Central Dogma of Molecular Biology powerpoint

Central Dogma of Molecular
Biology
“The central dogma of molecular biology deals with
the detailed residue-by-residue transfer of
sequential information. It states that such
information cannot be transferred back from
protein to either protein or nucleic acid.”
Francis Crick, 1958

… in other words
 Protein information
cannot flow back to
nucleic acids
 Fundamental
framework to
understanding the
transfer of sequence
information between
biopolymers

Presentation Outline
 PART I
 The Basics
 DNA Replication
 Transcription
 PART II
 Translation
 Protein Trafficking & Cell-cell communications
 Conclusion

The Basics: Cell Organization
Prokaryotes
Eukaryotes

The Basics: Additional Points
 DNA => A T C G, RNA => A U C G
 Almost always read in 5' and 3' direction
 DNA and RNA are dynamic - 2° structure
 Not all DNA is found in chromosomes
 Mitochondria
 Chloroplasts
 Plasmids
 BACs and YACs
 Some extrachromosomal DNA can be useful in Synthetic
Biology

… an example of a plasmid vector
 Gene of interest
 Selective
markers
 Origin of
replication
 Restriction sites

The Basics: Gene Organization
… now to the main course

DNA Replication
 The process of copying double-stranded DNA
molecules
 Semi-conservative replication
 Origin of replication
 Replication Fork
 Proofreading mechanisms

DNA Replication: Prokaryotic
origin of replication
 1 origin of replication; 2
replication forks

DNA Replication: Enzymes
involved
 Initiator proteins (DNApol clamp loader)
 Helicases
 SSBPs (single-stranded binding proteins)
 Topoisomerase I & II
 DNApol I – repair
 DNApol II – cleans up Okazaki fragments
 DNApol III – main polymerase
 DNA primase
 DNA ligase

DNA Replication: Proofreading
mechanisms
 DNA is synthesised from dNTPs. Hydrolysis of (two) phosphate
bonds in dNTP drives this reduction in entropy.
- Nucleotide binding error rate =>c.10−4, due to extremely short-lived imino and enol tautomery.
- Lesion rate in DNA => 10-9.
Due to the fact that DNApol has built-in 3’ →5’ exonuclease activity, can chew back
mismatched pairs to a clean 3’end.

Transcription
 Process of copying DNA to RNA
 Differs from DNA synthesis in that only one strand
of DNA, the template strand, is used to make
mRNA
 Does not need a primer to start
 Can involve multiple RNA polymerases
 Divided into 3 stages
 Initiation
 Elongation
 Termination

Transcription: The final product

Transcription: Transcriptional
control
 Different promoters for different sigma factors

… Case study – Lac operon
 For control of lactose metabolism
 Consists of three structural genes, a promoter, a
terminator and an operator
 LacZ codes for a lactose cleavage enzyme
 LacY codes for ß-galactosidase permease
 LacA codes for thiogalactoside transcyclase
 When lactose is unavailable as a carbon source, the
lac operon is not transcribed

 The regulatory response requires the lactose repressor
 The lacI gene encoding repressor lies nearby the lac operon
and it is consitutively (i.e. always) expressed
 In the absence of lactose, the repressor binds very tightly to a
short DNA sequence just downstream of the promoter near the
beginning of lacZ called the lac operator
 Repressor bound to the operator interferes with binding of
RNAP to the promoter, and therefore mRNA encoding LacZ
and LacY is only made at very low levels
 In the presence of lactose, a lactose metabolite called
allolactose binds to the repressor, causing a change in its shape
 The repressor is unable to bind to the operator, allowing
RNAP to transcribe the lac genes and thereby leading to high
levels of the encoded proteins.

End of Part I
 Q & A
 Coffeebreak?!

Central Dogma of Molecular Biology powerpoint

More Related Content

Similar to Central Dogma of Molecular Biology powerpoint

Recently uploaded

Central Dogma of Molecular Biology powerpoint