• 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

无证据表明线粒体DNA在精子活力中起作用:来自弱精子症男性全基因组测序的数据。

No evidence for an mtDNA role in sperm motility: data from complete sequencing of asthenozoospermic males.

作者信息

Pereira Luísa, Gonçalves João, Franco-Duarte Ricardo, Silva Júlia, Rocha Tiago, Arnold Christiane, Richards Martin, Macaulay Vincent

机构信息

Instituto de Patologia e Imunologia Molecular da Universidade do Porto, (IPATIMUP), Porto, Portugal.

出版信息

Mol Biol Evol. 2007 Mar;24(3):868-74. doi: 10.1093/molbev/msm004. Epub 2007 Jan 11.

DOI:10.1093/molbev/msm004
PMID:17218641
Abstract

The first complete mitochondrial DNA (mtDNA) sequences (approximately 16,569 bp) in 20 patients with asthenozoospermia and a comparison with 23 new complete mtDNA sequences in teratoasthenozoospermic individuals, confirmed no sharing of specific polymorphisms or specific mitochondrial lineages between these individuals. This is strong evidence against the accepted claim of a major role played by mtDNA in male fertility, once supported by haplogroup association studies based on the screening of hypervariable region I. The hypothesis of maternally driven selection acting in male reproductive success must thus be treated with caution.

摘要

对20例弱精子症患者的首个完整线粒体DNA(mtDNA)序列(约16,569 bp),以及与23例畸形精子症患者的23个新的完整mtDNA序列进行比较后,证实这些个体之间不存在特定多态性或特定线粒体谱系的共享。这有力地反驳了mtDNA在男性生育中起主要作用这一已被认可的观点,该观点曾得到基于高变区I筛选的单倍群关联研究的支持。因此,对于母系驱动的选择作用于男性生殖成功这一假说必须谨慎对待。

相似文献

1
No evidence for an mtDNA role in sperm motility: data from complete sequencing of asthenozoospermic males.无证据表明线粒体DNA在精子活力中起作用:来自弱精子症男性全基因组测序的数据。
Mol Biol Evol. 2007 Mar;24(3):868-74. doi: 10.1093/molbev/msm004. Epub 2007 Jan 11.
2
4,977-bp human mitochondrial DNA deletion is associated with asthenozoospermic infertility in Jordan.4977 个碱基对的人类线粒体 DNA 缺失与约旦弱精症不育有关。
Andrologia. 2020 Feb;52(1):e13379. doi: 10.1111/and.13379. Epub 2019 Nov 20.
3
Sperm mitochondrial DNA deletion in Iranian infertiles with asthenozoospermia.伊朗弱精子症不育男性的精子线粒体DNA缺失
Andrologia. 2017 Apr;49(3). doi: 10.1111/and.12627. Epub 2016 Jun 30.
4
Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population.芬兰人群中mtDNA单倍群TJ的系统发育分析。
J Hum Genet. 2001;46(2):64-9. doi: 10.1007/s100380170110.
5
Mitochondrial DNA haplogroup associated with sperm motility in the Han population.线粒体 DNA 单倍群与汉族人群精子活力相关。
Asian J Androl. 2013 Sep;15(5):630-3. doi: 10.1038/aja.2013.83. Epub 2013 Aug 5.
6
Human sperm motility: a molecular study of mitochondrial DNA, mitochondrial transcription factor A gene and DNA fragmentation.人类精子活力:线粒体 DNA、线粒体转录因子 A 基因和 DNA 碎片化的分子研究。
Mol Biol Rep. 2019 Aug;46(4):4113-4121. doi: 10.1007/s11033-019-04861-0. Epub 2019 May 14.
7
Differences of sperm motility in mitochondrial DNA haplogroup U sublineages.线粒体DNA单倍群U亚分支中精子活力的差异。
Gene. 2006 Mar 1;368:21-7. doi: 10.1016/j.gene.2005.09.015. Epub 2005 Dec 1.
8
Promoter targeted bisulfite sequencing reveals DNA methylation profiles associated with low sperm motility in asthenozoospermia.启动子靶向亚硫酸氢盐测序揭示了与弱精子症中精子活力低下相关的DNA甲基化谱。
Hum Reprod. 2016 Jan;31(1):24-33. doi: 10.1093/humrep/dev283. Epub 2015 Nov 30.
9
Oxidative stress and sperm mitochondrial DNA mutation in idiopathic oligoasthenozoospermic men.特发性少弱精子症男性的氧化应激与精子线粒体DNA突变
Indian J Biochem Biophys. 2009 Apr;46(2):172-7.
10
Sperm motility in Mytilus edulis in relation to mitochondrial DNA polymorphisms: implications for the evolution of doubly uniparental inheritance in bivalves.紫贻贝精子活力与线粒体DNA多态性的关系:对双壳贝类单亲二倍体遗传进化的启示
Evolution. 2008 Jan;62(1):99-106. doi: 10.1111/j.1558-5646.2007.00262.x. Epub 2007 Nov 26.

