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利用异源模型菌株鉴定和功能分析 的启动子。

Identification and Functional Analysis of the Promoter of Using Heterologous Model Strains.

机构信息

Department of Life Science, College of Natural Sciences, Hanyang University, Seoul 04763, Korea.

Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.

出版信息

Int J Mol Sci. 2018 Jul 6;19(7):1969. doi: 10.3390/ijms19071969.

DOI:10.3390/ijms19071969
PMID:29986409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6073903/
Abstract

has great potential as a bio-factory for production of value-added compounds. To produce the desired chemicals more efficiently in , genetic tools for modification of need to be developed, especially an endogenous promoter. In this study, the promoter of photosystem I protein D () from UTEX395 was identified. Computational analysis revealed the presence of several putative cis-acting elements, including a potential core element, and light-responsive or stress-responsive elements. Gene expression analysis in heterologous expression system in and showed that promoter can be used to drive the expression of genes. Functional analysis of this promoter suggested that the initiator element (Inr) is important for its function (i.e., TATA-less promoter) and that an additional factor (e.g., downstream of the transcriptional start site) might be needed for light response. We have shown that the promoter is functional, but not sufficiently strong, both in microalgae and higher plant.

摘要

具有作为生产增值化合物的生物工厂的巨大潜力。为了更有效地在 中生产所需的化学品,需要开发用于修饰 的遗传工具,特别是内源性启动子。在这项研究中,从 UTEX395 中鉴定出了光系统 I 蛋白 D ()的启动子。计算分析显示存在几个假定的顺式作用元件,包括一个潜在的核心元件,以及光响应或应激响应元件。在 和 中的异源表达系统中的基因表达分析表明, 启动子可用于驱动基因的表达。该启动子的功能分析表明,起始元件 (Inr) 对于其功能(即 TATA-less 启动子)很重要,并且可能需要额外的因子(例如,在转录起始位点的下游)来进行光响应。我们已经表明, 启动子在微藻和高等植物中均具有功能,但不够强。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/ab18356fb4f4/ijms-19-01969-g006.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/2e79b7085b37/ijms-19-01969-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/39ebdc1820e8/ijms-19-01969-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/ab18356fb4f4/ijms-19-01969-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/4f3570eb3276/ijms-19-01969-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/63808372daaf/ijms-19-01969-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/9121cf7a07ad/ijms-19-01969-g003a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/2e79b7085b37/ijms-19-01969-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/39ebdc1820e8/ijms-19-01969-g005a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f7c/6073903/ab18356fb4f4/ijms-19-01969-g006.jpg

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Biotechnol J. 2016 Oct;11(10):1244-1261. doi: 10.1002/biot.201500617. Epub 2016 Jul 28.
3
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4
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J Microbiol Biotechnol. 2020 Nov 28;30(11):1777-1784. doi: 10.4014/jmb.2007.07024.
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Site-Specific Gene Knock-Out and On-Site Heterologous Gene Overexpression in via a CRISPR-Cas9-Mediated Knock-in Method.通过CRISPR-Cas9介导的敲入方法在[具体生物]中进行位点特异性基因敲除和原位异源基因过表达。 (注:原文中“in via”表述有误,推测应该是“in [具体生物] via”,这里按推测完整表述翻译)
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Biotechnol J. 2016 Mar;11(3):384-92. doi: 10.1002/biot.201500269.
4
In Metabolic Engineering of Eukaryotic Microalgae: Potential and Challenges Come with Great Diversity.真核微藻的代谢工程:潜力与挑战并存于巨大的多样性之中。
Front Microbiol. 2015 Dec 15;6:1376. doi: 10.3389/fmicb.2015.01376. eCollection 2015.
5
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J Exp Bot. 2014 Dec;65(22):6563-76. doi: 10.1093/jxb/eru374. Epub 2014 Sep 10.
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