Literature DB >> 22450538

Functional cDNA expression cloning: pushing it to the limit.

Hiroto Okayama1.   

Abstract

The 1970s and the following decade are the era of the birth and early development of recombinant DNA technologies, which have entirely revolutionized the modern life science by providing tools that enable us to know the structures of genes and genomes and to dissect their components and understand their functions at the molecular and submolecular levels. One major objective of the life sciences is to achieve molecular and chemical understandings of the functions of genes and their encoded proteins, which are responsible for the manifestation of all biological phenomena in organisms. In the early 1980s, I developed, together with Paul Berg, a new technique that enables the cloning of full-length complementary DNAs (cDNAs) on the basis of their functional expression in a given cell of interest. I review the development, application and future implications in the life sciences of this gene-cloning technique.

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Year:  2012        PMID: 22450538      PMCID: PMC3365248          DOI: 10.2183/pjab.88.102

Source DB:  PubMed          Journal:  Proc Jpn Acad Ser B Phys Biol Sci        ISSN: 0386-2208            Impact factor:   3.493


  64 in total

1.  High-efficiency cloning of full-length cDNA; construction and screening of cDNA expression libraries for mammalian cells.

Authors:  H Okayama; M Kawaichi; M Brownstein; F Lee; T Yokota; K Arai
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

2.  High-efficiency transformation of mammalian cells by plasmid DNA.

Authors:  C Chen; H Okayama
Journal:  Mol Cell Biol       Date:  1987-08       Impact factor: 4.272

3.  A simple and very efficient method for generating cDNA libraries.

Authors:  U Gubler; B J Hoffman
Journal:  Gene       Date:  1983-11       Impact factor: 3.688

4.  Identification of clones that encode chicken tropomyosin by direct immunological screening of a cDNA expression library.

Authors:  D M Helfman; J R Feramisco; J C Fiddes; G P Thomas; S H Hughes
Journal:  Proc Natl Acad Sci U S A       Date:  1983-01       Impact factor: 11.205

5.  Efficient isolation of genes by using antibody probes.

Authors:  R A Young; R W Davis
Journal:  Proc Natl Acad Sci U S A       Date:  1983-03       Impact factor: 11.205

6.  Complementation used to clone a human homologue of the fission yeast cell cycle control gene cdc2.

Authors:  M G Lee; P Nurse
Journal:  Nature       Date:  1987 May 7-13       Impact factor: 49.962

7.  Isolation of a cDNA clone for the human HLA-DR antigen alpha chain by using a synthetic oligonucleotide as a hybridization probe.

Authors:  D Stetler; H Das; J H Nunberg; R Saiki; R Sheng-Dong; K B Mullis; S M Weissman; H A Erlich
Journal:  Proc Natl Acad Sci U S A       Date:  1982-10       Impact factor: 11.205

8.  Fission yeast Schizosaccharomyces pombe correctly excises a mammalian RNA transcript intervening sequence.

Authors:  N F Käufer; V Simanis; P Nurse
Journal:  Nature       Date:  1985 Nov 7-13       Impact factor: 49.962

9.  Simian virus 40 early- and late-region promoter functions are enhanced by the 72-base-pair repeat inserted at distant locations and inverted orientations.

Authors:  M Fromm; P Berg
Journal:  Mol Cell Biol       Date:  1983-06       Impact factor: 4.272

10.  Isolation and characterization of a full-length expressible cDNA for human hypoxanthine phosphoribosyl transferase.

Authors:  D J Jolly; H Okayama; P Berg; A C Esty; D Filpula; P Bohlen; G G Johnson; J E Shively; T Hunkapillar; T Friedmann
Journal:  Proc Natl Acad Sci U S A       Date:  1983-01       Impact factor: 11.205

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