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1.
Science ; 294(5547): 1719-23, 2001 Nov 23.
Article in English | MEDLINE | ID: mdl-11721056

ABSTRACT

Global patterns of human DNA sequence variation (haplotypes) defined by common single nucleotide polymorphisms (SNPs) have important implications for identifying disease associations and human traits. We have used high-density oligonucleotide arrays, in combination with somatic cell genetics, to identify a large fraction of all common human chromosome 21 SNPs and to directly observe the haplotype structure defined by these SNPs. This structure reveals blocks of limited haplotype diversity in which more than 80% of a global human sample can typically be characterized by only three common haplotypes.


Subject(s)
Chromosomes, Human, Pair 21/genetics , Haplotypes/genetics , Oligonucleotide Array Sequence Analysis/methods , Polymorphism, Single Nucleotide/genetics , Algorithms , Alleles , Animals , Ethnicity/genetics , Gene Frequency/genetics , Genetic Variation/genetics , Genome, Human , Humans , Hybrid Cells/metabolism , Mutation/genetics , Racial Groups/genetics , Random Allocation , Sensitivity and Specificity
2.
Genome Res ; 11(10): 1651-9, 2001 Oct.
Article in English | MEDLINE | ID: mdl-11591642

ABSTRACT

Comparison of human sequences with the DNA of other mammals is an excellent means of identifying functional elements in the human genome. Here we describe the utility of high-density oligonucleotide arrays as a rapid approach for comparing human sequences with the DNA of multiple species whose sequences are not presently available. High-density arrays representing approximately 22.5 Mb of nonrepetitive human chromosome 21 sequence were synthesized and then hybridized with mouse and dog DNA to identify sequences conserved between humans and mice (human-mouse elements) and between humans and dogs (human-dog elements). Our data show that sequence comparison of multiple species provides a powerful empiric method for identifying actively conserved elements in the human genome. A large fraction of these evolutionarily conserved elements are present in regions on chromosome 21 that do not encode known genes.


Subject(s)
Chromosomes, Human, Pair 21/genetics , Conserved Sequence/genetics , Evolution, Molecular , Animals , Chromosomes, Artificial, Bacterial/genetics , DNA/genetics , Dogs , Genes, Overlapping/genetics , Humans , Mice , Oligonucleotide Array Sequence Analysis/methods , Sensitivity and Specificity , Synteny/genetics
3.
Biophys J ; 76(6): 2922-33, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10354420

ABSTRACT

Atomic force microscopy (AFM) can be used to probe the mechanics of molecular recognition between surfaces. In the application known as "chemical force" microscopy (CFM), a chemically modified AFM tip probes a surface through chemical recognition. When modified with a biological ligand or receptor, the AFM tip can discriminate between its biological binding partner and other molecules on a heterogeneous substrate. The strength of the interaction between the modified tip and the substrate is governed by the molecular affinity. We have used CFM to probe the interactions between short segments of single-strand DNA (oligonucleotides). First, a latex microparticle was modified with the sequence 3'-CAGTTCTACGATGGCAAGTC and epoxied to a standard AFM cantilever. This DNA-modified probe was then used to scan substrates containing the complementary sequence 5'-GTCAAGATGCTACCGTTCAG. These substrates consisted of micron-scale, patterned arrays of one or more distinct oligonucleotides. A strong friction interaction was measured between the modified tip and both elements of surface-bound DNA. Complementary oligonucleotides exhibited a stronger friction than the noncomplementary sequences within the patterned array. The friction force correlated with the measured strength of adhesion (rupture force) for the tip- and array-bound oligonucleotides. This result is consistent with the formation of a greater number of hydrogen bonds for the complementary sequence, suggesting that the friction arises from a sequence-specific interaction (hybridization) of the tip and surface DNA.


