Topic 7 Nucleic Acids IBDP HL Notes
Topic 7 Nucleic Acids IBDP HL Notes
Topic 7 Nucleic Acids IBDP HL Notes
HL Biology
7 : Nucleic Acids
Student Notes
Name : ________________________________
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Revised
Covered in lesson
reference Syllabus
Checklist questions
7.1 U3 DNA polymerases can only add nucleotides to the 3’ end of a primer
DNA replication is continuous on the leading strand and discontinuous on the lagging
7.1 U4
strand
7.1 U6 Some regions of DNA do not code for proteins but have other important functions
Analysis of results of the Hershey and Chase experiment providing evidence that DNA
7.1 S1
is the genetic material
Utilisation of molecular visualisation software to analyse the association between
7.1 S2
protein and DNA within a nucleosome
Highly repetitive sequences were once classified as “junk DNA” showing a degree of
TOK confidence that it had no role. To what extent do the labels and categories used in the
pursuit of knowledge affect the knowledge we obtain?
Making careful observations—Rosalind Franklin’s X-ray diffraction provided crucial
NOS
evidence that DNA is a double helix. (1.8)
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Revised
Covered in lesson
reference Syllabus
Checklist questions
7.2 U4 Splicing of mRNA increases the number of different proteins an organism can produce
7.2 U5 Gene expression is regulated by proteins that bind to specific base sequences
7.2 U6 The environment of a cell and of an organism has an impact on gene expression
The nature versus nurture debate concerning the relative importance of an individual’s
TOK innate qualities versus those acquired through experiences is still under discussion. Is
it important for science to attempt to answer this question?
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Revised
Covered in lesson
reference Syllabus
Checklist questions
7.3 U1 Initiation of translation involves assembly of the components that carry out the process
7.3 U4 Free ribosomes synthesise proteins primarily for use within the cell
7.3 U5 Bound ribosomes synthesise proteins primarily for secretion of for use in lysosomes
7.3 U7 The sequence and number of amino acids in the polypeptide is the primary structure
The secondary structure is the formation of alpha helices and beta pleated sheets
7.3 U8
stabilised by hydrogen bonding
The tertiary structure is the further folding of the polypeptide stabilised by interaction
7.3 U9
between R groups
7.3 U10 The quaternary structure exists in proteins with more than one polypeptide chain
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7.1. S1 Analysis of results of the Hershey and Chase experiment providing evidence that DNA is the genetic
material.
1. Explain why was sulphur used in one experiment and phosphorus in the other.
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3. In both experiments state what separates into the supernatant and the pellet and explain why.
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4. Explain why most of the radioactive sulphur (35S) was found in the supernatant.
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5. Explain why little of the radioactive phosphorous (32P) was found in the supernatant, i.e. most remained in the pellet.
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Hershey and Chase used a bacteriophage (a virus that infects bacteria) to investigate the chemical nature of genes. The
diagram shows a bacteriophage.
The sulphur in the protein and the phosphorus in the DNA of the bacteriophage were radioactively labelled. The data
obtained after bacterial infection and centrifugation are shown in the table.
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7.1.A1 Rosalind Franklin’s and Maurice Wilkins’ investigation of DNA structure by X-ray diffraction.
When X-rays are directed at a material some is scattered by the material. This scattering is known as diffraction. For
X-ray diffraction to work well the material ideally should be crystallised so that the repeating pattern causes
diffraction to occur in a regular way. DNA cannot be crystallised but the molecules were arranged regularly enough
for the technique to work.
https://undsci.berkeley.edu/images/us101/xray.jpg
Nature of Science: Making careful observations—Rosalind Franklin’s X-ray diffraction provided crucial evidence that
DNA is a double helix. (1.8)
Rosalind Franklin’s careful observation and interpretation of the photographic evidence was crucial to Crick’s
and Watson’s successful discovery of the structure of DNA. Her work and her calculations were shown to Crick
and Watson without her permission and they subsequently published their model before she had an opportunity to
publish her work. Her work is now widely recognised as being as important to the discovery of DNA as Crick and
Watson, but unfortunately, she has never shared in the Nobel prize awarded to Crick and Watson as Nobel prizes
cannot be given posthumously (Franklin died in 1958 aged just 37).
What contribution did the X-ray diffraction conducted by Rosalind Franklin make to our understanding of DNA?
