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Natural Genetic Engineering of Genome Structure

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Natural Genetic Engineering of Genome Structure FOGA-III: HOW DOES GENETIC CHANGE HAPPEN? - NATURAL GENETIC ENGINEERING OF GENOME STRUCTURE • Cells have a large toolbox of biochemical systems that carry out genome restructuring at all levels of complexity • Sequenced genomes display structures and relationships that reveal the evolutionary importance of natural genetic engineering functions • Natural genetic engineering functions are subject to cellular regulation and control Outline • Personal history with natural genetic engineering • The mammalian immune system • Natural genetic engineering in evolution • Non-random features of natural genetic engineering • Advantages of evolution by natural genetic engineering gal+ Mobile DNA P E T K - IS elements epimerase transferase kinase galT::IS P E T K x x epimerase Shapiro JA. Mutations caused by the insertion of genetic material into the galactose operon of Escherichia coli. J Mol Biol. 1969 Feb 28;40(1):93-105. Replicative transposition and DNA rearrangements Shapiro, J. 1979. "A molecular model for the transposition and replication of bacteriophage Mu and other transposable elements." Proc. Nat. Acad. Sci. U.S.A. 76, 1933-1937. Differential Replicative Transposition of Mudlac in E. coli Colonies - Starvation Triggered Shapiro, J.A. and N.P. Higgins. 1989. Differential activity of a transposable element in E. coli colonies. J. Bacteriol. 171, 5975-5986. Stress-induced ara-lac fusions and adaptive mutation araB U118 lacZ 200 Derepression ClpPX, Lon RpoS (42C, starvation) Transposasome MuA, HU, IHF formation MCS2 (2 subclones) CDC/Target complex araB U118 lacZ 100 Strand transfer U118 Total fusion colonies MCS1366 (4 subclones) STC = strand transfer complex MuB for replication 0 (Crp-dependent starvation- 0 10 20 induced functions inhibit and/or replace MuB?) araB lacZ Days/32 DNA processing Replication (RpoS-, Crp-dependent (exponential growth) functions?) ClpX ClpX araB lacZ araB lacZ U118 Adjacent inversion (precludes fusion) araB-lacZ fusion Shapiro, J.A. 1997b. Genome organization, natural genetic engineering, and adaptive mutation. Trends in Genetics 13, 98-104 Immune Systems Receptors: How to generate virtually infinite diversity with finite coding capacity Combinatorial Diversity: assembling immunoglobulin coding sequences from cassettes Junctional Flexibility: Augmenting Diversity D. C. van Gent, J. H. Hoeijmakers, Fugmann et al. 2000. The RAG proteins R. Kanaar, Chromosomal Stability and V(D)J recombination: complexes, And The Dna Double-Stranded ends and transposition. Annu Rev Break Connection Nature Rev. Immunol 18:495-527. Genet. 2, 196 (2001) Antigen stimulation/selection: a rapid evolution system Post-selection (antigen stimulation): antibody improvement and functional diversification Nature Reviews Molecular Cell Biology 2; 493-503 (2001) LINKING CLASS- SWITCH RECOMBIN ATION WITH SOMATIC HYPERMUT ATION Transcriptional Targeting of Class Switch Recombination Nature Reviews Molecular Cell Biology 2; 493-503 (2001) LINKING CLASS- SWITCH RECOMBIN ATION WITH SOMATIC HYPERMUT ATION Immune System Lessons: cellular capabilities for controlled but non- determined DNA restructuring • Tight regulation of complex set of events as to cell type, sequence of particular DNA changes, and linkage to selection & cellular proliferation • Capacity for multiple types of DNA changes, including ability to incorporate untemplated sequences • Targeting of VDJ joining events to particular locations within coding regions while maintaining flexibility of novel sequences formed • Transcriptional activation and targeting of somatic hypermutation (base changes) to V regions of Ig coding sequences • Lymphokine-directed transcriptional activation and targeting of class switch recombination (breakage and rejoining) Natural genetic engineering of sequenced genomes - Pack-MULEs Ning Jiang, Zhirong Bao, Xiaoyu Zhang, Sean R. Eddy and Susan R. Wessler. 