Expression of fission yeast cdc25 driven by the wheat ADP-glucose pyrophosphorylase large subunit promoter reduces pollen viability and prevents transmission of the transgene in wheat

Copyright New Phytologist (2005).

Détails bibliographiques
Publié dans:The New phytologist. - 1979. - 166(2005), 1 vom: 01. Apr., Seite 185-92
Auteur principal: Chrimes, D (Auteur)
Autres auteurs: Rogers, H J, Francis, D, Jones, H D, Ainsworth, C
Format: Article
Langue:English
Publié: 2005
Accès à la collection:The New phytologist
Sujets:Journal Article Research Support, Non-U.S. Gov't Recombinant Fusion Proteins Nucleotidyltransferases EC 2.7.7.- Glucose-1-Phosphate Adenylyltransferase EC 2.7.7.27 cdc25 Phosphatases EC 3.1.3.48
Description
Résumé:Copyright New Phytologist (2005).
Cell number was to be measured in wheat (Triticum aestivum) endosperm expressing Spcdc25 (a fission yeast cell-cycle regulator) controlled by a supposedly endosperm-specific promoter, AGP2 (from the large subunit of ADP glucose pyrophosphorylase). Wheat was transformed by biolistics either with AGP2::GUS or AGP2::Spcdc25. PCR and RT-PCR checked integration and expression of the transgene, respectively. In cv. Chinese Spring, AGP2::GUS was unexpectedly expressed in carpels and pollen, as well as endosperm. In cv. Cadenza, three AGP2::Spcdc25 plants, AGP2::Spcdc25.1, .2 and .3, were generated. Spcdc25 expression was detected in mature leaves of AGP2::Spcdc25.1/.3 which exhibited abnormal spikes, 50% pollen viability and low seed set per plant; both were small compared with the nonexpressing and normal AGP2::Spcdc25.2. Spcdc25 was not transmitted to the T(1) in AGP2::Spcdc25.1 or .3, which developed normally. Spcdc25 was PCR-positive in AGP2::Spcdc25.2, using primers for a central portion, but not with primers for the 5' end, of the ORF, indicating a rearrangement; Spcdc25 was not expressed in either T(0) or T(1). The AGP2 promoter is not tissue-specific and Spcdc25 expression disrupted reproduction
Description:Date Completed 22.06.2005
Date Revised 10.03.2022
published: Print
Citation Status MEDLINE
ISSN:1469-8137