Unit 3 - Transcription (DNA and RNA synthesis) Flashcards
Transcription 3 process
1) initiation
2) elongation
3) termination
-occurs in nucleus + DNA is chemically rewritten as an RNA code
simple Initation
RNA polymerase binds to the DNA and unwind it
Elongation simple
RNA polymerase creat a complementary mRAN strand. it + on ribonucleotides in 5’ to 3’ direction
Termination simple
translation ceases, and the mRNA is relesed
STRAND terms
template strand = used as a template
coding stand = not used as a template
Initiation in depth
RNA polymerase enzyme used to synthesize an RNA stran while using DNA as a template and needs no primer
RNA polymerase
- binds to the promoter region located upstream of the gene
- and unzips the double strand in order to expose the bases
Promoter
a nucleotide sequence that lies just before a gene and allows for the binding of RNA polymerase
- high inn A=T bp
- only two H-bonds = easy to break needing less energy needed
TATA Box
a section of DNA with a high % of T and A bases, which recognized by RNA polymerase
Eukaryotes = TATA
Prokaryotes = TATAAT
two steps of initation
1) binding to promoter
2) unzipping the DNA
Elongation in depth
builds mRNA strand
- incorporates ribonucleotides that r complementary to template DNA (catalyzes the formation of phosphodiester bonds)
- no primer
- 5’ to 3’
- promoter does not get transcribed
where r mRNA found(+)
at 3’ end
which enzyme initiates transciption
RNA polymerase
RNA is synthesized from strand of DNA
DNA template strand
Termination in depth
- The terminator sequence is located at the end of the gene
- recognizes the terminator sequence (AAUAA) + releases mRNA strand
- transcription stops (DNA rewinds itself)
After transcription
- mRNA will exit nucleus
- transcription of mRNA = protein in cytoplasm
post transcriptional modification
- newly built mRNA but must be modified bf leaving the nucleus
- remove non-coding regions
- Protect the mRNA from cytoplasmic nucleases and phosphates
3 modifications
1) splicing
2) add 5’ cap
3) add poly-A tail
Splicing
removal of non coding regions (introns) in the transcript
a) excise the introns
b) ligate exons
c) degraded in the nucleus
3 splicing steps
1) small nuclear RiboNucleoProteins bond together to from splicesome
2) splicesome loops the intron bringing the exon close together
3) intron is cute and removed
5’ cap
made of 7-methyl guanosine
- protects mRNA from digestion by enzymes
- ribosomes recognizes this site as initial attachment
Poly (A) tail
- 200 A nucleotides r added to 3’ end of mRNA
- catalyzed by poly-a-polymerase
- prevent degradation
- aids in export from nucleus
quality control
- no proofreading mechanisms
- more errors in transcription than replication
- redundancy of the genetic code
first major step in transcription
recognition of the promoter sites
T or F
during initiation of transcription, RNA polymerase binds to the promoter region
T
T or F
RNA polymerase transcribes both strands of DNA at the same time
F
what is added to the 3’ end of mRNA
a poly-A-tail