Maintenance of Genetic Information Flashcards
Eukaryotic cell cycle?
M = mitosis G1 = Gap 1 (cells cease division) S phase = DNA synthesis G2 = Gap 2 (leads back to mitosis) Signal commits cell to replicate DNA received in G1, if no signal is received then G0 phase is entered
What is Semi-conservative replication?
Replication fork formed as DNA helicase unwinds the strand
immediate reformation of the helix is prevented by single strand binding proteins
pulling strands apart increases winding further down the molecules which is positive supercoiling
Topoisomerase breaks the phosphodiester bind in one of the parental strands ahead of the replication fork so the rest of the helix can unwind releasing DNA supercoils
DNA polymerase synthesises in 5’ to 3’ direction (one strand synthesised continuously and the other discontinuously
RNA polymerase initiates RNA synthesis so DNA synthesis begins with the synthesis of a short primer
DNA polymerase takes over extending the 3’ of the RNA primer
The lagging band consists of okazaki fragments, to join them, DNA polymerase extends DNA in 5’ to 3’ direction until it reaches the next primer.
Primer is then degraded by exonuclease leaving a gap and DNA ligase fills this, Okazaki fragments are now joined
DNA is now replicated
What removes the wrong nucleotides?
3’-5’ exonuclease removes the wrong nucleotide and adds the correct one
What is the end-replication paradox?
where a small amount of DNA is lost from each end of the linear chromosome after each round of DNA replication
How to stop the loss of information when DNA is shortened?
Telomeres extend DNA which maintain base pairing and allow DNA synthesis to continue
Uses of Telomerase?
Extends the chromosome ends as template RNA anneals to DNA
Telomerase adds nucleotides and then telomerase translocates further along DNA maintaining base pairing and allowing DNA synthesis to continue
What happens when telomerase is switched off in somatic cells?
With every DNA division, telomerase gets shorter, so eventually telomeric sequences are lost and useful DNA will be lost which contributes to ageing
What is a point mutation?
Where a single base is changed
What is a frame shift?
Where the reading frame is lost (if a multiple of 3 bases aren’t implemented)
What is Inversion?
Chromosome rearrangement where DNA segment breaks away and goes elsewhere
What is Deletion?
Where a section of DNA is removed
What is Duplication?
Where a section is duplicated
What is Translocation?
Where a portion reattaches to another chromosome
How are spontaneous mutations formed?
Errors in DNA replication, replication slippage and deamination where C to U now pairs with A
How are induced mutations formed?
Ionising radiation, ultraviolet light, distorting DNA, Nitrous acid, alkylating agent and free radicals