transcription, RNA processing, gene expression Flashcards
RNA vs DNA
RNA has ribose instead of deoxyribose
RNA has uracil instead of thymine
RNA is SS, DNA is DS
mRNA
protein transcription
Pol II
rRNA
component of ribosome/translation
Pol I: 28S, 18S, 5.8S
Pol III: 5S
80% of total RNA
tRNA
adapter between mRNA and AAs during protein synthesis
Pol III
Pol I
most of rRNA
nucleolus
Pol II
mRNA
nucleoplasm
Pol III
tRNA
5S rRNA
some snRNAs
nucleoplasm
transcription unit
space between start and end of gene
promoter region
area containing binding site for Pol II upstream of transcription unit TATA box = where transcription begins CAAT box binds NF1 GC regions bind SP-1 also gene specific elements, enhancers, silencers
what does binding of pol II determine?
where transcription begins
which DNA strand is used as template
in which direction transcription proceeds
amanitin poisoning
alpha amanitin binds to Pol II, inhibiting mRNA synthesis
rifampicin
inhibits RNA polymerase in bacteria
does not affect eukaryotic Pol I-III
effective against Mycobacterium tuberculosis
capping of pre-mRNA
m7Gppp = 7-methyguanidine
attached to first nucleotide of pre-mRNA (5’ cap)
important for cell to distinguish mRNA from other RNA, processing, export, and initiation of translation
polyadenylation
required for termination of transcription in eukaryotes
signal is encoded in DNA template, transcribed in pre-mRNA
GU rich element signals to Pol II to slip off transcript
CstF cleaves GU rich element
CPSF cleaves 10-30 nucleotides from poly-A signal, generating new 3’ end
poly-A tail is added to 3’ end
splicing of pre-mRNA
removal of introns and connecting of exons to form mature mRNA
catalyzed by spliceosome
involves 5’ splice site, 3’ splice site, branch point within intron
alternative splicing
different combinations of exons can be spliced together, forming different proteins
beta thalessemia
error in splicing of pre-mRNA that produces beta chain of hemoglobin
deficiency of beta chain leads to deficiency of hemoglobin and anemia
alters nucleotide sequence at first exon/intron boundary
PKU
base exchange at 5’ splice donor site of one intron
leads to incorrectly spliced mRNA and truncated protein lacking one exon
truncated protein is unstable and degraded, resulting in deficiency of phenylalanine hydroxylase