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Novel pristinamycin‐responsive expression systems for plant cells
Author(s) -
Frey Alexander D.,
Rimann Markus,
Bailey James E.,
Kallio Pauli T.,
Thompson Charles J.,
Fussenegger Martin
Publication year - 2001
Publication title -
biotechnology and bioengineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.136
H-Index - 189
eISSN - 1097-0290
pISSN - 0006-3592
DOI - 10.1002/bit.1105
Subject(s) - biology , cauliflower mosaic virus , repressor , operon , transactivation , streptomyces coelicolor , expression vector , gene , microbiology and biotechnology , nicotiana tabacum , gene expression , genetics , genetically modified crops , transgene , recombinant dna , escherichia coli , mutant
Novel gene regulation systems were designed for plant cells responsive to the streptogramin antibiotic pristinamycin. The pristinamycin‐repressible plant gene regulation concept (PIPpOFF) is based on a transcriptional activator (PIT) which consists of the Pip protein, the repressor of the pristinamycin resistance operon of Streptomyces coelicolor , fused to the VP16 transactivation domain of the Herpes simplex virus. PIT mediates pristinamycin‐repressible activation of a synthetic plant promoter (P pPIR ) in tobacco cells consisting of a nine Pip‐binding site‐containing artificial operator (PIR3) placed upstream of a TATA‐box derived from the cauliflower mosaic virus 35S promoter (P CaMV35S ). Pristinamycin interferes with induction by negatively regulating the DNA‐binding capacity of the Pip moiety of PIT. A second, streptogramin‐inducible plant gene regulation system (PIPpON) was constructed by combining Pip expression with a plant‐specific pristinamycin‐inducible promoter (P pPIRON ). P pPIRON consists of a PIR3 module cloned downstream of the strong constitutive plant promoter P CaMV35S . As in the native Streptomyces configuration, Pip binds to its cognate sequence within P pPIRON in the absence of regulating antibiotic and silences the chimeric plant promoter. Upon addition of pristinamycin, Pip is released from the PIR3 operator and full P CaMV35S ‐driven expression of desired plant genes is induced. The PIPpOFF and PIPpON systems performed well in Nicotiana tabacum suspension cultures and promise to provide an attractive extension of existing plant gene regulation technology for basic plant research or biopharmaceutical manufacturing using plant tissue culture. © John Wiley & Sons, Inc. Biotechnol Bioeng 74: 154–163, 2001.