Cite as: Cold Spring Harb. Protoc.; 2008; doi:10.1101/pdb.prot5002

This Protocol
Right arrow Full Text
Right arrow Update/discuss this protocolDiscussion icon
Right arrow Alert me when this protocol is cited
Right arrow Alert me when comments are published
Right arrow Alert me if a correction is posted
Services
Right arrow Similar protocols in this database
Right arrow Alert me to new releases of protocols
Right arrow Save to Personal Folders
Right arrow Download to citation manager
Right arrow Printer-friendly versionPrinter-friendly version
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Liu, C. L.
Right arrow Articles by Schreiber, S. L.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Liu, C. L.
Right arrow Articles by Schreiber, S. L.
Related Collections
Right arrow Bioinformatics/Genomics, general
Right arrow Genetics, general
Right arrow Genetic Variation
Right arrow Molecular Biology, general
Right arrow DNA Sequencing
Right arrow Genomic DNA
Right arrow Libraries
Right arrow Libraries, general
Right arrow Genomic Libraries
Right arrow RNA
Right arrow RNA, general
Right arrow Immunoprecipitation
Right arrow Genome Analysis
Right arrowRelated Article
Right arrowRelated Protocols
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati  
What's this?
Legend icon

protocolProtocol

Whole Genome Amplification by T7-Based Linear Amplification of DNA (TLAD): I. CIP Treatment of Samples and Tailing Reaction with Terminal Transferase

Chih Long Liu, Bradley E. Bernstein, and Stuart L. Schreiber

This protocol was adapted from "DNA Linear Amplification," Chapter 7, in Whole Genome Amplification: Methods Express (eds. Hughes and Laskin), from the Methods Express series. Scion Publishing Ltd., Oxfordshire, UK, 2005.


INTRODUCTION

T7-based linear amplification of DNA (TLAD) uses a linear amplification approach based on in vitro transcription (IVT) of template DNA by RNA polymerase from T7 phage. TLAD was designed for use with the ChIP-chip method (whereby DNA recovered from chromatin immunoprecipitation [ChIP] of cell lysate is used for subsequent analysis on DNA microarrays) and requires nanogram quantities of dsDNA to generate microgram amounts of amplified RNA. In Part I of the method, described here, a 3' conserved end is added to the template dsDNA, using terminal deoxynucleotidyl transferase (TdT) tailing. The initial treatment with calf intestinal phosphatase (CIP) is optional but strongly recommended for removing 3' phosphate groups, because most genomic DNA fragmentation methods (i.e., sonication, micrococcal nuclease digestion, and certain restriction digests) produce a significant proportion of 3' phosphate groups within the mixture of fragmented genomic DNA. This protocol is compatible with the presence of RNase A and can be carried out immediately after digestion of RNA carried over from ChIP, without any intermediate clean-up step. The tailing reaction involves the addition of a short (20-40 nucleotide [nt]) poly(dT) tail to the template DNA. The included dideoxynucleotide acts as a tail terminator in the reaction mixture and is necessary to maintain a tight size distribution. This poly(dT) tail provides a conserved 3' element that permits the addition of a T7 promoter sequence in the subsequent second-strand synthesis step. IVT can then use this newly appended T7 promoter and linearly amplify the template dsDNA, producing amplified RNA product.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati    What's this?

Related Article

Whole Genome Amplification by T7-Based Linear Amplification of DNA (TLAD): Overview
Chih Long Liu, Bradley E. Bernstein, and Stuart L. Schreiber
CSH Protocols 2008: 42. [Abstract] [Full Text]

Related Protocols

Whole Genome Amplification by T7-Based Linear Amplification of DNA (TLAD): II. Second-Strand Synthesis and In Vitro Transcription
Chih Long Liu, Bradley E. Bernstein, and Stuart L. Schreiber
CSH Protocols 2008: 5003. [Abstract] [Full Text]

Whole Genome Amplification by T7-Based Linear Amplification of DNA (TLAD): III. Sample Purification
Chih Long Liu, Bradley E. Bernstein, and Stuart L. Schreiber
CSH Protocols 2008: 5004. [Abstract] [Full Text]



This article has been cited by other articles:


Home page
CSH ProtocolsHome page
C. L. Liu, B. E. Bernstein, and S. L. Schreiber
Whole Genome Amplification by T7-Based Linear Amplification of DNA (TLAD): Overview
CSH Protocols, May 1, 2008; 2008(6): pdb.top42 - pdb.top42.
[Abstract] [Full Text]


Home page
CSH ProtocolsHome page
C. L. Liu, B. E. Bernstein, and S. L. Schreiber
Whole Genome Amplification by T7-Based Linear Amplification of DNA (TLAD): II. Second-Strand Synthesis and In Vitro Transcription
CSH Protocols, May 1, 2008; 2008(6): pdb.prot5003 - pdb.prot5003.
[Abstract] [Full Text]


Home page
CSH ProtocolsHome page
C. L. Liu, B. E. Bernstein, and S. L. Schreiber
Whole Genome Amplification by T7-Based Linear Amplification of DNA (TLAD): III. Sample Purification
CSH Protocols, May 1, 2008; 2008(6): pdb.prot5004 - pdb.prot5004.
[Abstract] [Full Text]