Literature DB >> 7874119

Cloning the shared components of complex DNA resources.

A J Brookes1, E M Slorach, K E Morrison, S J Qureshi, D Blake, K Davies, D J Porteous.   

Abstract

The complex and repetitive nature of mammalian genomes limits the ability of conventional molecular techniques to recover sequences of interest. Here we describe a rapid and simple procedure for the direct cloning of sequences which are coincident between DNA mixtures of whole genome complexity. The system, called end ligation coincident sequence cloning (EL-CSC), can enrich coincident DNA by greater than 10(6)-fold and overcomes problems associated with repetitive elements. Applying EL-CSC to various paired DNA resources enables the facile cloning of both genomic markers and novel genes. To demonstrate the power of the method we have i) selectively purified single copy sequences from a complete genome, and ii) isolated gene fragments from 260 kb of cloned genomic DNA.

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Year:  1994        PMID: 7874119     DOI: 10.1093/hmg/3.11.2011

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  3 in total

1.  Direct selection of cDNAs using whole chromosomes.

Authors:  S Rouquier; B J Trask; S Taviaux; G van den Engh; S Diriong; G G Lennon; D Giorgi
Journal:  Nucleic Acids Res       Date:  1995-11-11       Impact factor: 16.971

Review 2.  Coincidence cloning. Taking the coincidences out of genome analysis.

Authors:  R S Devon; A J Brookes
Journal:  Mol Biotechnol       Date:  1996-06       Impact factor: 2.695

3.  Rapid isolation of cDNA by hybridization.

Authors:  M Hamaguchi; E A O'Connor; T Chen; L Parnell; R W McCombie; M H Wigler
Journal:  Proc Natl Acad Sci U S A       Date:  1998-03-31       Impact factor: 11.205

  3 in total

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