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1
Deletion of many yeast introns reveals a minority of genes that require splicing for function.许多酵母内含子的缺失揭示了少数需要剪接才能发挥功能的基因。
Mol Biol Cell. 2008 May;19(5):1932-41. doi: 10.1091/mbc.e07-12-1254. Epub 2008 Feb 20.
2
Genome-wide analysis of pre-mRNA splicing: intron features govern the requirement for the second-step factor, Prp17 in Saccharomyces cerevisiae and Schizosaccharomyces pombe.全基因组范围的前体信使核糖核酸剪接分析:内含子特征决定了酿酒酵母和粟酒裂殖酵母中第二步剪接因子Prp17的需求。
J Biol Chem. 2004 Dec 10;279(50):52437-46. doi: 10.1074/jbc.M408815200. Epub 2004 Sep 27.
3
Normal mitochondrial function in has become dependent on inefficient splicing.已经依赖于低效剪接来维持正常的线粒体功能。
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4
Introns regulate RNA and protein abundance in yeast.内含子调控酵母中的RNA和蛋白质丰度。
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Introns within ribosomal protein genes regulate the production and function of yeast ribosomes.核糖体蛋白基因内的内含子调节酵母核糖体的产生和功能。
Cell. 2011 Oct 14;147(2):320-31. doi: 10.1016/j.cell.2011.08.044.
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Identification of essential intron sequences that enhance gene expression independently of splicing in the yeast Saccharomyces cerevisiae.鉴定在酵母酿酒酵母中独立于剪接增强基因表达的必需内含子序列。
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An intron in the YRA1 gene is required to control Yra1 protein expression and mRNA export in yeast.YRA1基因中的一个内含子对于控制酵母中Yra1蛋白的表达和mRNA输出是必需的。
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8
The Saccharomyces cerevisiae gene CDC40/PRP17 controls cell cycle progression through splicing of the ANC1 gene.酿酒酵母基因CDC40/PRP17通过ANC1基因的剪接来控制细胞周期进程。
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The Cbp2 protein stimulates the splicing of the omega intron of yeast mitochondria.Cbp2蛋白刺激酵母线粒体ω内含子的剪接。
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Expression of the essential mRNA export factor Yra1p is autoregulated by a splicing-dependent mechanism.必需的mRNA输出因子Yra1p的表达通过一种剪接依赖性机制进行自我调节。
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Autoregulation of RPL7B by inhibition of a structural splicing enhancer.通过抑制一种结构剪接增强子对RPL7B进行自动调节。
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Cells resist starvation through a nutrient stress splice switch.细胞通过营养应激剪接开关来抵抗饥饿。
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Domain acquisition enabled functional expansion of the TFIIS transcription factor family.结构域的获得促使了TFIIS转录因子家族的功能扩展。
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Horizontal transmission of functionally diverse transposons is a major source of new introns.功能多样的转座子的水平转移是新内含子的主要来源。
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Taxonomy of introns and the evolution of minor introns.内含子的分类和小内含子的演化。
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MAE-seq refines regulatory elements across the genome.MAE-seq 对基因组范围内的调控元件进行精细化分析。
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Impact on splicing in of random 50-base sequences inserted into an intron.插入内含子的随机 50 个碱基序列对剪接的影响。
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本文引用的文献

