Transcriptional Activators of Human Genes with Programmable DNA-Specificity

被引:118
作者
Geissler, Rene [1 ]
Scholze, Heidi [2 ]
Hahn, Simone [2 ]
Streubel, Jana [2 ]
Bonas, Ulla [2 ]
Behrens, Sven-Erik [1 ]
Boch, Jens [2 ]
机构
[1] Univ Halle Wittenberg, Inst Biochem & Biotechnol, Sect Microbial Biotechnol, Halle, Saale, Germany
[2] Univ Halle Wittenberg, Dept Genet, Inst Biol, Halle, Saale, Germany
来源
PLOS ONE | 2011年 / 6卷 / 05期
关键词
HERPES-SIMPLEX-VIRUS; DOUBLE-STRAND BREAKS; TAL EFFECTORS; III EFFECTORS; RESTRICTION ENZYMES; BINDING SPECIFICITY; BACTERIAL-BLIGHT; C-TERMINUS; ONE-POT; RECOGNITION;
D O I
10.1371/journal.pone.0019509
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
TAL (transcription activator-like) effectors are translocated by Xanthomonas bacteria into plant cells where they activate transcription of target genes. DNA target sequence recognition occurs in a unique mode involving a central domain of tandem repeats. Each repeat recognizes a single base pair in a contiguous DNA sequence and a pair of adjacent hypervariable amino acid residues per repeat specifies which base is bound. Rearranging the repeats allows the design of novel TAL proteins with predictable DNA-recognition specificities. TAL protein-based transcriptional activation in plant cells is mediated by a C-terminal activation domain (AD). Here, we created synthetic TAL proteins with designed repeat compositions using a novel modular cloning strategy termed "Golden TAL Technology". Newly programmed TAL proteins were not only functional in plant cells, but also in human cells and activated targeted expression of exogenous as well as endogenous genes. Transcriptional activation in different human cell lines was markedly improved by replacing the TAL-AD with the VP16-AD of herpes simplex virus. The creation of TAL proteins with potentially any desired DNA-recognition specificity allows their versatile use in biotechnology.
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页数:7
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