It is as a result of the combination of data from a range of investigations that this understanding came about.
Proponent Contribution
Franklin
Chagraff
1. Replication occurs via _________________________ base pairing (adenine pairs with thymine, guanine pairs with
cytosine)
2. Replication is bi-directional (proceeds in opposite directions on the two strands) due to the
________________________ nature of the strands
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7.2 U2 Nucleosomes help to supercoil the DNA.
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https://qph.fs.quoracdn.net/main-qimg-
6eea1244ddb25ceff916d5acfec15fcb
In the space below, draw and label the structure of a simplified nucleosome, including the H1 linker and octamer (which
consists of two copies of four different types of histone proteins).
Nucleosomes both protect DNA and allow it to be packaged, this in turn allows DNA to be supercoiled.
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https://ib.bioninja.com.au/_Media/organisation-of-dna_med.jpeg
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a. Outline how nucleosomes help regulate transcription.
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b. State the part of the cell cycle in which the most DNA would be supercoiled.
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7.1.S2 Utilization of molecular visualization software to analyse the association between protein and DNA within a
nucleosome.
Use the RCSB Protein Bank to read about nucleosomes and examine Jmol images of them.
a. Identify the two copies of each histone protein. This can be done by locating the ‘tail of each protein’.
The tails of the proteins are involved in regulating gene expression.
b. Suggest how the positive charges help to form the nucleosome with the negatively charged DNA molecule.
You may find it useful to add a labelled diagram.
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7.1.U3 DNA polymerases can only add nucleotides to the 3’ end of a primer.
Recap
Label the following diagram, including the carbon numbers.
Name Function
All three are ___________________ and so have a specific shape. This specific shape is especially important in their
____________ __________.
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7.1.U4 DNA replication is continuous on the leading strand and discontinuous on the lagging strand.
7.1.U5 DNA replication is carried out by a complex system of enzymes.
Complete the following table and label the diagram above to describe the enzymes involved in prokaryotic DNA
replication and their functions.
Enzyme Function
DNA Gyrase
(aka topoisomerase)
DNA Helicase
RNA Primase
DNA Polymerase I
DNA Ligase
Single Strand Binding
Proteins (SSBs)
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Some biochemists are making a mixture of enzymes for DNA replication in the lab. In each of these cases,
something was missing from the mixture. For each situation, deduce which enzyme was missing and justify your
choice.
a. The DNA produced came out as lots of short sections of DNA, a few hundred base-pairs long, rather
than one continuous strand.
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What are the functions of DNA primase and DNA polymerase I in DNA replication?
Meselson and Stahl conducted experiments using the isotopes 14N and 15N which showed that DNA replication is semi-
conservative. What would they have observed about the distribution of isotopes in the DNA after one round of replication
if DNA replication was conservative rather than semi-conservative?
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7.1.U6 Some regions of DNA do not code for proteins but have other important functions.
Type Function
https://cdn-
prod.servicemaster.com/-/media/Feature/Term
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Mnemonic
STING
7.1.A2 Use of nucleotides containing dideoxyribonucleic acid to stop DNA replication in preparation of
samples for base sequencing.
Identify the following molecules and justify your choices H
H H
HO https://cdn.kastatic.org/ka-perseus-images/64e1ccffde9ce9a25833188b2a07e51693a9f5b8.png
HO
- Image altered HO OH
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Draw a diagram showing the type of dideoxynucleotide used in the Sanger method of sequencing.
https://www.sigmaaldrich.com/content/dam/sigma-aldrich/articles/biology/marketing-assets/sanger-sequencing_steps_process_diagram.png
Sanger developed a method for determining DNA base sequences using terminating nucleotides called dideoxyribonucleotides.
After an incubation period, the DNA samples are run on an electrophoresis gel. Results are shown in the diagram.
A. A C G C C C G A G T A G C C C A G A T T
B. U G C G G G C U C A U C G G G U C U A A
C. A C G C C C G A G U A G C C C A G A U U
D. T G C G G G C T C A T C G G G T C T A A
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7.1.A3 Tandem repeats are used in DNA profiling
The main difference is one of size. STRs are between 4 and 13 bases long, whereas VNTRs are usually 10 – 100 bases long.
STRs have anywhere between 5 and 200 repeats, whereas VNTRs repeat from between 10 and 1,500 times.
Child
Mother
Father
Sketch what you would expect to see with the above samples when separated using gel electrophoresis.
