J Gen Virol Try Microbiology Online
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Gen Virol 78 (1997), 487-491
© 1997 Society for General Microbiology

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Toister-Achituv, M.
Right arrow Articles by Faktor, O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Toister-Achituv, M.
Right arrow Articles by Faktor, O.
Agricola
Right arrow Articles by Toister-Achituv, M.
Right arrow Articles by Faktor, O.

Journal of General Virology, Vol 78, 487-491, Copyright © 1997 by Society for General Microbiology


ARTICLES

Transcriptional analysis and promoter activity of the Spodoptera littoralis multicapsid nucleopolyhedrovirus ecdysteroid UDP- glucosyltransferase gene

M Toister-Achituv and O Faktor
Department of Entomology, Faculty of Agriculture, The Hebrew University of Jerusalem, Rehovot, Israel.

The ecdysteroid UDP-glucosyltransferase gene (egt) of Spodoptera littoralis multicapsid nucleopolyhedrovirus (SpliMNPV) is a homologue of the Autographa californica MNPV (AcMNPV) egt gene, which has been found to block insect moulting. Infection of larvae with an egt-deleted AcMNPV resulted in enhanced mortality as compared to infection with the wild-type virus. Consequently, deletion of an egt gene has been proposed as a tempting approach for enhancing the insecticidal properties of baculoviruses. In a previous report we described the mapping and sequencing of the SpliMNPV egt gene. Here we use time- course Northern blot and biochemical analyses to show the production of egt transcripts and protein. The SpliMNPV egt transcription start sites were mapped to 22 and 25 nucleotides downstream of the TATA box by primer extension. Transient expression assays of chimeric egt promoter- chloramphenicol acetyltransferase (cat) reporter gene constructs revealed low promoter activity that was transactivated by AcMNPV immediate-early viral protein IE-1.


This article has been cited by other articles:


Home page
J. Gen. Virol.Home page
N. Markine-Goriaynoff, L. Gillet, J. L. Van Etten, H. Korres, N. Verma, and A. Vanderplasschen
Glycosyltransferases encoded by viruses
J. Gen. Virol., October 1, 2004; 85(10): 2741 - 2754.
[Abstract] [Full Text] [PDF]


Home page
J. Gen. Virol.Home page
S. Gutierrez, I. Kikhno, and M. Lopez Ferber
Transcription and promoter analysis of pif, an essential but low-expressed baculovirus gene
J. Gen. Virol., February 1, 2004; 85(2): 331 - 341.
[Abstract] [Full Text] [PDF]


Home page
J. Virol.Home page
Q. Du, D. Lehavi, O. Faktor, Y. Qi, and N. Chejanovsky
Isolation of an Apoptosis Suppressor Gene of the Spodoptera littoralis Nucleopolyhedrovirus
J. Virol., February 1, 1999; 73(2): 1278 - 1285.
[Abstract] [Full Text]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 1997 by the Society for General Microbiology.