Transcriptional effects of a positive feedback circuit in Drosophila melanogaster

被引:3
作者
Bryk, Jaroslaw [1 ,2 ]
Reeves, R. Guy [1 ]
Reed, Floyd A. [1 ,3 ]
Denton, Jai A. [1 ,4 ]
机构
[1] Max Planck Inst Evolutionary Biol, Dept Evolutionary Genet, Plon, Germany
[2] Univ Huddersfield, Sch Appl Sci, Huddersfield HD1 3DH, W Yorkshire, England
[3] Univ Hawaii Manoa, Dept Biol, Honolulu, HI 96822 USA
[4] Grad Univ, Okinawa Inst Sci & Technol, Genom & Regulatory Syst Unit, Onna, Okinawa, Japan
来源
BMC GENOMICS | 2017年 / 18卷
关键词
Drosophila melanogaster; tTAV; Vector control; Transcriptome; Microarrays; Tetracycline; MITOCHONDRIAL-FUNCTION; GENE-EXPRESSION; LETHAL MUTANTS; SYSTEM; SUPPRESSION; DOMINANT; CELLS;
D O I
10.1186/s12864-017-4385-z
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Synthetic systems that use positive feedback have been developed to control human disease vectors and crop pests. The tTAV system, which has been deployed in several insect species, relies on a positive feedback circuit that can be inhibited via dietary tetracycline. Although insects carrying tTAV fail to survive until adulthood in the absence of tetracycline, the exact reason for its lethality, as well as the transcriptomic effects of an active positive feedback circuit, remain unknown. Results: We engineered the tTAV system in Drosophila melanogaster and investigated the effects of tTAV genome integration locus on the whole fly transcriptome during larval and adult life stages in four transgenic fly strains using gene expression microarrays. We found that while there were widespread effects on the transcriptome, the gene expression differences after removal of tetracycline were not consistent between integration sites. No specific region of the genome was affected, no common set of genes or pathways, nor did the integration site affect the transcripts in cis. Conclusion: Although the positive feedback tTAV system is effective at killing insect larvae regardless of where it is inserted in the genome, it does not exhibit a specific, consistent transcriptional signature. Instead, each insertion site is associated with broad, but different, transcriptional effects. Our results suggest that lethality may not be caused by a direct effect on transcription of a set of key genes or pathways. Instead, we propose that rather than a specific action of a tTAV protein, it is the stochastic transcriptional effects specific to each insertion site that contribute to the tTAV-induced mortality.
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页数:14
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