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Biosci 755  Genomics and Gene Expression 9 sessions: 7, 14, 21 &  28 March, 4 April, 2, 9, 16 & 23 May. Lecturers Associate Professor Brian Murray - course coordinator Associate Professor Rob Young Professor Russell Snell Each responsible for three sessions, the first will be an overview lecture of the general area and the second and third will be student seminars. Attendance at ALL sessions is compulsory.
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Genome structure, organization and evolution - the wider perspective ,[object Object],[object Object]
Overview of five topics today ,[object Object],[object Object],[object Object],[object Object],[object Object]
One key question to keep in mind is, why are eukaryote genomes so variable in some aspects and constant in others? ,[object Object],[object Object]
[object Object],[object Object],[object Object]
Nature 470: 289-294 10 February 2011
[object Object],[object Object],[object Object],1. Chromosome number and karyotype variation
[object Object],[object Object],[object Object],[object Object]
Variation in chromosome number and size in the plant family Aloaceae but the karyotypes are always bimodal.  This family shows karyotypic orthoselection. From: Brandham and Doherty (1998) Genome size variation in the Aloeaceae, an angiosperm family showing karyotypic orhtoselection. Annals of Botany  82  (Supplement A): 67-73.
Karyotypes of these three species from the Commelinaceae are highly diverse, in size, number and shape. From: Jones and Colden (1972) Chromosomes and the classification of the Commelinaceae. Botanical Journal of the Linnean Society  65 : 129-162.
How do differences in chromosome number arise? ,[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],2. Variation in genome size
[object Object],From: Leitch et al. (2007) Journal of Evolutionary Biology  20 : 2296-2308.
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What are the key mechanisms that affect genome size identified by recent genome analyses ?  ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Growing chromosomes in  Nicotiana  hybrids and mouse cell cultures
Gene duplication in  Arabidopsis ,[object Object],Dot plot showing location of duplicate genes Location of duplications on  Arabidopsis  chromosomes
[object Object],Duplicate segments in rice
Duplications can be dated by computing the number of substitutions per silent site (Ks), used here to identify segmental duplications in rice. ,[object Object],[object Object]
Transposable element activity - Retrotransposons ,[object Object],From: Griffiths et al. (2005) Introduction to Genetic Analysis, Freeman.
Molecular clock can be used to ‘date’ the time of insertion of LTR retrotransposons ,[object Object],[object Object]
Model for the evolution of the  Hv-elF4E  locus in barley  ,[object Object]
 
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
From: Lynch M (2007) The Origins of Genome Architecture, Sinauer.
[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],The microbial origin of genes in the  Arabidopsis  genome
What about mechanisms of reduction? ,[object Object],[object Object]
[object Object],From: Devos K et al. (2002) Genome size reduction through illegitimate recombination counteracts genome expansion in  Arabidopsis .  Genome Research 12: 1075-1079.
[object Object],Evidence for genome reduction in  Arabidopsis
Other possible mechanisms to prevent the proliferation of retroelements ,[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],3. Chromosome order in the nucleus
[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object]
[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object]
Mechanisms for the initiation of heterochromatin assembly. Grewal and Jia  Nature Reviews Genetics   8 , 35 –46 (January 2007) | doi:10.1038/nrg2008 Initiation by recognition of transcription factors (TF) or repetitive DNA, then recruit histone methyltransferase (HMT) and histone deacetylase (HDAC) that modify histone tails and change chromatin conformation.  Boundary elements prevent the spread of heterochromatin.
[object Object],[object Object],[object Object]
The multiple interactions of heterochromatin with chromosome structure, behaviour and gene activity Grewal and Jia  Nature Reviews Genetics   8 , 35 –46 (January 2007) | doi:10.1038/nrg2008
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[object Object]
From: KL Adams & JF Wendel (2005) Polyploidy and genome evolution in plants.  Current Opinion in Plant Biology 8: 135-141. Inferred polyploidy events during the evolution of angiosperms.
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Duplicate genes can either be preserved or lost ,[object Object],[object Object],[object Object],[object Object]
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[object Object],[object Object],[object Object]

