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植物在气候变化下的应激耐受中的表观基因组学。

Epigenomics in stress tolerance of plants under the climate change.

机构信息

AICRN On Potential Crops, ARS Mandor, Agriculture University, Jodhpur, 342 304, Rajasthan, India.

ICAR-National Bureau of Plant Genetic Resources (NBPGR), Regional Station, Jodhpur, 342 003, Rajasthan, India.

出版信息

Mol Biol Rep. 2023 Jul;50(7):6201-6216. doi: 10.1007/s11033-023-08539-6. Epub 2023 Jun 9.

Abstract

BACKGROUND

Climate change has had a tremendous impact on the environment in general as well as agricultural crops grown in these situations as time passed. Agricultural production of crops is less suited and of lower quality due to disturbances in plant metabolism brought on by sensitivity to environmental stresses, which are brought on by climate change. Abiotic stressors that are specific to climate change, including as drought, extremes in temperature, increasing CO, waterlogging from heavy rain, metal toxicity, and pH changes, are known to negatively affect an array of species. Plants adapt to these challenges by undergoing genome-wide epigenetic changes, which are frequently accompanied by differences in transcriptional gene expression. The sum of a cell's biochemical modifications to its nuclear DNA, post-translational modifications to histones, and variations in the synthesis of non-coding RNAs is called an epigenome. These modifications frequently lead to variations in gene expression that occur without any alteration in the underlying base sequence.

EPIGENETIC MECHANISMS AND MARKS

The methylation of homologous loci by three different modifications-genomic (DNA methylation), chromatin (histone modifications), and RNA-directed DNA methylation (RdDM)-could be regarded as epigenetic mechanisms that control the regulation of differential gene expression. Stresses from the environment cause chromatin remodelling, which enables plant cells to adjust their expression patterns temporarily or permanently. EPIGENOMICS' CONSEQUENCES FOR GENOME STABILITY AND GENE EXPRESSION: DNA methylation affects gene expression in response to abiotic stressors by blocking or suppressing transcription. Environmental stimuli cause changes in DNA methylation levels, either upward in the case of hypermethylation or downward in the case of hypomethylation. The type of stress response that occurs as a result also affects the degree of DNA methylation alterations. Stress is also influenced by DRM2 and CMT3 methylating CNN, CNG, and CG. Both plant development and stress reactions depend on histone changes. Gene up-regulation is associated with histone tail phosphorylation, ubiquitination, and acetylation, while gene down-regulation is associated with de-acetylation and biotinylation. Plants undergo a variety of dynamic changes to histone tails in response to abiotic stressors. The relevance of these transcripts against stress is highlighted by the accumulation of numerous additional antisense transcripts, a source of siRNAs, caused by abiotic stresses. The study highlights the finding that plants can be protected from a range of abiotic stresses by epigenetic mechanisms such DNA methylation, histone modification, and RNA-directed DNA methylation. TRANSGENERATIONAL INHERITANCE AND SOURCES OF EPIGENETIC VARIATION: Stress results in the formation of epialleles, which are either transient or enduring epigenetic stress memory in plants. After the stress is gone, the stable memory is kept for the duration of the plant's remaining developmental cycles or passed on to the next generations, leading to plant evolution and adaptability. The bulk of epigenetic changes brought on by stress are temporary and return to normal after the stress has passed. Some of the modifications, however, might be long-lasting and transmitted across mitotic or even meiotic cell divisions. Epialleles often have genetic or non-genetic causes. Epialleles can arise spontaneously due to improper methylation state maintenance, short RNA off-target effects, or other non-genetic causes. Developmental or environmental variables that influence the stability of epigenetic states or direct chromatin modifications may also be non-genetic drivers of epigenetic variation. Transposon insertions that change local chromatin and structural rearrangements, such copy number changes that are genetically related or unrelated, are two genetic sources of epialleles.

EPIGENOMICS IN CROP IMPROVEMENT

To include epigenetics into crop breeding, it is necessary to create epigenetic variation as well as to identify and evaluate epialleles. Epigenome editing or epi-genomic selection may be required for epiallele creation and identification. In order to combat the challenges given by changing environments, these epigenetic mechanisms have generated novel epialleles that can be exploited to develop new crop types that are more climate-resilient. Numerous techniques can be used to alter the epigenome generally or at specific target loci in order to induce the epigenetic alterations necessary for crop development. Technologies like CRISPR/Cas9 and dCas, which have recently advanced, have opened up new avenues for the study of epigenetics. Epialleles could be employed in epigenomics-assisted breeding in addition to sequence-based markers for crop breeding.

CONCLUSIONS AND FUTURE PROSPECTUS

A few of the exciting questions that still need to be resolved in the area of heritable epigenetic variation include a better understanding of the epigenetic foundation of characteristics, the stability and heritability of epialleles, and the sources of epigenetic variation in crops. Investigating long intergenic non-coding RNAs (lincRNAs) as an epigenetic process might open up a new path to understanding crop plant's ability to withstand abiotic stress. For many of these technologies and approaches to be more applicable and deployable at a lower cost, technological breakthroughs will also be necessary. Breeders will probably need to pay closer attention to crop epialleles and how they can affect future responses to climate changes. The development of epialleles suitable for particular environmental circumstances may be made possible by creating targeted epigenetic changes in pertinent genes and by comprehending the molecular underpinnings of trans generational epigenetic inheritance. More research on a wider variety of plant species is required in order to fully comprehend the mechanisms that produce and stabilise epigenetic variation in crops. In addition to a collaborative and multidisciplinary effort by researchers in many fields of plant science, this will require a greater integration of the epigenomic data gathered in many crops. Before it may be applied generally, more study is required.

