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Quiz about Great DNA Experiments
Quiz about Great DNA Experiments

Great DNA Experiments Trivia Quiz


This quiz takes a look at some key experiments and prominent figures in the history of the discovery of DNA's properties and structure.

A multiple-choice quiz by doublemm. Estimated time: 6 mins.
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Author
doublemm
Time
6 mins
Type
Multiple Choice
Quiz #
356,848
Updated
Jul 23 22
# Qns
10
Difficulty
Average
Avg Score
6 / 10
Plays
553
Awards
Top 5% quiz!
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Question 1 of 10
1. DNA first came to the attention of scientists when, in 1869, Johann Friedrich Miescher found a substance which was not protein in the pus cells he was examining. Miescher came to the conclusion that "nuclein" (as he called it) was not a protein by using pepsin. What is pepsin? Hint


Question 2 of 10
2. Following on from Frederick Griffith's work in 1928, Avery, MacLeod and McCarty claimed that their experiments showed that DNA could be taken up and expressed by bacteria. What is this process called? Hint


Question 3 of 10
3. The confirmation that DNA was the hereditary material came from the 1952 experiments carried out by Alfred Hershey and Martha Chase. They did this by labelling DNA with a certain isotope and then checking to see if the isotope (and therefore the DNA) had been taken up by the bacteria. Which element's isotope, found in the "backbone" of DNA, was used? Hint


Question 4 of 10
4. With the revelation that DNA was the hereditary material, Erwin Chargaff was puzzled by the fact that DNA was made of only four "letters", or nucleotides. Chargaff also discovered that the number of purines in a molecule of DNA was always equal to the number of pyrimidines. Which of the following is NOT true of purines and pyrimidines? Hint


Question 5 of 10
5. Just as Chargaff set down the rules for base pairing, Salvador Luria and Max Delbruck characterised the phenomenon of mutation. Their "fluctuation test" aimed to determine whether mutations arose spontaneously or in response to a selective force. What was their conclusion? Hint


Question 6 of 10
6. The components of DNA were now known, but the structure remained elusive. The breakthrough came from two groups working in parallel in the UK - Watson and Crick at Cambridge and Wilkins and Franklin in King's, London. Which of the following best describes the structure of DNA? Hint


Question 7 of 10
7. The discovery of the structure of DNA was followed by a hive of activity in the study of this molecule. The next major step came in 1958, when Matthew Meselson and Franklin Stahl demonstrated that DNA replicated semi-conservatively. Which of the following best describes the term "semi-conservative replication"? Hint


Question 8 of 10
8. Experiments involving synthetic mRNA in the 1950s and carried out by Nirenberg and Khorana (amongst other) were employed to determine which nucleotides coded for which amino acid. What principle, first put forward by George Gamow, was essential to the understanding of the genetic code? Hint


Question 9 of 10
9. Frederick Sanger pushed forward the field of DNA sequencing, using clever techniques in the 1970s to determine nucleotide sequences of DNA molecules. Which of these was used by Sanger to achieve this? Hint


Question 10 of 10
10. Sanger's sequencing techniques were effective, but time consuming. Several "next generation" methods of sequencing were used from 1990 as part of an international effort to identify and map every gene found in the human genome. What name was given to this venture? Hint



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Quiz Answer Key and Fun Facts
1. DNA first came to the attention of scientists when, in 1869, Johann Friedrich Miescher found a substance which was not protein in the pus cells he was examining. Miescher came to the conclusion that "nuclein" (as he called it) was not a protein by using pepsin. What is pepsin?

Answer: An enzyme that breaks down proteins

Miescher was Swiss born and was trained in medicine before becoming partially deaf. From then on, Miescher turned towards physiology and biochemistry. The enzyme used to test whether or not nuclein was a protein or not was pepsin - one of many proteases which cleaves polypeptide chains at specific site (i.e. at specific amino acid residues).
2. Following on from Frederick Griffith's work in 1928, Avery, MacLeod and McCarty claimed that their experiments showed that DNA could be taken up and expressed by bacteria. What is this process called?

Answer: Transformation

Griffith's experiment used two strains of bacteria - a dead virulent strain and a live non-virulent strain - and showed that a mixture of the two was capable of killing mice. This suggested that there was something which causes bacteria to be virulent which was transferred from the dead strain to the live strain, making the live strain virulent also.

The work was built upon by Oswald Avery, Colin MacLeod and Maclyn McCarty. This was the first method of gene transfer identified. The two other main methods of gene acquisition by bacteria are conjugation (directly from other bacteria) and transduction (from viruses). Both of the latter mechanisms were discovered by Joshua Lederberg.
3. The confirmation that DNA was the hereditary material came from the 1952 experiments carried out by Alfred Hershey and Martha Chase. They did this by labelling DNA with a certain isotope and then checking to see if the isotope (and therefore the DNA) had been taken up by the bacteria. Which element's isotope, found in the "backbone" of DNA, was used?

Answer: Phosphorus

This experiment employed the technique of transduction, which had been discovered only a year before. Bacteriophages (viruses which infect bacteria) had their proteins labelled with sulphur-35 and DNA labelled with phosphorus-32. There was one component that was being transferred to the bacteria from the bacteriophage. Analysis of the transformed bacteria showed them to contain P-32, but not S-35.