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Citations:
Allott, Andrew. Biology: Course Companion. S.l.: Oxford UP, 2014. Print.
Taylor, Stephen. "Essential Biology 03.3 07.1 DNA Structure.docx." Web. 1 Oct. 2014.
<http://www.slideshare.net/gurustip/essential-biology-33-71-dna-structure-core-ahl>.
Taylor, Stephen. "Essential Biology 03.4 07.2 DNA Replication.docx." Web. 1 Oct. 2014.
<http://www.slideshare.net/gurustip/essential-biology-34-72-dna-replication-core-ahl>
Bioninja – AHL Pages 7.1
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7.2.A1 The promoter as an example of non-coding DNA with a function.
Genes are made up of ________ main sections. The promoter and terminator sections are non-coding, but perform
specific functions.
https://ib.bioninja.com.au/higher-level/topic-7-nucleic-
acids/72-transcription-and-gene/sections-of-a-gene.html
Promoters are located upstream / downstream of the gene they are associated with.
It is responsible for the initiation of transcription / translation.
The promoter has a binding site for RNA / DNA polymerase.
In eukaryotes / prokaryotes there are also a number of transcription factors involved.
These factors can either bind near to (proximal / distal) or further from (proximal / distal) the promoter.
7.2.U5 Gene expression is regulated by proteins that bind to specific base sequences in DNA.
Transcription factors
Regulatory proteins
https://ib.bioninja.com.au/higher-level/topic-7-nucleic-acids/72-transcription-
and-gene/sections-of-a-gene.html
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Complete the table to outline the functions of the different types of gene expression regulation by proteins that occur in
eukaryotes.
Enhancers Activator
Silencers
7.2.U6 The environment of a cell and of an organism has an impact on gene expression.
https://ib.bioninja.com.au/higher-level/topic-7-nucleic-acids/72-transcription- http://www.essaywriterpros.com/environment-controls-gene-expression-sex-
and-gene/sections-of-a-gene.html determination-and-the-onset-of-genetic-disorders/
What is a morphogen?
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https://phys.org/news/2019-07-secrets-
sex-changing-fish-revealed.html
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7.2.U2 Nucleosomes help to regulate transcription in eukaryotes.
There are a number of changes which can be made to nucleosomes to either increase or decrease the ease with which the
DNA is transcribed.
DNA
Histone
miRNA
https://www.researchgate.net/figure/Simplified-overview-of-main-epigenetic-modifications-A-
20 Chromosomal-DNA-is-packaged_fig1_333836553
How can environmental factors affect the expression of genes?
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7.2.S1 Analysis of changes in the DNA methylation patterns.
The images show a mapping of chromosomal regions with differential DNA methylation in monozygotic (identical)
twins.
The numbers below each chromosome indicate which four chromosomes, from the twenty three pairs that humans
possess, are being analysed.
The diagrams maps changes between the twins’ levels of methylation of DNA across the chromosomes.
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a. Compare the diagrams (not the graphs) and summarise the evidence.
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b. Analyse the evidence and deduce conclusions that can be made using DNA methylation.
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Very soon after fertilization, parental epigenetic methylation is reversed in the DNA.
Later, tissue-specific epigenetic modifications are made to the embryonic DNA. The graph follows the degree of
methylation from different sources during embryonic development.
According to the graph, what are the changes in DNA methylation during embryonic development?
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7.2.U1 Transcription occurs in a 5’ to 3’ direction.
On the diagram, label the following: DNA, RNA, RNA polymerase, 5’, 3’, RNA nucleotides, 5’ to 3’ direction
https://ib.bioninja.com.au/_Media/tr
anscription-summary_med.jpeg
http://botanystudies.com/wp-
content/uploads/2017/09/Steps-of-Transcription.jpg
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7.2.U3 Eukaryotic cells modify mRNA after transcription.
1.
2.
3.
https://www.mun.ca/biology/sc
arr/iGen3_05-12_Figure-L.jpg
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Citations:
Allott, Andrew. Biology: Course Companion. S.l.: Oxford UP, 2014. Print.
Taylor, Stephen. "Essential Biology 7.3 & 7.4 Transcription and Translation (AHL).docx." Web. 1 Oct. 2014.
<http://www.slideshare.net/gurustip/essential-biology7-37-4transcriptiontranslationahl.docx>.
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