• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

线粒体 DNA 变体影响黑腹果蝇的线粒体生物能量学。

Mitochondrial DNA variants influence mitochondrial bioenergetics in Drosophila melanogaster.

机构信息

School of Biotechnology and Biomolecular Sciences, University of New South Wales, Sydney 2052, Australia.

出版信息

Mitochondrion. 2012 Jul;12(4):459-64. doi: 10.1016/j.mito.2012.06.005. Epub 2012 Jun 24.

DOI:10.1016/j.mito.2012.06.005
PMID:22735574
Abstract

The influence of mitochondrial DNA (mtDNA) mutations on human disease has been extensively studied, but the impact of mutations within the adaptive range is debated. We studied males from lines of Drosophila melanogaster that have a highly standardized nuclear genome but different mtDNA, at two ages. We measured mitochondrial respiration on permeabilized muscle fibers, hydrogen peroxide production of isolated mitochondria and mtDNA copy number of whole individuals. The results show that a small set of naturally occurring mtDNA mutations can have a significant influence on mitochondrial bioenergetics that may change as the organism ages.

摘要

线粒体 DNA(mtDNA)突变对人类疾病的影响已得到广泛研究,但突变在适应范围内的影响仍存在争议。我们研究了具有高度标准化核基因组但 mtDNA 不同的黑腹果蝇品系的雄性个体,分别在两个年龄段进行测量。我们测量了透化肌肉纤维的线粒体呼吸、分离线粒体的过氧化氢产生以及整个个体的 mtDNA 拷贝数。结果表明,一小部分自然发生的 mtDNA 突变可能对线粒体生物能量学产生重大影响,而这种影响可能会随着生物体的衰老而发生变化。

相似文献

1
Mitochondrial DNA variants influence mitochondrial bioenergetics in Drosophila melanogaster.线粒体 DNA 变体影响黑腹果蝇的线粒体生物能量学。
Mitochondrion. 2012 Jul;12(4):459-64. doi: 10.1016/j.mito.2012.06.005. Epub 2012 Jun 24.
2
Sympatric Drosophila simulans flies with distinct mtDNA show difference in mitochondrial respiration and electron transport.具有不同线粒体DNA的同域拟果蝇在线粒体呼吸和电子传递方面存在差异。
Insect Biochem Mol Biol. 2007 Mar;37(3):213-22. doi: 10.1016/j.ibmb.2006.11.002. Epub 2006 Nov 15.
3
Sex differences in survival and mitochondrial bioenergetics during aging in Drosophila.果蝇衰老过程中生存及线粒体生物能量学的性别差异
Aging Cell. 2007 Oct;6(5):699-708. doi: 10.1111/j.1474-9726.2007.00331.x. Epub 2007 Aug 24.
4
Mitochondrial DNA variants in Drosophila melanogaster are expressed at the level of the organismal phenotype.黑腹果蝇中的线粒体 DNA 变体在机体表型水平上表达。
Mitochondrion. 2011 Sep;11(5):756-63. doi: 10.1016/j.mito.2011.06.012. Epub 2011 Jul 5.
5
Mitochondrial DNA copy number and function decrease with age in the short-lived fish Nothobranchius furzeri.线粒体 DNA 拷贝数和功能随短生命周期鱼类非洲鲫鱼 Nothobranchius furzeri 的年龄增长而下降。
Aging Cell. 2011 Oct;10(5):824-31. doi: 10.1111/j.1474-9726.2011.00723.x. Epub 2011 Jun 27.
6
Variation in mitochondrial genotype has substantial lifespan effects which may be modulated by nuclear background.线粒体基因型的变异对寿命有显著影响,这种影响可能会受到核背景的调节。
Aging Cell. 2008 Dec;7(6):795-804. doi: 10.1111/j.1474-9726.2008.00428.x. Epub 2008 Aug 21.
7
The mitochondrial genome in human adaptive radiation and disease: on the road to therapeutics and performance enhancement.人类适应性辐射与疾病中的线粒体基因组:通往治疗与性能提升之路。
Gene. 2005 Jul 18;354:169-80. doi: 10.1016/j.gene.2005.05.001.
8
Diet influences the intake target and mitochondrial functions of Drosophila melanogaster males.饮食影响黑腹果蝇雄性的摄入目标和线粒体功能。
Mitochondrion. 2013 Nov;13(6):817-22. doi: 10.1016/j.mito.2013.05.008. Epub 2013 May 23.
9
The A8296G mtDNA mutation associated with several mitochondrial diseases does not cause mitochondrial dysfunction in cybrid cell lines.与几种线粒体疾病相关的A8296G线粒体DNA突变不会在胞质杂种细胞系中引起线粒体功能障碍。
Hum Mutat. 2002 Mar;19(3):234-9. doi: 10.1002/humu.10050.
10
Apoptosis in mitochondrial myopathies is linked to mitochondrial proliferation.线粒体肌病中的细胞凋亡与线粒体增殖有关。
Brain. 2006 May;129(Pt 5):1249-59. doi: 10.1093/brain/awl061. Epub 2006 Mar 14.

