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Summary All exercises/self study assigments and solutions from Genome Technology and Applications (19/20)

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Course
Genome technology and applications (2051FBDBMW)

Institution
Universiteit Antwerpen (UA)

All exercises/self study assigments and solutions from Genome Technology and Applications (19/20): This document includes all questions AND FULL answers to the exercises of the exercise session of Genome Technology and Applications. It has the answers given by professor Guy van Camp and is thus ver...

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Uploaded on September 20, 2023
Number of pages 37
Written in 2022/2023
Type Summary

genome
exam questions
gene and genome
genome technology
biomedical sciences
cloning
lectures
expression cloning
pcr
ngs
bionano
illumina
pacbio
seque
exam
ua
genome technology and applications
summary

Institution
Universiteit Antwerpen (UA)
Education
Biomedische Wetenschappen
Course
Genome technology and applications (2051FBDBMW)

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Full summary of all lectures
\'Genome Technology and
Applications\' (18/20)

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Genome technology and
applications
CELL-BASED DNA CLONING 29/9
= when you clone in cells. Sometimes techniques like PCR are called in vitro cloning. Cloning means
amplifying nucleic acids.

PRINCIPLES OF DNA CLONING
Cell based DNA cloning comprises 4 steps:

1. In vitro construction of a recombinant DNA molecule
2. Transformation
3. Selective propagation of clones
4. Isolation of recombinant DNA clones

1. IN VITRO CONSTRUCTION OF A RECOMBINANT DNA MOLECULE
This is always done in vitro. It requires cutting and pasting of DNA by enzymes:

- Resitriction endonucleases: cut DNA
- DNA ligase: seals cuts.

To make a recombinant DNA molecule, we require a replicon. This is a piece of DNA that makes
independent DNA replication possible.

- Replicon is specific for a host
- Usually a construct called “vector” is used
o = piece of DNA containing the replicon and many elements that make the cloning
process possible

In most cases an ORI is needed: origin of replication, a DNA sequence that makes a DNA polymerase
work. If the cell divides, extra DNA of the recombinant DNA molecule is made and is passed on to
daughter cells. If you don’t have an ORI, it will not be replicated and the recombinant DNA will be
lost.

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Plasmids are usually used in cloning as a vector. You cut the plasmid and target DNA open with the
same restriction enzyme after which you can ligate the target DNA in a recombinant DNA molecule.

2. TRANSFORMATION
The recombinant DNA molecule is introduced in a host cell. This is usually bacterium or yeast but can
also be eukaryotic cells. Bacteria and yeasts are very popular because they’re easy to grown and have
a fast reproduction.

For expression studies, cloning is often done in eukaryotic cells (mammalian cells, insect cells, see
later in this chapter). If you want to express human proteins you will need eukaryotic cells because
they’re often too big for bacteria. You will often still begin in cloning in a bacterium. Next, you put it
in the eukaryotic cells for the expression.

3. SELECTIVE PROPAGATION OF CLONES
After transformation, the cells are plated on agar. Each individual cell forms a colony. Each colony is a
clone: All cells are identical, and have the same ancestor cell. 1 colony can be grown in liquid medium
to obtain more cells. Usually the vector contains an antibiotic resistance genes, and the agar contains
this antibiotic, so only the transformed bacteria can survive.

4. ISOLATION OF RECOMBINANT DNA CLONES
If you want to isolate your construct and multiply it, you have to lyse the bacteria and purify the
plasmid: the recombinant DNA is purified from the cells. This is pretty easy since the bacterial
genome is bigger.

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E.g. Hemophilus
RESTRICTION ENDONUCLEASES aegypticus
 HaeIII
Nomenclature: 1 letter genus + 2 letters species + followed by number
Restriction endonucleases (RE) are a defence mechanism against bacteriophages. Bacteriophage DNA
enters the bacterium and is cleaved by RE. The bacteria has to make sure its own DNA is not cut.
That’s why a RE always has a matching methylase. This methylation will be of the same recognition
sequence. In bacteria, all sequences are methylated and restriction endonucleases never cut
methylated DNA.

RE are very specific and never make mistakes. The sequence that they recognize is 4-8 bp and is
usually a palindrome. RE can cut on the symmetry axis, but can also cut somewhere else. In this case,
it creates overhanging sticky ends which can base pair and form unstable double helices.
5’ prime overhang

The overhangs are complimentary so they can base pair. They’re not stable at room temperature but
can hybridize shortly. The short hybridization makes it easier to ligate the cut again. DNA ligase can
also ligate blunt ends, but it’s more difficult.

Some restriction enzyme give long DNA pieces and others give short pieces:
- Depending on length of recognition sequences
o Shorter recognition sequences  more present  shorter pieces
o Longer recognition sequences  less present  longer pieces
- The human genome has only 40% GC’s and 60% AT’s
o Recognition sequence with only G and C’s  less present  longer pieces
- CPG sequence (-CG-): site where methylation happens. Methylated C’s mutate away more
often to T’s so there aren’t that many.
o Recognition sequence with -CG- in it  less present  long pieces

Isoschizomeres: when different restriction enzymes have the same recognition sequence.
Some RE have compatible cohesive termini. After a cut they have compatible ends and can be ligated

DNA LIGASE

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