Unit 3 - Exam Review Flashcards
4.1 7 Historical figures in the discovery of DNA + discoveries
Frederich - puss, nuclein
Hammerling - algae cap, nuclein location
Griffith - mice, DNA transforming principle
Hershey/Chase - bacteriophage, DNA contains info not protein
Chargaff - nucleotides, A=T C=G
Rosalind/Wilkins - xray, DNA double helix
Watson/Crick - stole info to create 3D model
4.2 DNA vs RNA
DNA - double helix, CGAT, deoxyribose
RNA - single stranded, CGAU, ribose
4.3 Conservative vs. Semi-Conservative replication
Conservative - One daughter molecule is unchanged, parent strands recombine
Semi-Conservative - Each daughter cell is half parent and half new dna
4.3 3 Steps of DNA replication
Initiation, elongation, termination
4.3 What happens during DNA initiation + 3 enzymes
HELIICASE seperates 2 strands of double helix, creating a replication fork.
SSBs prevent parent DNA from reannealing
GYRASE untwist strands and relieve tension
PRIMASE adds RNA primers
4.3 What happens during DNA elongation + 3 enzymes
DNA POLYMERASE III brings nucleotides into the replication fork from 3’-5’ starting at primers
DNA POLYMERASE I replaces RNA primers with correct nucleotides
DNA LIGASE joins Okazaki fragments by phosphodiester bonds
4.3 What happens during DNA termination
Daughter DNA rewind. DNA POLYMERASE III and I exonuclease (proof read) new strands and splice out any mistakes and replace the correct nucleotide.
5.2 What happens during transcription and translation
Transcription - RNA POLYMERASE synthesizes mRNA by copying DNA, similar to DNA replication. mRNA leaves the nucleus.
Translation - mRNA clamps between the small subunit and large subunit of the ribosome, starting in the P site. Strand shifts left and tRNAs are added until a stop codon is reached. EPA site order
5.5 Types of mutation
Point (silent, nonsense, missense)
Frameshift (substitution, deletion)
Chromosomal (Abnormal Structure - Deletion, Inversion, Duplication, Translocation)(Abnormal Number - Nondisjunction, Polyploids)
5.7 Prokaryotes vs Eukaryotes
Genome
Transcription
Translation
Prokaryotes - Small and circular, all coding but promoters&operators, operons (genome), with translation, no excision (transcription), formylmethoinine, ShineDalgama binding site, small ribosomes (translation)
Eukaryotes - large chromosomes, coding and non coding, no operons (genome), in nucleus, splicing (transcription), methionine, 5’ cap binding site, cytoplasm, big ribosomes (translation)
5.8 Gene organization smallest to biggest
200 nucleotides + 8 histones -> nucleosomes -> chromatin -> chromosomes
6.1 Explain - Plasmids, restriction enzymes, vectors
Plasmid: circular pieces of bacteria DNA
Restriction Enzyme: protects against phages
Vectors: used to transport foreign DNA, usually plasmids
6.1 Explain - Gel electrophoresis, cloning
Gel electrophoresis: bacteria is shocked in a gel to loosen up cell wall allowing a vector to enter
Cloning: desired gene added to DNA vector, then added to bacteria, transformed bacteria is isolated and cultured
6.3 Explain – polymerase chain reaction, Sanger dideoxy method, CRISPR method + examples
PCR - Used to make copies of a gene with a small amount of DNA, fingerprinting
SDM - determine base pairs that makeup genes, human genome project
CRISPR - molecular scissors (Cas9) cut DNA to add or remove sections, treat diseases
6.4 Name 2 medical uses, agricultural uses, and forensic uses of cloning/DNA replication
Medical: gene therapy, gene screening
Agricultural: Bt toxin herbicide, Ti plasmid
Forsenic: fingerprinting, PCR investigations