1. Genomics Chapter 18

2. 2 Mapping Genomes Maps of genomes can be divided into 2 types -Genetic maps -Abstract maps that place the relative location of genes on chromosomes based on recombination frequency -Physical maps -Use landmarks within DNA sequences, ranging from restriction sites to the actual DNA sequence

3. 3 Physical Maps Distances between “landmarks” are measured in base-pairs -1000 basepairs (bp) = 1 kilobase (kb) Knowledge of DNA sequence is not necessary There are three main types of physical maps -Restriction maps -Cytological maps -Radiation hybrid maps

4. 4 Physical Maps Restriction maps -The first physical maps -Based on distances between restriction sites -Overlap between smaller segments can be used to assemble them into a contig -Continuous segment of the genome

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7. 7 Physical Maps Cytological maps -Employ stains that generate reproducible patterns of bands on the chromosomes -Divide chromosomes into subregions -Provide a map of the whole genome, but at low resolution -Cloned DNA is correlated with map using fluorescent in situ hybridization (FISH)

8. 8 Physical Maps

9. 9 Radiation hybrid maps -Use radiation to fragment chromosomes randomly -Fragments are then recovered by fusing irradiated cell to another cell -Usually a rodent cell -Fragments can be identified based on banding patterns or FISH

10. 10 Physical Maps Sequence-tagged sites -An STS is a small stretch of DNA that is unique in the genome -Only 200-500 bp -Boundary is defined by PCR primers -Identified using any DNA as a template -STSs essentially provide a scaffold for assembling genome sequences

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13. 13 Genetic Maps Genetic maps are measured in centimorgans -1 cM = 1% recombination frequency Linkage mapping can be done without knowing the DNA sequence of a gene -Limitations: 1. Genetic distance does not directly correspond to actual physical distance 2. Not all genes have obvious phenotypes

14. 14 Genetic Maps Most common markers are short repeat sequences called, short tandem repeats, or STR loci -Differ in repeat length between individuals -13 form the basis of modern DNA fingerprinting developed by the FBI -Cataloged in the CODIS database to identify criminal offenders

15. 15 Genetic Maps Genetic and physical maps can be correlated -Any cloned gene can be placed within the genome and can also be mapped genetically

16. 16 Genetic Maps All of these different kinds of maps are stored in databases -The National Center for Biotechnology Information (NCBI) serves as the US repository for these data and more -Similar databases exist in Europe and Japan

17. 17 Whole Genome Sequencing The ultimate physical map is the base-pair sequence of the entire genome -Requires use of high-throughout automated sequencing and computer analysis

18. 18 Whole Genome Sequencing Sequencers provide accurate sequences for DNA segments up to 800 bp long -To reduce errors, 5-10 copies of a genome are sequenced and compared Vectors use to clone large pieces of DNA: -Yeast artificial chromosomes (YACs) -Bacterial artificial chromosomes (BACs) -Human artificial chromosomes (HACs) -Are circular, at present

19. 19 Whole Genome Sequencing Clone-by-clone sequencing -Overlapping regions between BAC clones are identified by restriction mapping or STS analysis Shotgun sequencing -DNA is randomly cut into smaller fragments, cloned and then sequenced -Computers put together the overlaps -Sequence is not tied to other information

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22. 22 The Human Genome Project Originated in 1990 by the International Human Genome Sequencing Consortium Craig Venter formed a private company, and entered the “race” in May, 1998 In 2001, both groups published a draft sequence -Contained numerous gaps

23. 23 The Human Genome Project In 2004, the “finished” sequence was published as the reference sequence (REF-SEQ) in databases -3.2 gigabasepairs -1 Gb = 1 billion basepairs -Contains a 400-fold reduction in gaps -99% of euchromatic sequence -Error rate = 1 per 100,000 bases

24. 24 Characterizing Genomes The Human Genome Project found fewer genes than expected -Initial estimate was 100,000 genes -Number now appears to be about 25,000! In general, eukaryotic genomes are larger and have more genes than those of prokaryotes -However, the complexity of an organism is not necessarily related to its gene number

25. 25 Characterizing Genomes

26. 26 Finding Genes Genes are identified by open reading frames -An ORF begins with a start codon and contains no stop codon for a distance long enough to encode a protein Sequence annotation -The addition of information, such as ORFs, to the basic sequence information

27. 27 Finding Genes BLAST -A search algorithm used to search NCBI databases for homologous sequences -Permits researchers to infer functions for isolated molecular clones Bioinformatics -Use of computer programs to search for genes, and to assemble and compare genomes

