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标题:【分享】表观遗传“记忆” 在植物研究中的进展

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【分享】表观遗传“记忆” 在植物研究中的进展

Nature在7月24日报道,约翰英纳斯中心的研究人员发现了生物体对不同环境条件(如营养的质量或温度)形成记忆的证据,这一发现解释了记忆机制和记忆如何遗传给下一代。

约翰英纳斯中心 Martin Howard 教授和 Caroline Dean 教授共同领导这项研究。

Dean教授称,很多事例表明,基因的表达活性在一些地区长期受环境的影响;个体生存的环境能影响后代的生物学或生理学特征,但是在遗传过程中基因组却没有改变。一些研究表明,在家庭中,祖父母遭受严重的食物短缺,子孙后代患心血管疾病和糖尿病的风险就会更大,表观遗传学中通过基因是否表达获取的记忆能解释这一点。但是截止到目前,还没有一个清晰的机制能解释个体如何形成对可变因子(如营养)的“记忆”。

研究小组举出一个例子,植物如何“记住”寒冬期的天数以便在特定时期内开花。形成季节记忆后,植物的生命周期中授粉、发育、种子传播以及萌发才可在合适的时期内发生。

霍华德教授称,我们已经知道很多开花相关的基因,确定的是,这些基因根据寒冬期的长短发生特定的变化,最终影响植物的开花时间。

研究小组利用运算组合模型和实验分析方法揭示了一种记忆机制,在这种机制下,关键基因(FLC)在每一个细胞或分裂子细胞中要么完全“关闭”,要么完全“开启”。寒冷期越长,更高比例的细胞由FLC基因“开启”状态切换到“关闭”状态。开花时期被延迟,植物会形成对这一现象的表观遗传记忆。

表观遗传记忆会以不同方式出现,但是一个重要方式涉及由DNA序列缠绕的组蛋白。组蛋白会发生特定的化学修饰,这些修饰能影响附近基因的表达——“开启”或“关闭”。当细胞分裂时,这些修饰可由分裂出的新细胞继承,如果发生在生殖细胞中,组蛋白的化学修饰会遗传到后代中。

约翰英纳斯中心 Howard 教授和 Andrew Angel博士共同开发出FLC系统的运算模型,该模型可预测FLC基因在单个细胞中要么完全活化,要么完全沉默,以及寒冷期延长后,一部分细胞的FLC活跃状态切换到沉默状态。

为了提供对上述模型的实验支持,研究小组成员 Jie Song 博士使用一种可以观察细胞状态的技术,“开启”FLC基因的细胞在显微镜下呈现出蓝色。她的观察提供了明确结论:细胞要么完全“关闭”,要么完全“开启”,这一现象与理论保持一致。

Song 博士还发现,FLC基因附近的组蛋白在寒冷期被修饰,因而能够对该基因的“关闭”做出解释。

该研究由BBSRC、欧洲研究理事会和英国皇家学会资助。
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英文原文

Epigenetic 'Memory' Key to Nature Versus Nurture

Researchers at the John Innes Centre have made a discovery, reported this evening (24 July) in Nature, that explains how an organism can create a biological memory of some variable condition, such as quality of nutrition or temperature. The discovery explains the mechanism of this memory -- a sort of biological switch -- and how it can also be inherited by offspring.
The work was led by Professor Martin Howard and Professor Caroline Dean at the John Innes Centre.

Professor Dean said "There are quite a few examples that we now know of where the activity of genes can be affected in the long term by environmental factors. And in some cases the environment of an individual can actually affect the biology or physiology of their offspring but there is no change to the genome sequence."

For example, some studies have shown that in families where there was a severe food shortage in the grandparents' generation, the children and grandchildren have a greater risk of cardiovascular disease and diabetes, which could be explained by epigenetic memory. But until now there hasn't been a clear mechanism to explain how individuals could develop a "memory" of a variable factor, such as nutrition.

The team used the example of how plants "remember" the length of the cold winter period in order to exquisitely time flowering so that pollination, development, seed dispersal and germination can all happen at the appropriate time.

Professor Howard said "We already knew quite a lot about the genes involved in flowering and it was clear that something goes on in winter that affects the timing of flowering, according to the length of the cold period."

Using a combination of mathematical modelling and experimental analysis the team has uncovered the system by which a key gene called FLC is either completely off or completely on in any one cell and also later in its progeny. They found that the longer the cold period, the higher the proportion of cells that have FLC stably flipped to the off position. This delays flowering and is down to a phenomenon known as epigenetic memory.
Epigenetic memory comes in various guises, but one important form involves histones -- the proteins around which DNA is wrapped. Particular chemical modifications can be attached to histones and these modifications can then affect the expression of nearby genes, turning them on or off. These modifications can be inherited by daughter cells, when the cells divide, and if they occur in the cells that form gametes (e.g. sperm in mammals or pollen in plants) then they can also pass on to offspring.

Together with Dr Andrew Angel (also at the John Innes Centre), Professor Howard produced a mathematical model of the FLC system. The model predicted that inside each individual cell, the FLC gene should be either completely activated or completely silenced, with the fraction of cells switching to the silenced state increasing with longer periods of cold.

To provide experimental evidence to back up the model, Dr Jie Song in Prof. Dean's group used a technique where any cell that had the FLC gene switched on, showed up blue under a microscope. From her observations, it was clear that cells were either completely switched or not switched at all, in agreement with the theory.

Dr Song also showed that the histone proteins near the FLC gene were modified during the cold period, in such a way that would account for the switching off of the gene.

Funding for the project came from BBSRC, the European Research Council, and The Royal Society.

Professor Douglas Kell, Chief Executive, BBSRC said "This work not only gives us insight into a phenomenon that is crucial for future food security -- the timing of flowering according to climate variation -- but it uncovers an important mechanism that is at play right across biology. This is a great example of where the research that BBSRC funds can provide not only a focus on real life problems, but also a grounding in the fundamental tenets of biology that will underpin the future of the field. It also demonstrates the value of multidisciplinary working at the interface between biology, physics and mathematics."
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