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Riboswitches Region in mRNA, usually the 5’ UTR, that binds a ligand and affects expression. The ligand is usually a small molecule, e.g., flavin mononucleotide (FMN). The portion that directly binds the ligand is the aptamer. Expression can be affected transcriptionally or post-transcriptionally.
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Fig. 7.34 A riboswitch from the B. subtilis ribD operon that binds FMN and promotes transcription termination.
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Fig. 7.35
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REGULON Collection of genes that are not in the same operon but are co-regulated Example: Maltose (mal) regulon: genes needed to metabolize maltose (glucose-glucose) involves multiple promoters and operons Activated by: –MalT (a protein that requires the inducer, maltotriose) –and CAP for some promoters
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Extensive and global regulation of transcription in prokaryotes 1.Regulated transcription during sporulation in Bacillus subtilis 2. Circadian regulation of global transcription in Synechococcus, a cyanobacterium
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2 forms of Bacillus Vegetative cells (Growing and dividing) Mother cell forming endospore (Dormant stage or cell) endospore Spore resistant to heat and stress, and can turn back into a vegetative cell. Fig. 8.3
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Endospore formation 1.Occurs in certain species of soil bacteria. 2.Triggered by lack of nutrients. 3.Requires turning off of many vegetative genes, and turning on of spore-specific genes. 4.Requires 3 sigma factors (σ 29, σ 30 and σ 32 or σ E, σ H and σ C ) in addition to the vegetative sigma factor (σ 43 or σ A ).
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Specific transcription in vitro by σ A and σ E. The in vitro-synthesized (with 32 P- UTP) RNA was hybridized to Southern (DNA) blots of the above DNA digested with the indicated restriction enzymes. σ A σ E Conclusion: The σ A RNAP initiates only at the Veg. promoter, but the σ E RNAP initiates at the veg. and sporulation promoters Fig. 8.5 Similar to Fig. 8.5
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The function of the putative sporulation-specific gene in the previous experiment was unknown. So, transcription of a well- characterized sporulation gene was performed with 4 different RNAPs, each with a different sigma (σ A, σ B, σ C, and σ E ). Only σ E transcribed the spoDII promoter. Fig. 8.6
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What about genes that need to be expressed at high levels at more than one stage in development? One mechanism is to have 2 promoters: Example: The spoVG gene of B. subtilis has σ E and σ B promoters. Fig. 8.8
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Some sigma factors are, themselves, sporulation-specific genes. Sigma K is the product of 2 sporulation genes, spoIVCB and spoIIIC - recombination forms the gene - only happens in mother cell during spore formation; the endospore remains unrecombined
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Circadian Rhythms 1.Oscillate with a period of ~24 hours 2.Phase determined by light-dark cycle 3.Once entrained, continue in “constant conditions” 4.Show temperature compensation
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Circadian Bioluminescence Rhythm in Gonyaulax (a eukaryote) A natural rhythm Temp. compensation
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http://www.ucmp.berkeley.edu/history/linnaeus.html
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Gene expression
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An engineered circadian rhythm of bioluminescence in Synechoccocus. PpsbAI - promoter for psbAI gene luxA + luxB = bacterial (Vibrio) luciferase
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How many genes in Synechococcus are circadian regulated? Kondo et al. used promoter tagging approach: 1.Transform promoterless luxA-luxB gene fusion into Synechococcus so that it integrates randomly - when it integrates downstream of a promoter, get a bioluminescent transformant. 2.Screen transformants for bioluminescence. 3.Determine how many show circadian rhythm of bioluminescence.
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Promoterless DNA construct used for transforming Synechococcus Bioluminescent colonies that are tracked with a computer controlled imaging system – track ~100 colonies at a time. Mid-day Night-time
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Results & Conclusion 1.Of ~30,000 transformants, ~800 had high levels of bioluminescence. 2.Of the 800, all showed circadian rhythm of bioluminescence. 3.Circadian rhythms of different phases and amplitudes were observed. Conclusion: The transcription of most genes in Synechococcus are regulated by the circadian clock (in addition to their other modes of regulation).
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What is the Clock? - Regulatory proteins that form an autofeedback loop! Kai A,B,C genes in Synechococcus
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Transcription in Organelles α–Proteobacterium–like organism Mitochondrion Cyanobacterium-like organism Chloroplast What about transcription of these highly evolved and derived genomes? endosymbiosis
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Mitochondrion from Bean root tip Mito. from transfer cell
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Mitochondrial RNA Polymerase: A phage-like RNAP 1.Core enzyme: 1-subunit, phage-like enzyme. 2.Specificity factor needed to initiate at promoter - human POLRMT enzyme needs two factors - factors A (TFAM) and B (TFBM) 3.Similar core enzyme in animal, fungal and plant mitochondria, but different specificity factors. 4.Promoter is usually a 9-10 bp sequence. 5.Genes usually encoded in the nucleus.
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Evolutionary questions about the Mitochondrial RNA Polymerase How and when was the phage-like RNAP acquired? What happened to the bacterial RNAP (Rpo) genes in the original endosymbiont?
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Look at earlier eukaryotes Pylaiella, a eukaryotic brown alga Phage-like polymerase gene in the mitochondrial genome –suggests the nuclear- encoded RNAP came from the endosymbiont a.k.a. “Mung”
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Reclinomonas, primitive eukaryote Bacterial RNAP (rpo) genes in mitochrondrial genome (pseudogenes?) Suggests the endosymbiont also had rpo genes. During evolution, phage-like polymerase was transferred to the nucleus (from the endosymbiont), and the rpo genes were lost.
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