U3 Chapter 20: DNA Tools and Biotechnology Flashcards
Nucleic Acid Hybridization
The base pairing of one strand of a nucleic acid to the complementary sequence on a strand from another nucleic acid molecule, is widely used in DNA technology
DNA Sequencing
The general laboratory technique for determining the exact sequence of nucleotides, or bases, in a DNA molecule
-can be carried out by using the deoxy sequencing method in automated sequencing machines
Gene Cloning (or DNA Cloning)
Produces multiple copies of a gene (or DNA segment) that can be used to manipulate and analyze DNA and to produce useful new products or organisms with beneficial traits
Genetic Engineering
Where bacterial enzymes are used to cut DNA molecules within short, specific nucleotide sequences (restriction sites), yielding a set of double-stranded restriction fragments with single-stranded sticky ends
Recombinant DNA Molecules
Involves using enzymes and various laboratory techniques to manipulate and isolate DNA segments of interest. This method can be used to combine (or splice) DNA from different species or to create genes with new functions
Gel Electrophoresis
A laboratory method used to separate mixtures of DNA, RNA, or proteins according to molecular size. In gel electrophoresis, the molecules to be separated are pushed by an electrical field through a gel that contains small pores
Polymerase Chain Reaction (PCR)
Amplify (produce many copies of) a specific target segment of DNA, using primers that bracket the desired sequence and a heart-resistant DNA polymerase
Plasmids
A small, circular, double-stranded DNA molecule that is distinct from a cell’s chromosomal DNA
- recombinant plasmids: returned to host cells, each of which divides to form a clones of cells
Expression Vectors
Vector which is designed to allow expression (transcription and translation) of the inserted section of DNA. The vector carries a promoter (normally inducible) on one side of the cloning site, and a transcription terminator on the other side
Nucleic Acid Probe
Based on the detection of unique nucleotide sequences within the DNA or RNA of a microorganism; these unique nucleotide ‘signatures’ are surrogates for the presence of the organism itself
- detect the presence of specific mRNAs
Hybridization
The process in which two complementary single-stranded DNA and/or RNA molecules bond together to form a double-stranded molecule
- detect the presence of a given mRNA in tissue
RT-PCR
Technology by which RNA molecules are converted into their complementary DNA (cDNA) sequences by reverse transcriptase, followed by the amplification of the newly synthesized cDNA by standard PCR procedures
- detect the presence of a given mRNA in a RNA sample
RNA Sequencing (RNA-seq)
Sequencing the cDNAs corresponding to mRNAs from the cells
- DNA microarrays are also used for this purpose
Gene Drive
Dramatically increase the likelihood that a particular suite of genes will be passed onto the next generation, allowing the genes to rapidly spread through a population and override natural selection
Genome-Wide Association Studies
Identify and use single nucleotide polymorphisms (SNPs) as genetic markers for alleles that are associated with particular conditions