DNA and sometimes RNA are the primary sources of hereditary material
DNA
Wrapped around proteins known as histone proteins
Chromatin condensation
1. Nucleosomes
2. Chromatin
3. Chromosomes
Deoxyribose sugar
One less oxygen than ribose sugar
DNA directionality
From the 5 prime end to the 3 prime end with the hydroxyl, but new nucleotides aren't added from the 5' they are added from the 3'
The base pair rule is universal for DNA no matter the organism
Base pairing rules come from conserved evolution of Purines and Pyrimidines
Prokaryote DNA (bacteria)
Free-floating in the cytoplasm (cytosol) and specifically in the nucleoid region
Circular chromosomes, cannot clearly distinguish the start and end points
Smaller genomes
Contains plasmids located in the cytoplasm (some eukaryotes contain plasmids located in the nucleus)
Cloning DNA using bacteria
1. Obtain a plasmid
2. Insert foreign DNA, creating a recombinant DNA molecule plasmid
3. Dividing bacteria pass the recombinant DNA plasmid onto its descendents
Nucleosome
DNA wrapped around 8 histone proteins
Gene
A sequence of nucleotides coding for specific proteins
Purines
Have larger double-ring bases (Guanine and Adenine)
Pyrimidines
Have smaller single ring base (Cytosine, Thymine, and Uracil)
Genome
All genetic material
Plasmids
Small, circular, double stranded DNA molecules, existing independently of the bacterial chromosomes and are occasionally transferred between cells. They are used to confer resistance against environmental conditions
Enzymes used in DNA replication
Helicase
Ligase
DNA polymerase
Topoisomerase
New molecules are synthesized from 5' to the 3' → added onto the 3' hydroxyl group
All characteristics come from inheritance
DNA is a polynucleotide
DNA polymerase is adding bases antiparallel
Primer lays down to allow nucleotides to be added
Leading strand
Needs 1 RNA primer
Lagging strand
Needs many RNA primers (because of the many fragments)
DNA polymerase cannot start without primers
Purpose of RNA primer
To act as a binding site where DNA polymerase can add the nucleotide bases
Okazaki fragments
Fragments of the lagging strand
Semiconservative
Replicated DNA will have one new strand and one old strand
Primer
Short segment of RNA
Each codon codes for an amino acid
Not all sections of DNA code for proteins, only around 1% do but these sections are still important
1. RNA Polymerase adds nucleotides on the template strand
2. Section of DNA opens forming a transcription bubble
3. Adds uracil not thymine
4. Transcription factors will bind on to the promoter region to help RNA polymerase bind onto the gene and form transcription initiation factor
Bacteria do not have nuclei so mRNA in prokaryotes is immediately translated without additional processing. In eukaryotes, the original RNA called pre-mRNA is processed before leaving the nucleus
Pre-mRNA processing
1. Adds a modifying guanine nucleotide on the 5' end/cap
2. Adds a polyA tail
3. Introns are removed and exons are spliced
5' cap
Determines where the ribosomal area attaches and increases stability
PolyA tail
Increases the lifespan of the mRNA
The 5' end cap and the poly-A-tail both help in the attachment of the nucleotide bases
Mature transcript destination
If it goes to a ribosomes in the cytoplasm then it will code for proteins only inside the cell
If it goes to a ribosome in the rough endoplasmic reticulum then it will code for a protein used in the cell membrane or outside the cell
Alternative splicing
The process that clips different exons together to make new sequences
Gives different exon sequences making multiple proteins from one mature mRNA
Many genes can form two or more different polypeptides depending on which segments are treated as exons