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1
Transgenes are dispensable for the RNA degradation step of cosuppression.转基因对于共抑制的RNA降解步骤是可有可无的。
Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9675-80. doi: 10.1073/pnas.95.16.9675.
2
A Transcriptionally Active State Is Required for Post-Transcriptional Silencing (Cosuppression) of Nitrate Reductase Host Genes and Transgenes.转录活性状态是硝酸还原酶宿主基因和转基因转录后沉默(共抑制)所必需的。
Plant Cell. 1997 Aug;9(8):1495-1504. doi: 10.1105/tpc.9.8.1495.
3
Graft transmission of post-transcriptional gene silencing: target specificity for RNA degradation is transmissible between silenced and non-silenced plants, but not between silenced plants.转录后基因沉默的嫁接传递:RNA降解的靶标特异性可在沉默植物与未沉默植物之间传递,但不能在沉默植物之间传递。
Plant J. 2000 Jan;21(1):1-8. doi: 10.1046/j.1365-313x.2000.00645.x.
4
Arabidopsis mutants impaired in cosuppression.共抑制受损的拟南芥突变体。
Plant Cell. 1998 Oct;10(10):1747-58. doi: 10.1105/tpc.10.10.1747.
5
Activation of systemic acquired silencing by localised introduction of DNA.通过局部导入DNA激活系统获得性沉默
Curr Biol. 1999 Jan 28;9(2):59-66. doi: 10.1016/s0960-9822(99)80016-5.
6
Systemic acquired silencing: transgene-specific post-transcriptional silencing is transmitted by grafting from silenced stocks to non-silenced scions.系统获得性沉默:转基因特异性转录后沉默通过嫁接从沉默的砧木传递到未沉默的接穗。
EMBO J. 1997 Aug 1;16(15):4738-45. doi: 10.1093/emboj/16.15.4738.
7
Molecular and genetic analysis of nitrite reductase co-suppression in transgenic tobacco plants.转基因烟草植株中亚硝酸还原酶共抑制的分子与遗传分析
Mol Gen Genet. 1995 Aug 21;248(3):311-7. doi: 10.1007/BF02191598.
8
Specific degradation of 3' regions of GUS mRNA in posttranscriptionally silenced tobacco lines may be related to 5'-3' spreading of silencing.在转录后沉默的烟草品系中,GUS mRNA 3' 区域的特异性降解可能与沉默的 5'-3' 扩展有关。
RNA. 2002 Aug;8(8):1034-44. doi: 10.1017/s1355838202026080.
9
Co-suppression of nitrate reductase host genes and transgenes in transgenic tobacco plants.转基因烟草植株中硝酸盐还原酶宿主基因和转基因的共抑制
Mol Gen Genet. 1994 Jun 15;243(6):613-21. doi: 10.1007/BF00279570.
10
The capacity of transgenic tobacco to send a systemic RNA silencing signal depends on the nature of the inducing transgene locus.转基因烟草发送系统性RNA沉默信号的能力取决于诱导转基因位点的性质。
Plant J. 2003 Jul;35(1):82-92. doi: 10.1046/j.1365-313x.2003.01785.x.

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Efficient Generation of diRNAs Requires Components in the Posttranscriptional Gene Silencing Pathway.双链 RNA(diRNA)的高效产生需要转录后基因沉默途径中的成分。
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A 22-nt artificial microRNA mediates widespread RNA silencing in Arabidopsis.22 个核苷酸的人工 microRNA 在拟南芥中引发广泛的 RNA 沉默。
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Graft-transmitted siRNA signal from the root induces visual manifestation of endogenous post-transcriptional gene silencing in the scion.接穗中的根诱导的来自移植物的 siRNA 信号引发内源转录后基因沉默的可见表型。
PLoS One. 2011 Feb 9;6(2):e16895. doi: 10.1371/journal.pone.0016895.
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Stable expression and phenotypic impact of attacin E transgene in orchard grown apple trees over a 12 year period.在 12 年的时间里,稳定表达抗菌肽 attacin E 转基因对果园种植苹果树的表型影响。
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10
Developmentally early and late onset of Rps10 silencing in Arabidopsis thaliana: genetic and environmental regulation.拟南芥中核糖体蛋白S10(Rps10)沉默的发育早期和晚期起始:遗传和环境调控
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Nitrate Reductase mRNA Regulation in Nicotiana plumbaginifolia Nitrate Reductase-Deficient Mutants.烟草中硝酸盐还原酶缺陷型突变体的硝酸盐还原酶mRNA调控
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Introduction of a Chimeric Chalcone Synthase Gene into Petunia Results in Reversible Co-Suppression of Homologous Genes in trans.将嵌合查尔酮合酶基因导入矮牵牛导致同源基因的反式可逆共抑制。
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Induction of a Highly Specific Antiviral State in Transgenic Plants: Implications for Regulation of Gene Expression and Virus Resistance.转基因植物中高度特异性抗病毒状态的诱导:对基因表达调控和病毒抗性的影响。
Plant Cell. 1993 Dec;5(12):1749-1759. doi: 10.1105/tpc.5.12.1749.
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Suppression of Virus Accumulation in Transgenic Plants Exhibiting Silencing of Nuclear Genes.在表现出核基因沉默的转基因植物中病毒积累的抑制
Plant Cell. 1996 Feb;8(2):179-188. doi: 10.1105/tpc.8.2.179.
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RNA-Mediated Virus Resistance: Role of Repeated Transgenes and Delineation of Targeted Regions.RNA介导的病毒抗性:重复转基因的作用及靶向区域的界定
Plant Cell. 1996 Dec;8(12):2277-2294. doi: 10.1105/tpc.8.12.2277.
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A Transcriptionally Active State Is Required for Post-Transcriptional Silencing (Cosuppression) of Nitrate Reductase Host Genes and Transgenes.转录活性状态是硝酸还原酶宿主基因和转基因转录后沉默(共抑制)所必需的。
Plant Cell. 1997 Aug;9(8):1495-1504. doi: 10.1105/tpc.9.8.1495.
8
Characterization of Post-Transcriptionally Suppressed Transgene Expression That Confers Resistance to Tobacco Etch Virus Infection in Tobacco.赋予烟草对烟草蚀纹病毒感染抗性的转录后抑制转基因表达的特征分析
Plant Cell. 1997 Aug;9(8):1411-1423. doi: 10.1105/tpc.9.8.1411.
9
The Frequency and Degree of Cosuppression by Sense Chalcone Synthase Transgenes Are Dependent on Transgene Promoter Strength and Are Reduced by Premature Nonsense Codons in the Transgene Coding Sequence.有义查尔酮合酶转基因共抑制的频率和程度取决于转基因启动子强度,并因转基因编码序列中的过早无义密码子而降低。
Plant Cell. 1997 Aug;9(8):1357-1368. doi: 10.1105/tpc.9.8.1357.
10
Frequencies, Timing, and Spatial Patterns of Co-Suppression of Nitrate Reductase and Nitrite Reductase in Transgenic Tobacco Plants.转基因烟草植株中硝酸还原酶和亚硝酸还原酶共抑制的频率、时间及空间模式
Plant Physiol. 1996 Dec;112(4):1447-1456. doi: 10.1104/pp.112.4.1447.

