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Genomes & Genomics

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Genome, the entire genetic complement of an organismGenomics, research that addresses all or a substantial portion of an organism’s genome Includes physical mapping & sequencing of all or a large part

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Слайд 1Genomes & Genomics

Genomes & Genomics

Слайд 2Genome, the entire genetic complement of an organism
Genomics, research that

addresses all or a substantial portion of an organism’s genome


Includes physical mapping & sequencing of all or a large part of a genome or chromosome
Genome, the entire genetic complement of an organismGenomics, research that addresses all or a substantial portion of

Слайд 3Why Study Genomes of Different Organisms?
To understand the genetics behind

diseases (Homo sapien & Canis familiarus)
To

learn more about human pathogens & how to prevent or treat their infections (Clostridium tetani, Bacillus anthacis, & Haemophilus influenzae)
Understand & improve the genetics of commercial organisms (Lactococcus lactis, Oryza sativa, Bos taurus, & Gallus gallus)
To discover the workings of unusual or odd organisms (Bdellovibrio bacteriovorus & Deinococcus radiodurans)
To understand phyolegeny
Why Study Genomes of Different Organisms?To understand the genetics behind diseases 		    (Homo sapien

Слайд 4How Many Genomes Have Been Sequenced?
Completed Draft In Progress
Eukaryote 24 129 182
Archaea 46 4 27
Eubacteria 521 414 402
Viral

1703
(NCBI 9/4/07)

How Many Genomes Have Been Sequenced?		Completed	Draft		In ProgressEukaryote	 24		129		182Archaea	 46		4		27Eubacteria	 521		414		402Viral		 1703						(NCBI 9/4/07)

Слайд 5


How Do We Measure a Genome?

1 base=1 nucleotide=1basepair (bp)
1000bases=1kilobase

(Kb)
1000kb=1megabase (Mb)
1000mb=1gigabase (Gb)

How Do We Measure a Genome?	1 base=1 nucleotide=1basepair (bp)	1000bases=1kilobase (Kb)	1000kb=1megabase (Mb)	1000mb=1gigabase (Gb)

Слайд 6Genome Sizes (haploid)
Organism Genome in Mb
E. coli 4.64
Yeast 12
Nematode 97
Fruit Fly 170
Pufferfish 345
Human 3200
Lungfish 129000

Genome Sizes (haploid)Organism			Genome in MbE. coli				4.64Yeast				12Nematode			97Fruit Fly			170Pufferfish			345Human			3200Lungfish			129000

Слайд 7105 106 107 108 109 1010 1011

1012
basepairs
Amount of DNA in a Genome Does Not Correlate

with Complexity
105	106	107	108	109    1010   1011    1012basepairsAmount of DNA in a Genome

Слайд 8http://www.ornl.gov/sci/techresources/Human_Genome/publicat/primer/fig14.html

http://www.ornl.gov/sci/techresources/Human_Genome/publicat/primer/fig14.html

Слайд 9http://www.chromosome18.org/graphics/Slide.gif
http://uk.encarta.msn.com/media_121636626/Fruit_Fly_Chromosomes.html
Genomes Are Organized Into Chromosomes
Human
Fruit Fly

http://www.chromosome18.org/graphics/Slide.gifhttp://uk.encarta.msn.com/media_121636626/Fruit_Fly_Chromosomes.htmlGenomes Are Organized Into ChromosomesHumanFruit Fly

Слайд 10Chromosome Number Is Species Specific
Diploid Number 2n
Human 46
Mouse 40
Fruit Fly 8
Dog 78
Arabidopsis 10
Corn 20
Yeast 32
Crayfish 200

Chromosome Number Is Species Specific		Diploid Number 2nHuman		46Mouse			40Fruit Fly		8Dog			78Arabidopsis		10Corn			20Yeast			32Crayfish		200

Слайд 11How many genes do we have?
Original estimate was between 50

000 to 100 000 genes
We now think human have ~

25 000 genes
How does this compare to other organisms?
Mice have ~30 000 genes
Pufferfish have ~35 000 gene
The nematode (C. elegans), has ~19 000
Yeast (S. cerevisiae) there are ~6000 genes
The microbe responsible for tuberculosis has ~4000
How many genes do we have?Original estimate was between 50 000 to 100 000 genesWe now think

