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内含子介导了绿藻莱茵衣藻中核基因表达的转录后增强。

Introns mediate post-transcriptional enhancement of nuclear gene expression in the green microalga Chlamydomonas reinhardtii.

机构信息

Bielefeld University, Faculty of Biology, Center for Biotechnology (CeBiTec), Universitätsstrasse, Bielefeld, Germany.

Biological and Environmental Sciences and Engineering Division (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, Kingdom of Saudi Arabia.

出版信息

PLoS Genet. 2020 Jul 30;16(7):e1008944. doi: 10.1371/journal.pgen.1008944. eCollection 2020 Jul.

DOI:10.1371/journal.pgen.1008944
PMID:32730252
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7419008/
Abstract

Efficient nuclear transgene expression in the green microalga Chlamydomonas reinhardtii is generally hindered by low transcription rates. Introns can increase transcript abundance by a process called Intron-Mediated Enhancement (IME) in this alga and has been broadly observed in other eukaryotes. However, the mechanisms of IME in microalgae are poorly understood. Here, we identified 33 native introns from highly expressed genes in C. reinhardtii selected from transcriptome studies as well as 13 non-native introns. We investigated their IME capacities and probed the mechanism of action by modification of splice sites, internal sequence motifs, and position within transgenes. Several introns were found to elicit strong IME and found to be broadly applicable in different expression constructs. We determined that IME in C. reinhardtii exclusively occurs from introns within transcribed ORFs regardless of the promoter and is not induced by traditional enhancers of transcription. Our results elucidate some mechanistic details of IME in C. reinhardtii, which are similar to those observed in higher plants yet underly distinctly different induction processes. Our findings narrow the focus of targets responsible for algal IME and provides evidence that introns are underestimated regulators of C. reinhardtii nuclear gene expression.

摘要

在绿藻衣藻中,高效的核转基因表达通常受到转录率低的限制。在内含子可以通过一种称为内含子介导增强(IME)的过程增加转录本丰度,并且在其他真核生物中广泛观察到。然而,IME 在微藻中的机制还知之甚少。在这里,我们从转录组研究中选择的衣藻中高度表达的基因中鉴定了 33 个天然内含子,以及 13 个非天然内含子。我们研究了它们的 IME 能力,并通过修饰剪接位点、内部序列基序和转基因内的位置来探究其作用机制。发现几个内含子能够引发强烈的 IME,并在不同的表达构建体中广泛适用。我们确定 IME 在衣藻中仅从转录的 ORF 内的内含子发生,而与启动子无关,并且不受传统转录增强子的诱导。我们的结果阐明了 IME 在衣藻中的一些机制细节,这些细节与在高等植物中观察到的相似,但基础的诱导过程却截然不同。我们的研究结果缩小了负责藻类 IME 的靶标的范围,并提供了证据表明内含子是低估了衣藻核基因表达的调控因子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/8ac168a3beb1/pgen.1008944.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/505b63b47269/pgen.1008944.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/aa2875b7e064/pgen.1008944.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/7eb21b6e41f9/pgen.1008944.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/83384d9db203/pgen.1008944.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/8ac168a3beb1/pgen.1008944.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/505b63b47269/pgen.1008944.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/aa2875b7e064/pgen.1008944.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/7eb21b6e41f9/pgen.1008944.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/83384d9db203/pgen.1008944.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/722a/7419008/8ac168a3beb1/pgen.1008944.g005.jpg

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