2004. Pack-MULE transposable elements mediate gene evolution in plants. Nature 431, 569-573. Natural Genetic Engineering Modalities • Homology-dependent exchange & gene conversion: - DS break repair - Rearrangements by crossover at dispersed homologies - Cassette exchange, protein diversification • Non-homologous end joining (NHEJ) - DS break repair - Targeted and untargeted rearrangements • Mutator polymerases • Terminal transferase - insertion of novel sequences • Site-specific recombinases - Integration of horizontally transferred DNA - Regulation of protein synthesis, protein diversification • DNA transposons (replicative, cut-&-paste, rolling circle helitrons) - Amplification and insertion of repeat elements - Large-scale rearrangements (in particular, duplications) • Reverse transcription-dependent retrotransposons (retroviral-like, LINEs, SINEs) - Amplification and insertion of repeat elements - Integration of processed RNA cDNA copies - Small-scale movement of genomic segments (e.g. exon shuffling) • Homing and retrohoming introns Natural genetic engineering of sequenced genomes - protein coding sequences a. Coding region (codons) 0 50 150 100 19 LTR Chemokine 200 700 1000 600 500 400 300 0 100 900 800 mRNA (bp) b. Coding region (codons) Ion Channel 50 150 200 250 350 0 100 400 300 B1 RSINE1 23 21 34 20 24 32 24 27 3 B3 B1 B4 B1 B3 B4 B2 600 700 900 800 300 100 2800 2700 200 1800 2200 1700 2400 1000 400 1200 1300 2300 1900 500 2000 1600 1100 2600 1500 1400 0 2500 2100 mRNA (bp) Nekrutenko, A. and W.-H. Li. 2001. Transposable elements are found in a large number of human protein coding regions. Trends in Genetics 17: 619-625 Leaf wounding and retrotransposon transcription http://www-biocel.versailles.inra.fr/Anglais/03Transposon.html The expression of the tobacco Tnt1 retrotransposon is induced by wounding : the expression of the LTR-GUS construct is detected by a blue staining surrounding injury points in transgenic tomato (A), tobacco (B) and Arabidopsis (C) plants. M.-A. Grandbastien et al. Stress activation and genomic impact of Tnt1 retrotransposons in Solanaceae. Cytogenetic and Genome Research 2005;110:229-241 Targeting of natural genetic engineering Known molecular mechanisms: • Sequence recognition by proteins (yeast mating-type switching, ribosomal LINE elements, homing introns, VDJ joining); • Protein-protein interaction wth transcription factors or chromatin proteins (Ty retrotransposon targeting); • Sequence recognition by RNA (reverse splicing of group II retrohoming introns); • Transcriptional activation of target DNA (somatic hypermutation; class-switch recombination). Unknown mechanisms: • Telomere targeting of certain LINE elements in insects; • HIV & MLV targeting upstream of transcribed regions; • P factor homing directed by transcription, chromatin signals; • P factor targeting to heat-shock promoters. Shapiro, JA. 2005. A 21st Century View Of Evolution: Genome System Architecture, Repetitive DNA, And Natural Genetic Engineering. Gene 345: 91-100 Yeast Ty5 targeting S. Sandmeyer. Integration by design. PNAS, May 13, 2003; 100(10): 5586 - 5588. Advantages of non-random searches of genome space at evolutionary crises • Genome changes occur under stress or other conditions, when they are most likely to prove beneficial; • Multiple related changes can occur when a particular natural genetic engineering system is activated; • Rearrangement of proven genomic components increases the chance that novel combinations will be functional; • Targeting can increase the probability of functional integration and reduce the risk of system damage (ensure syntactically correct changes in the program architecture, as in GP); • Rearrangements followed by localized changes provide opportunities for fine tuning once novel function has been achieved..
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