引用本文的文献

1
Evolutionary genetics of the mitochondrial genome: insights from Drosophila.线粒体基因组的进化遗传学:来自果蝇的启示。
Genetics. 2023 Jul 6;224(3). doi: 10.1093/genetics/iyad036.
2
Stimulating the sir2-spargel axis rescues exercise capacity and mitochondrial respiration in a Drosophila model of Barth syndrome.刺激 sir2-spargel 轴可恢复 Barth 综合征果蝇模型的运动能力和线粒体呼吸。
Dis Model Mech. 2022 Oct 1;15(10). doi: 10.1242/dmm.049279. Epub 2022 Oct 5.
3
Mitonuclear interactions alter sex-specific longevity in a species without sex chromosomes.
线粒体与核基因互作改变了一种不含性染色体的物种的性别特异性寿命。
Proc Biol Sci. 2021 Nov 10;288(1962):20211813. doi: 10.1098/rspb.2021.1813. Epub 2021 Nov 3.
4
Mitonuclear Interactions Produce Diverging Responses to Mild Stress in Larvae.线粒体-细胞核相互作用在幼虫中对轻度应激产生不同反应。
Front Genet. 2021 Sep 16;12:734255. doi: 10.3389/fgene.2021.734255. eCollection 2021.
5
Presence of male mitochondria in somatic tissues and their functional importance at the whole animal level in the marine bivalve Arctica islandica.雄性线粒体在海洋双壳类贻贝 Arctica islandica 体组织中的存在及其在整个动物水平上的功能重要性。
Commun Biol. 2021 Sep 20;4(1):1104. doi: 10.1038/s42003-021-02593-1.
6
An atlas of mitochondrial DNA genotype-phenotype associations in the UK Biobank.英国生物银行线粒体DNA基因型-表型关联图谱。
Nat Genet. 2021 Jul;53(7):982-993. doi: 10.1038/s41588-021-00868-1. Epub 2021 May 17.
7
as a Model System to Investigate the Effects of Mitochondrial Variation on Innate Immunity.作为研究线粒体变异对固有免疫影响的模型系统。
Front Immunol. 2020 Mar 25;11:521. doi: 10.3389/fimmu.2020.00521. eCollection 2020.
8
PARIS induced defects in mitochondrial biogenesis drive dopamine neuron loss under conditions of parkin or PINK1 deficiency.巴黎诱导的线粒体生物发生缺陷在 parkin 或 PINK1 缺乏的情况下驱动多巴胺神经元丢失。
Mol Neurodegener. 2020 Mar 5;15(1):17. doi: 10.1186/s13024-020-00363-x.
9
Sex-specific effects of mitochondrial haplotype on metabolic rate in support predictions of the Mother's Curse hypothesis.线粒体单倍型对代谢率的性别特异性影响支持“母亲的诅咒”假说的预测。
Philos Trans R Soc Lond B Biol Sci. 2020 Jan 20;375(1790):20190178. doi: 10.1098/rstb.2019.0178. Epub 2019 Dec 2.
10
Age Dependent Dysfunction of Mitochondrial and ROS Metabolism Induced by Mitonuclear Mismatch.线粒体核错配诱导的年龄依赖性线粒体和活性氧代谢功能障碍。
Front Genet. 2019 Feb 20;10:130. doi: 10.3389/fgene.2019.00130. eCollection 2019.