Mitochondrial epigenetics and ORFan genes: exploiting the mitochondrial genetic system to fuel phenotypic variation and functional novelties
线粒体表观遗传学和 ORFan 基因:利用线粒体遗传系统促进表型变异和功能新颖性
基本信息
- 批准号:RGPIN-2019-04076
- 负责人:
- 金额:$ 3.06万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Discovery Grants Program - Individual
- 财政年份:2019
- 资助国家:加拿大
- 起止时间:2019-01-01 至 2020-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Organisms respond to environmental factors over time in two ways: (i) short-term changes during their lifetime (e.g. epigenetic modifications and gene expression changes) and (ii) long-term changes across generations, i.e. heritable evolutionary responses, resulting in genetically distinct populations potentially even new species. While empirical examples of rapid responses and evolutionary adaptations involving nuclear epigenetic variation (in the form of DNA methylation) and genetic variation (through the evolution of lineage-specific or adaptive genes or ORFan genes) exist from a range of animals and plants, the importance of mitochondria (the powerhouse of cells) and their genomes (mtDNA) in promoting adaptation to both short- and long-term environmental changes using the same mechanisms is still largely unexplored. This major knowledge gap is surprising given the pivotal role of mitochondria in cell survival and functions, aging and human diseases. The proposed research will address this fundamental knowledge gap in our understanding of adaptation and speciation processes through the use an integrative approach combining epigenomics, transcriptomics, physiology and cell biology to investigate the capacity of mitochondria and their genomes to adapt to changing environments.******This proposal builds on results from my previous Discovery Grant on the molecular mechanisms underlying doubly uniparental inheritance (DUI) of mitochondria and sex determination in bivalves, which suggested that bivalves likely exploit the mitochondrial genetic system to fuel phenotypic variation and evolutionary innovations. The proposal still focus on bivalves with DUI but also on two model organisms used to study human health and diseases (yeast and planarians). I propose four short-term objectives: 1) measure the mitochondrial epigenetic response to environmental changes; 2) measure the functional consequences of mitochondrial epigenetic variation; 3) estimate the prevalence of mtORFans; and 4) and test their function(s).******In objectives 1-2, planarians and bivalves will offer unique opportunities to study mitochondrial epigenetic and transcriptional changes under diverse environmental regimes respectively because of their absence of genetic variation (asexual reproduction in planarians) and the presence of two different mtDNAs in the same nuclear background (DUI).******In objectives 3-4, bivalves, with their sex-specific mt-encoded proteins with (still unknown) functions other than energy production, and yeast (S. cerevisiae), with their important mitochondrial genome size, will offer unique opportunities to test the hypothesis that like the nuclear DNA, the mtDNA possesses several overlooked small protein-coding genes that have key functions and are important sources of functional novelty.******The questions posited in the current proposal are unique and exciting, and have the potential for transforming our understanding of the role of mitochondria in living organisms.
随着时间的推移,生物以两种方式对环境因素作出反应:(I)生命周期中的短期变化(例如表观遗传修饰和基因表达变化)和(Ii)世代间的长期变化,即可遗传的进化反应,导致遗传上不同的种群,甚至可能是新物种。虽然从一系列动物和植物中已经存在涉及核表观遗传变异(以DNA甲基化的形式)和遗传变异(通过谱系特有或适应基因或ORFan基因的进化)的快速反应和进化适应的经验例子,但线粒体(细胞的动力库)及其基因组(MtDNA)在使用相同机制促进适应短期和长期环境变化方面的重要性在很大程度上仍未被探索。鉴于线粒体在细胞生存和功能、衰老和人类疾病中的关键作用,这一重大知识差距令人惊讶。这项拟议的研究将通过使用结合表观基因组学、转录学、生理学和细胞生物学的综合方法来研究线粒体及其基因组适应不断变化的环境的能力,来解决我们对适应和物种形成过程的基本知识差距。*这项建议建立在我之前的发现授予关于双壳类线粒体双亲单亲遗传(DUI)和性别决定的分子机制的结果的基础上,这表明双壳类可能利用线粒体遗传系统来推动表型变异和进化创新。该提案仍然将重点放在酒后驾车的双壳类上,但也关注用于研究人类健康和疾病的两种模式生物(酵母和浮游生物)。我提出了四个短期目标:1)测量线粒体对环境变化的表观遗传反应;2)测量线粒体表观遗传变异的功能后果;3)估计mtORFans的患病率;和4)并测试它们的功能(S)。*在目标1-2中,双壳类动物和双壳类动物将分别提供独特的机会来研究不同环境条件下线粒体的表观遗传和转录变化,因为它们没有遗传变异(浮游生物的无性繁殖),并且在相同的核背景(DUI)中存在两种不同的mtDNA。*在目标3-4中,双壳类动物及其性别特异的mt编码蛋白具有(尚不清楚)除能量生产之外的功能,以及酵母(酿酒酵母),其重要的线粒体基因组大小,将提供独特的机会来检验这一假设,即像核DNA一样,线粒体DNA拥有几个被忽视的小蛋白编码基因,这些基因具有关键功能,是功能新颖性的重要来源。当前提案中提出的问题是独特和令人兴奋的,并有可能改变我们对线粒体在生物体内作用的理解。
项目成果
期刊论文数量(0)
专著数量(0)
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Breton, Sophie其他文献
The effect of cryopreservation on mitochondrial function in freshwater mussel tissue samples (Bivalvia: Unionida)
- DOI:
10.1016/j.cryobiol.2019.04.006 - 发表时间:
2019-06-01 - 期刊:
- 影响因子:2.7
- 作者:
Bettinazzi, Stefano;Gendron, Andree D.;Breton, Sophie - 通讯作者:
Breton, Sophie
Putative Mitochondrial Sex Determination in the Bivalvia: Insights From a Hybrid Transcriptome Assembly in Freshwater Mussels
- DOI:
10.3389/fgene.2019.00840 - 发表时间:
2019-09-13 - 期刊:
- 影响因子:3.7
- 作者:
Capt, Charlotte;Renaut, Sebastien;Breton, Sophie - 通讯作者:
Breton, Sophie
Did doubly uniparental inheritance (DUI) of mtDNA originate as a cytoplasmic male sterility (CMS) system?
