Literature DB >> 15127224

Quantitative determination of mosaic GFP gene expression in tobacco.

M T Bastar1, Z Luthar, S Skof, B Bohanec.   

Abstract

A specific form of gene silencing that was observed visually as a mosaic distribution of fluorescent and non-fluorescent cells apparently dispersed at random within tissues was found in a few green fluorescent protein (GFP)-transformed tobacco lines. To characterize this event quantitatively, we studied flow cytometric measurements in GFP-expressing and -silenced cells in T1 and T2 progeny of four selected plants. The proportion of silenced cells varied considerably among the T1 lines but with notable genotype differences. Mosaic expression was inherited into the T2 generation in which the majority of progenies tested exhibited a level of silencing similar to that of their T1 parental plants. However, in some T2 progenies segregation, evident as a decrease or increase in the proportion of fluorescent cells, was observed. We discuss several factors, such as copy number, promoter activity or polyploidy, that may be the possible causes of the gene silencing, but none sufficiently explain the appearance of the mosaic distribution.

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Year:  2004        PMID: 15127224     DOI: 10.1007/s00299-004-0782-2

Source DB:  PubMed          Journal:  Plant Cell Rep        ISSN: 0721-7714            Impact factor:   4.570


  15 in total

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Journal:  Plant J       Date:  2002-07       Impact factor: 6.417

6.  Susceptibility of transgene loci to homology-dependent gene silencing.

Authors:  F Neuhuber; Y D Park; A J Matzke; M A Matzke
Journal:  Mol Gen Genet       Date:  1994-08-02

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  5 in total

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4.  The usefulness of the gfp reporter gene for monitoring Agrobacterium-mediated transformation of potato dihaploid and tetraploid genotypes.

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5.  Development and bioassay of transgenic Chinese cabbage expressing potato proteinase inhibitor II gene.

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  5 in total

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