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DNA Polymerase III
Enzyme that catalyzes the production of DNA, stranding in a 5’ to 3’ direction
requires a template and primer
DNA polymerase I
Enzyme that removes DNA from primer sequences and fills gaps with DNA during replication on the lagging strand, has 5’ to 3’ polymerase activity, exonuclease activity in both directions
Taq DNA polymerase
A thermostable enzyme used in DNA synthesis from the thermophilic organism Thermus aquaticus
DNA ligase
Enzyme that catalyzes the formation of phosphodiester bond between adjacent nucleotides
involved in sealing ‘nick's’ (gaps in a single strand of DNA)
Gyrase/topoisomerase
Enzymes that catalyze changes in the topological state of DNA, such as relaxing supercoiling
ssDNA
Single stranded DNA
Primase
ssDNA-dependent RNA polymerase that synthesizes RNA primers during DNA replication
Helicase
Enzyme that unwinds the double helix by breaking hydrogen bonds between bases
Single stranded (ss) binding protein
Protein that bind single stranded DNA facilitating access of DNA polymerases
MCM2-7 complex
A eukaryotic DNA helicase
Licensing factor
Protein or complex of proteins that allows an origin of replication to begin DNA replication at that site
Kinase
Protein that attaches phosphate group to another molecule, often for the purpose of regulation
Telomere
DNA-protein structures found at both ends of a chromosome, protect genome from degradation, unnecessary recombination, and inter-chromosomal fusion
Telomerase
The enzyme responsible for maintenance of the length of telomeres by addition of guanine-rich repetitive sequences
End replication hypothesis
Proposal that the ends of linear DNA cannot be replicated completely
Germ cell
Reproductive cell, such as egg or sperm produced by meiosis in sexually reproducing organisms
Somatic cell
Any cell that is not a reproductive cell
Mutagen
Compound which causes mutations to DNA
Carcinogen
Compound which causes cancer (can be naturally occurring or mad-made)
Auxotroph
Mutant organism unable to grow without provision of a nutrient
Insertion
Mutation involving insertion of one or more nucleotides within a sequence of DNA
Deletion
Mutation involving loss of one or more nucleotides within a sequence of DNA
Substitution
Mutation involving replacement of one nucleotide with another within a sequence of DNA
InDel
An abbreviation describing the type of mutation
“insertion or deletion”
Missense
Outcome of a mutation resulting in a change of the codon and resulting amino acid sequence of a gene
Nonsense
Outcome of a mutation resulting in generation of a stop codon
Silent
Outcome of a mutation that results in no change in the amino acid sequence of a protein
Reading frame
Specific choice out of three different ways to read a sequence of nucleotides
Frameshift
Outcome of a mutation caused by insertion or deletion of a nucleotide that changes which downstream sequences are read by the ribosome
Nick (DNA)
Gap in a double stranded DNA molecule where there is no phosphodiester bond between adjacent nucleotides of one strand
Mismatch (base pair)
Where two bases are paired together that do not match, introducing changes in DNA sequence
DNA adduct
Piece of DNA covalently bound to a chemical that can impede DNA replication
Base excision repair
Mechanism of repairing damage to individual base pairs involving removal and replacement
recognizes specific modifications and involves enzymes such as DNA glycoslyases
Nucleotide excision repair
Mechanism for repairing single stranded DNA damage caused by chemicals, UV radiation or other mutagens, through the removal and replacement of segments of DNA
Deamination
Loss of an amino group from 5-methylcytosine creating thymine or from cytosine creating uracil
Cyclins
Proteins that control the progression of a cell through the cell cycle by activating cyclin-dependent kinases (CDK)
Cyclin dependent kinase
A group of protein kinases (enzymes which catalyze addition of a phosphate group) which control progression through the cell cycle
p53
Protein involved in regulating cell cycle progression in response to DNA damage
Bengin tumor
Growth of cells that does not invade tissues or spread to different areas of the body (non-cancerous)
Malignant tumor
Cancerous tumor that can invade tissues and spread to other parts of the body
Angiogenesis
Formation of new blood cells
Tumor supressor gene
Gene which works to regulate cell division which when inactivated can cause cancer
these genes are recessive meaning both alleles must be inactive before inhibition of cell division is removed
Two-hit theory of cancer
Dominant pre-disposition to cancer comes from a germ-line mutation while tumorigenesis occurs through a second somatic mutation
Kinase
Enzyme which catalyzes the transfer of a phosphate group from ATP to another molecule
Rb (retinoblastoma protein)
Tumor suppressor protein involved in control of the G1 checkpoint
Checkpoint
Control point to pause the cell cycle to ensure necessary conditions have been met before progression
Proto-oncogene
Gene which causes cells to become cancerous when mutated
turns into an oncogene
Oncogene
Mutated gene which causes cancer
dominant, meaning that only allele needs to be activated to promote cell division
HER2
Human epidermal growth factor receptor
controls growth differentiation of cells in response to hormone signaling
ras
Group of genes which encode proteins that regulate cell proliferation as part of a signaling cascade
raf
Family of serine/theronine protein kinases involved in the cellular proliferation signaling cascade
activated by ras
v-src (SARK)
Viral src oncogene
c-src
Chromosomal src proto-oncogene
Sanger (dideoxy) sequencing
Method of DNA sequencing that involves electrophoresis and is based on the random incorporation of chain-terminating dideoxynucleotides
Dideoxy trinucleotide phosphates (ddNTPs)
Nucleic acids with bases A, T, C, or G attached, that lack a 3’ hydroxyl group
p53
Transcription factor involved in initiating DNA damage repair
p21
Protein which binds to and inhibits CDK-cyclin complexes, preventing cell-cycle progression
ATM kinase (Ataxia-Telangiectasia Mutated kinase)
Enzyme involved in detection of dsDNA breaks and stabilizing p53 through phosphorylation