Amplification and analysis of whole genome and whole transcriptome libraries generated by a DNA polymerization process

a polymerization and dna technology, applied in the field of amplify, can solve the problems of inability to amplify single stranded, short, or fragmented dna and rna molecules

Inactive Publication Date: 2007-03-08
KAMBEROV EMMANUEL +6
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0059] In specific embodiments, the invention provides a two-step procedure that can be performed in a single tube or in a micro-titer plate, for example, in a high throughput format. The first step (termed the “library synthesis step”) involves incorporation of known sequence at both ends of amplicons using highly degenerate primers and at least one enzyme possessing strand-displacement activity. The resulting branching process creates molecules ...

Problems solved by technology

This lack of primer complementarity overcomes major problems known in the art associated with DNA amplification by random primers, such as excessive primer-dimer formation, comp...

Method used

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  • Amplification and analysis of whole genome and whole transcriptome libraries generated by a DNA polymerization process
  • Amplification and analysis of whole genome and whole transcriptome libraries generated by a DNA polymerization process
  • Amplification and analysis of whole genome and whole transcriptome libraries generated by a DNA polymerization process

Examples

Experimental program
Comparison scheme
Effect test

example 1

Design of Degenerate Pyrimidine Primers and Analysis of Self-Priming and Extension

[0254] Pyrimidine primers comprising a constant 18 base sequence, followed by 10 random pyrimidines and between 0 and 6 completely random bases at the 3′ end (Table III, primers 1-7), are compared for their ability to self prime and to extend a model template oligonucleotide.

TABLE IIIOLIGONUCLEOTIDE SEQUENCESNoCodeSequence 5′-3′ *1.YCCTTTCTCTCCCTTCTCTYYYYYYYYYY(SEQ ID NO:11)2.YNCCTTTCTCTCCCTTCTCTYYYYYYYYYYN(SEQ ID NO:12)3.Y(N)2CCTTTCTCTCCCTTCTCTYYYYYYYYYYNN(SEQ ID NO:13)4.Y(N)3CCTTTCTCTCCCTTCTCTYYYYYYYYYYNNN(SEQ ID NO:14)5.Y(N)4CCTTTCTCTCCCTTCTCTYYYYYYYYYYNNNN(SEQ ID NO:15)6.Y(N)5CCTTTCTCTCCCTTCTCTYYYYYYYYYYNNNNN(SEQ ID NO:16)7.Y(N)6CCTTTCTCTCCCTTCTCTYYYYYYYYYYNNNNNN(SEQ ID NO:17)8.YuCCTTTCTCTCCCTTCTCT(SEQ ID NO:18)9.TemplateGTAATACGACTCACTATAGGRRRRRRRRRR(SEQ ID NO:19)10.R(N)2AGAGAAGGGAGAGAAAGGRRRRRRRRRRNN(SEQ ID NO:20)11.RuAGAGAAGGGAGAGAAAGG(SEQ ID NO:21)12.M(N)2CCAAACACACCCAACACAMMMMMMMMMMNN(SEQ I...

example 2

Comparison of Different Degenerate Pyrimidine Primers Used in the Library Synthesis with Klenow Exo− Fragment of DNA Polymerase-I and Subsequent Whole Genome Amplification

[0256] Human lymphocyte genomic DNA isolated by standard procedures was randomly fragmented in TE buffer to an average size of 1.5 Kb using the Hydro Shear™ device (Gene Machines; Palo Alto, Calif.). The reaction mixture contained 50 ng of fragmented DNA in 1× EcoPol buffer (NEB), 200 μM of each dNTP, 360 ng of Single Stranded DNA Binding Protein (USB), 500 nM of known YU primer (Table III, primer 8), and 1 μM of degenerate pyrimidine primers with 0 to 6 random 3′ bases (Table III, primers 1-7) or 1 μM of T7 primer with six random N bases at the 3′ end (Table III, T7(N)6 primer 16,) in a final volume of 25 μl. After a denaturing step of 2 min at 95° C., the samples were cooled to 16° C., and the reaction was initiated by adding 5 units of Klenow enzyme that lacks 3′-5′ exonuclease activity (NEB). WGA library synth...

example 3

Whole Genome Amplification of Thermally Fragmented Genomic DNA Converted into an Amplifiable DNA Library Using Klenow Exo− Fragment of DNA Polymerase-I or Sequenase Version-2 and Degenerate Primers Y(N)2

[0260] Human lymphocyte genomic DNA isolated by standard procedures was randomly fragmented in TE-L buffer (10 mM Tris, 0.1 mM EDTA, pH 7.5) by heating at 95° C. for 5 min. The reaction mixture contained 100 ng of thermally fragmented DNA in 1× EcoPol buffer (NEB) or 1× Sequenase buffer (USB), 200 μM of each dNTP, 360 ng of Single Stranded DNA Binding Protein (USB), 200 nM of known YU primer (Table III, primer 8), and 500 nM of degenerate Y(N)2 primer (Table III, primer 3) in a final volume of 25 μl. After a denaturing step of 2 min at 95° C., the samples were cooled to 16° C., and the reaction initiated by adding 2.5 units or 6.5 units of Klenow Exo− polymerase (NEB) or Sequenase version 2 (USB), respectively. WGA library synthesis was carried out in a three-step protocol for 10 mi...

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Abstract

The present invention regards a variety of methods and compositions for whole genome amplification and whole transcriptome amplification. In a particular aspect of the present invention, there is a method of amplifying a genome comprising a library generation step followed by a library amplification step. In specific embodiments, the library generating step utilizes specific primer mixtures and a DNA polymerase, wherein the specific primer mixtures are designed to eliminate ability to self-hybridize and/or hybridize to other primers within a mixture but efficiently and frequently prime nucleic acid templates.

Description

[0001] This application claims priority to U.S. Provisional Patent Application Ser. No. 60 / 453,060, filed Mar. 7, 2003, which is incorporated by reference herein in its entirety.FIELD OF THE INVENTION [0002] The present invention is directed to the fields of genomics, molecular biology, genotyping, and expression profiling. In some embodiments, the present invention relates to methods for the amplification of DNA or cDNA yielding a product that is a non-biased representation of the original genomic or transcribed sequences, wherein the methods utilize primers substantially incapable of forming primer dimers. BACKGROUND OF THE INVENTION [0003] For genomic studies, the quality and quantity of DNA samples is crucial. High-throughput genetic analysis requires large amounts of template for testing. However, the amount of DNA extracted from individual patient samples, for example, is limited. DNA sample size also limits forensic and paleobiology work. Thus, there has been a concerted effo...

Claims

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Application Information

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IPC IPC(8): C12Q1/68C12P19/34C12N15/10
CPCC12N15/10C12N15/1093C12Q1/686C40B40/06C40B50/06C12Q2525/161C12Q2525/179C12Q2525/15
Inventor KAMBEROV, EMMANUELSUN, TONGBRUENING, ERICPINTER, JONATHON H.SLEPTSOVA, IRINAKURIHARA, TAKAOMAKAROV, VLADIMIR L.
Owner KAMBEROV EMMANUEL
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