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Ch2. Genome Organization and Evolution 阮雪芬 Nov21, 2002 NTUST.

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Presentation on theme: "Ch2. Genome Organization and Evolution 阮雪芬 Nov21, 2002 NTUST."— Presentation transcript:

1 Ch2. Genome Organization and Evolution 阮雪芬 Nov21, 2002 NTUST

2 Protein Array Detection of specific antibody–antigen interactions on the hEx1 cDNA array.

3 DNA Microarray 或稱 DNA chip For checking a sample of DNA simultaneously for the presence of many sequences. Can be used –To determine expression patterns of different proteins by detection of mRNA. –For genotyping The correlation between the abundance of an mRNA and the corresponding protein is imperfect.

4 DNA Microarray A DNA array may contain 100000 probe oligomers. The spot size ~150 u in diameter Oligomers of length ~50-80 bp For genotype, genomic DNA fragments of length 500-5000 bp.

5 Application of DNA Microarray Investigating cellular states and processes. Diagnosis of disease: – Huntington disease: expanded repeats of CAG In normal, 11-28 CAG repeats >41 CAG repeats, huntington disease Genetic warning signs Drug selection Classification of disease: –Different types of leukaemia can be identified by different patterns of gene expression Target selection for drug design Pathogen resistance

6 Chip Technology Eur J Nucl Med 2002, 29, 115-32 Control or treatment mRNA Reverse transcriptase to generate Cy3/Cy5 cDNA probes Hybridization to the gene chip Data analysis Fluorescently labeled DNA or RNA hybridization

7 cDNA Microarray Chip

8 From the point of view of bioinformatics. DNA arrays are yet another profilic stream of data creation

9 Eavesdropping on the Transmission of Genetic Information Three types of maps have been essential –Linkage maps of genes Classically determined by observed patterns of heredity. The unit of length in a gene map is the Morgan. 1 cM~1% recombination frequency~1x10 6 bp in humans –Banding patterns of chromosomes –DNA sequences

10 Linkage maps of genes Example: Cross 1: a + b x ab +  1773 a + b, 1747 ab +, 104 a + b +, 96 ab Cross 2: b + c x bc +  1348 b + c., 1312 bc +, 124 b + c +, 108 bc Cross 3: a + c x ac +  1443 a + c, 1483 ac +, 51a + c +, 55 ac

11 Recombination Frequency R a-b = (104 + 96 )/3720 = 0.054 =5.4% R b-c = (124 + 108)/2892 = 0.080 =80% R a-c = (51+55)/ 3031 = 0.035 = 3.5% b a c 5.43.5

12 Eavesdropping on the Transmission of Genetic Information Three types of maps have been essential –Linkage maps of genes Classically determined by observed patterns of heredity. The unit of length in a gene map is the Morgan. 1 cM~1% recombination frequency~1x10 6 bp in humans –Banding patterns of chromosomes –DNA sequences

13 Banding Patterns of Chromosomes Chromosome –Physical objects p: petite ( 短 ) q: queue ( 長 ) centromere 8p1.2 17q2.2

14 Restriction Enzymes –1970, Smith 發現第二類核酸 限切酵素 , 可以很準確分割 DNA –1973, Boyer-Cohen-Chang 完 成第一基因選殖的工作

15 第二類核酸限切酵素 鈍端 (blunt end ) 黏端 (sticky end)

16 連接酵素 (ligase)

17 載體 (vector)

18 Restriction Map

19

20 Cystic Fibrosis Knowing the general region of the chromosome Search the DNA of that region to identify candidate genes Pinpoint the particular gene responsible and sequence it

21 Cystic Fibrosis In 1989 the gene was isolated and sequenced. CFTR: cystic fibrosis transmembrane conductance regulator CFTR codes for a 1480 amino acids protein that normally forms a cyclicAMP-regulated epithelial Cl - channel. The mutation is a three base pair deletion--- deleting the residue 508Phe from the protein

22 Mappings Between The Maps Several approaches to coordinating chromosome banding patterns with individual DNA sequences of genes –In Fluorescent In Situ Hybridization (FISH) –Somatic Cell Hybrids FISH

23 Somatic Cell Hybrids

24 High-resolution Maps (I) Variable number tandem repeats (VNTRs) –Minisatellites –10-100 bp long, repeated a variable number of times –Genetic fingerprints –RFLPs (restriction fragment length polymorphisms) –Southern blotting –PCR (polymerase chain reaction)

25 Southern Blotting

26 Multiple Cycles of PCR (I)

27 Multiple Cycles of PCR (II)

28 Multiple Cycles of PCR (III)

29 High-resolution Maps (II) Short tandem repeat polymorphisms (STRPs) –Microsatellites –Regions of only 2-5 bp but repeated many times A conting (contiguous clone map): –A series of overlapping DNA clones of known order along a chromosome from an organism of interest –Human-stored in yeast or bacterial cells as YAC or BAC A sequence tagged site (STS) –A short, sequenced region of DNA, typically 200-60 bp long, that appears in a unique location in the genome. –EST (expressed sequence tag)


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