Subject(s)
DNA/chemistry , Microscopy, Atomic Force/methods , Nucleic Acid Hybridization , Base Sequence , Biophysical Phenomena , Biophysics , DNA/ultrastructure , DNA Probes/chemistry , DNA Probes/genetics , Latex , Microscopy, Atomic Force/instrumentation , Microspheres
4.
Nat Genet ; 22(2): 164-7, 1999 Jun.
Article in English | MEDLINE | ID: mdl-10369258

ABSTRACT

Here we report the application of high-density oligonucleotide array (DNA chip)-based analysis to determine the distant history of single nucleotide polymorphisms (SNPs) in current human populations. We analysed orthologues for 397 human SNP sites (identified in CEPH pedigrees from Amish, Venezuelan and Utah populations) from 23 common chimpanzee, 19 pygmy chimpanzee and 11 gorilla genomic DNA samples. From this data we determined 214 proposed ancestral alleles (the sequence found in the last common ancestor of humans and chimpanzees). In a diverse human population set, we found that SNP alleles with higher frequencies were more likely to be ancestral than less frequently occurring alleles. There were, however, exceptions. We also found three shared human/pygmy chimpanzee polymorphisms, all involving CpG dinucleotides, and two shared human/gorilla polymorphisms, one involving a CpG dinucleotide. We demonstrate that microarray-based assays allow rapid comparative sequence analysis of intra- and interspecies genetic variation.


Subject(s)
Hominidae/genetics , Polymorphism, Genetic , Alleles , Animals , Dinucleoside Phosphates/chemistry , Dinucleoside Phosphates/genetics , Genotype , Gorilla gorilla/genetics , Humans , Models, Genetic , Pan troglodytes/genetics , Pedigree
5.
Nat Genet ; 21(1 Suppl): 20-4, 1999 Jan.
Article in English | MEDLINE | ID: mdl-9915496

ABSTRACT

Experimental genomics involves taking advantage of sequence information to investigate and understand the workings of genes, cells and organisms. We have developed an approach in which sequence information is used directly to design high-density, two-dimensional rays of synthetic oligonucleotides. The GeneChipe probe arrays are made using spatially patterned, light-directed combinatorial chemical synthesis and contain up to hundreds of thousands of different oligonucleotides on a small glass surface. The arrays have been designed and used for quantitative and highly parallel measurements of gene expression, to discover polymorphic loci and to detect the presence of thousands of alternative alleles. Here, we describe the fabrication of the arrays, their design and some specific applications to high-throughput genetic and cellular analysis.


Subject(s)
Gene Expression , Genotype , Oligonucleotide Array Sequence Analysis/methods , Oligonucleotides/chemical synthesis , Animals , Base Sequence , Database Management Systems , Humans
6.
Nucleic Acids Res ; 26(21): 4975-82, 1998 Nov 01.
Article in English | MEDLINE | ID: mdl-9776762

ABSTRACT

Pairs of high density oligonucleotide arrays (DNA chips) consisting of >96 000 oligonucleotides were designed to screen the entire 5.53 kb coding region of the hereditary breast and ovarian cancer BRCA1 gene for all possible sequence changes in the homozygous and heterozygous states. Single-stranded RNA targets were generated by PCR amplification of individual BRCA1 exons using primers containing T3 and T7RNA polymerase promoter tails followed by in vitro transcription and partial fragmentation reactions. Fluorescent hybridization signals from targets containing the four natural bases to >5592 different fully complementary 25mer oligonucleotide probes on the chip varied over two orders of magnitude. To examine the thermodynamic contribution of rU.dA and rA.dT target.probe base pairs to this variability, modified uridine [5-methyluridine and 5-(1-propynyl)-uridine)] and modified adenosine (2,6-diaminopurine riboside) 5'-triphosphates were incorporated into BRCA1 targets. Hybridization specificity was assessed based upon hybridization signals from >33 200 probes containing centrally localized single base pair mismatches relative to target sequence. Targets containing 5-methyluridine displayed promising localized enhancements in hybridization signal, especially in pyrimidine-rich target tracts, while maintaining single nucleotide mismatch hybridization specificities comparable with those of unmodified targets.


