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Lecture notes

Introduction to genetics

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Simple introduction of what genetics are and how to calculate them










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Uploaded on
February 5, 2021
Number of pages
10
Written in
2020/2021
Type
Lecture notes
Professor(s)
Amanda jones
Contains
All classes

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DNA
Electrophoresis
Electrophoresis : using electricity to separate DNA fragments by
length
 DNA is negatively charged
 Attach a fluorescent label or stain DNA fragments
 Put DNA fragments into well at negative end
 Turn on current
 DNA fragments are attached at positive electrode
 Small fragments move faster ( therefore further away)
 Calibrate scale by using pieces of DNA of known length
 Logarithm will process bigger things move slower than smaller
 Stick it under UV light and it will show you the fragments


Prokaryotic Chromosome

 Each gene encodes
for a different
function
 Genes with related
function often form
operon




Eukaryotic Chromosome

 Typical chromosome with
centromere and telomeres
 Spliceosome will splice out
the intron and let the exon
be.




Replication

, The DNA unwinds and unzips by the help of DNA helicase which
breaks hydrogen bonds between complementary bases

The free nucleotides will pair with complementary bases on the
template strand

The DNA Polymerase joins nucleotides together in a condensation
reaction

DNAS is antiparallel so the nucleotides are arranged differently

DNA polymerase is an enzyme is its active site can only bind to
nucleotides at one end

DNA replication is semi-conservative as half of the DNA is retained
and the other half is new



Transcription
DNA helicase separates the strands as it breaks down the hydrogen
bonds

The free RNA nucleotides attach to the template strands with
complementary base pairing

RNA polymerase joins nucleotides together by a condensation
reaction forming phosphodiester bonds

H-bonds between base pairs reform (3 between C-G and 2 between A-
T)

First bit of RNA contains introns which must be removed via splicing
which is the removal of introns so MiRNA forms which will code for the
polypeptide.

Prokaryotes  Transcription goes directly from DNA- MRNA so no
splicing

Eukaryotes  Transcription goes from DNA-pre-Mrna – Mrna so
splicing occurs



Translation
Codon: triplet of bases on Mrna that codes for a specific amino acid

Anticodon: triplet of bases on TRNA that is complementary to the
codon on Mrna

tRNA: polynucleotide that’s folded by hydrogen bonds and the
anticodon is specific to the amino acid that it carries

The riboso0me binds to the Mrna at the start codon

Codon is matched to an anticodon by complementary base pairing
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