转基因对于共抑制的RNA降解步骤是可有可无的。

Transgenes are dispensable for the RNA degradation step of cosuppression.

作者信息

Palauqui J C, Vaucheret H

机构信息

Laboratoire de Biologie Cellulaire, Institut National de la Recherche Agronomique, 78026 Versailles Cedex, France.

出版信息

Proc Natl Acad Sci U S A. 1998 Aug 4;95(16):9675-80. doi: 10.1073/pnas.95.16.9675.

DOI:10.1073/pnas.95.16.9675
PMID:9689140
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC21398/
Abstract

Cosuppression results in the degradation of RNA from host genes and homologous transgenes after transcription in the nucleus. By using grafting experiments, we have shown previously that a systemic signal mediates the propagation of cosuppression of Nia host genes and 35S-Nia2 transgenes from silenced 35S-Nia2 transgenic stocks to nonsilenced 35S-Nia2 transgenic scions but not to wild-type scions. Here, we examined the requirements for triggering and maintenance of cosuppression in various types of scions. Grafting-induced silencing occurred in 35S-Nia2 transgenic lines over-accumulating Nia mRNA whether they are able to spontaneously trigger cosuppression or not and in 35S-Nia2 transgene-free plants over-accumulating host Nia mRNA caused by metabolic derepression. When grafting-induced silenced scions were removed from the silenced stocks and regrafted onto wild-type plants, silencing was not maintained in the 35S-Nia2 transgene-free plants and in the 35S-Nia2 transgenic lines that are not able to trigger cosuppression spontaneously. Conversely, silencing was maintained in the 35S-Nia2 transgenic lines that are able to trigger cosuppression spontaneously. Our results indicate that the presence of a 35S-Nia2 transgene is dispensable for the RNA degradation step of posttranscriptional silencing when host Nia mRNA over-accumulate above the level of wild-type plants. They also suggest that grafting-induced RNA degradation does not result in the production of the systemic silencing signal required for spontaneous triggering and maintenance.

摘要

共抑制导致细胞核转录后宿主基因和同源转基因的RNA降解。通过嫁接实验,我们先前已经表明,一种系统性信号介导了Nia宿主基因和35S-Nia2转基因从沉默的35S-Nia2转基因砧木到未沉默的35S-Nia2转基因接穗的共抑制传播,但不介导到野生型接穗。在这里,我们研究了在各种类型接穗中引发和维持共抑制的条件。嫁接诱导的沉默发生在过量积累Nia mRNA的35S-Nia2转基因株系中,无论它们是否能够自发引发共抑制,也发生在因代谢抑制而过量积累宿主Nia mRNA的无35S-Nia2转基因的植物中。当将嫁接诱导沉默的接穗从沉默的砧木上移除并重新嫁接到野生型植物上时,在无35S-Nia2转基因的植物和不能自发引发共抑制的35S-Nia2转基因株系中,沉默不能维持。相反,在能够自发引发共抑制的35S-Nia2转基因株系中,沉默得以维持。我们的结果表明,当宿主Nia mRNA积累量超过野生型植物水平时,35S-Nia2转基因的存在对于转录后沉默的RNA降解步骤是不必要的。它们还表明,嫁接诱导的RNA降解不会导致自发引发和维持所需的系统性沉默信号的产生。