Green fluorescent protein as a vital marker for non-destructive detection of transformation events in transgenic plants

被引:38
作者
Hraska, Marek
Rakousky, Slavomir
Curn, Vladislav
机构
[1] Univ S Bohemia, Fac Hlth & Social Studies, CZ-37005 Ceske Budejovice, Czech Republic
[2] Univ S Bohemia, Dept Genet, Fac Biol Sci, CZ-37005 Ceske Budejovice, Czech Republic
[3] Univ S Bohemia, Ctr Biotechnol, Fac Agr, CZ-37005 Ceske Budejovice, Czech Republic
关键词
Agrobacterium tumefaciens; green fluorescent protein; particle bombardment; plant transformation; selection;
D O I
10.1007/s11240-006-9131-1
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Transformation of plants is a popular tool for modifying various desirable traits. Marker genes, like those encoding for bacterial beta-glucuronidase (GUS), firefly luciferase (LUC) or jellyfish green fluorescent protein (GFP) have been shown to be very useful for establishing of efficient transformation protocols. Due to favourable properties such as no need of exogenous substrates and easy visualization, GFP has been found to be superior in to other markers in many cases. However, the use of GFP fluorescence is associated with some obstacles, mostly related to the diminishing of green fluorescence in older tissues, variation in fluorescence levels among different tissues and organs, and occasional interference with other fluorescing compounds in plants. This paper briefly summarizes basic GFP properties and applications, and describes in more detail the contribution of GFP to the establishment, evaluation and improvement of transformation procedures for plants. Moreover, features and possible obstacles associated with monitoring GFP fluorescence are discussed.
引用
收藏
页码:303 / 318
页数:16
相关论文
共 129 条
[1]   Green fluorescent protein as a reporter system in the transformation of barley cultivars [J].
Ahlandsberg, S ;
Sathish, P ;
Sun, CX ;
Jansson, C .
PHYSIOLOGIA PLANTARUM, 1999, 107 (02) :194-200
[2]   Green fluorescent protein as an efficient selection marker for Agrobacterium rhizogenes mediated carrot transformation [J].
Baranski, R ;
Klocke, E ;
Schumann, G .
PLANT CELL REPORTS, 2006, 25 (03) :190-197
[3]   HISTOCHEMICAL ANALYSIS OF CAMV 35S PROMOTER-BETA-GLUCURONIDASE GENE-EXPRESSION IN TRANSGENIC RICE PLANTS [J].
BATTRAW, MJ ;
HALL, TC .
PLANT MOLECULAR BIOLOGY, 1990, 15 (04) :527-538
[4]  
Baucher M, 1998, CRIT REV PLANT SCI, V17, P125, DOI 10.1016/S0735-2689(98)00360-8
[5]   Simultaneous visualization of the yellow and green forms of the green fluorescent protein in living cells [J].
Baumann, CT ;
Lim, CS ;
Hager, GL .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1998, 46 (09) :1073-1076
[6]   Jellyfish green fluorescent protein as a useful reporter for transient expression and stable transformation in Medicago sativa L. [J].
Bellucci, M ;
De Marchis, F ;
Mannucci, R ;
Arcioni, S .
PLANT CELL REPORTS, 2003, 22 (05) :328-337
[7]   THE CAMV S-35 ENHANCER CONTAINS AT LEAST 2 DOMAINS WHICH CAN CONFER DIFFERENT DEVELOPMENTAL AND TISSUE-SPECIFIC EXPRESSION PATTERNS [J].
BENFEY, PN ;
REN, L ;
CHUA, NH .
EMBO JOURNAL, 1989, 8 (08) :2195-2202
[8]   Plant transformation: Problems and strategies for practical application [J].
Birch, RG .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1997, 48 :297-326
[9]   Increased Agrobacterium-mediated transformation and rooting efficiencies in canola (Brassica napus L.) from hypocotyl segment explants [J].
Cardoza, V ;
Stewart, CN .
PLANT CELL REPORTS, 2003, 21 (06) :599-604
[10]   Visual screening of microspore-derived transgenic barley (Hordeum vulgare L.) with green-fluorescent protein [J].
Carlson, AR ;
Letarte, J ;
Chen, J ;
Kasha, KJ .
PLANT CELL REPORTS, 2001, 20 (04) :331-337