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RNA processing and export.RNA 加工和输出。
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Testing the IMEter on rice introns and other aspects of intron-mediated enhancement of gene expression.在水稻内含子和内含子介导的基因表达增强的其他方面测试 IMEter。
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Characterization of EMU, the Arabidopsis homolog of the yeast THO complex member HPR1.拟南芥 THO 复合物成员 HPR1 的酵母同源物 EMU 的特性分析。
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Pre-mRNA processing reaches back to transcription and ahead to translation.前体信使核糖核酸(pre-mRNA)加工可追溯到转录阶段,并延伸至翻译阶段。
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A reduction in RNA polymerase II initiation rate suppresses hyper-recombination and transcription-elongation impairment of THO mutants.RNA聚合酶II起始速率的降低可抑制THO突变体的过度重组和转录延伸损伤。
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The splicing factor SC35 has an active role in transcriptional elongation.剪接因子SC35在转录延伸中发挥着积极作用。
Nat Struct Mol Biol. 2008 Aug;15(8):819-26. doi: 10.1038/nsmb.1461. Epub 2008 Jul 20.
9
Gene expression enhancement mediated by the 5' UTR intron of the rice rubi3 gene varied remarkably among tissues in transgenic rice plants.水稻rubi3基因5'UTR内含子介导的基因表达增强在转基因水稻植株的不同组织间存在显著差异。
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内含子的存在对于拟南芥中 ERECTA 的表达是必不可少的。

The presence of multiple introns is essential for ERECTA expression in Arabidopsis.

机构信息

Department of Biochemistry, Cellular and Molecular Biology, University of Tennessee, Knoxville, TN 37996, USA.

出版信息

RNA. 2011 Oct;17(10):1907-21. doi: 10.1261/rna.2825811. Epub 2011 Aug 31.

DOI:10.1261/rna.2825811
PMID:21880780
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3185922/
Abstract

Gene expression in eukaryotes is often enhanced by the presence of introns. Depending on the specific gene, this enhancement can be minor or very large and occurs at both the transcriptional and post-transcriptional levels. The Arabidopsis ERECTA gene contains 27 exons encoding a receptor-like kinase that promotes cell proliferation and inhibits cell differentiation in above-ground plant organs. The expression of ERECTA very strongly depends on the presence of introns. The intronless ERECTA gene does not rescue the phenotype of erecta mutant plants and produces about 500-900 times less protein compared with the identical construct containing introns. This result is somewhat surprising as the region upstream of the ERECTA coding sequence effectively promotes the expression of extraneous genes. Here, we demonstrate that introns are essential for ERECTA mRNA accumulation and, to a lesser extent, for mRNA utilization in translation. Since mRNA produced by intronless ERECTA is degraded at the 3' end, we speculate that introns increase mRNA accumulation through increasing its stability at least in part. No individual intron is absolutely necessary for ERECTA expression, but rather multiple introns in specific locations increase ERECTA expression in an additive manner. The ability of introns to promote ERECTA expression might be linked to the process of splicing and not to a particular intron sequence.

摘要

真核生物的基因表达通常会受到内含子的增强。具体取决于特定的基因,这种增强可能很小或非常大,发生在转录和转录后水平。拟南芥 ERECTA 基因包含 27 个外显子,编码一种受体样激酶,该激酶促进地上植物器官的细胞增殖并抑制细胞分化。EREcta 的表达强烈依赖于内含子的存在。无内含子的 ERECTA 基因不能挽救 erecta 突变体植物的表型,与包含内含子的相同构建体相比,产生的蛋白大约少 500-900 倍。这一结果有点令人惊讶,因为 ERECTA 编码序列上游的区域有效地促进了外源基因的表达。在这里,我们证明内含子是 ERECTA mRNA 积累所必需的,并且在较小程度上,对于翻译中 mRNA 的利用也是必需的。由于无内含子的 ERECTA 产生的 mRNA 在 3'端被降解,我们推测内含子通过至少部分增加其稳定性来增加 mRNA 的积累。没有单个内含子对于 ERECTA 的表达是绝对必需的,而是多个特定位置的内含子以累加的方式增加 ERECTA 的表达。内含子促进 ERECTA 表达的能力可能与剪接过程有关,而不是与特定的内含子序列有关。