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Supplement request for 1F32GM116361-01

1F32GM116361-01 的补充请求

基本信息

批准号：
9403361
负责人：
Justin C Havird
金额：
$ 0.06万
依托单位：
COLORADO STATE UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2015
资助国家：
美国
起止时间：
2015-07-01 至 2018-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/9403361
关键词：
Address Affect Age of Onset Aging Animals Backcrossings Bacteria Biological Assay Categories Cell Nucleus Cell physiology Cells Characteristics Chloroplast DNA Complement Complex DNA Disease Distant Droughts Ecology Environment Eukaryota Evolution Exhibits Female Fertility Fertilization in Vitro Financial compensation Gene Expression Genes Genome Genomics Glycolysis Growth Health Human Hybrids Individual Inherited Lead Life Metabolic Metabolic Pathway Mitochondria Mitochondrial DNA Modeling Mutate Mutation Nuclear Organelles Organism Oxidative Phosphorylation Parents Pattern Phenotype Photosynthetic Complexes Physiology Plants Population Population Sizes Production Published Comment Regulation Replacement Therapy Research Severities Silene Symbiosis System Testing Time Tissue-Specific Gene Expression Tissues Work age related base biological adaptation to stress complex IV differential expression environmental stressor falls fitness functional genomics insight male metabolic rate mitochondrial DNA mutation mitochondrial genome oxidative damage public health relevance response sex theories transcriptome sequencing virtual

项目摘要

DESCRIPTION (provided by applicant): All eukaryotes have or once had mitochondria. These organelles are the remains of an ancient symbiosis with a bacterium early in eukaryotic evolution some 2 billion years ago. As such, mitochondria retain their own genome (mtDNA). Although it only encodes a small fraction of the genes encoded by nuclear DNA (nucDNA), its products must interact closely with their nucDNA-encoded counterparts in order to generate the energy needed for maintaining eukaryotic cellular functions. Mutations in mtDNA can lead to a breakdown in this interaction, with dire consequences for organismal health. Mutations in mtDNA accumulate rapidly compared to nucDNA in animals, and one general theory of ageing posits that the accumulation of somatic mtDNA mutations leads to ageing and the onset of age-related diseases. However, not all eukaryotes have elevated mtDNA mutation rates. To understand how underlying mtDNA mutations influence organismal health and fitness, the proposed research will examine mito-nuclear mismatch in the plant genus Silene, which occurs when mtDNA from one population/species is expressed against the nuclear background of a distant relative. Silene contains species with both slowly and rapidly evolving mtDNA, making it an ideal model for this research. The overarching question addressed by the proposed research is to determine how mito-nuclear interactions influence organismal physiology, ecology, and evolution. Silene species and populations with varying degrees of evolutionary relatedness will be crossed in order to produce progeny with a range of predicted mito-nuclear mismatch severities. Standard growth phenotypes, metabolic rates, and fecundities will be assayed in these hybrids. Oxidative phosphorylation (OXPHOS) proficiency will be assessed in both control and mismatched individuals by assessing OXPHOS complex II and IV activity. Complex IV consists of both mtDNA and nucDNA-ecoded subunits and should show reduced activity in mismatched individuals, while complex II serves as a negative control, since it is composed solely of nucDNA-encoded subunits. Furthermore, differential gene expression will be assessed between a subset of control and mismatched individuals via RNA-Seq to test between several alternative hypotheses for how mismatch affects organismal function. Finally, control and mismatched individuals will be assessed under variable drought regimes to determine if specific mito-nuclear backgrounds may be adapted to particular environments. This work will extend our understanding of mito-nuclear genomic interactions by utilizing a well- suited model that complements previous studies. Its results will be relevant to ongoing issues in human health including advancing theories of ageing and commenting on ongoing debates regarding the long-term consequences of mitochondrial replacement therapy (aka, "three-parent" in-vitro fertilization).

