Abstract
In previous work, we selected a particular transcription factor, designated VP16-HRU, from a pool of zinc finger artificial transcription factors (ZF-ATFs) used for genome interrogation. When expressed in Arabidopsis thaliana under control of the ribosomal protein S5A promoter, the RPS5A::VP16-HRU construct led to a 200- to 300-fold increase in the frequency of somatic intrachromosomal homologous recombination (iHR). Because the expression of each ZF-ATF leads to a large number of transcriptional changes, we designed a strategy employing a collection of structurally similar ZF-ATFs to filter out the transcriptional changes relevant to the phenotype by deep sequencing. In that manner, 30 transcripts were found to be consistently induced in plants with enhanced homologous recombination (HR). For 25 of the cognate genes, their effect on the HR process was assessed using cDNA/gDNA expression constructs. For three genes, ectopic expression indeed led to enhanced iHR frequencies, albeit much lower than the frequency observed when a HR-inducing ZF-ATF was present. Altogether, our data demonstrate that despite the large number of transcriptional changes brought about by individual ZF-ATFs, causal changes can be identified. In our case, the picture emerged that a natural regulatory switch for iHR does not exist but that ZF-ATFs-like VP16-HRU act as an ectopic master switch, orchestrating the timely expression of a set of plant genes that each by themselves only have modest effects, but when acting together support an extremely high iHR frequency. © 2013 Society for Experimental Biology, Association of Applied Biologists and John Wiley & Sons Ltd.
Original language | English |
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Pages (from-to) | 1069-1079 |
Number of pages | 11 |
Journal | Plant Biotechnology Journal |
Volume | 11 |
Issue number | 9 |
DOIs | |
Publication status | Published - 1 Dec 2013 |
Keywords
- synthetic DNA
- transcription factor
- zinc finger protein
- Arabidopsis
- article
- DNA sequence
- gene expression
- gene expression profiling
- genetics
- genome interrogation
- high throughput sequencing
- homologous recombination
- mutagenesis
- mutation
- next generation sequencing
- phenotype
- plant genome
- promoter region
- somatic intrachromosomal homologous recombination
- transcriptome analysis
- transgenic plant
- zinc finger artificial transcription factor