Chapter 17 - Expression of Genes Flashcards
functional RNA
tRNA, rRNA
central dogma
explanation of the flow of genetic material:
DNA –> RNA –> protein
transcription & translation
Beadle and Tatum’s experiment
- bombarded red bread mold with X-rays
- analyzed relationship between metabolic pathway of arginine biosynthesis and mutated genes
- explained the “one gene one enzyme” hypothesis
degeneracy/redundancy of codons
many-to-one structure-function relationship
e.g. more than on codons (synonymous codons) code for a particular amino acid
Sense strand
(coding strand)
- DNA strand that is not used for mRNA transcription
- directed in 5’-3’ direction
- contains same sequence as mRNA (except T)
Antisense strand
(non-coding, template strand)
- template used for transcription to make mRNA
- antisense because its direction is 3’-5’ as the mRNA needs to be transcribed in 5’-3’ direction
Start codon
AUG - methionine
Stop codon
UAA / UAG /UGA
Site of transcription
eukaryotes - in the nucleus
prokaryotes - in the cytoplasm (nucleoid region)
RNA polymerase (II)
- enzyme for transcription
- binds to promoter region on DNA
- acts like helicase: unwinds DNA double helix
- acts like DNA polymerase III: adds RNA nucleotides to 3’ OH end of transcript
Transcription factors
mediate binding of RNA polymerase
+
initiation of transcription
1) general TF - responsible for all transcriptions in every cell
2) specific TF - works specifically at specific time in a specific cell
Stages of transcription
1) Initiation
- formation of transcription initiation complex
a) RNA polymerase (II) on promotor
b) general, specific transcription factors
c) transcription unit - DNA region downstream of promotor
2) Elongation
- RNA polym II moves along template strand and adds complementary RNA nucleotides to 3’ OH end of transcript
3) Termination
a) in prokaryotes: terminator sequence transcribed, RNA polymerase detaches from DNA template
b) in eukaryotes: polyadenylation signal recognized by nuclease which cleave mRNA from RNA polymerase II
RNA processing in eukaryotes
1) 5’ capping
- adding modified guanine to 5’ end of pre-mRNA
2) 3’ poly A tail
- adding 50-250 adenine nucleotides to 3’ OH end of pre-mRNA
3) RNA splicing
Intron
INTervening RegiON
- non-coding segments
- removed during RNA splicing
- increases probability of crossing over
Exon
Expressed regiON
-coding segments