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the central dogma
how we go from DNA to a protein
transcription
gene of DNA to mRNA strand
occurs in nucleus
translation
mRNA to a protein
occurs in the cytoplasm
gene
a segment of DNA that encodes for a protein
structure of DNA nucleotides
deoxyribose (DNA) or ribose (RNA) sugar
phosphate (has negative oxygens which help it bind to other things)
a nitrogenous base (ATCG)
nitrogenous base pairing
A & T (adenine and thymine)
C & G (guanine and cytosine)
what does DNA separate into during transcription
a coding strand and a template strand
what strand is used to transcribe into mRNA
template strand
differences between DNA and RNA
nitrogenous bases (U instead of T in RNA)
two-stranded vs. one-stranded
sugar: deoxyribose vs. ribose
why is it mRNA
the code of a single gene
messenger RNA because it is created in the nucleus and transported into the cytoplasm
how does the mRNA become a protein
ribosomes put together amino acids based on the mRNA sequence (codes of three bases correspond to types of amino acids)
codon
group of 3 nitrogenous bases that code for 1 amino acid
groups of amino acids
grouped by functionality/chemical properties
charged, polar, nonpolar, special cases
charged amino acids
attracted to other charged molecules
polar amino acids
hydrophilic
nonpolar amino acids
hydrophobic
special case amino acids
ex: cysteine has a sulfur which allows for disulfide bonds
codon chart
shows how to convert 3 RNA nucleotides into an amino acid
start codon
AUG/Met
beginning of every protein - tells the ribosome to start making the protein
stop codons
UAA, UAG, UGA
tells the ribosome that the prior amino acid is the last in the chain
stop codons are not amino acids, just stop signs
another name for a protein
polypeptide
tRNA
transfer RNA - like a shuttle that helps ribosomes assemble the protein by carrying the corresponding amino acid of the anticodon
once it drops off the amino acid, it leaves to go find another one
purpose of extra bases on the sides of an mRNA
insulation to help protect the strand from damage during movement from the nucleus to the cytoplasm
what connects the amino acids
peptide bonds
genetic mutations
changes in the nucleotide sequence that cause the ribosome to bring a different amino acid which leads to a different protein with a different (wrong) function
example of a genetic mutation
sickle cell disease
the mutated amino acid is now hydrophobic instead of charged, which changes the shape of an RBC to a sickle