Слайд 12http://www.mun.ca/biology/desmid/brian/BIOL2250/Week_Two/genespac.jpg
Gene Spacing in Various Species

http://www.mun.ca/biology/desmid/brian/BIOL2250/Week_Two/genespac.jpgGene Spacing in Various Species

Слайд 13Even the Amount of DNA a Gene Spans Differs Amongst

Species

Even the Amount of DNA a Gene Spans Differs Amongst Species

Слайд 14Comparative Genomics

Comparative Genomics

Слайд 15Yeast
70 human genes are known to repair mutations in

yeast
Nearly all we know about cell cycle and cancer comes

from studies of yeast
Advantages:
fewer genes (6000)
few introns
31% of yeast genes give same products as human homologues
Yeast 70 human genes are known to repair mutations in yeastNearly all we know about cell cycle

Слайд 16Drosophila
nearly all we know of how mutations affect gene

function come from Drosophila studies
We share 50% of their genes
61%

of genes mutated in 289 human diseases are found in fruit flies
68% of genes associated with cancers are found in fruit flies
Knockout mutants
Homeobox genes
Drosophila nearly all we know of how mutations affect gene function come from Drosophila studiesWe share 50%

Слайд 17C. elegans
959 cells in the nervous system
131 of

those programmed for apoptosis
apoptosis involved in several human genetic

neurological disorders
Alzheimers
Huntingtons
Parkinsons
C. elegans 959 cells in the nervous system 131 of those programmed for apoptosis apoptosis involved in

Слайд 18Mouse
known as “mini” humans
Very similar physiological systems
Share 90% of

their genes

Mouse known as “mini” humansVery similar physiological systemsShare 90% of their genes

Слайд 19What is the rest of the human genome made up

of?
Regulatory regions of DNA that turn genes on or off
Repetitive

DNA sequences:
Tandem Repetitive Sequences (~10%)
Microsatellite DNA: 2 to 4bp long repeats
Minisatellite DNA: 20bp or longer repeats
Macrosatellite DNA: megabase long repeats
Transposable elements SINEs and LINEs 35%
Retroviral fossils
What is the rest of the human genome made up of?Regulatory regions of DNA that turn genes

Слайд 21Genetic vs. Physical Mapping

Genetic vs. Physical Mapping

Слайд 22Genetic mapping based on genetic techniques, maps show the positions

of diseases or traits based on recombination frequencies
Genetic techniques include

cross-breeding experiments or, the examination of family histories (pedigrees)

Physical mapping uses molecular biology techniques to examine DNA molecules directly to construct maps showing the positions of sequence features, including genes
Physical techniques include DNA restriction enzyme analysis & fluorescent tagging of chromosomal regions
Genetic mapping based on genetic techniques, maps show the positions of diseases or traits based on recombination

Слайд 23http://www.ornl.gov/TechResources/Human_Genome/graphics/slides/images/98-1455.jpg
Genetic Map showing the location of disease genes on human

chromosome 4

http://www.ornl.gov/TechResources/Human_Genome/graphics/slides/images/98-1455.jpgGenetic Map showing the location of disease genes on human chromosome 4

Слайд 24Human chromosomes stained to show bands of different DNA
These bands

are the roughest markers for physical mapping

Human chromosomes stained to show bands of different DNAThese bands are the roughest markers for physical mapping

Слайд 25Fluorescent Labeling of Chromosomes
http://www.mun.ca/biology/scarr/FISH_chromosome_painting.htm

Fluorescent Labeling of Chromosomeshttp://www.mun.ca/biology/scarr/FISH_chromosome_painting.htm

Слайд 26http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=hmg.figgrp.1556
Types of Physical Maps
For Chromosome 21

http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=hmg.figgrp.1556Types of Physical MapsFor Chromosome 21

Слайд 27http://freepages.genealogy.rootsweb.com/~patafordgenealogy/images/usmaphyperlinks.jpg
http://socialstudies.ccswebacademy.net/CivicsEconomicsJenkins/images/Map_Outline_US_Outline.jpg
The more markers better the resolution, the more useful the

http://freepages.genealogy.rootsweb.com/~patafordgenealogy/images/usmaphyperlinks.jpghttp://socialstudies.ccswebacademy.net/CivicsEconomicsJenkins/images/Map_Outline_US_Outline.jpgThe more markers better the resolution, the more useful the map