The transforming material was therefore DNA, not protein.
4. With the revelation that DNA was the hereditary material, Erwin Chargaff was puzzled by the fact that DNA was made of only four "letters", or nucleotides. Chargaff also discovered that the number of purines in a molecule of DNA was always equal to the number of pyrimidines. Which of the following is NOT true of purines and pyrimidines?

Answer: Uracil is a purine

Cytosine, thymine and uracil (C, T and U) are all derived from the molecule pyrimidine, and so are called the pyrimidines. They are single-ringed structures. Purines are double ringed structure which include guanine and adenine (G and A). As well as the number of purines being equal to the number of pyrimidines, Chargaff stated that the number of C and G nucleotides were equal and that the number of A and T nucleotides are equal (U is not found in DNA).

This can be explained by the fact that C always pairs with G and A always pairs with T.
5. Just as Chargaff set down the rules for base pairing, Salvador Luria and Max Delbruck characterised the phenomenon of mutation. Their "fluctuation test" aimed to determine whether mutations arose spontaneously or in response to a selective force. What was their conclusion?

Answer: That mutations arise spontaneously

Luria and Delbruck tested this hypothesis by growing several cultures before exposing them to a selective media (e.g. a plate containing an antibiotic). If mutations were induced by the exposure to this media, then a similar number of colonies would survive on each plate.

However, there was much fluctuation between the number of surviving colonies on each plate, suggesting that antibiotic resistance mutations arose spontaneously.
6. The components of DNA were now known, but the structure remained elusive. The breakthrough came from two groups working in parallel in the UK - Watson and Crick at Cambridge and Wilkins and Franklin in King's, London. Which of the following best describes the structure of DNA?

Answer: Double helix, with bases pointing inwards and a sugar-phosphate backbone

The triple helix model was proposed by a group led by Linus Pauling in America, but this was obviously incorrect to the eyes of the groups in Britain, who favoured a double helix model. X-ray diffraction images (especially those from Rosalind Franklin) were proof that the double helix model was correct and that the bases pointed inwards.

The 1962 Nobel Prize was awarded to Watson, Crick and Wilkins.
7. The discovery of the structure of DNA was followed by a hive of activity in the study of this molecule. The next major step came in 1958, when Matthew Meselson and Franklin Stahl demonstrated that DNA replicated semi-conservatively. Which of the following best describes the term "semi-conservative replication"?

Answer: Two "daughter" DNA molecules contain one strand from the "parent" DNA molecule

Meselson and Stahl showed this by growing cells on a medium containing nitrogen-15 (a heavy isotope). After several divisions, the DNA of these cells contained no nitrogen-14 (the usual isotope), but only the heavier nitrogen-15. By transferring these cells onto a medium containing nitrogen-14, the DNA was allowed one round of replication before the density of the DNA was measured.

The density was shown to be in between the DNA containing only nitrogen-15 and the DNA containing only nitrogen-14, supporting the semi-conservative hypothesis.
8. Experiments involving synthetic mRNA in the 1950s and carried out by Nirenberg and Khorana (amongst other) were employed to determine which nucleotides coded for which amino acid. What principle, first put forward by George Gamow, was essential to the understanding of the genetic code?

Answer: That three nucleotides code for one amino acid

It had already been established that there were 20 naturally occurring amino acids in living organisms, and four nucleotides found in DNA. The first attempt to explain this problem was a rather convoluted system involving an overlapping code in which two nucleotides coded for one amino acid.

The reality was much simpler - that three nucleotides code for one amino acid. The number of combinations of the four nucleotides into a triplet would mean 64 combinations, showing that some amino acids are coded for by more than one triplet (called a codon).

For example, tyrosine is coded for by UAU and UAC.
9. Frederick Sanger pushed forward the field of DNA sequencing, using clever techniques in the 1970s to determine nucleotide sequences of DNA molecules. Which of these was used by Sanger to achieve this?

Answer: A nucleotide which terminated DNA elongation when added to a growing chain

Sanger used radiolabelled dideoxynucleotides, which, when added to a growing DNA chain, would prevent elongation. Only one form of dideoxynucleotide was used at a time (e.g. ddA, ddT, ddG or ddC). For example, if ddA was used, this meant that wherever a chain terminated, the nucleotide found at that point was an A nucleotide. By doing this with each type of dideoxynucleotide, the full sequence could be determined.
10. Sanger's sequencing techniques were effective, but time consuming. Several "next generation" methods of sequencing were used from 1990 as part of an international effort to identify and map every gene found in the human genome. What name was given to this venture?

Answer: The Human Genome Project

The Human Genome Project (HGP) identified and sequenced every gene in the human genome, but did not sequence the entire sequence of DNA, as is often thought. Much of the human genome is non-coding/serves structural or unknown purposes, rather than to code for RNA or proteins. Several next generation techniques such as 454 pyrosequencing, Solexa, and SOLiD sequence by synthesis, and the reading is performed by computers.

This is in comparison to Sanger's technique of analysing DNA fragments on a gel.
Source: Author doublemm

This quiz was reviewed by FunTrivia editor WesleyCrusher before going online.
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