1
Transcript specificity in yeast pre-mRNA splicing revealed by mutations in core spliceosomal components.核心剪接体成分突变揭示酵母前体mRNA剪接中的转录本特异性
PLoS Biol. 2007 Apr;5(4):e90. doi: 10.1371/journal.pbio.0050090.
2
The effects of camptothecin on RNA polymerase II transcription: roles of DNA topoisomerase I.喜树碱对RNA聚合酶II转录的影响:DNA拓扑异构酶I的作用
Biochimie. 2007 Apr;89(4):482-9. doi: 10.1016/j.biochi.2007.01.001. Epub 2007 Jan 21.
3
YRA1 autoregulation requires nuclear export and cytoplasmic Edc3p-mediated degradation of its pre-mRNA.YRA1自身调控需要其前体mRNA进行核输出以及细胞质中Edc3p介导的降解。
Mol Cell. 2007 Feb 23;25(4):559-73. doi: 10.1016/j.molcel.2007.01.012.
4
High-density yeast-tiling array reveals previously undiscovered introns and extensive regulation of meiotic splicing.高密度酵母平铺阵列揭示了先前未发现的内含子以及减数分裂剪接的广泛调控。
Proc Natl Acad Sci U S A. 2007 Jan 30;104(5):1522-7. doi: 10.1073/pnas.0610354104. Epub 2007 Jan 23.
5
Splicing regulation in neurologic disease.神经疾病中的剪接调控
Neuron. 2006 Oct 5;52(1):93-101. doi: 10.1016/j.neuron.2006.09.017.
6
Defective splicing, disease and therapy: searching for master checkpoints in exon definition.剪接缺陷、疾病与治疗:探寻外显子定义中的关键检查点
Nucleic Acids Res. 2006 Jul 19;34(12):3494-510. doi: 10.1093/nar/gkl498. Print 2006.
7
Introns regulate RNA and protein abundance in yeast.内含子调控酵母中的RNA和蛋白质丰度。
Genetics. 2006 Sep;174(1):511-8. doi: 10.1534/genetics.106.058560. Epub 2006 Jul 2.
8
A high-throughput method to measure the sensitivity of yeast cells to genotoxic agents in liquid cultures.一种用于测量液体培养物中酵母细胞对基因毒性试剂敏感性的高通量方法。
Mutat Res. 2006 Jul 14;606(1-2):92-105. doi: 10.1016/j.mrgentox.2006.03.006. Epub 2006 May 19.
9
Autoregulation of the mRNA export factor Yra1p requires inefficient splicing of its pre-mRNA.mRNA输出因子Yra1p的自调控需要其前体mRNA的低效剪接。
RNA. 2006 Jun;12(6):994-1006. doi: 10.1261/rna.6706. Epub 2006 Apr 17.
10
Identification and evolutionary analysis of novel exons and alternative splicing events using cross-species EST-to-genome comparisons in human, mouse and rat.利用人、小鼠和大鼠跨物种的EST与基因组比对进行新型外显子和可变剪接事件的鉴定及进化分析。
BMC Bioinformatics. 2006 Mar 15;7:136. doi: 10.1186/1471-2105-7-136.

许多酵母内含子的缺失揭示了少数需要剪接才能发挥功能的基因。

Deletion of many yeast introns reveals a minority of genes that require splicing for function.

作者信息

Parenteau Julie, Durand Mathieu, Véronneau Steeve, Lacombe Andrée-Anne, Morin Geneviève, Guérin Valérie, Cecez Bojana, Gervais-Bird Julien, Koh Chu-Shin, Brunelle David, Wellinger Raymund J, Chabot Benoit, Abou Elela Sherif

机构信息

Laboratoire de génomique fonctionnelle de l'Université de Sherbrooke, Département de microbiologie et d'infectiologie, Faculté de médecine et des sciences de la santé, Université de Sherbrooke, Sherbrooke, QC J1H 5N4, Canada.

出版信息

Mol Biol Cell. 2008 May;19(5):1932-41. doi: 10.1091/mbc.e07-12-1254. Epub 2008 Feb 20.

DOI:10.1091/mbc.e07-12-1254
PMID:18287520
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2366882/
Abstract

Splicing regulates gene expression and contributes to proteomic diversity in higher eukaryotes. However, in yeast only 283 of the 6000 genes contain introns and their impact on cell function is not clear. To assess the contribution of introns to cell function, we initiated large-scale intron deletions in yeast with the ultimate goal of creating an intron-free model eukaryote. We show that about one-third of yeast introns are not essential for growth. Only three intron deletions caused severe growth defects, but normal growth was restored in all cases by expressing the intronless mRNA from a heterologous promoter. Twenty percent of the intron deletions caused minor phenotypes under different growth conditions. Strikingly, the combined deletion of all introns from the 15 cytoskeleton-related genes did not affect growth or strain fitness. Together, our results show that although the presence of introns may optimize gene expression and provide benefit under stress, a majority of introns could be removed with minor consequences on growth under laboratory conditions, supporting the view that many introns could be phased out of Saccharomyces cerevisiae without blocking cell growth.

摘要

剪接调控基因表达,并有助于高等真核生物蛋白质组的多样性。然而,在酵母中,6000个基因中只有283个含有内含子,它们对细胞功能的影响尚不清楚。为了评估内含子对细胞功能的贡献,我们在酵母中启动了大规模的内含子缺失,最终目标是创建一个无内含子的模式真核生物。我们发现,约三分之一的酵母内含子对生长并非必需。只有三个内含子缺失导致严重的生长缺陷,但在所有情况下,通过从异源启动子表达无内含子的mRNA都恢复了正常生长。20%的内含子缺失在不同生长条件下导致轻微表型。令人惊讶的是,15个细胞骨架相关基因的所有内含子的联合缺失并不影响生长或菌株适应性。总之,我们的结果表明,虽然内含子的存在可能会优化基因表达并在应激条件下带来益处,但在实验室条件下,大多数内含子可以被去除,对生长的影响较小,这支持了许多内含子可以在不阻碍细胞生长的情况下从酿酒酵母中逐步淘汰的观点。