描述（由申请人提供）：所有真核生物都有或曾经有线粒体。这些细胞器是大约20亿年前真核生物进化早期与细菌共生的古老遗迹。因此，线粒体保留自己的基因组（mtDNA）。虽然它只编码一小部分由核DNA（nucDNA）编码的基因，但其产物必须与其nucDNA编码的对应物密切相互作用，以产生维持真核细胞功能所需的能量。线粒体DNA的突变可能导致这种相互作用的破坏，对生物体健康造成可怕的后果。在动物中，线粒体DNA的突变比核DNA积累得更快，一种关于衰老的一般理论认为，体细胞线粒体DNA突变的积累会导致衰老和与年龄相关的疾病的发生。然而，并不是所有的真核生物都有较高的mtDNA突变率。为了了解潜在的mtDNA突变如何影响生物体的健康和适应性，拟议的研究将研究植物属Silene中的线粒体核错配，当来自一个种群/物种的mtDNA在远亲的核背景下表达时，就会发生这种错配。Silene包含具有缓慢和快速进化mtDNA的物种，使其成为这项研究的理想模型。拟议研究解决的首要问题是确定线粒体-核相互作用如何影响生物生理学，生态学和进化。将杂交具有不同程度进化相关性的蝇子草物种和种群，以产生具有一系列预测的线粒体-核错配严重性的后代。将在这些杂种中测定标准生长表型、代谢率和繁殖力。通过评估OXPHOS复合物II和IV活性，在对照和错配个体中评估氧化磷酸化（OXPHOS）能力。复合体IV由mtDNA和nucDNA编码的亚基组成，并且在错配个体中应显示降低的活性，而复合体II用作阴性对照，因为它仅由nucDNA编码的亚基组成。此外，将通过RNA-Seq评估对照和错配个体的子集之间的差异基因表达，以测试错配如何影响生物体功能的几种替代假设之间的差异。最后，控制和不匹配的个人将在可变的干旱制度下进行评估，以确定特定的线粒体核背景是否可以适应特定的环境。这项工作将扩大我们的理解线粒体核基因组相互作用，利用一个非常适合的模型，补充以前的研究。其结果将与人类健康中正在发生的问题有关，包括推进衰老理论，并评论有关线粒体替代疗法（又名“三亲”体外受精）长期后果的持续辩论。

项目成果

期刊论文数量（15）

专著数量（0）

科研奖励数量（0）

会议论文数量（0）

专利数量（0）

Salinity-induced changes in gene expression from anterior and posterior gills of Callinectes sapidus (Crustacea: Portunidae) with implications for crustacean ecological genomics.

DOI：
10.1016/j.cbd.2016.06.002
发表时间：
2016-09
期刊：
Comparative biochemistry and physiology. Part D, Genomics & proteomics
影响因子：
0
作者：
Havird JC;Mitchell RT;Henry RP;Santos SR
通讯作者：
Santos SR

Sex, Mitochondria, and Genetic Rescue.

性、线粒体和基因拯救。

DOI：
10.1016/j.tree.2015.11.012
发表时间：
2016
期刊：
Trends in ecology & evolution
影响因子：
16.8
作者：
Havird,JustinC;Fitzpatrick,SarahW;Kronenberger,John;Funk,WChris;Angeloni,LisaM;Sloan,DanielB
通讯作者：
Sloan,DanielB

Do angiosperms with highly divergent mitochondrial genomes have altered mitochondrial function?

线粒体基因组高度分化的被子植物是否改变了线粒体功能？

DOI：
10.1016/j.mito.2019.06.005
发表时间：
2019
期刊：
Mitochondrion
影响因子：
4.4
作者：
Havird,JustinC;Noe,GregoryR;Link,Luke;Torres,Amber;Logan,DavidC;Sloan,DanielB;Chicco,AdamJ
通讯作者：
Chicco,AdamJ

The on-again, off-again relationship between mitochondrial genomes and species boundaries.