Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector

The promoter sequences of the encoding genes for the three most abundant hexamerins of the Lepidoptera Trichoplusia ni were isolated and cloned into the Autographa californica multiple nucleopolyhedrovirus (AcMNPV)-derived baculovirus expression vector. >From the sequences analyzed, the DNA region driving the expression of the Basic juvenile hormone-suppressible protein 2 (BJHSP-2), denominated pB2, presented the highest promoter strength in the context of the baculovirus vector in Sf21 insect cells. This promoter activity occurred earlier in baculovirus-infected cells than that achieved by a conventional polyhedrin promoter (polh), but surprisingly stopped at 48h post-infection. A mapping of pB2 essential promoter elements determined that a region of about 400bp, denominated pB29, retained and even increased the transcriptional activity with respect to the parental full-length sequence. Finally, several chimeric combinations of the insect-derived pB2 with the virus-derived conventional polh or p10 promoters were constructed and incorporated into an AcMNPV baculovirus vector. The pB2-p10 combination showed increased recombinant protein expression at early times post-infection and similar expression levels at very late times post-infection in Sf21 cells with respect to conventional late promoters. To the best of our knowledge, pB2 is the first promoter isolated from the Lepidoptera T. ni, the natural host of AcMNPV, to be assayed in a baculovirus expression vector. © 2013 Elsevier B.V.

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Bibliographic Details
Main Authors: López-Vidal, J., Gómez-Sebastián, S., Sánchez Ramos, Ismael Ignacio, Escribano, J. M.
Format: artículo biblioteca
Language:English
Published: Elsevier 2013
Subjects:Baculovirus expression vector system, AcMNPV, Recombinant protein expression, Promoter, Trichoplusia ni, Basic juvenile hormone-suppressible protein 2,
Online Access:http://hdl.handle.net/20.500.12792/2498
http://hdl.handle.net/10261/291192
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spelling dig-inia-es-10261-2911922023-02-20T07:15:33Z Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector López-Vidal, J. Gómez-Sebastián, S. Sánchez Ramos, Ismael Ignacio Escribano, J. M. Baculovirus expression vector system AcMNPV Recombinant protein expression Promoter Trichoplusia ni Basic juvenile hormone-suppressible protein 2 The promoter sequences of the encoding genes for the three most abundant hexamerins of the Lepidoptera Trichoplusia ni were isolated and cloned into the Autographa californica multiple nucleopolyhedrovirus (AcMNPV)-derived baculovirus expression vector. >From the sequences analyzed, the DNA region driving the expression of the Basic juvenile hormone-suppressible protein 2 (BJHSP-2), denominated pB2, presented the highest promoter strength in the context of the baculovirus vector in Sf21 insect cells. This promoter activity occurred earlier in baculovirus-infected cells than that achieved by a conventional polyhedrin promoter (polh), but surprisingly stopped at 48h post-infection. A mapping of pB2 essential promoter elements determined that a region of about 400bp, denominated pB29, retained and even increased the transcriptional activity with respect to the parental full-length sequence. Finally, several chimeric combinations of the insect-derived pB2 with the virus-derived conventional polh or p10 promoters were constructed and incorporated into an AcMNPV baculovirus vector. The pB2-p10 combination showed increased recombinant protein expression at early times post-infection and similar expression levels at very late times post-infection in Sf21 cells with respect to conventional late promoters. To the best of our knowledge, pB2 is the first promoter isolated from the Lepidoptera T. ni, the natural host of AcMNPV, to be assayed in a baculovirus expression vector. © 2013 Elsevier B.V. 2023-02-20T07:15:33Z 2023-02-20T07:15:33Z 2013 artículo Journal of Biotechnology 165: 201-208 (2013) 0168-1656 http://hdl.handle.net/20.500.12792/2498 http://hdl.handle.net/10261/291192 10.1016/j.jbiotec.2013.03.012 en none Elsevier
institution INIA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-inia-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del INIA España
language English
topic Baculovirus expression vector system
AcMNPV
Recombinant protein expression
Promoter
Trichoplusia ni
Basic juvenile hormone-suppressible protein 2
Baculovirus expression vector system
AcMNPV
Recombinant protein expression
Promoter
Trichoplusia ni
Basic juvenile hormone-suppressible protein 2
spellingShingle Baculovirus expression vector system
AcMNPV
Recombinant protein expression
Promoter
Trichoplusia ni
Basic juvenile hormone-suppressible protein 2
Baculovirus expression vector system
AcMNPV
Recombinant protein expression
Promoter
Trichoplusia ni
Basic juvenile hormone-suppressible protein 2
López-Vidal, J.
Gómez-Sebastián, S.
Sánchez Ramos, Ismael Ignacio
Escribano, J. M.
Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector
description The promoter sequences of the encoding genes for the three most abundant hexamerins of the Lepidoptera Trichoplusia ni were isolated and cloned into the Autographa californica multiple nucleopolyhedrovirus (AcMNPV)-derived baculovirus expression vector. >From the sequences analyzed, the DNA region driving the expression of the Basic juvenile hormone-suppressible protein 2 (BJHSP-2), denominated pB2, presented the highest promoter strength in the context of the baculovirus vector in Sf21 insect cells. This promoter activity occurred earlier in baculovirus-infected cells than that achieved by a conventional polyhedrin promoter (polh), but surprisingly stopped at 48h post-infection. A mapping of pB2 essential promoter elements determined that a region of about 400bp, denominated pB29, retained and even increased the transcriptional activity with respect to the parental full-length sequence. Finally, several chimeric combinations of the insect-derived pB2 with the virus-derived conventional polh or p10 promoters were constructed and incorporated into an AcMNPV baculovirus vector. The pB2-p10 combination showed increased recombinant protein expression at early times post-infection and similar expression levels at very late times post-infection in Sf21 cells with respect to conventional late promoters. To the best of our knowledge, pB2 is the first promoter isolated from the Lepidoptera T. ni, the natural host of AcMNPV, to be assayed in a baculovirus expression vector. © 2013 Elsevier B.V.
format artículo
topic_facet Baculovirus expression vector system
AcMNPV
Recombinant protein expression
Promoter
Trichoplusia ni
Basic juvenile hormone-suppressible protein 2
author López-Vidal, J.
Gómez-Sebastián, S.
Sánchez Ramos, Ismael Ignacio
Escribano, J. M.
author_facet López-Vidal, J.
Gómez-Sebastián, S.
Sánchez Ramos, Ismael Ignacio
Escribano, J. M.
author_sort López-Vidal, J.
title Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector
title_short Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector
title_full Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector
title_fullStr Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector
title_full_unstemmed Characterization of a Trichoplusia ni hexamerin-derived promoter in the AcMNPV baculovirus vector
title_sort characterization of a trichoplusia ni hexamerin-derived promoter in the acmnpv baculovirus vector
publisher Elsevier
publishDate 2013
url http://hdl.handle.net/20.500.12792/2498
http://hdl.handle.net/10261/291192
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