A base sequence of DNA that codes for a polypeptide or functional RNA
Locus
The position of a gene on a chromosome
Intron
A non-coding sequence that is found within a gene
Exon
A sequence of DNA that codes for a polypeptide
Chromosome
The DNA double helix combined with histones, coiled up, forming chromatin
Homologous
2 chromosomes that carry the same genes
Allele
An alternative form of a gene
Histone
A circular protein combined with DNA to make a chromosome
Genome
The complete set of genes in a cell
Proteome
The full range of proteins produced by the genome
Triplet Code
3 bases form a triplet code; each triplet codes for 1 amino acid
Universal
The triplet code codes for the same amino acid in organsims
Non-overlapping
The bases are read in triplets and then the next 3 triplets are read
Degenerate
When amino acids are coded for by more than one triplet code
Chromosome structure
mRNA Structure and Function
Structure: Single strand of RNA nucleotides
Function: Carries the triplet code cor a specific polypeptide
rRNA Structure and Function
Structure: 2 subunits (large&small) combined with protein -> ribosome
Function: Site of protein synthesis
tRNA Structure & Function
Structure: Small single strand of RNA folded into a clover-leaf shape
Function: Carry amino acids to ribosome
Why is the Genetic Code Universal?
Every organisms DNA is made up of the same 4 bases
Every 3 bases forms a triplet code
Each triplet code determines 1 amino acid
Each triplet code codes for the SAME amino acid in all organisms
The sequence of bases and quantity of DNA determines the organisms characteristics
Why is Genetic Code degenerate?
A number of different triplet codes/codons can code for the same amino acid
Why is Genetic Code Non-overlapping?
Each base in the DNA molecule is only read once- as a series of 3/in triplets
If all cells contain the same DNA in the nucleus, why are cells in the body different?
All cells have potential to produce all proteins as they have the DNA present in their nuclei
Each cell expresses (transcribes and translates) a limited number of those genes & in a different combo
-> because some genes are "switched on"/ expresses and others are not
Semi-Conservative Replication
A representative portion of DNA, about to undergo Replication
The 2 strands of DNA separate. The H bonds between the basesbreak
Free nucleotides are attracted to their complementary bases
Once lined up, they are joined by enzyme DNA polymerase
Finally, all nucleotides have joined to form complete nucleotides chain. Two identical strands of DNA formed. Each strand retains ½ genetic material ∴ this replication is semi-conservative
Meselson and Stahl
Steps:
They grew bacteria for many generations on a medium with ¹⁵N
Then transferred bacteria to medium of ¹⁴N & allowed it to replicate once, for single gen
The transferred bacteria again to ¹⁴N allowed & allowed it to replicate once, for a 2nd gen
Repeated again for 3rd gen
At each step, sample was centrifuged in special solution to different DNA could be separated
Lighter DNA nearer to top
Meselson and Stahl explanation
All bases in DNA contain N
There are two isotopes, normal ¹⁴N and heavy ¹⁵N
Bacteria will incorporate N from growth media into any new DNA made
Bacteria grown on ¹⁴N would be lighter/less dense that bacteria grown on medium containing ¹⁵N
So when samples are centrifuged, they will collect as band in different positions according to density
DNA Semi-Conservative
Let bacteria divide and replicate their DNA
Grow E-Coli with heavier ¹⁵N
Move bacteria to medium with lighter ¹⁴N. All new DNA will now be lighter
Check bacterial DNA & found all DNA molecules were same density (half ¹⁴N, half ¹⁵N) so not conservative
To distinguish between semi-conservative and dispersive, DNA divided again. If same density, dispersive, if ½contained ¹⁵N + ¹⁴N and half ¹⁴N, semi
-> Found it was semi-conservative
Features of DNA + how they are important for semi-conservative replication
Complementary base pairings- allows accurate replication
Weak/easily broken H bonds between bases- allows 2 strands to separate/unzip
Two strands- both can act as template
Roles of Mitosis
Growth of tissues
Repair of tissues (by replacing cells)
Asexual reproduction
Development of body plan
Proliferation of WBC (clonal expansion)
Production of new STEM cells
Cell Cycle
Most cells do not divide continously
Instead undergo regular cycle of division, separated by periods of growth
This is known as the cell cycle
Interphase
Mitosis
Cytokinesis
Steps
Interphase(95%)
G1: Growth phase 1- protein synthesis/transcription/formation of mRNA, organelles replicate ATP required
S: Synthesis phase- DNA replication, ATP required
G2: Growth phase 2- cell growth, cell increases in size
Mitosis:
PMAT
Checking the cell
To prevent mistakes & mutations the cell can only progress through cell cycle after passing checkpoints
If there is a problem, cell will pause cell cycle until fixed
If it cannot be fixed, cell will kill itself, preventing a tumour developing. Called apoptosis
Cell Checkpoints
Cell growth checkpoint: Occurs towards the end of G1- checks whether cell is big enough + has made proper proteins for S phase. If not, cell goes through resting (G0) period until ready
DNA synthesis checkpoint: occurs during S phase. Checks whether DNA has been replicated correctly. If so, carried on to M
Mitosis checkpoint: occurs during M phase. Checks whether chromosomes are attached correctly to the spindle
Cancer & Mitosis
Cancer is uncontrolled cell division leading to formation of a tumour
Causes by mutations in the genes that control mitosis
Mutant cells formed are structurally & functionally different from normal cells and generally die
However, those that survive clone themselves (mitosis( and form tumours
Malignant tumours grow rapidly, less compact, more likely to be life-threatening
Benign grow more slowly, more compact, less likely to be life-threatening
Methotrexate: stops replication of DNA. Also works in fast dividing cells (eg hair cells leading to hair loss)
Vinblastine: Inhibits metaphase stage of mitosis by interfering with spindle fibre formationn
P
Spindle fibres form
Nuclear membrane breaks down
Chromatin condenses (coils & shortens) to form chromosomes
M(etaphase)
Controversial join the chromosomes onto each spindle fibre at the metaphase plate (equator)
A
Centromere splits in two
The sister chromatids are pulled to opposite poles as spindle fibres shorten (they contract)
T
Nuclear membranes reform at the two poles
Chromatids uncoil back into chromatin
Prophase
Chromosomes shorten/thicken/condense and become visible; due to DNA replication, chromosomes appear as 2 identical sister chromatids joined at the centromere