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Revealing the alternative promoter usage of SAF/MAZ gene by bichromatic fluorescent reporter construct
Author(s) -
Jianbo Ren,
Dawei Guo,
Xiaoyi Wang,
Chao Zhang,
Bo Wang,
Zhe Gao
Publication year - 2019
Publication title -
bioscience reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.938
H-Index - 77
eISSN - 1573-4935
pISSN - 0144-8463
DOI - 10.1042/bsr20171668
Subject(s) - promoter , reporter gene , transactivation , green fluorescent protein , biology , gene , transcription factor , gene expression , transcription (linguistics) , zinc finger , plasmid , regulation of gene expression , microbiology and biotechnology , genetics , linguistics , philosophy
The large-scale identification of putative alternative promoters study shows more than 52% of human genes are regulated by alternative promoters. The human myc -associated zinc finger protein (SAF/MAZ) gene have SAF-1 and SAF-3 variants transcripted from two transcription start sites (TSSs). By using SAF/MAZ promoter as a model, we set up an approach to probe how the alternative promoters are regulated in real time. We have constructed the bichromatic fluorescent reporter driven by SAF/MAZ 5'-proximal promoter plasmids from which transactivation status of SAF-1 and SAF-3 alternative promoter could be monitored by EGFP and DsRed expression respectively. The results showed that the SAF-3 expression is regulated by alternative promoters. When the bichromatic fluorescent reporter was driven by -1692/+277 or -1401/+277 SAF/MAZ promoter the dominant expression of SAF-3 would be observed in comparison with SAF-1 expression. We also identified that Elk-1 is an inhibitory transcription factor for SAF-3 expression. The temporal diversity of SAF-1 and SAF-3 expressions can be observed via bichromatic fluorescent reporters. These imply that the bichromatic fluorescent reporter driven by alternative promoter construct might be a useful tool for decoding the temporal regulatory repertoire of alternative promoter in human genes.

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