Слайд 28DNA Sequencing

DNA Sequencing

Слайд 29Polyacrylamide gel electrophoresis can resolve ssDNA molecules that differ in

length by just one nucleotide
A banding pattern is produced after

separation of ssDNA molecules by denaturing polyacrylamide gel electrophoresis

Polyacrylamide gel electrophoresis can resolve ssDNA molecules that differ in length by just one nucleotideA banding pattern

Слайд 31Automatic Sequencing Machines use fluorescent dyes

Automatic Sequencing Machines use fluorescent dyes

Слайд 32Fluorescent Dye Dideoxy-sequencing

Fluorescent Dye Dideoxy-sequencing

Слайд 33http://www.ornl.gov/TechResources/Human_Genome/graphics/slides/ttseqfacility.html
DNA Sequencers in Action

http://www.ornl.gov/TechResources/Human_Genome/graphics/slides/ttseqfacility.htmlDNA Sequencers in Action

Слайд 34First Complete Sequence of a Free-Living Organism

First Complete Sequence of a Free-Living Organism

Слайд 351995, the Haemophilus influenzae genome sequenced
Genome size=1830 kb
1st genome

sequenced using the shotgun method
28,643 sequencing experiments totaling 11,631,485 bp
This

equaled 6x the length of the H. influenzae genome
Sequence assembly 30 hrs on a computer with 512 Mb of RAM
Resulted in 140 lengthy contiguous sequences
Each sequence contig represented, non-overlapping portion of the genome
1995, the Haemophilus influenzae genome sequencedGenome size=1830 kb 1st genome sequenced using the shotgun method28,643 sequencing experiments

Слайд 391st proposed by the DoE 1984
By 1990, the Human

Genome Project was launched
The Human Genome Organization (HUGO) was

founded to provide a forum for international coordination of genomic research
The program was proposed to include:
The creation of genetic & physical maps to be used in the generation of a complete genome sequence

Human Genome Project

1st proposed by the DoE 1984 By 1990, the Human Genome Project was launched The Human Genome

Слайд 40First Steps of the Human Genome Project

1) Construct genetic &

physical maps of the haploid human & mouse genomes
These would

provide key tools for identification of disease genes and anchoring points for genomic sequence
2) Sequence the yeast and worm genomes, as well as targeted regions of mammalian genomes
First Steps of the Human Genome Project1) Construct genetic & physical maps of the haploid human &

Слайд 41Sequencing Plan of HUGO
1) Isolate each human chromosome
2) Physical mapping

of each chromosome
The banding pattern of visible through staining
Location of

known genes already mapped
Location of restriction enzyme sites
Chromosome fragmented into large pieces of DNA and inserted into BAC or YAC libraries
Fragments overlap such that they can be ordered into a rough assembly of the chromosome

DNA from 5 humans
2 males, 3 females
2 caucasians, one each of asian, african, hispanic

Sequencing Plan of HUGO1) Isolate each human chromosome2) Physical mapping of each chromosome	The banding pattern of visible

Слайд 42Each YAC or BAC is fragmented into smaller 1 to

2 kb pieces of DNA which are sequenced
Each of these

fragments slightly overlaps with each other
A computer takes the DNA sequences & looks for regions of overlap these are connected to form a sequence contig for the entire BAC or YAC
The sequence of all the YACs or BACs are assembled through the same process to give the sequence of the chromosome
This is repeated for all 22 chromosomes plus the X & Y
Each YAC or BAC is fragmented into smaller 1 to 2 kb pieces of DNA which are

Слайд 43Hierarchical Shotgun Approach
http://www.genome.ou.edu/3653/3653-101705.html
Separate Individual Chromosomes

Hierarchical Shotgun Approachhttp://www.genome.ou.edu/3653/3653-101705.htmlSeparate Individual Chromosomes

Слайд 45http://www.csmc.edu/csri/korenberg/chroma11.html
Chromosome 11 BACs

http://www.csmc.edu/csri/korenberg/chroma11.htmlChromosome 11 BACs

Слайд 461999, Celera Genomics, set out to sequence the human genome

using a whole-genome shotgun method - more riskier - goal

to patent some seq.
There would be no isolation of individual chromosomes & no subcloning into BACs or YACs
They skipped straight to the 1 to 2 kb fragments
The $300 million Celera effort was intended to proceed at a faster pace and at a fraction of the cost of the roughly $3 billion HUGO project.