28. 28 Genome Organization Genomes consist of two main regions -Coding DNA -Contains genes than encode proteins -Noncoding DNA -Regions that do not encode proteins

29. 29 Coding DNA in Eukaryotes Four different classes are found: -Single-copy genes : Includes most genes -Segmental duplications : Blocks of genes copied from one chromosome to another -Multigene families : Groups of related but distinctly different genes -Tandem clusters : Identical copies of genes occurring together in clusters -Also include rRNA genes

30. 30 Noncoding DNA in Eukaryotes Each cell in our bodies has about 6 feet of DNA stuffed into it -However, less than one inch is devoted to genes! Six major types of noncoding human DNA have been described

31. 31 Noncoding DNA in Eukaryotes Noncoding DNA within genes -Protein-encoding exons are embedded within much larger noncoding introns Structural DNA -Called constitutive heterochromatin -Localized to centromeres and telomeres Simple sequence repeats (SSRs) -One- to six-nucleotide sequences repeated thousands of times

32. 32 Noncoding DNA in Eukaryotes Segmental duplications -Consist of 10,000 to 300,000 bp that have duplicated and moved Pseudogenes -Inactive genes

33. 33 Noncoding DNA in Eukaryotes Transposable elements (transposons) -Mobile genetic elements -Four types: -Long interspersed elements (LINEs) -Short interspersed elements (SINEs) -Long terminal repeats (LTRs) -Dead transposons

34. 34 Noncoding DNA in Eukaryotes

35. 35 Expressed Sequence Tags ESTs can identify genes that are expressed -They are generated by sequencing the ends of randomly selected cDNAs ESTs have identified 87,000 cDNAs in different human tissues -But how can 25,000 human genes encode three to four times as many proteins? -Alternative splicing yields different proteins with different functions

36. 36 Alternative Splicing

37. 37 Variation in the Human Genome Single-nucleotide polymorphisms (SNPs) are sites where individuals differ by only one nucleotide -Must be found in at least 1% of population Haplotypes are regions of the chromosome that are not exchanged by recombination -Tendency for genes not to be randomized is called linkage disequilibrium -Can be used to map genes

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41. 41 Genomics Comparative genomics, the study of whole genome maps of organisms, has revealed similarities among them -For example, over half of Drosophila genes have human counterparts Synteny refers to the conserved arrangements of DNA segments in related genomes -Allows comparisons of unsequenced genomes

42. 42 Genomics

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44. 44 Genomics Organellar genomes -Mitochondria and chloroplasts are descendants of ancient endosymbiotic bacterial cells -Over time, their genomes exchanged genes with the nuclear genome -Both organelles contain polypeptides encoded by the nucleus

45. 45 Genomics Functional genomics is the study of the function of genes and their products DNA microarrays (“gene chips”) enable the analysis of gene expression at the whole-genome level -DNA fragments are deposited on a slide -Probed with labeled mRNA from different sources -Active/inactive genes are identified

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48. 48 Genomics Transgenics is the creation of organisms containing genes from other species (transgenic organisms -Can be used to determine whether: -A gene identified by an annotation program is really functional in vivo -Homologous genes from different species have the same function

49. 49 Genomics

50. 50 Genomics

51. 51 Genomics

52. 52 Genomics

53. 53 Proteomics Proteomics is the study of the proteome -All the proteins encoded by the genome The transcriptome consists of all the RNA that is present in a cell or tissue

54. 54 Proteomics Proteins are much more difficult to study than DNA because of: -Post-translational modifications -Alternative splicing However, databases containing the known protein structural motifs exist -These can be searched to predict the structure and function of gene sequences

55. 55 Proteomics

56. 56 Proteomics Protein microarrays are being used to study large numbers of proteins simultaneously -Can be probed using: -Antibodies to specific proteins -Specific proteins -Small molecules The yeast two-hybrid system has generated large-scale maps of interacting proteins

57. 57 Applications of Genomics The genomics revolution will have a lasting effect on how we think about living systems The immediate impact of genomics is being seen in diagnostics -Identifying genetic abnormalities -Identifying victims by their remains -Distinguishing between naturally occurring and intentional outbreaks of infections

58. 58 Applications of Genomics

59. 59 Applications of Genomics Genomics has also helped in agriculture -Improvement in the yield and nutritional quality of rice -Doubling of world grain production in last 50 years, with only a 1% cropland increase

60. 60 Applications of Genomics Genome science is also a source of ethical challenges and dilemmas -Gene patents -Should the sequence/use of genes be freely available or can it be patented? -Privacy concerns -Could one be discriminated against because their SNP profile indicates susceptibility to a disease?