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
[51]  
HU W, 1995, FEBS LETT, V369, P331, DOI 10.1016/0014-5793(95)00776-6
[52]   High transformation frequencies obtained from a commercial wheat (Triticum aestivum L. cv. 'Combi') by microbombardment of immature embryos followed by GFP screening combined with PPT selection [J].
Huber, M ;
Hahn, R ;
Hess, D .
MOLECULAR BREEDING, 2002, 10 (1-2) :19-30
[53]   Cell-to-cell trafficking of cucumber mosaic virus movement protein green fluorescent protein fusion produced by biolistic gene bombardment in tobacco [J].
Itaya, A ;
Hickman, H ;
Bao, YM ;
Nelson, R ;
Ding, B .
PLANT JOURNAL, 1997, 12 (05) :1223-1230
[54]  
JEFFERSON RA, 1987, EMBO J, V6, P3901
[55]   Optimization of sorghum transformation parameters using genes for green fluorescent protein and β-glucuronidase as visual markers [J].
Jeoung, JM ;
Krishnaveni, S ;
Muthukrishnan, S ;
Trick, HN ;
Liang, GH .
HEREDITAS, 2002, 137 (01) :20-28
[56]   Green fluorescent protein as a visual marker for wheat transformation [J].
Jordan, MC .
PLANT CELL REPORTS, 2000, 19 (11) :1069-1075
[57]   Transgenic oat plants via visual selection of cells expressing green fluorescent protein [J].
Kaeppler, HF ;
Menon, GK ;
Skadsen, RW ;
Nuutila, AM ;
Carlson, AR .
PLANT CELL REPORTS, 2000, 19 (07) :661-666
[58]   Transformation of floral organs with GFP in Medicago truncatula [J].
Kamaté, K ;
Rodriguez-Llorente, ID ;
Scholte, M ;
Durand, P ;
Ratet, P ;
Kondorosi, E ;
Kondorosi, A ;
Trinh, TH .
PLANT CELL REPORTS, 2000, 19 (07) :647-653
[59]   Agrobacterium tumefaciens-mediated transformation of Rosa hybrida using the green fluorescent protein (GFP) gene [J].
Kim, CK ;
Chung, JD ;
Park, SH ;
Burrell, AM ;
Kamo, KK ;
Byrne, DH .
PLANT CELL TISSUE AND ORGAN CULTURE, 2004, 78 (02) :107-111
[60]   Transgenic medaka with brilliant fluorescence in skeletal muscle under normal light [J].
Kinoshita, M .
FISHERIES SCIENCE, 2004, 70 (04) :645-649