Literature DB >> 12239419

Approaching the Lower Limits of Transgene Variability.

L. Mlynarova1, LCP. Keizer, W. J. Stiekema, J. P. Nap.   

Abstract

The inclusion of chicken lysozyme matrix-associated regions (MARs) in T-DNA has been demonstrated to reduce the variation in [beta]-glucuronidase (GUS) gene expression among first-generation transformed plants. The residual variation observed between transgenic plant lines with MARs at the T-DNA borders was investigated. By definition, any phenotypic variance between or within genetically identical plants is caused by random or environmental variation. This variation therefore sets a lower limit to the variation in GUS activities. The variance of GUS activity in offspring plant populations of genetically identical individuals was used as an estimate of environmental variation. For transgenic plants with MARs at the T-DNA borders, the variation between independent transformants could not be distinguished from the environmental variation. The variation could be attributed mainly to the variation in the GUS activity measurement. Therefore, the MAR element approached the maximal possible reduction of transgene variability given current technology and sample sizes. The role of MARs in offspring plants was evaluated by comparing such populations of transgenic plants for the magnitude of and variation in GUS activity. Pairwise comparisons showed that the presence of MARs reduced variation in offspring generations in the same manner as demonstrated for primary transformants. The populations carrying a doubled cauliflower mosaic virus 35S promoter-GUS gene tended to be more variable than the Lhca3.St.1 promoter-GUS gene-carrying populations. This tendency indicated an intrinsic susceptibility of the doubled cauliflower mosaic virus 35S promoter to variation. Homozygous plants were approximately twice as active as the corresponding hemizygous plants and tended to be more variable than the hemizygous plants. We hypothesized that the magnitude of environmental variations is related to a higher susceptibility to transgene silencing.

Entities:  

Year:  1996        PMID: 12239419      PMCID: PMC161300          DOI: 10.1105/tpc.8.9.1589

Source DB:  PubMed          Journal:  Plant Cell        ISSN: 1040-4651            Impact factor:   11.277


  14 in total

1.  Nuclear Matrix Attachment Regions and Transgene Expression in Plants.

Authors:  S. Spiker; W. F. Thompson
Journal:  Plant Physiol       Date:  1996-01       Impact factor: 8.340

2.  How and Why Do Plants Inactivate Homologous (Trans)genes?

Authors:  M. A. Matzke; AJM. Matzke
Journal:  Plant Physiol       Date:  1995-03       Impact factor: 8.340

3.  Transgene expression variability (position effect) of CAT and GUS reporter genes driven by linked divergent T-DNA promoters.

Authors:  C Peach; J Velten
Journal:  Plant Mol Biol       Date:  1991-07       Impact factor: 4.076

4.  Transgene copy number can be positively or negatively associated with transgene expression.

Authors:  S L Hobbs; T D Warkentin; C M DeLong
Journal:  Plant Mol Biol       Date:  1993-01       Impact factor: 4.076

5.  A nuclear DNA attachment element mediates elevated and position-independent gene activity.

Authors:  A Stief; D M Winter; W H Strätling; A E Sippel
Journal:  Nature       Date:  1989-09-28       Impact factor: 49.962

6.  Scaffold attachment regions increase reporter gene expression in stably transformed plant cells.

Authors:  G C Allen; G E Hall; L C Childs; A K Weissinger; S Spiker; W F Thompson
Journal:  Plant Cell       Date:  1993-06       Impact factor: 11.277

7.  Expansions of transgene repeats cause heterochromatin formation and gene silencing in Drosophila.

Authors:  D R Dorer; S Henikoff
Journal:  Cell       Date:  1994-07-01       Impact factor: 41.582

8.  Reduced Position Effect in Mature Transgenic Plants Conferred by the Chicken Lysozyme Matrix-Associated Region.

Authors:  L. Mlynarova; A. Loonen; J. Heldens; R. C. Jansen; P. Keizer; W. J. Stiekema; J. P. Nap
Journal:  Plant Cell       Date:  1994-03       Impact factor: 11.277

9.  Activity of the promoter of the Lhca3.St.1 gene, encoding the potato apoprotein 2 of the light-harvesting complex of Photosystem I, in transgenic potato and tobacco plants.

Authors:  J P Nap; M van Spanje; W G Dirkse; G Baarda; L Mlynarova; A Loonen; P Grondhuis; W J Stiekema
Journal:  Plant Mol Biol       Date:  1993-11       Impact factor: 4.076

10.  Binary Agrobacterium vectors for plant transformation.

Authors:  M Bevan
Journal:  Nucleic Acids Res       Date:  1984-11-26       Impact factor: 16.971

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  18 in total

1.  Matrix attachment region binding protein MFP1 is localized in discrete domains at the nuclear envelope.

Authors:  F Gindullis; I Meier
Journal:  Plant Cell       Date:  1999-06       Impact factor: 11.277

Review 2.  Enabling technologies for manipulating multiple genes on complex pathways.

Authors:  C Halpin; A Barakate; B M Askari; J C Abbott; M D Ryan
Journal:  Plant Mol Biol       Date:  2001-09       Impact factor: 4.076

Review 3.  Plants as bioreactors for protein production: avoiding the problem of transgene silencing.

Authors:  C De Wilde; H Van Houdt; S De Buck; G Angenon; G De Jaeger; A Depicker
Journal:  Plant Mol Biol       Date:  2000-06       Impact factor: 4.076

Review 4.  Use of matrix attachment regions (MARs) to minimize transgene silencing.

Authors:  G C Allen; S Spiker; W F Thompson
Journal:  Plant Mol Biol       Date:  2000-06       Impact factor: 4.076

5.  Elevation of transgene expression level by flanking matrix attachment regions (MAR) is promoter dependent: a study of the interactions of six promoters with the RB7 3' MAR.

Authors:  S Luke Mankin; George C Allen; Thomas Phelan; Steven Spiker; William F Thompson
Journal:  Transgenic Res       Date:  2003-02       Impact factor: 2.788

6.  Quantitative determination of mosaic GFP gene expression in tobacco.

Authors:  M T Bastar; Z Luthar; S Skof; B Bohanec
Journal:  Plant Cell Rep       Date:  2004-05-04       Impact factor: 4.570

7.  Heritable transgene expression pattern imposed onto maize ubiquitin promoter by maize adh-1 matrix attachment regions: tissue and developmental specificity in maize transgenic plants.

Authors:  François Torney; Anne Partier; Véronique Says-Lesage; Isabelle Nadaud; Pierre Barret; Michel Beckert
Journal:  Plant Cell Rep       Date:  2004-05-04       Impact factor: 4.570

8.  Conservation of matrix attachment region-binding filament-like protein 1 among higher plants.

Authors:  P A Harder; R A Silverstein; I Meier
Journal:  Plant Physiol       Date:  2000-01       Impact factor: 8.340

9.  TM2, a novel strong matrix attachment region isolated from tobacco, increases transgene expression in transgenic rice calli and plants.

Authors:  Hua Xue; Yu-Tao Yang; Chang-Ai Wu; Guo-Dong Yang; Meng-Meng Zhang; Cheng-Chao Zheng
Journal:  Theor Appl Genet       Date:  2005-01-20       Impact factor: 5.699

10.  Matrix attachment region from the chicken lysozyme locus reduces variability in transgene expression and confers copy number-dependence in transgenic rice plants.

Authors:  S-J Oh; J S Jeong; E-H Kim; N R Yi; S-I Yi; I-C Jang; Y S Kim; S-C Suh; B H Nahm; J-K Kim
Journal:  Plant Cell Rep       Date:  2005-02-16       Impact factor: 4.570

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