Module 11 Flashcards
Gene Cloning
Technique of isolating and making many copies of a gene
Utilized in DNA sequencing, gene editing, DNA probes, and expression of clones
Insertion of DNA into Vector
Requires cutting (restriction endonucleases) and joining of DNA fragments
Restriction enzymes can digest DNA into fragments with “sticky ends” that can bind to complementary strand, while others have “blunt ends”
Complementary DNA (cDNA)
A DNA strand that does not contain introns and only exons (protein-encoding genes), formed from reverse transcriptase on mRNA
DNA Library
Variety of DNA fragments inserted into vectors produces a collection of recombinant vectors
If starting was chromosomal DNA: genomic library
If starting was cDNA: cDNA library
Polymerase Chain Reaction (PCR)
Copies DNA without vectors or host cells, requiring template DNA, oligonucleotide primers, deoxynucleotide triphosphates (dNTPs), and Taq polymerase
3 Steps of PCR
- Denaturation: DNA strands are separated
- Primer Annealing: Oligonucleotide primers bind to DNA strands
- Primer Extension: Nucleotides are added to primers, extending their lengths
Reverse Transcriptase PCR
Used to detect and quantify the amount of RNA in living cells, beginning with RNA isolated from a sample, mixed with reverse transcriptase and a primer which anneals to 3’ end of RNA
Generates ss cDNA which can be used as a template
Real-Time PCR
Used to quantitate the amount of specific gene or mRNA in a sample, carried out in a thermocycler that can determine fluorescent changes using the TaqMan system
TaqMan System
Detects oligonucleotide with a fluorescent reporter molecule and a quencher molecule at either end. As the replicated length increases the fluorescence gets brighter, eventually reaching the cycle threshold
Cycle Threshold (Ct)
The point at which the accumulation of fluorescence in real-time PCR is significantly greater than the background level
Dideoxy DNA Sequencing
Based on DNA replication, a single tube contains all 4 nucleotides along with 4 fluorescently tagged ddNTPs without 3’ OH groups
Sanger sample is loaded onto single gel lane after polymerization, color fluoresces at each location identifying the specific nucleotide at that spot in the sequence
Gene Editing
Altering the sequence of a gene experimentally
CRISPR-Cas Editing Technology
Creates single guide RNA complex made of tracrRNA and crRNA. sgRNA then guides Cas9 to gene sequence using its spacer region which is complementary to the target gene
Cas9 cut can be repaired either through ____ which deactivates gene, or through ____ which allows for the insertion of donor DNA (causing point mutation)
non homologous end joining (NHEJ), homologous recombination repair (HRR)
Northern Blotting
Used to identify a specific RNA in a mixture to determine if a gene is transcribed within a cell type, at a development stage, and also observe if the pre-mRNA is alternatively spliced
Extract RNA mixture, separate via gel electrophoresis, blot onto nitrocellulose fiber, place in solution containing a probe, complementary DNA appears as a dark band