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Plang functional genome

  • 1. Biosci 755 Genomics and Gene Expression 9 sessions: 7, 14, 21 & 28 March, 4 April, 2, 9, 16 & 23 May. Lecturers Associate Professor Brian Murray - course coordinator Associate Professor Rob Young Professor Russell Snell Each responsible for three sessions, the first will be an overview lecture of the general area and the second and third will be student seminars. Attendance at ALL sessions is compulsory.
  • 2.
  • 3.
  • 4.  
  • 5.  
  • 6.  
  • 7.
  • 8.
  • 9.
  • 10.
  • 11. Nature 470: 289-294 10 February 2011
  • 12.
  • 13.
  • 14. Variation in chromosome number and size in the plant family Aloaceae but the karyotypes are always bimodal. This family shows karyotypic orthoselection. From: Brandham and Doherty (1998) Genome size variation in the Aloeaceae, an angiosperm family showing karyotypic orhtoselection. Annals of Botany 82 (Supplement A): 67-73.
  • 15. Karyotypes of these three species from the Commelinaceae are highly diverse, in size, number and shape. From: Jones and Colden (1972) Chromosomes and the classification of the Commelinaceae. Botanical Journal of the Linnean Society 65 : 129-162.
  • 16.
  • 17.
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  • 23. Growing chromosomes in Nicotiana hybrids and mouse cell cultures
  • 24.
  • 25.
  • 26.
  • 27.
  • 28.
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  • 30.  
  • 31.
  • 32. From: Lynch M (2007) The Origins of Genome Architecture, Sinauer.
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  • 34.
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  • 45. Mechanisms for the initiation of heterochromatin assembly. Grewal and Jia Nature Reviews Genetics 8 , 35 –46 (January 2007) | doi:10.1038/nrg2008 Initiation by recognition of transcription factors (TF) or repetitive DNA, then recruit histone methyltransferase (HMT) and histone deacetylase (HDAC) that modify histone tails and change chromatin conformation. Boundary elements prevent the spread of heterochromatin.
  • 46.
  • 47. The multiple interactions of heterochromatin with chromosome structure, behaviour and gene activity Grewal and Jia Nature Reviews Genetics 8 , 35 –46 (January 2007) | doi:10.1038/nrg2008
  • 48.
  • 49.
  • 50. From: KL Adams & JF Wendel (2005) Polyploidy and genome evolution in plants. Current Opinion in Plant Biology 8: 135-141. Inferred polyploidy events during the evolution of angiosperms.
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  • 54.

Editor's Notes

  1. Three plant genomes sequenced in full but many smaller regions of many species have also been sequenced. Need to appreciate that this is a dynamic process and can go in either direction, up or down.
  2. Pre full sequence of Arabidopsis showing that many genes are present in duplicate locations but their order has not been well conserved. Duplicated regions are represented on the different chromosomes in the same colour. Suggestion here of ancient polyploidy in this diploid species.
  3. More recently published sequence in rice also shows extensive segmental duplication .
  4. Duplication events can be dated by looking at the rate of synonymous site substitutions in the duplicated segments. In rice there is a sub-set of more recent duplications.
  5. Can also study retrotransposons and these can also be used to date genomic changes - genome archaeology. Many retrotransposons have long terminal repeats that have the same sequence at insertion. Use molecular clock on number of changes between LTRs to date their insertion. Dot plot alingment of contig with itself. Parallel or perpendicular lines show repeats.
  6. History of the region presented here showing duplication (D), deletion (L) and insertion of transposable elements (T).
  7. Detail of previous figure, gene in grey, Xalas has inserted into Rada in ancestor locus.
  8. Transposons are also important in Triticeae. Also shows that many of the elements are active, not methylated.
  9. Hybrid derived species have 50% more DNA than parents, despite multiple origins hybrid species (except H. deserticola) are constant across range. Natural and synthetic hybrids don’t show increased values of hybrid species.
  10. Similarity of c. 25000 Arabidopsis proteins to c. 52000 proteins from 20 reference genomes. Suggests that c. 4500 Arabidopsis genes were acquired from a cyanobacterial ancestor of plastids. Black bars how many trees homologue shares in common with Arabidopsis, grey bars are number of best matches in genome at different degrees of stringency.
  11. Genome size increase may be counterbalanced by illegitimate recombination, can be identified by finding solo LTRs as in B or clearly different LTRs as in C.
  12. Frequency of a variety of different events observed in the Arabidopsis sequence.