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杜氏利什曼原虫转录起始区域染色质在生命周期各阶段的可及性

Life Cycle Stage-Specific Accessibility of Leishmania donovani Chromatin at Transcription Start Regions.

作者信息

Grünebast Janne, Lorenzen Stephan, Zummack Julia, Clos Joachim

机构信息

Leishmaniasis Group, Bernhard Nocht Institute for Tropical Medicinegrid.424065.1, Hamburg, Germany.

Department of Tropical Epidemiology, Bernhard Nocht Institute for Tropical Medicinegrid.424065.1, Hamburg, Germany.

出版信息

mSystems. 2021 Aug 31;6(4):e0062821. doi: 10.1128/mSystems.00628-21. Epub 2021 Jul 20.

Abstract

Leishmania donovani is a parasitic protist that causes the lethal Kala-azar fever in India and East Africa. Gene expression in is regulated by gene copy number variation and inducible translation while RNA synthesis initiates at a small number of sites per chromosome and proceeds through polycistronic transcription units, precluding a gene-specific regulation (C. Clayton and M. Shapira, Mol Biochem Parasitol 156:93-101, 2007, https://doi.org/10.1016/j.molbiopara.2007.07.007). Here, we analyze the dynamics of chromatin structure in both life cycle stages of the parasite and find evidence for an additional, epigenetic gene regulation pathway in this early branching eukaryote. The assay for transposase-accessible chromatin using sequencing (ATAC-seq) analysis (J. D. Buenrostro, P. G. Giresi, L. C. Zaba, H. Y. Chang, and W. J. Greenleaf, Nat Methods 10:1213-1218, 2013, https://doi.org/10.1038/nmeth.2688) predominantly shows euchromatin at transcription start regions in fast-growing promastigotes, but mostly heterochromatin in the slowly proliferating amastigotes, the mammalian stage, reflecting a previously shown increase of histone synthesis in the latter stage. parasites are important pathogens with a global impact and cause poverty-related illness and death. They are devoid of classic - and -acting transcription regulators but use regulated translation and gene copy number variations to adapt to hosts and environments. In this work, we show that transcription start regions present as open euchromatin in fast-growing insect stages but as less-accessible heterochromatin in the slowly proliferating amastigote stage, indicating an epigenetic control of gene accessibility in this early branching eukaryotic pathogen. This finding should stimulate renewed interest in the control of RNA synthesis in and related parasites.

摘要

杜氏利什曼原虫是一种寄生原生生物,在印度和东非引发致命的黑热病。其基因表达受基因拷贝数变异和诱导翻译调控,而RNA合成在每条染色体的少数位点起始,并通过多顺反子转录单元进行,这排除了基因特异性调控(C. 克莱顿和M. 沙皮拉,《分子生物化学寄生虫学》156:93 - 101,2007年,https://doi.org/10.1016/j.molbiopara.2007.07.007)。在此,我们分析了该寄生虫两个生命周期阶段染色质结构的动态变化,并发现了这种早期分支真核生物中存在另一种表观遗传基因调控途径的证据。使用测序法分析转座酶可及染色质(ATAC - seq)分析(J. D. 布恩罗斯特罗、P. G. 吉雷西、L. C. 扎巴、H. Y. 张和W. J. 格林利夫,《自然方法》10:1213 - 1218,2013年,https://doi.org/10.1038/nmeth.2688)主要显示,在快速生长的前鞭毛体中转录起始区域为常染色质,但在缓慢增殖的无鞭毛体(哺乳动物阶段)中大多为异染色质,这反映了先前在后一阶段显示的组蛋白合成增加。杜氏利什曼原虫是具有全球影响的重要病原体,会导致与贫困相关的疾病和死亡。它们缺乏经典的顺式和反式作用转录调节因子,但利用调控翻译和基因拷贝数变异来适应宿主和环境。在这项工作中,我们表明转录起始区域在快速生长的昆虫阶段呈现为开放的常染色质,但在缓慢增殖的无鞭毛体阶段则为难以接近的异染色质,这表明在这种早期分支真核病原体中存在对基因可及性的表观遗传控制。这一发现应会激发对杜氏利什曼原虫及相关寄生虫中RNA合成控制的新兴趣。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e446/8409730/f365ac0d9f7a/msystems.00628-21-f001.jpg

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