DNA Replication
Transcription
Translation
Mutations
100

Why does DNA need to replicate?

growth and maintenance 

100

What is the ultimate goal of transcription?

use DNA as a template to make mRNA so it can be translated

100

what are codons and what are the different types?

segments of mRNA molecules made of 3 nucleotides

- sense codons: code for amino acid (includes start codon AUG)

- stop codons

100

What is a mutation and what are they caused by?

- any permanent change to the DNA sequence

- caused by replication errors and environmental factors (like UV)


200

How does DNA replicate?

semiconservatively 

200

What is central dogma?

DNA --> (transcription) --> RNA --> (translation) --> protein

200

Describe a ribosome.

Made of two parts (only come together during translation):

- Large subunit – has 3 sites where tRNA can bind

• A = “amino acid”
• P = “polypeptide”
• E = “exit"
- Small subunit – checks codon and anticodon pairing; if incorrect, tRNA is ejected

200

What is incorporation error rate?

probability that an incorrect base will be inserted into a new strand of DNA, resulting in mismatch

300

Draw out initiation of DNA replication and include all components.

should include:

- DNA helicase

- replication fork (2)

- RNA primer and primase

- ori (origin of replication)

300

Draw out initiation of transcription and include all components.

should include:

- RNA polymerase

- promoter

- transcription initiation site

- transcription factors

- coding strand

- template strand

300

Draw out the initiation of translation and include all components.

should include:

- tRNA and small ribosome subunit bind to mRNA
(together = initiation complex) at the start codon
- Large subunit joins, with tRNA in P site

300

Describe mismatch repair.

- After replication, a mismatch repair complex checks the new strands of DNA
- If mismatch is found, it cuts out a small section from the new half of the DNA
- DNA polymerase comes back to redo that section
- Ligase connects the repair to the rest of the strand

400

Draw out elongation of DNA replication and include all components.

should include:

- DNA polymerase and its directionality (3' and 5')

- leading strand (made continuously)

- lagging strand (discontinuous)

- RNA primer 

- Okazaki fragments

- Ligase

400

Draw out elongation of transcription and include all components.

should include:

- RNA polymerase and its directionality (3' and 5')

- mRNA

400

Draw out elongation of translation and include all components.

should include:

- Polypeptide synthesized as ribosome
moves along mRNA from 5’ to 3’
- Large subunit breaking one bond (amino acid
to tRNA) and forming another (amino acid to amino acid on next tRNA)
- Catalyst of this reaction a ribozyme
(ribonucleic acid and enzyme)

400

What are ways mutations can affect phenotype?

- Silent mutation: The change in the DNA sequence doesn’t change the amino acid that section codes for
- Loss-of-function: Causes the function of that gene to be lost, because the resulting protein is not functional
anymore
- Gain-of-function: Creates a new/different function for the gene by creating a different version of the protein
- Conditional mutation:  Affect the phenotype in some
environmental conditions, but not others

500

Draw out termination of DNA replication and include all components.

should include:

- full length leading strand

- gap at end of lagging strand (shorter than parental strand)

500

Draw out termination of transcription and mRNA processing and include all components.

should include:

- termination ending at termination site

- pre-mRNA

- introns and exons 

- mRNA splicing: spliceosome made of snRNPs, consensus sequence, splice sites

- alteration of ends: 5' cap and poly A tail

500

Draw out termination of translation and include all components.

should include:

- Ribosome reaching stop codon in
the A site, no tRNAs can base pair with it
- Polypeptide chain released, the tRNA, mRNA, and
ribosome subunits all separate

500

What are the types of mutations?

point mutations: one changed pair of bases

- substitutions: A pair of bases get substituted for a different pair

- deletions: deletes single base pair

- insertions: inserts single base pair

chromosomal mutations: 

- deletions: loss of a section of a chromosome

- duplications: repetition of a segment of a chromosome, so there is an extra copy of the genes in that segment

- inversions: segment of a chromosome gets flipped around in the original location

- translocations: transfer of a chromosome segment to a different chromosome