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Genome architecture and evolution
Key considerations: Genes Chromosomes C value paradox Gene regulation Epigenetics Transposable elements
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Genes Other RNAs? DNA ……..……..mRNA……….…….Protein Plant
Transcription tRNA rRNA Translation Plant Estimated # genes Arabidposis thaliana 27,000 Fragaria vesca 35,000 Theobroma cacao 29,000 Zea mays 40,000 Other RNAs?
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Genes (classically..) DNA specifying a protein 200 – 2,000,000 nt (bp)
promoter Coding region Exon Intron Exon Intron Exon Start codon Stop codon 5’UTR 3’UTR Basal promoter +1 Termination signal ORF mRNA CDS
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Chromosomes Plant 2n = _X = _ Arabidposis thaliana 2n = 2x = 10 Fragaria vesca 2n = 2x = 14 Theobroma cacao 2n = 2x = 20 Zea mays F. vesca: 35,000 genes/7 chromosomes = 5,000 genes/chromosome?
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Genes, chromosomes, and genomes
F. vesca: 2n = 2x = 14 genome = 240 Mb average gene ~ 3kb 79,333 genes? 11,333 genes/chromosome? 35,000 genes….. ~ 5,000 genes/chromosome What’s the rest of the genome???????
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C-value paradox “Organisms of similar evolutionary complexity
differ vastly in DNA content” Federoff, N Science. 338: 1 pg = 978 Mb
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The C-value paradox Fig. 1.The C-value paradox. The range of haploid genome sizes is shown in kilobases for the groups of organisms listed on the left. [Adapted from an image by Steven M. Carr, Memorial University of Newfoundland] Fedoroff Science 2012;338:
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C-value paradox Plant Genome size # Genes Arabidposis thaliana 135 Mb
27,000 Fragaria vesca 240 Mb 35,000 Theobroma cacao 415 Mb 29,000 Zea mays 2,300 Mb 40,000 Pinus taeda 23,200Mb 50,000 Paris japonica 148,852Mb ??
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C-value paradox Junk??????? Shining a Light on the
Genome’s ‘Dark Matter’
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40% of all human disease-related SNPs are OUTSIDE of genes
Gene regulation Pennisi, E Science 330:1614. 40% of all human disease-related SNPs are OUTSIDE of genes The dark matter is conserved and therefore must have a function DNA sequences in the dark matter are involved in gene regulation ~80% of the genome is transcribed but “genes” account for ~2% RNAs of all shapes and sizes: RNAi lncRNA
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Epigenetics Observe changes in phenotype without changes in genotype - due to alternative regulation ( 0 – 100%) of the gene Methylation expression Acetylation expression
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Epigenetics Facultative heterochromatin:
Holoch and Moazed Nature Genetics
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Transposable elements
DNA sequences that can move to new sites in the genome More than half the DNA in many eukaryotes Two major classes: Transposons: Move via a DNA cut-and-paste mechanism Retrotransposons: Move via an RNA intermediate Potentially disruptive – can eliminate gene function. Therefore, usually epigenetically silenced
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Transposable elements
Federoff (2012) argues that TE’s, via altering gene regulation, account for the “evolvability” of the “massive and messy genomes” characteristic of higher plants Create new genes Modify genes Program and re-program genes Transposition events lead to genome expansion and help to explain the C value paradox
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Transposable elements
Transposition events lead to genome expansion and help to explain the C value paradox: TEs nested within TEs nested within TEs
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Transposable elements
The arrangement of retrotransposons in the maize adh1-F region Fig. 6.The arrangement of retrotransposons in the maize adh1-F region. The short lines represent retrotransposons, with the internal domains represented in orange and the LTRs in yellow. Younger insertions within older insertions are represented by the successive rows from the bottom to the top of the diagram. Small arrows show the direction of transcription of the genes shown under the long blue line that represents the sequence in the vicinity of the adh1 gene. [Adapted with permission from (102)] N V Fedoroff Science 2012;338: Published by AAAS
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Transposable elements
Sequence adjacent to the bronze (bz) gene in different lines of maize Fig. 7.The organization of the sequence adjacent to the bronze (bz) gene in eight different lines (haplotypes) of maize. The genes in this region are shown in the top diagram: bz, stc1, rpl35A, tac6058, hypro1, znf, tac7077, and uce2. The orientation of the gene is indicated by the direction of the green pentagon, pointing in the direction of transcription; exons are represented in dark green and introns in light green. Each haplotype is identified by its name and the size of the cloned NotI fragment. The same symbols are used for gene fragments carried by Helitrons (Hels), which are represented as bidirectional arrows below the line for each haplotype. Vacant sites for HelA and HelB are provided as reference points and marked by short vertical red bars. Dashed lines represent deletions. Retrotransposons are represented by yellow bars. DNA transposons and TAFTs (TA-flanked transposons), which are probably also DNA transposons, are represented by red triangles; small insertions are represented by light blue triangles. [Redrawn with permission from (113)] N V Fedoroff Science 2012;338: Published by AAAS
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Transposable elements
85% of the maize genome consists of transposons Transposition events are in real time: differences between maize inbreds Transposons can move large bocks of intervening DNA Transposases are the products of the most abundant genes on earth
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Transposable elements
~ 24% of the cacao genome ~ 21% of the Fragaria genome ~68,000 TE-related sequences in cacao “Gaucho” is a retrotransposon ~ 11Kb in length and present ~1,000 times “The lack of highly abundant LTR transposons is likely to be the reason F. vesca has a relatively small-size genome”
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Transposable elements
Reid and Ross. Mendel’s genes….An Ac/Ds-like 0.8 kb insertion: round vs. wrinkled peas Transposon tagging – find genes by mutation due to TE Holoch and Moazed. RNAi….Transposons held in check by epigenetic mechanisms
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Genome architecture and evolution
Plant #genes (est) 2n = _x = _ Genome size Arabidposis thaliana 27,000 2n = 2x = 10 135 Mb Fragaria vesca 35,000 2n = 2x = 14 240 Mb Theobroma cacao 29,000 2n = 2x = 20 415 Mb Zea mays 40,000 2,300 Mb Pinus taeda 50,000 2n = 2x =24 23,200Mb Paris japonica ?? 2n = 8x = 40 148,852Mb S. Wessler on Transposable elements: Review of retroviruses: Review of cut and past transposition:
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