Subject(s)
Genes, BRCA1 , Oligonucleotide Array Sequence Analysis/methods , Base Pair Mismatch , Base Sequence , Breast Neoplasms/genetics , DNA Primers/genetics , DNA, Neoplasm/genetics , Female , Heterozygote , Homozygote , Humans , In Vitro Techniques , Nucleic Acid Hybridization , Nucleotides , Oligonucleotide Probes/genetics , Ovarian Neoplasms/genetics , RNA, Neoplasm/genetics , Transcription, Genetic
7.
Nucleic Acids Res ; 26(16): 3865-6, 1998 Aug 15.
Article in English | MEDLINE | ID: mdl-9685507

ABSTRACT

High density oligonucleotide arrays (DNA chips) have been used in two color mutational analysis of the 3.43 kb exon 11 of the hereditary breast and ovarian cancer gene BRCA1 . Two color analysis allows competitive hybridization between a reference standard and an unknown sample, improving the performance of the assay. Fluorescein and phycoerythrin dyes werepreviously used due to their compatibility with a single line 488 nm excitation source. Here we show that an alternative dye combination, containing the energy transfer dye system phycoerythrin*cy5 along with phycoerythrin, provides more evenly matched signal intensities and decreased spectral overlap between the two fluorophores, while maintaining compatibility with a 488 nm excitation source.


Subject(s)
Coloring Agents , DNA Mutational Analysis/methods , Genes, BRCA1 , Nucleic Acid Hybridization/methods , Oligodeoxyribonucleotides/genetics , Base Sequence , Exons , Female , Fluorescent Dyes , Heterozygote , Humans , Phycoerythrin , Polymorphism, Genetic
8.
Nat Genet ; 18(2): 155-8, 1998 Feb.
Article in English | MEDLINE | ID: mdl-9462745

ABSTRACT

We explored the utility of high-density oligonucleotide arrays (DNA chips) for obtaining sequence information from homologous genes in closely related species. Orthologues of the human BRCA1 exon 11, all approximately 3.4 kb in length and ranging from 98.2% to 83.5% nucleotide identity, were subjected to hybridization-based and conventional dideoxysequencing analysis. Retrospective guidelines for identifying high-fidelity hybridization-based sequence calls were formulated based upon dideoxysequencing results. Prospective application of these rules yielded base-calling with at least 98.8% accuracy over orthologous sequence tracts shown to have approximately 99% identity. For higher primate sequences with greater than 97% nucleotide identity, base-calling was made with at least 99.91% accuracy covering a minimum of 97% of the sequence. Using a second-tier confirmatory hybridization chip strategy, shown in several cases to confirm the identity of predicted sequence changes, the complete sequence of the chimpanzee, gorilla and orangutan orthologues should be deducible solely through hybridization-based methodologies. Analysis of less highly conserved orthologues can still identify conserved nucleotide tracts of at least 15 nucleotides and can provide useful information for designing primers. DNA-chip based assays can be a valuable new technology for obtaining high-throughput cost-effective sequence information from related genomes.


Subject(s)
BRCA1 Protein/genetics , Evolution, Molecular , Genes, BRCA1 , Primates/genetics , Alouatta , Animals , Base Sequence , DNA Primers , Dogs , Exons , Galago , Genetic Techniques , Gorilla gorilla , Hominidae , Humans , Lemur , Macaca mulatta , Molecular Sequence Data , Polymerase Chain Reaction , Pongo pygmaeus , Primates/classification
9.
Genome Res ; 8(12): 1245-58, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9872980

ABSTRACT

Mutational analysis of large genes with complex genomic structures plays an important role in medical genetics. Technical limitations associated with current mutation screening protocols have placed increased emphasis on the development of new technologies to simplify these procedures. High-density arrays of >90,000-oligonucleotide probes, 25 nucleotides in length, were designed to screen for all possible heterozygous germ-line mutations in the 9.17-kb coding region of the ATM gene. A strategy for rapidly developing multiexon PCR amplification protocols in DNA chip-based hybridization analysis was devised and implemented in preparing target for the 62 ATM coding exons. Improved algorithms for interpreting data from two-color experiments, where reference and test samples are cohybridized to the arrays, were developed. In a blinded study, 17 of 18 distinct heterozygous and 8 of 8 distinct homozygous sequence variants in the assayed region were detected accurately along with five false-positive calls while scanning >200 kb in 22 genomic DNA samples. Of eight heterozygous sequence changes found in more than one sample, six were detected in all cases. Five previously unreported sequence changes, not found by other mutational scanning methodologies on these same samples, were detected that led to either amino acid changes or premature truncation of the ATM protein. DNA chip-based assays should play a valuable role in high throughput sequence analysis of complex genes.


