Literature DB >> 8932395

Expression of peptides encoded by exons in cloned mammalian DNA.

S Kreissig1, K Schüddekopf, N Dear, T Boehm.   

Abstract

New synthetic approaches, such as combinatorial chemistry, provide a rich source of potential drug candidates. At the same time, the human genome initiative and other large-scale sequencing projects provide a large number of novel drug targets. However, the functional analysis of thousands of new genes remains a major challenge for the future. A systematic strategy for genome-wide functional analysis of genes could employ the fact that at least some modules in multi-domain proteins are encoded in individual exons. Exon amplification provides information about coding regions of most genes that is independent of their transcriptional status; exon amplification from entire mammalian genomes has been demonstrated. Here, we describe the development of an exon-trap system, lambdaGEE (for genomic exon expression), that couples exon amplification with the expression of exon-encoded peptides.

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Year:  1996        PMID: 8932395      PMCID: PMC146242          DOI: 10.1093/nar/24.21.4358

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  17 in total

1.  Exon trapping: a genetic screen to identify candidate transcribed sequences in cloned mammalian genomic DNA.

Authors:  G M Duyk; S W Kim; R M Myers; D R Cox
Journal:  Proc Natl Acad Sci U S A       Date:  1990-11       Impact factor: 11.205

Review 2.  Exons--original building blocks of proteins?

Authors:  L Patthy
Journal:  Bioessays       Date:  1991-04       Impact factor: 4.345

Review 3.  Applications of combinatorial technologies to drug discovery. 2. Combinatorial organic synthesis, library screening strategies, and future directions.

Authors:  E M Gordon; R W Barrett; W J Dower; S P Fodor; M A Gallop
Journal:  J Med Chem       Date:  1994-05-13       Impact factor: 7.446

Review 4.  Applications of combinatorial technologies to drug discovery. 1. Background and peptide combinatorial libraries.

Authors:  M A Gallop; R W Barrett; W J Dower; S P Fodor; E M Gordon
Journal:  J Med Chem       Date:  1994-04-29       Impact factor: 7.446

5.  The sequence complexity of exons trapped from the mouse genome.

Authors:  M Nehls; D Pfeifer; G Micklem; C Schmoor; T Boehm
Journal:  Curr Biol       Date:  1994-11-01       Impact factor: 10.834

6.  A versatile expression vector for the in vitro study of protein-protein interactions: characterization of E47 mutant proteins.

Authors:  T Hainzl; T Boehm
Journal:  Oncogene       Date:  1994-03       Impact factor: 9.867

7.  Exon amplification from complete libraries of genomic DNA using a novel phage vector with automatic plasmid excision facility: application to the mouse neurofibromatosis-1 locus.

Authors:  M Nehls; D Pfeifer; T Boehm
Journal:  Oncogene       Date:  1994-08       Impact factor: 9.867

8.  Establishment of a highly sensitive and specific exon-trapping system.

Authors:  M Hamaguchi; H Sakamoto; H Tsuruta; H Sasaki; T Muto; T Sugimura; M Terada
Journal:  Proc Natl Acad Sci U S A       Date:  1992-10-15       Impact factor: 11.205

9.  Exon amplification: a strategy to isolate mammalian genes based on RNA splicing.

Authors:  A J Buckler; D D Chang; S L Graw; J D Brook; D A Haber; P A Sharp; D E Housman
Journal:  Proc Natl Acad Sci U S A       Date:  1991-05-01       Impact factor: 11.205

10.  A new homeobox gene contributes the DNA binding domain of the t(1;19) translocation protein in pre-B ALL.

Authors:  M P Kamps; C Murre; X H Sun; D Baltimore
Journal:  Cell       Date:  1990-02-23       Impact factor: 41.582

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