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Summary Lecture Notes DNA & Gene Expression | CBI10806 | Wageningen

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Lecture notes from Week 2 of Introduction to Cell Biology (CBI10806) at Wageningen University, covering DNA replication, transcription, translation, and gene expression regulation. Topics include DNA structure and the double helix, mechanisms of DNA and RNA polymerase, Okazaki fragments and telomeres, the lac operon, and an introduction to bioinformatics with sequence analysis. These notes provide clear explanations of complex molecular processes with key mechanisms highlighted, making them essential for understanding foundational cell biology concepts and preparing for exams.

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Week 2: DNA: replication, transcription and translation
Cells functionally specialize through expressing unique genes
 Gene structure
 Mechanisms of action of DNA and RNA polymerased
 Protein synthesis
 Regulation of gene expression in bacteria
 Introduction to bioinformatics
DNA structure
 DNA (deoxy-ribonucleic acid) is a polymer
 The polymer is built form nucleotides (A, C, G, T)
 Each nucleotide has a base (green), a sugar (blue) and a
phosphate (yellow)
 The polymer has a direction (5’ to 3’)
 Base complementarity ensures formation of a double helix
 The backbone of a DNA chain connects nucleotides via their sugar
and phosphate groups
 Adenine forms two hydrogen bonds with Thymine and Cystosine
makes three hydrogen bonds with Guanine
 DNA is a double-helix. This helix has a major and a minor groove
 Many DNA-binding proteins also bind to DNA through an interaction
of some of their alfa-helices with phosphate groups of the DNA
backbone
DNA replication
 The chain is extended at its 3’ end
 Synthesis occurs form 5’ to 3’ end
 The template strand is “read” from 3’ end to 5’ end
 Semi-conservative synthesis
 Starts at fixed positions: the origins of replication initiation (ORI)
DNA synthesis by DNA polymerase

,  Proofreading activity in DNA polymerase  only 1 mistake every 107
nucleotides (human genome = 6,4x109 nucleotides)
 DNA polymerase can only synthesize in 5’ to 3’ direction (how to
synthesis the other strand 3’ to 5’)


Solution 
 one half of the DNA
is replicated in
short strechtes, that
are later joined
 Okazaki fragments
start from RNA
primer
o Primase joins
together two




ribonucleotides
o Primase synthesizes in 5’-3’ direction
o it forms a RNA primer

 discontinuous synthesis: multiple enzymes
 RNA primer removed by nucleases and replaced with DNA by repair
polymerase  the end of the one strand and the beginning are
combined by DNA ligase
 DNA helicase opens up the DNA strand for replication
A mechanism is needed for maintaining chromosome ends
 Since Okazaki fragments start form RNA primer, which start at
random positions, and are themselves removed, it is impossible to
synthesize the lagging strand to the end
 The and of a DNA strand ends with telomere which are repeat
sequences
 Telomerase binds to template strand, it adds additional telomere
repeats  completion of lagging strand by DNA polymerase (there is
a bit loss or extra length but it is not significant)


 DNA = Deoxy-ribonucleic acid (RNA minus O)

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