Subject(s)
DNA Mutational Analysis/methods , Leucine Zippers/genetics , Oligonucleotide Array Sequence Analysis/methods , Phosphatidylinositol 3-Kinases/genetics , Protein Serine-Threonine Kinases , Proteins/genetics , Ataxia Telangiectasia Mutated Proteins , Cell Cycle Proteins , DNA-Binding Proteins , Exons/genetics , Female , Human Genome Project , Humans , Male , Mutation/genetics , Sensitivity and Specificity , Tumor Suppressor Proteins
10.
Nat Genet ; 14(4): 441-7, 1996 Dec.
Article in English | MEDLINE | ID: mdl-8944024

ABSTRACT

The ability to scan a large gene rapidly and accurately for all possible heterozygous mutations in large numbers of patient samples will be critical for the future of medicine. We have designed high-density arrays consisting of over 96,600 oligonucleotides 20-nucleotides (nt) in length to screen for a wide range of heterozygous mutations in the 3.45-kilobases (kb) exon 11 of the hereditary breast and ovarian cancer gene BRCA1. Reference and test samples were co-hybridized to these arrays and differences in hybridization patterns quantitated by two-colour analysis. Fourteen of fifteen patient samples with known mutations were accurately diagnosed, and no false positive mutations were identified in 20 control samples. Eight single nucleotide polymorphisms were also readily detected. DNA chip-based assays may provide a valuable new technology for high-throughput cost-efficient detection of genetic alterations.


Subject(s)
BRCA1 Protein/genetics , DNA Probes , Heterozygote , Mutation , False Negative Reactions , Feasibility Studies , Fluorescein , Fluoresceins , Fluorescence , Genetic Carrier Screening , Humans , Nucleic Acid Hybridization , Sensitivity and Specificity
11.
Science ; 274(5287): 610-4, 1996 Oct 25.
Article in English | MEDLINE | ID: mdl-8849452

ABSTRACT

Rapid access to genetic information is central to the revolution taking place in molecular genetics. The simultaneous analysis of the entire human mitochondrial genome is described here. DNA arrays containing up to 135,000 probes complementary to the 16.6-kilobase human mitochondrial genome were generated by light-directed chemical synthesis. A two-color labeling scheme was developed that allows simultaneous comparison of a polymorphic target to a reference DNA or RNA. Complete hybridization patterns were revealed in a matter of minutes. Sequence polymorphisms were detected with single-base resolution and unprecedented efficiency. The methods described are generic and can be used to address a variety of questions in molecular genetics including gene expression, genetic linkage, and genetic variability.


Subject(s)
DNA, Mitochondrial/genetics , Genome , Mitochondria/genetics , Nucleic Acid Hybridization , Oligonucleotide Probes , Algorithms , Base Composition , Base Sequence , Cloning, Molecular , Fluorescein , Fluoresceins , Gene Expression , Genetic Variation , Humans , Phycoerythrin , Polymerase Chain Reaction , Polymorphism, Genetic , Sequence Analysis, DNA
12.
Biotechniques ; 19(3): 442-7, 1995 Sep.
Article in English | MEDLINE | ID: mdl-7495558

ABSTRACT

As the Human Genome Project and related efforts identify and determine the DNA sequences of human genes, it is important that highly reliable and efficient mechanisms are found to access individual genetic variation. It is only through a greater understanding of genetic diversity that the true benefit of the Human Genome Project will be realized. One approach, hybridization to high-density arrays of oligonucleotides, is a fast and effective means of accessing this genetic variation. Light-directed chemical synthesis has been used to generate miniaturized, high-density arrays of oligonucleotide probes. Application-specific oligonucleotide probe array designs have been developed for the rapid screening of characterized genes. Dedicated instrumentation and software have been developed for array hybridization, fluorescence detection and data acquisition and analysis. In a specific and challenging application, oligonucleotide probe arrays have been used to screen the reverse transcriptase and protease genes of the highly polymorphic HIV-1 genome to explore genetic diversity and detect mutations conferring resistance to antiviral drugs. Results from this application strongly suggest that oligonucleotide probe arrays will be a powerful tool for rapid investigations in sequence checking, pathogen detection, expression monitoring and DNA molecular recognition.


