1 / 46

Shiri Freilich Janet Thornton’s group, EBI Cambridge University

Relating the evolution of gene content to tissue specialization. Shiri Freilich Janet Thornton’s group, EBI Cambridge University. “...And when he was 93, Grandpa decided that the time had come for a man-to-man conversation. (I was 36 at the time, I have been married for 15 years).

denna
Download Presentation

Shiri Freilich Janet Thornton’s group, EBI Cambridge University

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Relating the evolution of gene content to tissue specialization ShiriFreilich Janet Thornton’s group, EBI Cambridge University

  2. “...And when he was 93, Grandpa decided that the time had come for a man-to-man conversation. (I was 36 at the time, I have been married for 15 years). ‘All my life I am all the time looking at woman, looking and learning. Nu, and what I learned, I want to learn to you now also.’ ‘Woman,in some ways is just like us exactly the same. But in some other ways a woman is entirely different.’ ‘But you know what? In which ways a woman is just like us and in which ways she is very different – nu, on this I am still working’.” (Amos Oz, A Tale of Love and Darkness)

  3. The full genome sequence from various species can highlight the common versus unique

  4. What’s new?

  5. The transition from unicellularity to multicellularity as an interior design challenge - gene

  6. Overview • Part 1: Expression pattern of ‘old’ and ‘new’ proteins in mouse tissues • Part 2: Expression pattern of singleton and duplicate proteins in mouse tissues • Part 3: The evolution of tissue-specific metabolic pathways in mammals

  7. Part 1: Relating age and function of a protein to its expression pattern in mouse tissues A collaboration with Tom Freeman’s group (MRC RFCGR) Freilich et al, Genome Biol. 2005;6(7):R56.

  8. Processing mouse expression and sequence data

  9. Classification of mouse proteins into phylogenetic groups

  10. enzymes transporters signal transduction transcription regul. Fraction Tissue type Tissues have a similar composition of functional classes

  11. universal eukaryote sp. metazoan sp. mammalian sp. Fraction Tissue type Tissues have a similar composition of phylogenetic classes

  12. Fraction Expression distribution of proteins from different categories • Tissues have almost identical functional/ phylogenetic composition • Tissue diversity must be achieved through differences in the protein composition within each category • Do proteins from different categories duffer in their expression pattern? Number of tissues where protein is expressed

  13. enzymes Metabolic proteins transporters Mouse proteins classified into functional groups signal transduction Regulatory proteins transcription regul. ~1/3 ~1/10 Fraction Number of tissues where is expressed Regulatory proteins are more specifically expressed

  14. universal Present in a unicellular ancestor of metazoa eukaryote sp. Mouse proteins classified into phyletic groups metazoan sp. Specific to metzoa mammalian sp. Fraction Number of tissues where protein is expressed Metazoan-specific proteins are more specifically expressed

  15. Functional categories overlap with phylogenetic categories • Most of the pre-metazoan proteins are metabolic proteins (transporters and enzymes) • Most of the metazoan-specific proteins are regulatory proteins (signal transduction and transcription regulation)

  16. Identifying the dominant influence: function or age Fraction Number of tissues where protein is expressed • Obvious differences between ‘old’ and ‘new’ proteins, within the metabolic functional group • Yet, less than 1/3 of the pre-metazoa proteins are expressed in all tissues

  17. Still, some of the pre-metazoa proteins are tissue specific • Functions occurring in the unicellular cell become tissue-specific in multicellular species (Ldh example) • Universal genes that have been duplicated become specific to a tissue whilst a second copy maintains its original expression pattern(Pgk-2 example)

  18. Part 2: Relating duplication events to expression pattern in mouse tissues Freilich et al, Genome Biol. 2006;7. “…duplication events had contributed greatly to the attainment of the complex body organisation in metazoa, where cells having identical genetic material can differentiate … due to the presence of duplicated genes in their genomes” Ohno S. (1970). Evolution by gene duplication.

  19. The subfunctionalization model Lynch M & Force A, Genetics. 154 (2000): The division of expression of an ancestor gene between its daughter duplicates promotes the retention of a gene in the genome

  20. Microarray expression data provide support to the subfunctionalization model • Gu et al: expression divergence between duplicate genes increases with evolutionary time (differentiation modes in yeast).Trends Genet. 2002;18: 609-13. • Makova et al: spatial expression divergence between duplicate genes increases with evolutionary time (human tissues).Genome Res. 2003;13:1638-45 . • Huminiecki and Wolfe: a general trend for increased tissue-specificity of expression as family size increasewas observed for mammalian genes. Genome Res. 2004;14:1870-79 .

