Literature DB >> 21444239

Transposable element origins of epigenetic gene regulation.

Damon Lisch1, Jeffrey L Bennetzen.   

Abstract

Transposable elements (TEs) are massively abundant and unstable in all plant genomes, but are mostly silent because of epigenetic suppression. Because all known epigenetic pathways act on all TEs, it is likely that the specialized epigenetic regulation of regular host genes (RHGs) was co-opted from this ubiquitous need for the silencing of TEs and viruses. With their internally repetitive and rearranging structures, and the acquisition of fragments of RHGs, the expression of TEs commonly makes antisense RNAs for both TE genes and RHGs. These antisense RNAs, particularly from heterochromatic reservoirs of 'zombie' TEs that are rearranged to form variously internally repetitive structures, may be advantageous because their induction will help rapidly suppress active TEs of the same family. RHG fragments within rapidly rearranging TEs may also provide the raw material for the ongoing generation of miRNA genes. TE gene expression is regulated by both environmental and developmental signals, and insertions can place nearby RHGs under the regulation (both standard and epigenetic) of the TE. The ubiquity of TEs, their frequent preferential association with RHGs, and their ability to be programmed by epigenetic signals all indicate that RGHs have nearly unlimited access to novel regulatory cassettes to assist plant adaptation.
Copyright © 2011. Published by Elsevier Ltd.

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Year:  2011        PMID: 21444239     DOI: 10.1016/j.pbi.2011.01.003

Source DB:  PubMed          Journal:  Curr Opin Plant Biol        ISSN: 1369-5266            Impact factor:   7.834


  53 in total

Review 1.  Co-evolution of plant LTR-retrotransposons and their host genomes.

Authors:  Meixia Zhao; Jianxin Ma
Journal:  Protein Cell       Date:  2013-06-23       Impact factor: 14.870

2.  Parent-of-origin control of transgenerational retrotransposon proliferation in Arabidopsis.

Authors:  Jon Reinders; Marie Mirouze; Joël Nicolet; Jerzy Paszkowski
Journal:  EMBO Rep       Date:  2013-07-09       Impact factor: 8.807

3.  FT-like proteins induce transposon silencing in the shoot apex during floral induction in rice.

Authors:  Shojiro Tamaki; Hiroyuki Tsuji; Ayana Matsumoto; Akiko Fujita; Zenpei Shimatani; Rie Terada; Tomoaki Sakamoto; Tetsuya Kurata; Ko Shimamoto
Journal:  Proc Natl Acad Sci U S A       Date:  2015-02-09       Impact factor: 11.205

4.  Birth and Death of LTR-Retrotransposons in Aegilops tauschii.

Authors:  Xiongtao Dai; Hao Wang; Hongye Zhou; Le Wang; Jan Dvořák; Jeffrey L Bennetzen; Hans-Georg Müller
Journal:  Genetics       Date:  2018-08-29       Impact factor: 4.562

Review 5.  Dynamics and innovations within oomycete genomes: insights into biology, pathology, and evolution.

Authors:  Howard S Judelson
Journal:  Eukaryot Cell       Date:  2012-08-24

6.  The dynamics of LTR retrotransposon accumulation across 25 million years of panicoid grass evolution.

Authors:  M C Estep; J D DeBarry; J L Bennetzen
Journal:  Heredity (Edinb)       Date:  2013-02       Impact factor: 3.821

7.  Control of transposon activity by a histone H3K4 demethylase in rice.

Authors:  Xiekui Cui; Ping Jin; Xia Cui; Lianfeng Gu; Zhike Lu; Yongming Xue; Liya Wei; Jianfei Qi; Xianwei Song; Ming Luo; Gynheung An; Xiaofeng Cao
Journal:  Proc Natl Acad Sci U S A       Date:  2013-01-14       Impact factor: 11.205

Review 8.  Epigenetics: Beyond Chromatin Modifications and Complex Genetic Regulation.

Authors:  Steven R Eichten; Robert J Schmitz; Nathan M Springer
Journal:  Plant Physiol       Date:  2014-05-28       Impact factor: 8.340

9.  Chromosomal distribution and evolution of abundant retrotransposons in plants: gypsy elements in diploid and polyploid Brachiaria forage grasses.

Authors:  Fabíola Carvalho Santos; Romain Guyot; Cacilda Borges do Valle; Lucimara Chiari; Vânia Helena Techio; Pat Heslop-Harrison; André Luís Laforga Vanzela
Journal:  Chromosome Res       Date:  2015-09       Impact factor: 5.239

10.  Dicer-like 3 produces transposable element-associated 24-nt siRNAs that control agricultural traits in rice.

Authors:  Liya Wei; Lianfeng Gu; Xianwei Song; Xiekui Cui; Zhike Lu; Ming Zhou; Lulu Wang; Fengyi Hu; Jixian Zhai; Blake C Meyers; Xiaofeng Cao
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-19       Impact factor: 11.205

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