Subject(s)
Genetic Variation , Oligonucleotide Probes , Base Sequence , Fluorescent Dyes , HIV-1/genetics , Humans , Molecular Sequence Data , Nucleic Acid Hybridization , Polymorphism, Genetic
13.
Biophys J ; 68(5): 1653-60, 1995 May.
Article in English | MEDLINE | ID: mdl-7612807

ABSTRACT

We describe here a method for constructing ordered molecular arrays and for detecting binding of biomolecules to these arrays using atomic force microscopy (AFM). These arrays simplify the discrimination of surface-bound biomolecules through the spatial control of ligand presentation. First, photolithography is used to spatially direct the synthesis of a matrix of biological ligands. A high-affinity binding partner is then applied to the matrix, which binds at locations defined by the ligand array. AFM is then used to detect the presence and organization of the high-affinity binding partner. Streptavidin-biotin arrays of 100 x 100 microns and 8 x 8 microns elements were fabricated by this method. Contact and noncontact AFM images reveal a dense lawn of streptavidin specific to the regions of biotin derivatization. These protein regions are characterized by a height profile of approximately 40 A over the base substrate with a 350-nm edge corresponding to the diffraction zone of the photolithography. High resolution scans reveal a granular topography dominated by 300 A diameter features. The ligand-bound protein can then be etched from the substrate using the AFM tip, leaving an 8 A shelf that probably corresponds to the underlying biotin layer.


Subject(s)
Bacterial Proteins/chemistry , Biotin/chemistry , Microscopy, Atomic Force/methods , Molecular Conformation , Protein Conformation , Streptavidin
15.
Proc Natl Acad Sci U S A ; 91(11): 5022-6, 1994 May 24.
Article in English | MEDLINE | ID: mdl-8197176

ABSTRACT

In many areas of molecular biology there is a need to rapidly extract and analyze genetic information; however, current technologies for DNA sequence analysis are slow and labor intensive. We report here how modern photolithographic techniques can be used to facilitate sequence analysis by generating miniaturized arrays of densely packed oligonucleotide probes. These probe arrays, or DNA chips, can then be applied to parallel DNA hybridization analysis, directly yielding sequence information. In a preliminary experiment, a 1.28 x 1.28 cm array of 256 different octanucleotides was produced in 16 chemical reaction cycles, requiring 4 hr to complete. The hybridization pattern of fluorescently labeled oligonucleotide targets was then detected by epifluorescence microscopy. The fluorescence signals from complementary probes were 5-35 times stronger than those with single or double base-pair hybridization mismatches, demonstrating specificity in the identification of complementary sequences. This method should prove to be a powerful tool for rapid investigations in human genetics and diagnostics, pathogen detection, and DNA molecular recognition.


Subject(s)
Light , Sequence Analysis, DNA/methods , Base Sequence , Humans , Microscopy, Fluorescence , Molecular Sequence Data , Molecular Structure , Nucleic Acid Hybridization , Oligodeoxyribonucleotides/radiation effects , Oligonucleotide Probes
17.
Trends Biotechnol ; 12(1): 19-26, 1994 Jan.
Article in English | MEDLINE | ID: mdl-7765338

ABSTRACT

Combinatorial methods in biology and chemistry are proving to be powerful methods for generating molecular diversity. One approach, light-directed chemical synthesis, combines semiconductor-based photolithography technologies with solid-phase organic chemistry to synthesize large arrays of molecules with potential biological activity. This novel technology has the potential to provide libraries of both natural and synthetic molecules that might be screened rapidly for biological activity.


