2005
DOI: 10.1271/bbb.69.1014
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Homologous Region 3 fromBombyx moriNucleopolyhedrovirus Enhancing the Transcriptional Activity of Heat Shock Cognate 70-4 Promoter fromBombyx moriandBombyx mandarinain Vitroandin Vivo

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Cited by 12 publications
(4 citation statements)
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“…On the other hand, it has been supposed that HSPs act to chaperone viruses, are involved with the assembly and production of progeny virus, and thereby facilitate viral replication [34] . In addition, Tang et al [35] found that the homologous region 3 from Bombyx mori nucleopolyhedrovirus (BmNPVhr3) can significantly increase the transcriptional activity of BmHSC70-4p and HSC70-4p from Bombyx mandarina (BmandHSC70-4p). Taken together, we hold that protein HSP70 is not the result of virus infection, but an accomplice to the infection.…”
Section: Identification Of Host-derived Proteinsmentioning
confidence: 99%
“…On the other hand, it has been supposed that HSPs act to chaperone viruses, are involved with the assembly and production of progeny virus, and thereby facilitate viral replication [34] . In addition, Tang et al [35] found that the homologous region 3 from Bombyx mori nucleopolyhedrovirus (BmNPVhr3) can significantly increase the transcriptional activity of BmHSC70-4p and HSC70-4p from Bombyx mandarina (BmandHSC70-4p). Taken together, we hold that protein HSP70 is not the result of virus infection, but an accomplice to the infection.…”
Section: Identification Of Host-derived Proteinsmentioning
confidence: 99%
“…Previous studies have shown that B. mori baculovirus promoters are functional in expression vectors and display expected transcriptional activity when injected into silkworm larvae (Zhou et al 2002;Chen et al 2004;Tang et al 2005). To assess the efficiency of this method in the pupal wing, we generated a constitutive reporter encoding the luciferase gene under the control of the previously described ie-1 promoter and hr3 enhancer (pBacPAK8-ie-1-luc-hr3; Chen et al 2004).…”
Section: Resultsmentioning
confidence: 99%
“…The cycling protocol for PCR was the following: 1 cycle at 94°C for 3 min; 5 cycles at 94°C for 30 s, 50°C for 30 s and 72°C for 30 s; then 30 cycles at 94°C for 30 s, 55°C for 30 s and 72°C for 30 s; and a final extension step of 10 min at 72°C. The PCR products were analysed on 1% agarose gels and purified using the glass-milk method 30 . The purified fragment was then cloned into the pMD18-T vector and sequenced.…”
Section: Molecular Cloning Of Rmhe Cdnamentioning
confidence: 99%