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1
Different strategies to persist: the pogo-like Lemi1 transposon produces miniature inverted-repeat transposable elements or typical defective elements in different plant genomes.不同的持续存在策略:类似弹簧单高跷的Lemi1转座子在不同植物基因组中产生微型反向重复转座元件或典型的缺陷元件。
Genetics. 2008 Sep;180(1):83-92. doi: 10.1534/genetics.108.089615. Epub 2008 Aug 30.
2
The proteins encoded by the pogo-like Lemi1 element bind the TIRs and subterminal repeated motifs of the Arabidopsis Emigrant MITE: consequences for the transposition mechanism of MITEs.类pogo的Lemi1元件编码的蛋白质与拟南芥迁移微型反向重复转座元件(MITE)的末端反向重复序列(TIR)和亚末端重复基序结合:对MITE转座机制的影响
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3
Evidence that a family of miniature inverted-repeat transposable elements (MITEs) from the Arabidopsis thaliana genome has arisen from a pogo-like DNA transposon.来自拟南芥基因组的一个微型反向重复转座元件(MITE)家族起源于一种类似pogo的DNA转座子的证据。
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Identification of novel MITEs (miniature inverted-repeat transposable elements) in Coxiella burnetii: implications for protein and small RNA evolution.鉴定柯克斯体中的新型 MITEs(微型反向重复转座元件):对蛋白质和小 RNA 进化的影响。
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本文引用的文献

1
DNA transposons and the evolution of eukaryotic genomes.DNA转座子与真核生物基因组的进化
Annu Rev Genet. 2007;41:331-68. doi: 10.1146/annurev.genet.40.110405.090448.
2
Diversity and structure of PIF/Harbinger-like elements in the genome of Medicago truncatula.蒺藜苜蓿基因组中PIF/类先驱因子元件的多样性与结构
BMC Genomics. 2007 Nov 9;8:409. doi: 10.1186/1471-2164-8-409.
3
State II dissociation element formation following activator excision in maize.玉米中激活子切除后II型解离元件的形成。
Genetics. 2007 Oct;177(2):737-47. doi: 10.1534/genetics.107.075770. Epub 2007 Aug 24.
4
Transposition of the rice miniature inverted repeat transposable element mPing in Arabidopsis thaliana.水稻微型反向重复转座元件mPing在拟南芥中的转座
Proc Natl Acad Sci U S A. 2007 Jun 26;104(26):10962-7. doi: 10.1073/pnas.0702080104. Epub 2007 Jun 19.
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PAML 4: phylogenetic analysis by maximum likelihood.PAML 4:基于最大似然法的系统发育分析。
Mol Biol Evol. 2007 Aug;24(8):1586-91. doi: 10.1093/molbev/msm088. Epub 2007 May 4.
6
The ancient mariner sails again: transposition of the human Hsmar1 element by a reconstructed transposase and activities of the SETMAR protein on transposon ends.古老的水手再次启航:通过重组转座酶对人类Hsmar1元件进行转座以及SETMAR蛋白在转座子末端的活性。
Mol Cell Biol. 2007 Jun;27(12):4589-600. doi: 10.1128/MCB.02027-06. Epub 2007 Apr 2.
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Transposition of a fungal miniature inverted-repeat transposable element through the action of a Tc1-like transposase.一种真菌微型反向重复转座元件通过类Tc1转座酶的作用进行转座。
Genetics. 2007 Jan;175(1):441-52. doi: 10.1534/genetics.106.064360. Epub 2006 Dec 18.
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Positive selection of yeast nonhomologous end-joining genes and a retrotransposon conflict hypothesis.酵母非同源末端连接基因的正向选择与逆转座子冲突假说
Proc Natl Acad Sci U S A. 2006 Nov 21;103(47):17614-9. doi: 10.1073/pnas.0605468103. Epub 2006 Nov 13.
9
Analysis of retrotransposon structural diversity uncovers properties and propensities in angiosperm genome evolution.逆转座子结构多样性分析揭示了被子植物基因组进化的特性和倾向。
Proc Natl Acad Sci U S A. 2006 Nov 21;103(47):17638-43. doi: 10.1073/pnas.0605618103. Epub 2006 Nov 13.
10
Ogre elements--a distinct group of plant Ty3/gypsy-like retrotransposons.食人魔元件——一类独特的植物Ty3/类吉普赛逆转座子。
Gene. 2007 Apr 1;390(1-2):108-16. doi: 10.1016/j.gene.2006.08.007. Epub 2006 Aug 23.

不同的持续存在策略:类似弹簧单高跷的Lemi1转座子在不同植物基因组中产生微型反向重复转座元件或典型的缺陷元件。

Different strategies to persist: the pogo-like Lemi1 transposon produces miniature inverted-repeat transposable elements or typical defective elements in different plant genomes.

作者信息

Guermonprez Hélène, Loot Céline, Casacuberta Josep M

机构信息

Centre de Recerca en Agrigenòmica CSIC-IRTA-UAB, 08034 Barcelona, Spain.

出版信息

Genetics. 2008 Sep;180(1):83-92. doi: 10.1534/genetics.108.089615. Epub 2008 Aug 30.

DOI:10.1534/genetics.108.089615
PMID:18757929
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2535724/
Abstract

Miniature inverted-repeat transposable elements (MITEs) are a particular type of defective class II elements present in genomes as high-copy-number populations of small and highly homogeneous elements. While virtually all class II transposon families contain non-autonomous defective transposon copies, only a subset of them have a related MITE family. At present it is not known in which circumstances MITEs are generated instead of typical class II defective transposons. The ability to produce MITEs could be an exclusive characteristic of particular transposases, could be related to a particular structure of certain defective class II elements, or could be the consequence of particular constraints imposed by certain host genomes on transposon populations. We describe here a new family of pogo-like transposons from Medicago truncatula closely related to the Arabidopsis Lemi1 element that we have named MtLemi1. In contrast to the Arabidopsis Lemi1, present as a single-copy element and associated with hundreds of related Emigrant MITEs, MtLemi1 has attained >30 copies and has not generated MITEs. This shows that a particular transposon can adopt completely different strategies to colonize genomes. The comparison of AtLemi1 and MtLemi1 reveals transposase-specific domains and possible regulatory sequences that could be linked to the ability to produce MITEs.

摘要

微型反向重复转座元件(MITEs)是基因组中存在的一类特殊的缺陷型II类元件,以高拷贝数的小而高度同源的元件群体形式存在。虽然几乎所有II类转座子家族都包含非自主缺陷型转座子拷贝,但只有其中一部分有相关的MITE家族。目前尚不清楚在何种情况下会产生MITEs而非典型的II类缺陷型转座子。产生MITEs的能力可能是特定转座酶的独特特征,可能与某些缺陷型II类元件的特定结构有关,也可能是某些宿主基因组对转座子群体施加特定限制的结果。我们在此描述了一个来自蒺藜苜蓿的与拟南芥Lemi1元件密切相关的类pogo转座子新家族,我们将其命名为MtLemi1。与作为单拷贝元件存在并与数百个相关的Emigrant MITEs相关联的拟南芥Lemi1不同,MtLemi1有超过30个拷贝且未产生MITEs。这表明特定的转座子可以采用完全不同的策略来定殖于基因组。对AtLemi1和MtLemi1的比较揭示了转座酶特异性结构域和可能与产生MITEs的能力相关的调控序列。