Unit 6 Flashcards
Chapters 16 + 17
Transformation
The change in genotype and phenotype due to assimilation of foreign DNA
Bacteriophages
Viruses that infect and replicate within bacteria/archaea; used for genetic research
Virus
DNA (sometimes RNA) enclosed by a protective coat that is often a protein
Double Helix
The twisted structure of the DNA molecule
Sugar-Phosphate Backbone
Describes the alternating pattern of deoxyribose and phosphate group that makes up the sides of DNA molecule
Nitrogenous Bases
Make up the “rungs” of DNA ladder; adenine, thymine, guanine, cytosine, (uracil)
Antiparallel
The tendency of DNA backbones to run in opposite directions
Purines
Double-ringed (larger) nitrogenous bases; adenine and guanine
Pyrimidines
Single-ringed (smaller) nitrogenous bases; thymine and cytosine
Origin of Replication
Specific points along the DNA molecules where the strands are separated to form a “bubble” where replication can start
Replication Fork
Where new DNA strands are elongated
Helicase
An enzyme responsible for untwisting the double helix at the replication forks
Single-Strand Binding Proteins
Proteins that bind to the untwisted strands of DNA for stabilization
Topoisomerase
Enzyme that corrects over winding ahead of the replication fork
DNA Polymerase
Enzyme that attaches new nucleotides; cannot start the chain of replicated DNA; works only in the 5’ to 3’ direction
Primase
Enzyme that attaches a short segment known as an RNA primer to unraveled DNA so that polymerase has an open 3’ to attach new nucleotides to
Leading Strand
The strand of new DNA that is being replicated towards the replication fork; typically faster
Lagging Strand
The strand of new DNA that is being replicated away from the replication fork; typically slower due to additional synthesis of Okazaki fragments
Okazaki Fragments
Segments of 3 nucleotides added to the lagging strand in units
DNA Ligase
Enzyme responsible for joining together Okazaki fragments
DNA Replication Machine
Proteins used in DNA replication form a large, stationary complex
Mismatch Repair
Ability of some polymerase enzymes to proofread DNA and replace incorrect nucleotides
Carcinogens
Harmful chemicals/physical agents that can damage DNA and cause cancers
Mutations
Spontaneous changes to DNA sequence
Nuclease
Enzyme that cuts out and replaces damaged stretches of DNA
Telomeres
Nucleotide sequences at the ends of chromosomal DNA used to slow the erosion of genes; lengthened by telomerase
Chromatin
Complex of DNA and protein (often more loose and linear)
Euchromatin
Loosely packed chromatin
Heterochromatin
Highly condensed regions of chromatin (centromeres/telomers)
Histones
Basic proteins in the nucleus that help condense DNA into chromatin (early formation of chromosomes)
Gene Expression
Process in which DNA directs protein synthesis through transcription and translation of certain segments of genetic cod
“One-Gene, One-Protein” Hypothesis
Idea that each gene dictates the synthesis of a different protein
Transcription
The synthesis of RNA using DNA; produces mRNA
Translation
The synthesis of a polypeptide using mRNA; occurs in the ribosomes
RNA Processing
Sequence of alterations the initial strand of mRNA undergoes before leaving the nucleus of eukaryotes
Primary Transcript
The initial RNA strand produced in the nucleus from the DNA
Central Dogma
DNA –> RNA –> Protein
Triplet Code
Way of reading DNA in segments of 3 non-overlapping nucleotides
Codon
Segment of mRNA that is 3 nucleotides long to correspond with DNA triplet
Template Strand
One of the 2 DNA strands that the mRNA is transcribed off of
Reading Frame
The correct grouping of mRNA codons that begins at the first AUG
RNA Polymerase
Enzyme that catalyzes the synthesis of RNA in transcription
Promoter
Regions of DNA that indicate where RNA transcription will begin for a certain gene
Terminator
Regions of DNA that indicate where RNA transcription for a specific gene will end
Transcription Unit
Stretch of DNA being transcribed
Transcription Factors
Proteins that bind upstream of the starting point to mediate the binding of RNA Polymerase
TATA Box
Sequence of nucleotides in eukaryotes that the initiation complex is formed around and signals the beginning of transcription
5’ Cap
Modification added to the 5’ end of transcribed RNA that allows for recognition during translation (helps ribosome attach)
Poly-A Tail
Modification to the 3’ end of the transcribed RNA that protects mRNA from hydrolytic enzymes
Introns
Noncoding regions that are removed during RNA splicing
Exons
The regions of the RNA molecule that are necessary for the synthesis of the polypeptide chain that are joined together during RNA splicing
Spliceosomes
Configuration of enzymes that recognize splice sites on exons
Ribozymes
Catalytic RNA that function as an enzyme and assist in splicing process
Alternative RNA Splicing
Phenomena that some genes can encode more than 1 kind of polypeptide depending on which segments are deemed exons or introns during splicing
Domains (of proteins)
Discrete regions of proteins that vary in function
Anticodon
Segment of 3 tRNA nucleotides that complements RNA codons and attaches the amino acid to the growing polypeptide chain during translation
Aminoacyl-tRNA Synthetase
Enzyme responsible for matching tRNA molecules with their respective amino acids
Release Factor
Protein coded by stop codon that causes the addition of water to the growing polypeptide chain in place of an another amino acid
Signal-Recognition Particle (SRP)
Molecule that binds to signal peptide and brings it and the free ribosome to the ER for binding
Polyribosome
When multiple ribosomes translate a single mRNA simultaneously
Point Mutation
Chemical changes in just 1 base pair of a gene which can lead to the possible production of an abnormal protein
Nucleotide-Pair Substitution
Replacing of one nucleotide (and its partner) with another pair of nucleotides
Silent Mutation
When a mutation has no effect on the amino acid
Missense Mutation
When a mutation codes for an amino acid but not the correct one
Nonsense Mutation
When a codon is changed that normally codes for an amino acid into a codon that codes for a stop which most often leads to nonfunctional proteins
Frameshift Mutation
The addition/deletion of nucleotides that alters the reading frame
Mutagens
Physical/chemical agents that can cause mutations