引用本文的文献

1
Mother's Curse effects on lifespan and aging.母亲的诅咒对寿命和衰老的影响。
Front Aging. 2024 Mar 8;5:1361396. doi: 10.3389/fragi.2024.1361396. eCollection 2024.
2
Refining the Global Phylogeny of Mitochondrial N1a, X, and HV2 Haplogroups Based on Rare Mitogenomes from Croatian Isolates.基于克罗地亚分离株的罕见线粒体基因组,对线粒体 N1a、X 和 HV2 单倍群的全球系统发育进行精细化研究。
Genes (Basel). 2023 Aug 12;14(8):1614. doi: 10.3390/genes14081614.
3
Natural and Artificial Mechanisms of Mitochondrial Genome Elimination.线粒体基因组消除的自然和人工机制
Life (Basel). 2021 Jan 20;11(2):76. doi: 10.3390/life11020076.
4
Impact of Mitochondrial Genetic Variants in ND1, ND2, ND5, and ND6 Genes on Sperm Motility and Intracytoplasmic Sperm Injection (ICSI) Outcomes.线粒体 ND1、ND2、ND5 和 ND6 基因的遗传变异对精子活力和卵胞浆内单精子注射(ICSI)结局的影响。
Reprod Sci. 2021 May;28(5):1540-1555. doi: 10.1007/s43032-020-00449-3. Epub 2021 Jan 21.
5
Ancient DNA of Phoenician remains indicates discontinuity in the settlement history of Ibiza.腓尼基人遗骸的古 DNA 表明伊比萨岛的定居历史存在不连续性。
Sci Rep. 2018 Dec 4;8(1):17567. doi: 10.1038/s41598-018-35667-y.
6
'Infertile' studies on mitochondrial DNA variation in asthenozoospermic Tunisian men.关于突尼斯弱精子症男性线粒体DNA变异的“不育”研究。
Biochem Biophys Rep. 2016 Aug 11;8:114-119. doi: 10.1016/j.bbrep.2016.08.002. eCollection 2016 Dec.
7
Associations between male infertility and ancestry in South Americans: a case control study.南美洲男性不育与祖先之间的关联:一项病例对照研究。
BMC Med Genet. 2017 Jul 26;18(1):78. doi: 10.1186/s12881-017-0438-z.
8
Phylogenetic and population-based approaches to mitogenome variation do not support association with male infertility.基于系统发育和群体的线粒体基因组变异研究方法并不支持其与男性不育症有关联。
J Hum Genet. 2017 Mar;62(3):361-371. doi: 10.1038/jhg.2016.130. Epub 2016 Dec 1.
9
Mitochondrial-Nuclear Interactions Mediate Sex-Specific Transcriptional Profiles in Drosophila.线粒体-细胞核相互作用介导果蝇性别特异性转录谱
Genetics. 2016 Oct;204(2):613-630. doi: 10.1534/genetics.116.192328. Epub 2016 Aug 24.
10
Mitonuclear Epistasis for Development Time and Its Modification by Diet in Drosophila.果蝇发育时间的线粒体-细胞核上位效应及其饮食调节
Genetics. 2016 May;203(1):463-84. doi: 10.1534/genetics.116.187286. Epub 2016 Mar 10.