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Transcription
occurs in nucleus,
synthesis of RNA,
information for the process: a segment of one DNA strand,
product: one RNA molecule (e.g. mRNA, tRNA, rRNA),
Major Enzyme or structure involved in the process: RNA polymerase
type of base paring required: RNA with DNA- RNA bases pair with the DNA bases as an RNA molecule is synthesized
Translation
occurs in the cytoplasm
synthesis of protein
information for the process- mRNA,
product- one protein molecule,
major enzymes or structure involved in the process- ribosomes (also requires tRNA),
type of base paring required- mRNA with tRNA- a codon in mRNA forms base pairs with anticodon in tRNA
What is transcription?
transcription if a gene produces an mRNA with a nucleotide sequence complementary to one of the DNA strands
What is translation?
translation of the mRNA produces a protein with an amino acid sequence determined by the nucleotide sequence of the mRNA
Steps in translation
unwind DNA and one strand serves as a template to make RNA ,
complimentary base paring occurs, attaching RNA nucleotides => mRNA rolls off (e.g. TCAGATCT—AGUCUAGA)
mRNA is processed = edited,
Completed mRNA leaves nucleus for translation
Players involved for translation
mRNA- “messenger” RNA, carries a transcript gene,
Amino acid= building blocks (monomer) of protein,
Ribosome= make protein, attach amino acids together,
tRNA= Transfer RNA, brings amino acids to the ribosomes,
rRNA= ribosomal RNA, main component of ribosomes.
Steps in translation (mRNA-- protein)
initiation- “players arrive”- ribosomes attaches to the mRNA (at START codon) and the tRNA brings the 1st amino acid.
Elongation- “play game”- next tRNA brings an amino acid, and the ribosomes attaches amino acid, etc. building a protein,
termination- “game’s over”- ribosomes reaches a STOP codon, everything is released—> protein is made
Consequences of mutation
deletion and insertion mutation both result in a frameshift
(e.g. THE CAT ATE – THE eCAT ATE --- THE eCA Tat E – insertion),
a different sequence of amino acids = nonfunctional proteins
nucleotide substitution- substitution-> changes mRNA codon-> different amino acid -
e.g. sickle cell anemia,
silent mutation- substitution -> changes codon-> same animo acid
e.g. normal, functional protein.
Nonsense substitution -> STOP codon
e.g. nonfunctional, incomplete protein
DNA vs RNA
DNA
2 strands
nucleotide
phosphate
nitrogenous base
A,T, C, G
RNA
1 strand
nucleotide
phosphate'
ribose
A, U, C, G *no thymmine, uracil instead