vocab
transcription - the 1st step in gene expression
is a process where genetic info encoded in the DNA is copied in order to produce mRNA
this mRNA is used to produce proteins
eukaryotic cells - transcription takes place in nucleus
prokaryotic cells - transcription takes place in cytoplasm
occurs in 5’ to 3’ direction
RNA polymerase is one enzyme involved in transcription
occurs in 3 stages
initiation
elongation
termination
template/antisense strand - DNA strand that’s being used as the template to synthesize complementary RNA molecule
coding/sense strand - DNA strand that has same sequences as RNA molecule (except thymine replaced with uracil)
gene expression - process where genetic info encoded in genes is used to synthesize proteins
translation - the 2nd step in gene expression?
process by which ribosomes use the genetic info carried by mRNA to synthesize proteins
so basically the base sequence of mRNA is translated into the amino acid sequence of a polypeptide
has same 3 stages as transcription
occurs at free ribosomes in cytoplasm or ribosomes attached to ER
tRNA - a type of RNA molecule that has amino acids attached to it, and will bring these amino acids to the ribosome during translation
tRNA’s will bind based on the mRNA sequence, so the order of the amino acids is dictated by the mRNA sequence
codon - a set of 3 adjacent nucleotides in DNA or mRNA that code for a particular amino acid
anticodon - located on the tRNA & is complementary to the matching codon
anticodons & codons are complementary = the correct tRNA with the correct amino acid binds to the correct codon, so the amino acid is placed correctly in the sequence
degeneracy - the redundancy of the genetic code, as multiple codons can code for the same amino acid
i think this is important cuz it reduces the potential for mutations
universal - genetic code is found in most organisms
mutation - a mistake made when synthesizing either RNA or RNA
play an important role in introducing genetic variation
so are essential for survival
point mutation - a type of mutation where a single nucleotide is changed (either deleted, added, or replaced with another)
ex - sickle cell anaemia
this results in frameshift mutation
frameshift mutation - all the codons following that mutation are altered, as there’s been a change in the base sequence
silent mutation - type of mutation where there is no difference in produced protein, even if there has been a mutation
degeneracy of genetic code means that the change in nucleotide could result in a codon that codes for the same amino acid
promoter - a non-coding region of DNA that’s located right before a gene?
transcription factors - a group of proteins that bind to promoter, initiating transcription (& gene expression)
if these are missing or are unable to bind, then transcription doesn’t occur & gene isn’t expressed
non-coding regions of DNA/non-coding DNA - DNA sequences with a genome, that dont consist of info needed to synthesize a protein
include: promoters, introns, telomeres, genes for tRNAs & rRNAs
introns - sections in eukaryotic DNA that’re transcribed into mRNA but are edited out before translation
telomeres - repeated nucleotide sequences that protect end of chromosomes
help ensure DNA correctly replicated
maintain chromosome stability during DNA replication
genes for tRNAs & rRNAs - genes that code for RNA molecules that form tRNA or rRNA (which forms part of structure of ribosome)
exons - coding sections within gene that contain instructions for synthesizing a protein & are kept in the mature RNA molecule
post-transcriptional modification - changes are made to mRNA after transcription, to change pre-mRNA into mature mRNA
5’ cap & poly-A tail are added
introns are excised (using spliceosome)
exons are ligated
alternative splicing - is when a gene is spliced in different ways by combining different exons & omitting others
the result is different versions of proteins that function differently
important as it means that one gene can code for different polypeptides
post-translational modification - many polypeptides undergo modification in order to become functional
occurs in Golgi apparatus (in eukaryotes?)
ex: modification of pre-proinsulin into insulin
proteasomes - protein complexes that’re involved in breaking down/recycling unwanted proteins or damaged proteins, to amino acids
found in nucleus & cytoplasm in eukaryotes