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易位有利于产生可能促进快速适应的大效应突变。

Transposition favors the generation of large effect mutations that may facilitate rapid adaption.

机构信息

Institut de Biologie de l'Ecole Normale Supérieure (IBENS), Centre National de la Recherche Scientifique (CNRS), Institut National de la Santé et de la Recherche Médicale (INSERM), Ecole Normale Supérieure, PSL Research University, Paris, 75005, France.

Genoscope, Institut de biologie François-Jacob, Commissariat à l'Energie Atomique (CEA), Universite Paris-Saclay, F-91057, Evry, France.

出版信息

Nat Commun. 2019 Jul 31;10(1):3421. doi: 10.1038/s41467-019-11385-5.

Abstract

Transposable elements (TEs) are mobile parasitic sequences that have been repeatedly coopted during evolution to generate new functions and rewire gene regulatory networks. Yet, the contribution of active TEs to the creation of heritable mutations remains unknown. Using TE accumulation lines in Arabidopsis thaliana we show that once initiated, transposition produces an exponential spread of TE copies, which rapidly leads to high mutation rates. Most insertions occur near or within genes and targets differ between TE families. Furthermore, we uncover an essential role of the histone variant H2A.Z in the preferential integration of Ty1/copia retrotransposons within environmentally responsive genes and away from essential genes. We also show that epigenetic silencing of new Ty1/copia copies can affect their impact on major fitness-related traits, including flowering time. Our findings demonstrate that TEs are potent episodic (epi)mutagens that, thanks to marked chromatin tropisms, limit the mutation load and increase the potential for rapid adaptation.

摘要

转座元件 (TEs) 是可移动的寄生序列,它们在进化过程中被反复利用,以产生新的功能并重新构建基因调控网络。然而,活跃的 TEs 对可遗传突变的产生的贡献仍不清楚。通过拟南芥中的 TEs 积累系,我们表明,一旦启动,转座就会产生 TE 拷贝的指数级扩散,这会迅速导致高突变率。大多数插入发生在基因附近或内部,并且 TE 家族之间的靶标不同。此外,我们揭示了组蛋白变体 H2A.Z 在 Ty1/copia 反转录转座子优先整合在环境响应基因内并远离必需基因中的重要作用。我们还表明,新的 Ty1/copia 拷贝的表观遗传沉默会影响它们对主要与适应度相关的性状的影响,包括开花时间。我们的研究结果表明,TEs 是强大的爆发性 (epi) 突变源,由于明显的染色质趋向性,它们限制了突变负荷并增加了快速适应的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1e18/6668482/6c4843265a8e/41467_2019_11385_Fig1_HTML.jpg

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