Module 2 - The Molecular Basis of Inheritance Flashcards

1
Q

Genetic material must perform three essential functions. What are they?

A

Replication - the genotypic function. Each cell must be replicated from a single cell into daughter cells.
Gene expression - the phenotypic function. Genes control colour and shape.
Mutation - the evolutionary function. Through mutations different phenotypes (colours) are achieved.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Purines are _____ _____ structures, and are nucleotides ___ and ___. Pyrimidines are _____ _____ structures and are nucleotides ___ and ___. A and T have _____ hydrogen bonds while C and G have _____. New nucleotides must connect to the ____ ____ ____.

A

Double ring, A, G, single ring, T, C, two, three, free 3’OH group.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What is Chargaff’s rule?

A

States that DNA from any cell of all organisms should have a 1:1 ration (base pair rule) of pyrimidine and purine bases, and that the amount of guanine should equal cytosine and and the amount of adenine should equal thymine.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

There is a two step process by which the information in genes flows into proteins. Describe this model.

A

The Central Dogma

    DNA   ->    RNA    ->    Protein
       ^       ^                  ^
       |        ^                  ^    replic.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Name three forces that stabilise the DNA double helix.

A

Covalent bonds - sugar phosphate backbone
Hydrogen bonds - between bases
Hydrophobic interactions - bases

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

In the structure of DNA, DNA is negatively charged and histones are positively charged. The Solenoid & Zigzag models describes the condensation of DNA. How is the DNA mitotic chromosome formed from simple DNA molecules? How do positivity and negativity influence this process?

A

The DNA molecules (single histone proteins) start off at 2nm in length. These condense into nucleosomes, which consist of eight histone proteins wound together with linker DNA (think beads-on-a-string structure) - these make up the 11nm fibre. In vivo, these nucleosomes interact with each other to coil more tightly and produce the 30nm chromatin fibres. Finally, these chromatin fibres are densely coiled together to produce the 300nm mitotic metaphase chromosome.
As the positivity of the surrounding chemical environment increases, the condesation also increases. As the positivity decreases, condensation decreases.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

What causes ageing in terms of molecular DNA? Describe the structure and function of these.

A

Ageing is caused by the shortening of telomeres over time (the ends of a eukaryotic chromosome). Telomeres of cancer cells and germ-line cells do not deteriorate.

Telomeres form structures called t-loops which function to protect the free end of a DNA molecule from deoxyribonucleases and fusion with other chromosomes. They also facilitate the complete replecation of the ends of linear DNA molecules.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

DNA replication is semi-conservative - name the three stages of DNA replication in order.

A

Initiation, elongation, termination.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Describe bacterial replication.

A
  1. dsDNA bidirectionally unwinds at the oricyte, producing ssDNA templates for synthesis of new DNA.
  2. A replication bubble forms, usually having a replication for at each end.
  3. The forks proceed around the circle.
  4. Eventually two circular DNA molecules are produced.
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

Describe the requirements and functions of DNA polymerase I.

A

DNA polymerase I requires a primer with a free 3’OH, template DNA, substrates and Mg2+.

It synthesises the phosphorus trinucleotide at the terminus of the primer strand. It contains exonuclease activity that cuts (corrects) DNA strands. It is also able to proofread strands (mostly removes primers).

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Describe continuous and discontinuous DNA synthesis.

A

The synthesis of the leading strand is continuous as it must progress in a 5’ - 3’ direction. The synthesis of the lagging strand is discontinuous and is synthesised in short segments called Okazaki fragments.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

The Replication Apparatus
Formation of replication fork. Synthesis of new DNA strands initiated by ____ ____ and synthesised by _____ _____.
The discontinuous replication of the ______ strand requires an _____ _____ to start the synthesis of each _____ _____.
DNA _____ unwinds the double helix and DNA _____ synthesises the RNA ______ for successive Okazaki fragments. RNA primers are covalently ______ with ______ by DNA _____ ___. RNA primers are replaced with DNA by _____ _____ ___. Single stranded _____ left by polymerase are sealed with _____ ____.

A

RNA primers, DNA primase. Lagging, RNA primer, Okazaki fragment. Helicase, primase, primers. Extended, deoxyribonucleotides, polymerase III. DNA polymerase I. Breaks, DNA ligase.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

What is the function of telomerase?

A

To extend telomere length on the lagging strand’s 3’ end, so the whole DNA sequence can be synthesised.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What are the three functional units of a gene?

A

Promoter - DNA sequence. “Upstream” of coding sequence. Acts as “on/off” or “dimmer” switch (high/low).
Coding sequences - sequence when transcribed into RNA contains information to synthesise proteins.
Termination sequence - end point.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

What are the three additional features of eukaryotic transcription?

A
  1. 7 methyl guanosine cap added to the 5’ of primary transcript
  2. poly(A) tail added to the 3’ of the primary transcript
  3. removal of intron sequences
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Describe the structure and function of the 7 methyl guanosine cap.

A

The cap contains a guanosine that is methylated at position 7, and is added after a chain is ~30 nucleotides long.
The cap has two functions: to prevent degradation of the RNA transcript from RNases (ribosome bonding), and to be recognised by the proteins that initiate translation of the RNA transcript into a protein (stability of RNA).

17
Q

Describe the structure and function of the poly(A) tail.

A

After a sequence is cleaved downstream of the polyadenylation sequence, the polyA tail is added (up to 200bp’s long) by polyApolymerase.
The polyA tail enhances stability of mRNAs and plays important roles in their transport from nucleus to cytoplasm.

18
Q

What are the three tRNA binding sites on each ribosome. What are they?

A

EPA

A or aminoacyl site: binds incoming aminoglycyl-tRNA, the tRNA carrying the next amino acid to be added to the growing polypeptide chain.
P or petidyl sute: binds the tRNA to which the growing polypeptide is attached.
E or exit site: binds to the departing uncharged tRNA.

Enter - Pair - Stabilise

19
Q

Explain the numbering of a Transcription Unit using the following terms: +1, -10, -35, upstream, downstream, TATA box, transcription factor.

A

Transcription initiation site is +1 and it is the first nucleotide to be used for transcription. Bases preceding the intiation site are given (-) prefixes and are referred to as upstream sequences. Bases following the initiation site are given (+) prefixes and are downstream.
A DNA sequence has two key regions:
-10: “TATA” box - 2H bonds between T and A where DNA is unwound/separated
-35: “Transcription factors” - proteins that enhance transcription (RNA pol. binds here).

20
Q

There are _____ tRNA binding sites on each ribosome. Remember a ribosome is composed of ______ and ______, and have a _______ and _______ subunit.

A

Three, RNA, protein, large, small.