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1
Stable transcription activities dependent on an orientation of Tam3 transposon insertions into Antirrhinum and yeast promoters occur only within chromatin.依赖于 Tam3 转座子插入拟南芥和酵母启动子的方向的稳定转录活性仅发生在染色质内。
Plant Physiol. 2009 Nov;151(3):1557-69. doi: 10.1104/pp.109.142356. Epub 2009 Sep 16.
2
A pair of transposons coordinately suppresses gene expression, independent of pathways mediated by siRNA in Antirrhinum.一对转座子协同抑制基因表达,这一过程独立于金鱼草中 siRNA 介导的途径。
New Phytol. 2013 Jan;197(2):431-440. doi: 10.1111/nph.12041. Epub 2012 Nov 28.
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Resistance to gap repair of the transposon Tam3 in Antirrhinum majus: a role of the end regions.金鱼草中转座子Tam3的缺口修复抗性:末端区域的作用
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4
The temperature-dependent change in methylation of the Antirrhinum transposon Tam3 is controlled by the activity of its transposase.金鱼草转座子Tam3甲基化的温度依赖性变化受其转座酶活性的控制。
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Transposon-induced inversion in Antirrhinum modifies nivea gene expression to give a novel flower color pattern under the control of cycloidearadialis.转座子诱导的金鱼草倒位改变了nivea基因的表达,从而在cycloidearadialis的控制下产生了一种新的花色模式。
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Phenotypic effects of short-range and aberrant transposition in Antirrhinum majus.金鱼草中短程和异常转座的表型效应。
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Temperature shift coordinately changes the activity and the methylation state of transposon Tam3 in Antirrhinum majus.温度变化协同改变金鱼草中转座子Tam3的活性和甲基化状态。
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How to establish a mutually beneficial relationship between a transposon and its host: lessons from Tam3 in Antirrhinum.转座子与其宿主之间如何建立互利关系:金鱼草 Tam3 的启示。
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Tam3 in Antirrhinum majus is exceptional transposon in resistant to alteration by abortive gap repair: identification of nested transposons.金鱼草中的Tam3是一种特殊的转座子,对无效缺口修复引起的改变具有抗性:嵌套转座子的鉴定。
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DNA methylation is not necessary for the inactivation of the Tam3 transposon at non-permissive temperature in Antirrhinum.在金鱼草中,DNA甲基化对于Tam3转座子在非许可温度下的失活并非必需。
J Plant Physiol. 2005 Nov;162(11):1292-6. doi: 10.1016/j.jplph.2005.03.003.

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Nucleosome positioning and gene regulation: advances through genomics.核小体定位与基因调控:基因组学的进展
Nat Rev Genet. 2009 Mar;10(3):161-72. doi: 10.1038/nrg2522.
2
Multiple regulatory mechanisms influence the activity of the transposon, Tam3, of Antirrhinum.多种调控机制影响金鱼草转座子Tam3的活性。
New Phytol. 2008 Jul;179(2):343-355. doi: 10.1111/j.1469-8137.2008.02477.x.
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Predicting human nucleosome occupancy from primary sequence.从一级序列预测人类核小体占据情况。
PLoS Comput Biol. 2008 Aug 22;4(8):e1000134. doi: 10.1371/journal.pcbi.1000134.
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A barrier nucleosome model for statistical positioning of nucleosomes throughout the yeast genome.一种用于酵母全基因组核小体统计定位的屏障核小体模型。
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5
A Mutator transposon insertion is associated with ectopic expression of a tandemly repeated multicopy Myb gene pericarp color1 of maize.一个Mutator转座子插入与玉米中一个串联重复多拷贝Myb基因果皮颜色1的异位表达相关。
Genetics. 2008 Apr;178(4):1859-74. doi: 10.1534/genetics.107.082503.
6
Nucleosome organization in the Drosophila genome.果蝇基因组中的核小体组织
Nature. 2008 May 15;453(7193):358-62. doi: 10.1038/nature06929. Epub 2008 Apr 13.
7
Large-scale survey of cytosine methylation of retrotransposons and the impact of readout transcription from long terminal repeats on expression of adjacent rice genes.反转录转座子胞嘧啶甲基化的大规模调查以及来自长末端重复序列的读出转录对相邻水稻基因表达的影响。
Genetics. 2007 Dec;177(4):1975-85. doi: 10.1534/genetics.107.080234.
8
Transposase-derived transcription factors regulate light signaling in Arabidopsis.转座酶衍生的转录因子调控拟南芥中的光信号传导。
Science. 2007 Nov 23;318(5854):1302-5. doi: 10.1126/science.1146281.
9
Give-and-take: interactions between DNA transposons and their host plant genomes.相互作用:DNA转座子与其宿主植物基因组之间的相互作用
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10
ROSINA (RSI) is part of a CACTA transposable element, TamRSI, and links flower development to transposon activity.ROSINA(RSI)是CACTA转座元件TamRSI的一部分,并将花的发育与转座子活性联系起来。
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依赖于 Tam3 转座子插入拟南芥和酵母启动子的方向的稳定转录活性仅发生在染色质内。

