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anticodon
located on tRNA - corresponding to a complementary codon on mRNA
point mutation
alteration of a single nucleotide base
transcription factors
proteins that control rate of gene transcription
wobble
describes the loose bind that you may see between a tRNA and an mRNA. Shown of the codon chart as multiple codons coding for the same amino acid
base-pair substitution
genetic mutation where one single nucleotide base is replaced by another
missense mutation
point mutation where a different amino acid is coded for
transcription
DNA code is turned into mRNA code
nonsense mutation
mutation signaling the cell to stop building a protein
mRNA
carries genetic instructions in DNA from nucleus to cytoplasm
TATA box
located in the promoter region - “calls” RNA polymerase to the site
rRNA
ribosomal - made up of RNA and protein
insertion
mutation where one or more nucleotide base pairs are added to a DNA sequence
tRNA
bring amino acids to the ribosomes during translation to be assembled into polypeptide chains
deletion
mutation where a segment of DNA is removed
translation
convert mRNA code into a primary sequence of protein structure
snRNPs
recognize the splicing signals at the ends of introns
frameshift mutation
mutation caused by insertion/deletion of nucleotide bases not in multiples of 3
RNA processing
post transcription modification of newly made pre mRNA to functional mRNA
snRNA
a ribozyme - RNA that has catalytic properties to cut and splice
RNA splicing
removal of introns so you're left with exons
triplet code
using 3 nucleotides to code for 1 amino acid
intron
non coding section of pre mRNA that is removed by RNA processing
exon
give code that turns into a protein
codon
each 3 nucleotides of mRNA
spliceosome
collective mass of snRNA and snRNP that function in creating functional mRNA
RNA polymerase
creates mRNA (no lagging strand)
phages
type of virus that infects and replicates within bacteria
DNA polymerase
enzyme that adds new nucleotides to the growing strand 5’ to 3’
mismatch repair
any kind of small scale mistake
primase
joins RNA nucleotides together to make the primer
nuclease
identifies and cuts out the problem
double helix
physical shape of DNA
leading strand
goes straight into the fork
helicase
untwists and unwinds DNA
excision repair
specific kind of mismatch repairs (base excision/nucleotide excision)
semi conservative model
describes how DNA double helix separates into two single strands, each acting as a template for a new complementary strand
lagging strand
works away from the fork
single stranded binding protein (SSBP)
molecules that keep DNA strands apart from eachother
telomerase
makes telomeres
primer
shrot nucleic acid sequence that provides a starting point for DNA synthesis and replication
DNA ligase
joins fragments of DNA to one another
replication fork
the opening in the DNA where replication will occur