摘要

背景

随着时间的推移,气候变化对环境和在这些环境中生长的农作物产生了巨大影响。由于气候变化引起的环境胁迫会导致植物代谢紊乱,从而使农作物的农业生产不太适应,质量也较低。气候变化引起的特定非生物胁迫因素,如干旱、极端温度、CO 增加、暴雨导致的水涝、金属毒性和 pH 值变化,已知会对多种物种产生负面影响。植物通过经历全基因组的表观遗传变化来适应这些挑战,这些变化通常伴随着转录基因表达的差异。细胞对其核 DNA 的生化修饰、组蛋白的翻译后修饰以及非编码 RNA 合成的变化的总和被称为表观基因组。这些修饰通常会导致基因表达的变化,而不会改变潜在的基础序列。

表观遗传机制和标记

通过三种不同的修饰——基因组(DNA 甲基化)、染色质(组蛋白修饰)和 RNA 指导的 DNA 甲基化(RdDM)——同源基因座的甲基化可以被视为控制差异基因表达调节的表观遗传机制。环境应激引起染色质重塑,使植物细胞能够暂时或永久地调整其表达模式。

表观基因组学对基因组稳定性和基因表达的影响

DNA 甲基化通过阻止或抑制转录来响应非生物胁迫因子影响基因表达。环境刺激会导致 DNA 甲基化水平的上升(超甲基化)或下降(低甲基化)。发生的应激反应类型也会影响 DNA 甲基化变化的程度。DRM2 和 CMT3 甲基化 CNN、CNG 和 CG 也会影响胁迫。组蛋白变化既影响植物发育,也影响应激反应。基因上调与组蛋白尾巴磷酸化、泛素化和乙酰化有关,而基因下调与去乙酰化和生物素化有关。植物对非生物胁迫因子会发生多种动态的组蛋白尾巴变化。大量额外的反义转录本的积累突出了这些转录本对胁迫的相关性,这些转录本是由非生物胁迫引起的 siRNA 的来源。该研究强调了这样一个发现,即植物可以通过 DNA 甲基化、组蛋白修饰和 RNA 指导的 DNA 甲基化等表观遗传机制来保护自己免受多种非生物胁迫的影响。

转代遗传和表观遗传变异的来源

应激导致形成 epialleles,这些 epialleles 在植物中是暂时的或持久的表观遗传应激记忆。应激消失后,稳定的记忆会在植物剩余的发育周期中保持,或者传递给下一代,从而导致植物的进化和适应性。应激引起的大部分表观遗传变化是暂时的,应激过去后会恢复正常。然而,一些修饰可能是持久的,并在有丝分裂甚至减数分裂细胞分裂中传递。epialleles 通常有遗传或非遗传的原因。由于不正确的甲基化状态维持、短 RNA 非靶标效应或其他非遗传原因,epialleles 可能会自发产生。影响表观遗传状态稳定性或直接染色质修饰的发育或环境变量也可能是非遗传驱动表观遗传变异的因素。插入改变局部染色质和结构重排的转座子,如与遗传或非遗传相关的拷贝数变化,是 epialleles 的两个遗传来源。

在作物改良中的表观基因组学

为了将表观遗传学纳入作物育种,有必要创造表观遗传变异,并识别和评估 epialleles。epiallele 的创建和识别可能需要表观基因组编辑或表观基因组选择。为了应对不断变化的环境带来的挑战,这些表观遗传机制产生了新的 epialleles,可以利用这些 epialleles来开发更具气候适应性的新型作物类型。通常可以使用多种技术来改变整个基因组或特定靶标基因座的表观基因组,以诱导对作物发育必要的表观遗传变化。最近取得进展的 CRISPR/Cas9 和 dCas 等技术为研究表观遗传学开辟了新的途径。epialleles 可以与基于序列的标记一起用于作物育种的表观基因组学辅助育种。

结论和未来展望

在可遗传的表观遗传变异领域仍有一些令人兴奋的问题需要解决,包括更好地理解特征的表观遗传基础、epialleles 的稳定性和遗传性,以及作物中表观遗传变异的来源。研究长非编码 RNA(lncRNA)作为一种表观遗传过程可能为理解作物植物对非生物胁迫的耐受能力开辟新途径。为了使许多这些技术和方法更具适用性和可部署性,成本更低,还需要技术突破。育种者可能需要更加关注作物 epialleles 以及它们如何影响未来对气候变化的反应。通过在相关基因中创建靶向表观遗传变化并理解跨代际表观遗传遗传的分子基础,可以实现针对特定环境条件的 epialleles 的开发。需要对更多植物物种进行更广泛的研究,以充分理解在作物中产生和稳定表观遗传变异的机制。这需要研究人员在植物科学的许多领域进行协作和多学科努力,并更深入地整合在许多作物中收集的表观基因组学数据。在它可以普遍应用之前,还需要更多的研究。

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