1/38
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced |
---|
No study sessions yet.
deoxyribonucleic acid
made and found in nucleus, carries cell hereditary information
nucleic acid
macromolecule with cell’s genetic blueprint and instructions for cell functions
nucleotide
monomer of nucleic acids, made of a sugar, a nitrogenous base, and at least one phosphate group
purine
nitrogenous bases with 2 carbon-nitrogen rings— adenine and guanine
pyrimidine
nitrogenous base with 1 carbon-nitrogen ring— cytosine, thymine/uracil
ribonucleic acid
single-stranded, base paired molecule involved in protein synthesis
helicase
enzyme that “unzips” DNA during replication by breaking the hydrogen bonds
lagging strand
the strand of DNA that is replicated in fragments— going away from replication fork 5’-3’
leading strand
the strand of DNA that is continuously synthesized— going towards the replication fork 5’-3’
ligase
enzyme that joins the fragments in the lagging strand by repairing the hydrogen bonds, also occasionally fixes UV/chemically damaged DNA, is always present
Okazaki fragment
DNA fragment synthesized on the lagging strand
primase
RNA primer needed for DNA to start synthesis of a new strand
replication fork
y-shaped structure formed by “replication bubble” where replication is happening
DNA replication
helicase unzips DNA, single stranded binding protein keeps the strands separated, primase begins synthesis and DNA polymerase adds nucleotides, ligase joins and fixes the synthase
single stranded binding protein
protein that binds to a separated DNA to keep the two strands from reconnecting during replication
DNA polymerization
nucleotides join together via the phosphate group and 3’ carbon— growing always in the 5’-3’ direction
phosphate and sugar
make DNA backbone
Chargaff’s rule
base pairings— A=T, G=C
Rosalind Franklin
studied x-rays of DNA to show size that was only possible if it was a double helix
watson and crick
used Chargaff and Franklin’s work to build a model of DNA
to the right
direction DNA twists
initiation
transcription factors bind onto genes and “turn on” the ones necessary for the function
RNA polymerase
unzips DNA identified by transcription factors, copies the template and adds corresponding bases without the help of any enzyme or primer
transcription process
gene initiation, elongation, termination
elongation
RNA poly builds transcript from template, only one strand of DNA is copied and only one strand of RNA is created
coding strand
the strand of DNA that is directly copied, but is identical to the resulting RNA strand because that’s just how copying works
termination
RNA poly jumps off at the “terminator” sequence in the DNA, the transcript separates and DNA rezips
transfer RNA
final RNA product used in protein production
ribosomal RNA
final RNA product used to make ribosomes
messenger RNA
RNA product that carries coding genes and needs to go through maturation before it is usedma
maturation
5’ and 3’ caps are added to transcript, introns are excised and exons bind together
intron
“junk” section of gene that is basically gibberish
exon
portion of gene with important information that will get expressed
genetic code
triplets of mRNA codons- start/stop or code for amino acids
anti-codon
found on tRNA, makes amino acid attachment site by recognizing the codon
DNA translation
initiation, elongation, and termination
initiation
first step of translation- anti-codon recognizes the start codon and brings in the amino acid
elongation
second step of translation- next codon is read, anti-codon matches amino acid, 2 tRNA are held in the protein at a time
termination
third step of translation- the stop codon is recognized, amino acid chain breaks off and the system disassembles