Subject(s)
Oligonucleotides/chemical synthesis , Peptides/chemical synthesis , Photochemistry/methods , Amino Acid Sequence , Base Sequence , Biotechnology/methods , Carbamates/chemistry , DNA/genetics , Dynorphins/analogs & derivatives , Dynorphins/chemical synthesis , Dynorphins/chemistry , Dynorphins/genetics , Endorphins/chemical synthesis , Endorphins/chemistry , Endorphins/genetics , Molecular Sequence Data , Oligonucleotides/chemistry , Oligonucleotides/genetics , Peptides/chemistry , Peptides/genetics
18.
Science ; 261(5126): 1303-5, 1993 Sep 03.
Article in English | MEDLINE | ID: mdl-7689747

ABSTRACT

A highly efficient method has been developed for the solid-phase synthesis of an "unnatural biopolymer" consisting of chiral aminocarbonate monomers linked via a carbamate backbone. Oligocarbamates were synthesized from N-protected p-nitrophenyl carbonate monomers, substituted with a variety of side chains, with greater than 99 percent overall coupling efficiencies per step. A spatially defined library of oligocarbamates was generated by using photochemical methods and screened for binding affinity to a monoclonal antibody. A number of high-affinity ligands were then synthesized and analyzed in solution with respect to their inhibition concentration values, water/octanol partitioning coefficients, and proteolytic stability. These and other unnatural polymers may provide new frameworks for drug development and for testing theories of protein and peptide folding and structure.


Subject(s)
Biopolymers , Carbonates/chemical synthesis , Amino Acid Sequence , Animals , Antibodies, Monoclonal/immunology , Carbonates/chemistry , Carbonates/immunology , Epitopes , Mice , Mice, Inbred BALB C , Molecular Sequence Data , Oligopeptides/chemistry
19.
Nature ; 364(6437): 555-6, 1993 Aug 05.
Article in English | MEDLINE | ID: mdl-7687751

ABSTRACT

High density peptide and oligonucleotide chips are fabricated using semiconductor-based technologies. These chips have a variety of biological applications.


Subject(s)
Biochemistry/methods , Semiconductors , Amino Acid Sequence , Base Sequence , Biopolymers , DNA , Epitopes/analysis , Fluorescence , Lasers , Light , Miniaturization , Molecular Sequence Data , Oligonucleotides , Peptides , Sequence Analysis, DNA/methods
20.
Photochem Photobiol ; 53(3): 341-6, 1991 Mar.
Article in English | MEDLINE | ID: mdl-2062880

ABSTRACT

Detergent solubilized bacteriorhodopsin (BR) proteins which contain alterations made by site-directed mutagenesis (Asp-96----Asn, D96N; Asp-85----Asn, D85N; and Arg-82----Gln, R82Q) have been studied with resonance Raman spectroscopy. Raman spectra of the light-adapted (BRLA) and M species in D96N are identical to those of native BR, indicating that this residue is not located near the chromophore. The BRLA states of D85N and especially R82Q contain more of the 13-cis, C = N syn (BR555) species under ambient illumination compared to solubilized native BR. Replacement of Asp-85 with Asn causes a 25 nm red-shift of the absorption maximum and a frequency decrease in both the ethylenic (-7 cm-1) and the Schiff base C = NH+ (-3 cm-1) stretching modes of BRLA. These changes indicate that Asp-85 is located close to the protonated retinal Schiff base. The BRLA spectrum of R82Q exhibits a slight perturbation of the C = NH+ band, but its M spectrum is unperturbed. The Raman spectra and the absorption properties of D85N and R82Q suggest that the protein counterion environment involves the residues Asp-85-, Arg-82+ and presumably Asp-212-. These data are consistent with a model where the strength of the protein-chromophore interaction and hence the absorption maximum depends on the overall charge of the Schiff base counterion environment.


Subject(s)
Arginine , Aspartic Acid , Bacteriorhodopsins/chemistry , Mutagenesis, Site-Directed , Amino Acid Sequence , Bacteriorhodopsins/genetics , Halobacterium/metabolism , Spectrum Analysis, Raman/methods
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