watson

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9
Q

What does pus have a lot of?

A

RBC

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10
Q

What does DNA have? (2)

A
  1. Both acidic and basic parts
    - but mostly acidic
  2. Lots of phosphorus
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11
Q

What did Miescher suspect was involved in heredity? And why?

A

Thought that nuclein might be involved in heredity because the significance of nuclei in hereditary had been established

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12
Q

What did Miescher think might be hereditary variants?

A

Isomers of nuclein

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13
Q

What did Albrencht Kossel find out?

A

That there are 5 kinds of bases

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14
Q

What are the 5 kinds of bases?

A
  1. Adenine
  2. Guanine
  3. Cytosine
  4. Thymine
  5. Uracil
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15
Q

What did Phoebus Aaron Leven do? (3)

A
  1. Elucidated the structure of nucleotides
  2. Determined the difference between DNA and RNA and their sugars
  3. Proposed the tetranucleotide model of DNA
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16
Q

What did Leven’s analysis suggest?

A

That the 4 bases of DNA were present in equimolar amounts

- in equal numbers

17
Q

What was discovered about Leven’s model?

A

That it was wrong

  • thought it was proteins instead of DNA
  • proteins are not hereditary
18
Q

What did Archibald Garrod study?

A

Alcaptonuria

- soon after the rediscovery of Mendels law

19
Q

What did studying family pedigrees show?

A

That alcaptonuria is inherited as a Mendelian recessive trait

20
Q

Alcaptonuria

A

Is a rare inherited genetic disorder in which the body cannot process the amino acids phenylalanine and tyrosine, which occur in protein

21
Q

What are alcaptonuria not able to get ride of?

A

Homogentisic acid

22
Q

What happens when homogentistic acid builds up? (2)

A
  1. It is excreted in the urine

2. Turns black upon exposure to air

23
Q

What did Garrod suspect about alcaptonuria?

A

A deficiency in a pathway which lacked enzymatic function since it could not encode for that enzyme

24
Q

What did Garrod conclude?

A

That a normal allele somehow produced an enzyme for the metabolism of homogentisic acid
- the alcaptonuric allele produced a defective or missing enzyme

25
What did Franz Moewus study?
The genetics of sexuality in chlamydomonas eugametos | - which is a green unicellular alga
26
What did Moewus associated with Mendelian mutations?
With an inability to produce sex hormones, thus associating genes with biochemical functions - same as Garrod had done
27
What was Moewus accused of?
Making up data
28
What were mutations in Neurospora Crassa (a fungus) associated with?
Deficiencies in pathways that synthesize amino acids from precursor molecules
29
Mutagenesis
Ia a process by which the genetic information of an organism is changed, resulting in mutation
30
How might mutagenesis occur in nature? (2)
1. Spontaneously 2. As a result of exposure to mutagens - can also be achieved in the lab
31
Genetic dissections
A major tool of developmental geneticists is the ordering of gene in functional pathways
32
What did George Beadle and Edward Tatum perform?
The famous experiment of mutants having deficiencies in certain precursor pathways to synthesize amino acids for later precursor molecules - one gene = one enzyme (idea)
33
What was the first protein to be studied in structural and functional detail?
Hemoglobin (Hb) | - modle molecule
34
Why is Hb a model molecule? (3)
1. Can get a lot of it in pure substance 2. Easily accessible 3. Ability to quickly purify
35
What could Pauling and co-workers show?
That a disease known to be inherited in simple Mendelian fashion, sickle cell anemia, was associated with a malformed version of a protein, Hb
36
What do mutated proteins have? (3)
1. Different structures 2. Different functions 3. Can move at different migration speeds