Expression of Vectors for High Level of Expression of Cloned Genes

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  Cloning and Expression Vectors

  Cloning Vectors for Recombinant DNA

  Plasmids as Vectors

 pBR322 and pBR327 Vectors

 pUC Vectors

  Yeast Plasmid Vectors

  Examples of Yeast Plasmid Vectors

  Retriever Vectors

  Cosmids as Vectors

  Phagemids as Vectors

  Bluescript II KS

  PI Cloning Vectors for Cloning Large DNA Segments

  F-factor Based Vectors

  Plant and Animal Viruses as Vectors

  Plant Viruses ( Cauliflower Mosaic Virus OR CaMV and Geminivirus

  Important Geminiviruses

  Animal Viruses

  Transposons as Vectors

  Artificial Chromosome ( YAC and MAC) Vectors for Cloning Large DNA Segments

 Expression Vectors for High Level of Expression of Cloned Genes

  Promoters

  Nopaline Synthase (nos) Promoter from T-DNA

  Dual Promoter of Mannopine Synthase (mas) Genes 1 and 2

  35S RNA Promoter of CaMV

  Polyhedrin Promoter from Baculovirus

  Expression Cassettes

  Baculovirus and Expression Vector System for Insect Cells

  Virus Expression Vector for Mammalian Cells

 Transforming Viruses Used as Vectors in Mammalian Cells

  Binary and Shuttle Vectors

 

Expression of Vectors for High Level of Expression of Cloned Genes

Expression of Vectors for High Level of Expression of Cloned Genes - In a number of cloning vectors described earlier in this chapter, the main utility has been to clone a gene or a DNA sequence. In other words, they are used for obtaining millions of copies of the cloned DNA segment, for further use in either the genetic engineering experiments or for further basic studies.

With this objective in mind, the cloned genes in these vectors need not express themselves either at the transcription level (production of mRNA) or at the translation level (production of protein).

But, when the cloned gene is used for transformation to generate transgenic plants or animals or for production of microbes to be used in industry, then the cloned gene must be expressed.

Sometimes, a high level of expression of gene is desirable, if the product of cloned gene is to be recovered as a commercial product.

This objective can be achieved through the use of promoters and expression cassettes (an expression cassette is a combination of DNA sequences, which allow faithful expression of the cloned gene).

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  Ti and Ri Plasmids as Vectors for Higher Plants

  Bacteriophage as Vectors

  Lambda Phage Vectors

  EMBL3 and EMBL4 (Replacement Vectors)

 Charon 34 and Charon 35

  M13 Phage as Vector for DNA Sequencing