Production of Retroviral Constructs for Effective Transfer and Expression of T-cell Receptor Genes using Golden Gate Cloning
Author(s) -
Lori V. Coren,
Sumiti Jain,
Matthew T. Trivett,
Claes Öhlén,
David E. Ott
Publication year - 2015
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/000114265
Subject(s) - t cell receptor , biology , cloning (programming) , gene , expression cloning , complementary dna , expression cassette , vector (molecular biology) , genetics , computational biology , t cell , microbiology and biotechnology , recombinant dna , computer science , immune system , programming language
Here we present an improved strategy for producing T-cell receptor (TCR)-expressing retroviral vectors using a Golden Gate cloning strategy. This method takes advantage of the modular nature of TCR genes by directly amplifying TCR α and β variable regions from RNA or cDNA, then cloning and fusing them with their respective constant region genes resident in a retroviral TCR expression vector. Our one-step approach greatly streamlines the TCR vector production process in comparison to the traditional three-step procedure that typically involves cloning whole TCR genes, producing a TCR expression cassette, and constructing a retroviral construct. To date, we have generated TCR vectors that transferred seven functional human/rhesus macaque TCRs into primary T cells. The approach also holds promise for the assembly of other genes with defined variable regions, such as immunoglobulins.
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