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anti parallel
run in opposite directions
origin of replication
specific sequence on a DNA molecule where replication begins
replication bubble
open region of DNA where replication occurs when helicase enzymes separate two parental strands at ORI
replication fork
ends of Replication Bubble
helicase
enzyme that breaks hydrogen bonds and unzips molecules
single-stranded binding proteins
bind to unpaired DNA strands to keep them from re-pairing
topoisomerases
break bonds ahead of replication fork to relieve strain and prevent supercoiling as DNA unzips
RNA primers
provides a 3’-OH group that allows for DNA polymerase to begin DNA replication
RNA primase
RNA polymerase that synthesizes short RNA primers on single-stranded DNA
DNA polymerase III
attaches at primer and moves along DNA from 3’ towards the 5’ end. reads existing DNA single strand and pairs up free complementary nucleotides with them
leading strand
built continuously following helicase away from origin of replication and toward the fork
lagging strand
built in Okazaki fragments in the opposite direction as the fork keeps moving
DNA polymerase I
removes RNA primers and replaces them with DNA nucleotides
DNA ligase
“glue” that joins sugar-phosphate backbones of Okazaki fragments into continuous DNA strand
mismatch repair
enzymes remove and replace incorrectly paired nucleotides resulting from replication errors
nucleotide excision repair
damaged DNA segment cut out (excised) by a nuclease and gap filled with nucleotides using undamaged (complementary) strand as template
telomeres
repeating code at ends of strand that shorten after replication
telomerase
can extend telomeres
genetic engineering
Insert new gene into organism’s gene
Polymerase Chain Reaction
amplify DNA
Gel Electrophoresis
Use restriction enzymes to cut DNA → separate by size to compare
CRISPR
Can introduce a segment from a functional gene, which will be used as a template by repair enzymes to edit defective gene so it’s corrected
mRNA
“messenger”
copy of DNA for a gene that goes to a ribosome
tRNA
“transfer”
bring amino acids to ribosome
complementary to codon (mRNA)
rRNA
“ribosomal”
makes up part of the ribosome
transcription
read DNA sequence of a gene on template strand using RNA polymerase and make RNA transcript
promoter
specific DNA sequence where RNA Polymerase attaches and initiates transcription
transcription factors
in eukaryotes, a collection of proteins mediate the binding of RNA polymerase and the initiation of transcription
introns
noncoding DNA
“interrupt” code
exons
coding DNA
“expressed”
“exit the nucleus”
5’ cap
facilitate export of mature mRNA from nucleus
help ribosomes attach to 5’ end
3’ Poly-A Tail
protect mRNA from degradation by hydrolytic enzymes
alternative splicing
splice different combinations of exons to create different shaped proteins (ex. antibodies)
translation
read mRNA code using ribosomes to produce polypeptides
wobble
mutation where 3rd base of codon can change and may not affect amino acid
post-translational modifications
after translation, polypeptide may be modified in many ways before it becomes a final protein
enzymes may remove one or more amino acids from leading end of polypeptide chain
enzymes may cleave polypeptide chain into 2 or more piecces
may join up with other polypeptides (quaternary structure)
may get sugars phosphate groups
point mutations
changes in DNA
silent
new codon is swapped out for a different one
missense
changes the amino acid. may or may not affect protein (depends on R group properties)
nonsense
changes a codon in the middle to a STOP codon
frameshift
addition or deletion/removal of 1+ nucleotides
operons
a group of genes in a region of a prokaryotic chromosome that can be controlled in a unified manner
operator
on/off switch where repressor protein binds to prevent transcription
strucutral genes
sequences that actually code for proteins (usually enzymes)
regulatory gene
(located anywhere on a chromosome) codes for repressor protein, which controls gene expression
inducible operon
normally off, but can be turned on when needed
lac operon
bacteria’s ability to break down lactose in glucose-deprived environment
repressible operon
normally on, but can be turned off when not needed
trp operon
bacteria make tryptophan from precursor molecule when nutrient medium lacks this amino acid
epigenetics
inheritance of traits transmitted by mechanisms not directly involving nucleotide sequence of a genome
histone acetylation
+ acetyl groups to histones → DNA unwind/loosen → turns genes on
DNA methylation
+ methyl groups to DNA → DNA wind tighter → turns genes off (long-term inactivation)
microRNA and Small Interfering RNAs
small RNA molecules that regulate gene expression by degrading mRNA or blocking translation