  21. Project Overview:The relationship between gene duplication and breadth of expression Protein’s perspective: • Does duplication event lead to an increase in tissue specificity? Time of duplication perspective: • Does the date of duplication event matters? (i.e., do duplication events occurring in the ancestral unicellular lead to an increase in tissue specificity) Protein-family perspective: • does a protein family maintain a non-specific expression pattern? (i.e., is a specific expression of proteins from big families complementary) (Freilich et al,Genome Biol. 2006;7(10):R89)

  22. Proteins with many close homologues (417) Singleton proteins are more globally expressed Singletons (570) Duplicate proteins (1886) Fraction Number of tissues in which protein is expressed

  23. Singletons Duplicate proteins Mean number of tissues Groups of proteins, ordered by their number of homologues Negative correlation between expression breadth and number of homologues

  24. Singletons Correlation -0.20 P-value 1.5e-55 Correlation -0.20 P-value 1.5e-55 Duplicate proteins Mean number of expressed tissues Number of tissues Number of homologues proteins Large variation

  25. Increase in tissue specificity ? Global expression Does the date of duplication event matter?(i.e., do duplication events occurring in the ancestral unicellular lead to an increase in tissue specificity)

  26. Identifying ‘old’ and ‘new’ duplications

  27. Only post-multicelullarity duplication events lead to expression specificity

  28. Complementary expression ? Overlapping expression The protein-family perspective:Is the specific expression of family members complementary? Proteins from big families tend to be more specifically expressed. Does a protein family maintain a non specific expression pattern?

  29. Calculating the cumulative tissue distribution of protein families

  30. Singletons Families with any expression information Average tissue-coverage of protein families Families with >=75% expression information Protein families, ordered by size Cumulative tissue distribution of protein families is not correlated with family size Complementary expression pattern in protein families: While a duplication event leads to a tissue specialisation of one or both copy, the total tissue-distribution of the protein family remains constant.

  31. The findings support the subfunctionalization model Protein’s perspective: • Does duplication event lead to an increase in tissue specificity? Yes Time of duplication perspective: • Does the date of duplication event maters? only duplication events that that place in a multicellular species lead to a specific expression -> suggests that expression divergence, following gene duplication, promotes the retention of a gene in the genome Protein-family perspective: • Does a protein family maintain a non-specific expression pattern? Yes -> suggests the division of expression between family members

  32. STEROID HORMONE METABOLISM Part 3:The evolution of the mammalian metabolic pathways Some of the tissue-specific pathways are specific to mammals. Can we understand how tissue-differentiation of animals’ metabolism reflects their evolution? Freilich et al, BMC evolutionary biology 2008, 8:247.

  33. Why studying metabolic networks? • Metabolic networks’ structure and composition are well defined • Available metabolic databases • Genotype is highly related to phenotype

  34. STEROID HORMONE METABOLISM The structure of the KEGG database

  35. The reactions within a pathway can be absent/present in a species Arabidopsis Thaliana Homo Sapiens

  36. Project overview: • Identification of pathways absent/present in a species • Classification of human pathways according to their phyletic origin • Characterization of lineage-specific metabolic pathways

  37. All pathways in human (metabolic) Universal pathways Metazoan-specific pathways Eukaryota-specific pathways Mammalian-specific pathways Phylogenetic classification of human pathways

  38. Phylogenetic classification of human pathways 10 Metazoan-specific pathways 33 Universal pathways Tissue specific activities: Neuronal guidance, hormonal activity, digestion Metabolic skeleton: sugars, nucleotides, some amino-acids, energy 8 Eukaryota-specific pathways 14 Mammalian-spc. pathways Tissue specific activities and intracellular signaling (blood cell recognition) Components of the Eukaryotic membrane (sphingolipids, glycosaminoglycan)

  39. The pathways can be linked to form a network

  40. Universal pathways Eukaryota-spc. pathways Metazoan-spc. pathways Mammalian-spc. pathways The network structure of the metabolic pathways

  41. The integration of the steroid biosynthesis pathway into the sterol biosynthesis pathway Universal Eukaryota Human sterol cholesterol steroid hormone bile acid

  42. From manually selected examples to a computational approach Creating a list of adjacent reactions: 2.7.4.2 -> 4.1.1.33 4.1.1.33->2.5.1.1 .. 2.5.1.1->2.5.1.21 2.5.1.21->1.14.99.7

  43. Using the adjacency list for a large-scale characterizationof the metabolic network

  44. What’s new (metabolic pathways)?

  45. Summary • ‘New’ genes tend to be more tissue-specific, ‘ancient’ genes tend to be globally expressed • Despite this trend, many metazoan genes are ubiquitous and many universal proteins are tissue specific • ‘New’ duplications of ‘old’ and ‘new’ proteins lead to a more specific expression, and therefore can facilitate the evolution of new, tissue-specific, functions • The core of metabolic-pathways, inherited from a uniclellular ancestor, provides a platform for the evolution of mammalian-specific, tissue-specific pathways

  46. Thanks Thornton Group Janet Thornton Tim Massingham Eric Blanc Expression data: Tom Freeman Sumit Bhattacharyya

More Related