[Day 2] Designing DNA circuits


#1

Fri 12 Oct 13:58:52 +08 2018

Convenor/facilitator: Juanma
Convenor/facilitator: Minerva
Notes: Harold

DNA coding

Intro

DNA in everything with cells, encodes information. Resistant to
degradation. From fossils. RNA also codes information. Work
done in 30s, 50s (structure), more work in 70s (genetics work,
insulin). 80s: improved agriculture. 2000: human genome
decoded. Private vs public institutes involved in work.
Restriction enzymes to edit genes, as a chemical reaction.
CRISPR: insert a protein that can edit in vivo.

Slides distributed:

Eukaryote vs prokaryotes. Prokaryotes are easier, DNA is not
protected by nucleus. Eukaryotes have DNA in nucleus as
chromosomes.

That makes editing eukaryotic DNA difficult.

Endosymbiotics, mitochondria in human cells.

Central dogma of molecular biology: DNA transcribed into RNA,
which is translated into proteins.

RNA is not stable, degrades quickly. Is transported outside
the nucleus. Going through slides. Chromosomes need to be
disentangled before transcription or replicated. If transcribed
by RNA polymerase, mRNA is produced which floats off.

C-G bonds are stronger than A-t bonds.

Genetic code: need 3 letters per amino acid. Some amino acods
are coded by more than 1 triplet. Most errors are due to
DNA-to-DNA replication. Errors in transcription rarely serious.

Multiple proteins per gene coded for prokaryotes. For eukaryotes,
splicing occurs to create multiple proteins.

So, easier to work with bacteria. They have genome DNA amd plasmid
DNA (small circles of DNA) (these can cause resistance to antibiotics
for example).

Origin of replication in vector.

Slide: example plasmid vector of 2784bp.

Can add or remove genes.

  1. Download a gene from genbank.
    To get plasmid into the bacteria: Add salt at 40 degrees (other types of environmental shock can also be used).

Order DNA from company.
Standard plasmids, can order.

Talk on issues of security, bioterrorism, etc. Involvement of
FBI, CIA.


#2