Dr. Craig Venter (founder) Celera Genomics

Human Genome Whole-Genome Shotgun Method

1999, Celera Genomics, set out to sequence the human genome using a whole-genome shotgun method - more

Слайд 47
14.8-billion bp of DNA sequence was generated over 9 months
This

equaled 5x the human genome
Resulting sequence contigs spanned >99% of

the genome
In March 2000, President Clinton announced that the genome sequences could not be patented, and should be made freely available to all researchers. The statement sent Celera's stock plummeting.
The competition proved to be very good for the project, spurring the public groups to modify their strategy in order to accelerate progress.
In February 2001 Celera Genomics published their draft of the human genome in the journal Science
The same month HUGO published its draft of the human genome in the journal Nature
The rivals initially agreed to pool their data, but the agreement fell apart when Celera refused to deposit its data in the unrestricted public database GeneBank.

14.8-billion bp of DNA sequence was generated over 9 monthsThis equaled 5x the human genomeResulting sequence contigs

Слайд 48http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=genomes.figgrp.6211
Hierarchical Shotgun Approach
Whole-Genome Shotgun Approach

http://www.ncbi.nlm.nih.gov/books/bv.fcgi?rid=genomes.figgrp.6211Hierarchical Shotgun ApproachWhole-Genome Shotgun Approach

Слайд 49Celera took multiple copies of the genome fragmented them into

1 to 2kb fragments which where sequenced without concern for

what chromosome they belonged to
Celera took multiple copies of the genome fragmented them into 1 to 2kb fragments which where sequenced

Слайд 50
What did they learn?
1.1% of the genome is spanned by

exons
24% is in introns
75% of the genome is intergenic DNA
A

random pair of human haploid genomes differs on average at a rate of 1 bp per 1250 bp
What did they learn?1.1% of the genome is spanned by exons24% is in introns75% of the genome

Слайд 51Preliminary Functional Analysis of >26 000 genes
>12 000 (41%) have

no known function
S. Barnum, 2005 Biotechnology, An Introduction. Brookes/Cole

Preliminary Functional Analysis of >26 000 genes>12 000 (41%) have no known functionS. Barnum, 2005 Biotechnology, An

Слайд 52Diploid Genome Sequence of an Individual Human
On September 4th, 2007,

a team led by Craig Venter, published his (ovn) complete

DNA sequence, unveiling the six-billion-letter genome of a single individual for the first time.
44% of known genes had one or more alterations
>0.5% variation between two haploid genomes



Diploid Genome Sequence of an Individual HumanOn September 4th, 2007, a team led by Craig Venter, published

Слайд 53How Do We Differ?
Total of 4.1 million DNA variations
3.2 million

single nucleotide changes
53,800 block substitutions (2 to 206bp)
292,000 heterozygous insertion/deletions

(1 to 571bp)
559,000 homozygous insertion/deletions (1 to 82,711bp)
90 inversions
Numerous duplications & copy number variations
How Do We Differ?Total of 4.1 million DNA variations3.2 million single nucleotide changes53,800 block substitutions (2 to

Слайд 54The UCSC Genome Browser

The UCSC Genome Browser

Слайд 55The browser takes you from early maps of the genome

. . .

The browser takes you from early maps of the genome . . .

Слайд 56. . . to a multi-resolution view . . .

. . . to a multi-resolution view . . .

Слайд 57. . . at the gene cluster level . .

. . . at the gene cluster level . . .

Слайд 58. . . the single gene level . . .

. . . the single gene level . . .

Слайд 59. . . the single exon level . . .

. . . the single exon level . . .

Слайд 60. . . and at the single base level
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caggcggactcagtggatctagccagctgtgacttgacaag

. . . and at the single base level caggcggactcagtggatctggccagctgtgacttgacaag caggcggactcagtggatctagccagctgtgacttgacaag

Слайд 61Other –omics
Proteomics
Transcriptomics
Metabolomics
Glycomics
Epigenomics
Metagenomics

Other –omicsProteomicsTranscriptomicsMetabolomicsGlycomicsEpigenomicsMetagenomics

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