Extracellular calmodulin acceleratesrbcS-GUS expression in suspension-cultured transgenic tobacco cell

2000 ◽  
Vol 45 (22) ◽  
pp. 2089-2092 ◽  
Author(s):  
Ligeng Ma ◽  
Junli Zhou ◽  
Suqiao Zhang ◽  
Qiang Liu ◽  
Daye Sun
2001 ◽  
Vol 42 (10) ◽  
pp. 1049-1055 ◽  
Author(s):  
Junli Zhou ◽  
Ligeng Ma ◽  
Suqiao Zhang ◽  
Yuxian Zhu ◽  
Daye Sun

2005 ◽  
Vol 86 (6) ◽  
pp. 1851-1860 ◽  
Author(s):  
Naomi Shirasawa-Seo ◽  
Yoshitaka Sano ◽  
Shigeo Nakamura ◽  
Taka Murakami ◽  
Shigemi Seo ◽  
...  

Predicted promoter regions of Milk vetch dwarf virus (MDV) components (C1–C11) were isolated and fused with a β-glucuronidase (GUS) reporter gene and the characteristics of the promoters were examined. In transgenic tobacco calli, promoters of MDV C4 (encoding a cell-cycle link protein), C5 and C7 (both encoding unknown proteins), C6 (encoding a nuclear-shuttle protein) and C8 (encoding a movement protein) generated a stronger level of GUS expression than the Cauliflower mosaic virus 35S RNA promoter (P35S). In leaves of transgenic tobacco plants, the promoters of C5 and C8 conferred a level of GUS activity comparable to that of P35S. Histochemical GUS analysis showed that the promoters of C4–C9, the latter encoding a capsid protein, were active in phloem and meristematic tissue. The promoter of C8 was also active in mesophyll and cortex cell types. A low level of activity was found for the promoters of C11, which encodes a master replication-initiator protein (Rep), and C1, C2, C3 and C10, which encode additional Reps, in both transgenic tobacco calli and plants.


2017 ◽  
Vol 16 (17) ◽  
pp. 945-952
Author(s):  
Mubeen Hira ◽  
Bashir Aftab ◽  
Ameen Ayesha ◽  
Masood Ammara ◽  
Raza Shahid

2007 ◽  
Vol 164 (4) ◽  
pp. 521-524 ◽  
Author(s):  
Elisabeth Moyano ◽  
Javier Palazón ◽  
Mercedes Bonfill ◽  
Lidia Osuna ◽  
Rosa M. Cusidó ◽  
...  

2006 ◽  
Vol 41 (3) ◽  
pp. 201-222 ◽  
Author(s):  
MAREN BODE ◽  
MATTHIAS HAAS ◽  
TANYA FAYMONVILLE ◽  
BRIGITTE THIEDE ◽  
INGOLF SCHUPHAN ◽  
...  

2009 ◽  
Vol 102 (2) ◽  
pp. 508-520 ◽  
Author(s):  
Ting-Kuo Huang ◽  
Michael A. Plesha ◽  
Bryce W. Falk ◽  
Abhaya M. Dandekar ◽  
Karen A. McDonald

2014 ◽  
Vol 56 (1) ◽  
pp. 73-79 ◽  
Author(s):  
Martin Jopcik ◽  
Ildiko Matusikova ◽  
Jana Moravcikova ◽  
Jana Libantova

Abstract Current biotechnology research is focused on tissue-specific expression of genes of interest in plants. Promoters with specific spatial and temporal expression profiles in targeted organisms are in wide use for this. This study investigated whether the Arabidopsis thaliana seed- and pollen-specific promoter MXL maintains its specificity in transgenic tobacco plants. Histochemical analysis revealed that the MXL fusion promoter drives slightly different GUS expression in that heterologous organism. GUS staining was clearly detected in the bicellular stage of pollen development and later in germinating tobacco pollen grains. Unlike in A. thaliana, where the MXL promoter is active during the whole period of embryo development, in tobacco its activity was restricted to a short temporal and spatial window from late-heart to mid-torpedo stages, mainly in the apical part of the developing embryo. These results point to the need to test the expression profiles of heterologous promoters in targeted species before they are used in particular biotechnological programs.


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