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Functional Analysis of the Promoter Region of Japanese Flounder (Paralichthys olivaceus) ?-actin Gene: A Useful Tool for Gene Research in Marine Fish.


ABSTRACT: A newly isolated Japanese flounder (Paralichthys olivaceus) β-actin promoter and its derivative compact construct Poβ-actinΔ−1080/−801Δ−500/−201 have recently been demonstrated to promote ectopic gene expression in cell lines. Different Poβ-actin promoter deletion mutants were constructed and functionally characterized. Mutational analyses by dual-luciferase detected that three regulatory elements, including one enhancer (−1399/−1081) and two silencers (−1080/−801, −500/−201) in the first intron. The sequence located at −1399/−1081 was determined to significantly affect promoter activity. Additionally, the first exon (−1489/−1400) could also remarkably promote the β-actin promoter activity. In the following transduction application, we removed the two silencers and generated a compact reconstruct promoter/enhancer (Poβ-actinΔ−1080/−801Δ−500/−201), which exhibited relatively stronger promoter activity compared with Poβ-actin. Furthermore, the green fluorescent protein (GFP) transgenic stable flounder cell line was obtained by the reconstructed Poβ-actinΔ−1080/−801Δ−500/−201 promoter. Our study provided the potential application of Japanese flounder β-actin, particularly Poβ-actinΔ−1080/−801Δ−500/−201, in ectopic gene expression in the future.

SUBMITTER: Wang B 

PROVIDER: S-EPMC5983668 | biostudies-literature | 2018 May

REPOSITORIES: biostudies-literature

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Functional Analysis of the Promoter Region of Japanese Flounder (<i>Paralichthys olivaceus</i>) <i>β-actin</i> Gene: A Useful Tool for Gene Research in Marine Fish.

Wang Bo B   Wang Huizhen H   Gao Chen C   Liu Yuxiang Y   Jin Chaofan C   Sun Minmin M   Zhang Quanqi Q   Qi Jie J  

International journal of molecular sciences 20180508 5


A newly isolated Japanese flounder (<i>Paralichthys olivaceus</i>) &beta;-actin promoter and its derivative compact construct Po&beta;-actin&Delta;&minus;1080/&minus;801&Delta;&minus;500/&minus;201 have recently been demonstrated to promote ectopic gene expression in cell lines. Different Po&beta;-actin promoter deletion mutants were constructed and functionally characterized. Mutational analyses by dual-luciferase detected that three regulatory elements, including one enhancer (&minus;1399/&min  ...[more]

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