CONJOINT 541 Translating a Transcriptome at Specific Times and Places David Morris Department of Biochemistry http://faculty.washington.edu/dmorris/ Lecture 1 The Biology and Experimental Analysis of mrna Translation
Lecture 1 Translational control what and why? Genome-wide evaluation translation Global assessment of gene expression Polyribosomes as a tool Measurement of translational efficiency Translation states across a transcriptome Gene-specific translational control Sites of regulation of translation initiation Cis-acting elements in mrnas Regulation of Gene Expression DNA NUCLEUS Polymerase II Primary Transcript Capping Methylation Polyadenylation Splicing Editing Proofreading Transport Mature mrna CYTOSOL mrnp Particles Mature mrna Localization Protein REGULATION AT MANY SITES Degradation
Regulation of Expression of a Gene Network DNA NUCLEUS Polymerase II Primary Transcript Capping Methylation Polyadenylation Splicing Editing Proofreading Transport Mature mrna CYTOSOL mrnp Particles Mature mrna Localization Protein Degradation Why regulate gene expression at the translational level? Regulation of expression from stable mrnas Rapid response Both on and off Reversible Fine tuning expression at levels beyond transcription Issues unique to big cells Localized expression in a cell
Transcriptome-Wide Evaluation of Translation Genetic Regulatory Networks Particular Cellular State Transcription Pattern mrna 1 mrna 2 mrna 3... mrna n TRANSCRIPTOME Large-scale cdna sequencing SAGE Microarray Oligo cdna
Classic Expression Array Experiment Cell Population #1 Cell Population #2 Extract mrna Extract mrna Make cdna Label w/ Green Fluor Make cdna Label w/ Red Fluor Co-hybridize Gene 1.. Slide with DNA from different genes Gene n Scan R. Bumgarner Gene Expression Networks Particular Cellular State Transcription Pattern mrna 1 mrna 2 mrna 3... mrna n 1 2 3 T e T e T e n T e prot 1 prot 2 prot 3... prot n TRANSCRIPTOME PROTEOME PHENOTYPE
Approaches to High-Throughput Analysis of Molecular Phenotype DNA mrna Large-scale cdna sequencing SAGE Microarray TSAA Protein Proteome Analysis 2-D gels Mass spect POLYRIBOSOME GYMNASTICS
mrnas are Translated on Polyribosomes (Polysomes) Open Reading Frame (ORF) initiation elongation termination Rates of elongation and termination are constant for most transcripts, therefore rate of synthesis of the encoded protein is proportional to ribosome spacing [ribosome spacing] x k = rate of synthesis mrna Translation in Eukaryotes cap A n Translatable mrna cap A n cap mrnp Masked mrna A n Translating Polysome For a transcript species, want to know: fraction of mrna associated with ribosomes average polysome size (# ribosomes)
Two parameters dictate number of ribosomes loaded on an mrna: Size of the ORF Rate of ribosome loading Initiation is key How to measure number of ribosomes on a transcript?
Sucrose Gradient Centrifugation 7% sucrose Extract polysomes and load on a sucrose gradient 47% sucrose Spin gradients in an ultracentrifuge to separate polysomes mrnp 1 A260 Messages with different average numbers of ribosomes will sediment to different parts of the gradient 2 3 A northern analysis of polysome fractions, using a well translated gene as a probe.
Norm alized Cy3 : Cy5 ratio TOP 2.5 2 1.5 1 0.5 ACT1, 1128 nt CMD1, 444 nt TDH3, 999 nt 3.6 5.8 8.0 BOTTOM 0 0 5 10 15 20 25 mrnp Particles Fraction Average number of ribosomes per mrna / ORF length yields ribosome density: CMD1: 3.6 ribosomes / 444-nt ORF = 0.81 ribs / 100 nts TDH3: 8.0 ribosomes / 999-nt ORF = 0.80 ribs / 100 nts ACT1: 5.8 ribosomes / 1128-nt ORF = 0.51 ribs / 100 nts High throughput analysis TSAA
Ribosome Density Across a Transcriptome Ribosomes per 1000 nt in polysomes 12 10 8 6 4 2 Maximum density = 80-100 nts/ribosome Therefore, >20X difference across this transcriptome Minimum density = ~2000 nts/ribosome 0 0 4 8 12 16 20 Relative abundance - truncated scale MacKay et al., 2004 Occurrence of Transcripts in mrnp Particles Fraction Transcript in mrnp 1 0.8 0.6 0.4 0.2 0 Most of the mrnp particles contain low-abundance transcripts 0 5 10 Transcript Abundance MacKay et al., 2004
Synthetic Rates of Individual Proteins For protein x x dp dt = x. T e [mrna ] x T e = (polypeptide chains completed) mrna -1 min -1 Translation of the transcriptome of growing yeast Translational Efficiency 0 0.1 1.0 10 Enriched in environmentalresponse genes: Poised? Osmotic stress (18) 7% Nitrogen of 4549 stress transcripts (22) have T.E. Pheromone < 0.25 X mean response (11) DNA repair (11) 0 10 Metal uptake (12) 20 Transcript Abundance Sulfur utilization (9) Law et al., 2005
Two Poorly Translated mrnas: GCN4 and HAC1 14 12 mrnp GCN4 HAC1 Mean Cy3 : Cy5 ratio 10 8 6 4 1 ribosome 2 0 0 5 10 15 20 25 Fraction number MacKay et al., 2004 Sucrose gradient analysis of the response of YSP3 transcripts to nitrogen starvation mrnp+monos Polysomes Relative Transcript Amount Unstarved Nitrogen Starved 0 12 24 Fraction Number Lynn Law
Translation is generally regulated at initiation Scanning Sites of regulation: Accessibility of mrna mrnp Activity of eif4e Phosphorylation of eif2α Scheper et al., 2006 MECHANISMS What are the cis-acting elements that confer unique translational properties to individual mrnas? How are the these regulated?
mrna cis Elements Located in Non-Protein-Coding Regions Repressor Initiation Repressor Localization cap 5 Leader ORF 3 UTR (A) n 2 o structure Stability uorf uorf Adenylation