Stable transcription activities dependent on an orientation of Tam3 transposon insertions into Antirrhinum and yeast promoters occur only within chromatin.

机构信息

Laboratories of Plant Breeding, Research Faculty of Agriculture, Hokkaido University, Sapporo 060-8589, Japan.

出版信息

Plant Physiol. 2009 Nov;151(3):1557-69. doi: 10.1104/pp.109.142356. Epub 2009 Sep 16.

DOI:10.1104/pp.109.142356
PMID:19759347
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2773084/
Abstract

Transposon insertions occasionally occur in the promoter regions of plant genes, many of which are still capable of being transcribed. However, it remains unclear how transcription of such promoters is able to occur. Insertion of the Tam3 transposon into various genes of Antirrhinum majus can confer leaky phenotypes without its excision. These genes, named Tam3-permissible alleles, often contain Tam3 in their promoter regions. Two alleles at different anthocyanin biosynthesis loci, nivea(recurrensTam3) (niv(rec)) and pallida(recurrensTam3) (pal(rec)), both contain Tam3 at a similar position immediately upstream of the promoter TATA-box; however, these insertions had different phenotypic consequences. Under conditions where the inserted Tam3 is immobilized, the niv(rec) line produces pale red petals, whereas the pal(rec) line produces no pigment. These pigmentation patterns are correlated with the level of transcripts from the niv(rec) or pal(rec) alleles, and these transcriptional activities are independent of DNA methylation in their promoter regions. In niv(rec), Tam3 is inserted in an orientation that results in the 3' end of Tam3 adjacent to the 5' region of the gene coding sequence. In contrast, the pal(rec) allele contains a Tam3 insertion in the opposite orientation. Four of five different nonrelated genes that are also Tam3-permissible alleles and contain Tam3 within the promoter region share the same Tam3 orientation as niv(rec). The different transcriptional activities dependent on Tam3 orientation in the Antirrhinum promoters were consistent with expression of luciferase reporter constructs introduced into yeast chromosomes but not with transient expression of these constructs in Antirrhinum cells. These results suggest that for Tam3 to sustain stable transcriptional activity in various promoters it must be embedded in chromatin.

摘要

转座子插入偶尔发生在植物基因的启动子区域,其中许多仍然能够被转录。然而,目前尚不清楚这些启动子的转录是如何发生的。Tam3 转座子插入金鱼草的各种基因中,即使没有切除,也能赋予渗漏表型。这些基因被命名为 Tam3 允许等位基因,它们的启动子区域通常含有 Tam3。在不同的花色素生物合成基因座上的两个等位基因,nivea(recurrensTam3)(niv(rec))和 pallida(recurrensTam3)(pal(rec)),都在启动子 TATA 框的上游类似位置含有 Tam3;然而,这些插入具有不同的表型后果。在插入的 Tam3 被固定的情况下,niv(rec)系产生淡红色花瓣,而 pal(rec)系则不产生色素。这些色素沉着模式与来自 niv(rec)或 pal(rec)等位基因的转录本水平相关,并且这些转录活性与它们启动子区域的 DNA 甲基化无关。在 niv(rec)中,Tam3 以插入的方向导致 Tam3 的 3' 末端与基因编码序列的 5' 区域相邻。相比之下,pal(rec)等位基因含有相反方向的 Tam3 插入。在同样含有 Tam3 位于启动子区域的五个不同的、非相关基因中,有四个基因具有与 niv(rec)相同的 Tam3 取向。在金鱼草启动子中,Tam3 取向依赖性的不同转录活性与酵母染色体中引入的荧光素酶报告基因构建体的表达一致,但与这些构建体在金鱼草细胞中的瞬时表达不一致。这些结果表明,为了使 Tam3 在各种启动子中维持稳定的转录活性,它必须嵌入染色质中。