- DOI:
10.1002/bies.202100283 - 发表时间:
2022-04 - 期刊:
- 影响因子:4
- 作者:
Breton, Sophie;Stewart, Donald T.;Bremaud, Julie;Havird, Justin C.;Smith, Chase H.;Hoeh, Walter R. - 通讯作者:
Hoeh, Walter R.
Comparative Mitochondrial Genomics of Freshwater Mussels (Bivalvia: Unionoida) With Doubly Uniparental Inheritance of mtDNA: Gender-Specific Open Reading Frames and Putative Origins of Replication
- DOI:
10.1534/genetics.109.110700 - 发表时间:
2009-12-01 - 期刊:
- 影响因子:3.3
- 作者:
Breton, Sophie;Beaupre, Helene Doucet;Hoeh, Walter R. - 通讯作者:
Hoeh, Walter R.
The human mitochondrial genome may code for more than 13 proteins
- DOI:
10.3109/19401736.2014.1003924 - 发表时间:
2016-01-01 - 期刊:
- 影响因子:0
- 作者:
Capt, Charlotte;Passamonti, Marco;Breton, Sophie - 通讯作者:
Breton, Sophie
Breton, Sophie的其他文献
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{{ truncateString('Breton, Sophie', 18)}}的其他基金
Evolutionary Mitochondrial Biology
进化线粒体生物学
- 批准号:
CRC-2018-00049 - 财政年份:2022
- 资助金额:
$ 3.06万 - 项目类别:
Canada Research Chairs
Mitochondrial epigenetics and ORFan genes: exploiting the mitochondrial genetic system to fuel phenotypic variation and functional novelties
线粒体表观遗传学和 ORFan 基因:利用线粒体遗传系统促进表型变异和功能新颖性
- 批准号:
RGPIN-2019-04076 - 财政年份:2022
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Mitochondrial epigenetics and ORFan genes: exploiting the mitochondrial genetic system to fuel phenotypic variation and functional novelties
线粒体表观遗传学和 ORFan 基因:利用线粒体遗传系统促进表型变异和功能新颖性
- 批准号:
RGPIN-2019-04076 - 财政年份:2021
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Evolutionary Mitochondrial Biology
进化线粒体生物学
- 批准号:
CRC-2018-00049 - 财政年份:2021
- 资助金额:
$ 3.06万 - 项目类别:
Canada Research Chairs
Mitochondrial epigenetics and ORFan genes: exploiting the mitochondrial genetic system to fuel phenotypic variation and functional novelties
线粒体表观遗传学和 ORFan 基因:利用线粒体遗传系统促进表型变异和功能新颖性
- 批准号:
RGPIN-2019-04076 - 财政年份:2020
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Evolutionary Mitochondrial Biology
进化线粒体生物学
- 批准号:
CRC-2018-00049 - 财政年份:2020
- 资助金额:
$ 3.06万 - 项目类别:
Canada Research Chairs
Evolutionary Mitochondrial Biology
进化线粒体生物学
- 批准号:
CRC-2018-00049 - 财政年份:2019
- 资助金额:
$ 3.06万 - 项目类别:
Canada Research Chairs
Novel mtDNA-encoded proteins and mitochondrial sex determination in the Bivalvia (Mollusca)
双壳纲(软体动物)中新型 mtDNA 编码蛋白和线粒体性别决定
- 批准号:
435656-2013 - 财政年份:2018
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Novel mtDNA-encoded proteins and mitochondrial sex determination in the Bivalvia (Mollusca)
双壳纲(软体动物)中新型 mtDNA 编码蛋白和线粒体性别决定
- 批准号:
435656-2013 - 财政年份:2017
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Novel mtDNA-encoded proteins and mitochondrial sex determination in the Bivalvia (Mollusca)
双壳纲(软体动物)中新型 mtDNA 编码蛋白和线粒体性别决定
- 批准号:
435656-2013 - 财政年份:2016
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
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