Open AccessActivation domains for controlling plant gene expression using designed transcription factors
Author(s) -
Li Jianquan,
Blue Ryan,
Zeitler Bryan,
Strange Tonya L.,
Pearl Jocelynn R.,
Huizinga David H.,
Evans Steve,
Gregory Philip D.,
Urnov Fyodor D.,
Petolino Joseph F.
Publication year - 2013
Publication title -
plant biotechnology journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.525
H-Index - 115
eISSN - 1467-7652
pISSN - 1467-7644
DOI - 10.1111/pbi.12057
Subject(s) - biology , reporter gene , upstream activating sequence , promoter , transcriptional regulation , gene , gene expression , transcription (linguistics) , transcription factor , regulation of gene expression , eukaryotic transcription , rna polymerase ii , microbiology and biotechnology , genetics , linguistics , philosophy
Summary Targeted gene regulation via designed transcription factors has great potential for precise phenotypic modification and acceleration of novel crop trait development. To this end, designed transcriptional activators have been constructed by fusing transcriptional activation domains to DNA ‐binding proteins. In this study, a transcriptional activator from the herpes simplex virus, VP 16 , was used to identify plant regulatory proteins. Transcriptional activation domains were identified from each protein and fused with zinc finger DNA ‐binding proteins ( ZFP s) to generate designed transcriptional activators. In addition, specific sequences within each transcriptional activation domain were modified to mimic the VP 16 contact motif that interacts directly with RNA polymerase II core transcription factors. To evaluate these designed transcriptional activators, test systems were built in yeast and tobacco comprising reporter genes driven by promoters containing ZFP ‐binding sites upstream of the transcriptional start site. In yeast, transcriptional domains from the plant proteins ERF 2 and PTI 4 activated MEL 1 reporter gene expression to levels similar to VP 16 and the modified sequences displayed even greater levels of activation. Following stable transformation of the tobacco reporter system with transcriptional activators derived from ERF 2 , GUS reporter gene transcript accumulation was equal to or greater than those derived from VP 16 . Moreover, a modified ERF 2 domain displayed significantly enhanced transcriptional activation compared with VP 16 and with the unmodified ERF 2 sequence. These results demonstrate that plant sequences capable of facilitating transcriptional activation can be found and, when fused to DNA ‐binding proteins, can enhance gene expression.