• 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

Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis.

作者信息

Tiranti V, Rossi E, Ruiz-Carrillo A, Rossi G, Rocchi M, DiDonato S, Zuffardi O, Zeviani M

机构信息

Divisione di Biochimica e Genetica, Milano, Istituto Nazionale Neurologico Carlo Besta, Italy.

出版信息

Genomics. 1995 Jan 20;25(2):559-64. doi: 10.1016/0888-7543(95)80058-t.

DOI:10.1016/0888-7543(95)80058-t
PMID:7789991
Abstract

By using a PCR-based screening of a somatic cell hybrid panel and FISH, we have assigned the loci of mitochondrial single-stranded DNA-binding protein (SSBP), mitochondrial transcription factor A (TCF6), and mitochondrial endonuclease G (ENDOG) genes to human chromosomes 7q34, 10q21, and 9q34.1, respectively. The products of these three genes are involved in fundamental aspects of mitochondrial biogenesis, such as replication and transcription of the mitochondrial genome. The chromosomal localization of these genes is important to testing whether the corresponding proteins may play a role in the etiopathogenesis of human disorders associated with qualitative or quantitative abnormalities of mitochondrial DNA.

摘要

相似文献

1
Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesis.
Genomics. 1995 Jan 20;25(2):559-64. doi: 10.1016/0888-7543(95)80058-t.
2
Autophagy restricts mitochondrial DNA damage-induced release of ENDOG (endonuclease G) to regulate genome stability.自噬限制线粒体 DNA 损伤诱导的 ENDOG(核酸内切酶 G)释放以调节基因组稳定性。
Autophagy. 2021 Nov;17(11):3444-3460. doi: 10.1080/15548627.2021.1874209. Epub 2021 Jan 19.
3
Familial mitochondrial DNA depletion in liver: haplotype analysis of candidate genes.
Hum Genet. 1998 Mar;102(3):327-31. doi: 10.1007/s004390050700.
4
Endonuclease G is a novel determinant of cardiac hypertrophy and mitochondrial function.核酸内切酶 G 是心脏肥大和线粒体功能的一个新决定因素。
Nature. 2011 Oct 5;478(7367):114-8. doi: 10.1038/nature10490.
5
Assessment of the Role of Nuclear ENDOG Gene and mtDNA Variations on Paternal Mitochondrial Elimination (PME) in Infertile Men: An Experimental Study.评估核内 ENDOG 基因和 mtDNA 变异对男性不育患者父系线粒体清除(PME)的作用:一项实验研究。
Reprod Sci. 2022 Aug;29(8):2208-2222. doi: 10.1007/s43032-022-00953-8. Epub 2022 Apr 27.
6
Endonuclease G promotes hepatic mitochondrial respiration by selectively increasing mitochondrial tRNA production.核酸内切酶G通过选择性增加线粒体tRNA的产生来促进肝脏线粒体呼吸。
Proc Natl Acad Sci U S A. 2025 Jan 7;122(1):e2411298122. doi: 10.1073/pnas.2411298122. Epub 2025 Jan 3.
7
Human mitochondrial transcription factor A (mtTFA): gene structure and characterization of related pseudogenes.人类线粒体转录因子A(mtTFA):基因结构及相关假基因的特征
Gene. 2002 May 29;291(1-2):223-32. doi: 10.1016/s0378-1119(02)00600-5.
8
Biallelic Variants in Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions.与线粒体肌病和多种 mtDNA 缺失相关的双等位基因变异。
Cells. 2022 Mar 12;11(6):974. doi: 10.3390/cells11060974.
9
Endonuclease G is required for early embryogenesis and normal apoptosis in mice.小鼠早期胚胎发育和正常细胞凋亡需要核酸内切酶G。
Proc Natl Acad Sci U S A. 2003 Dec 23;100(26):15782-7. doi: 10.1073/pnas.2636393100. Epub 2003 Dec 8.
10
An autosomal locus predisposing to deletions of mitochondrial DNA.一个易导致线粒体DNA缺失的常染色体位点。
Nat Genet. 1995 Feb;9(2):146-51. doi: 10.1038/ng0295-146.

引用本文的文献

1
A case with bilateral C-shaped autofluorescence in retinal degeneration.一例视网膜变性伴双侧C形自发荧光的病例。
Am J Ophthalmol Case Rep. 2025 May 2;38:102351. doi: 10.1016/j.ajoc.2025.102351. eCollection 2025 Jun.
2
Skeletal muscle proteome differs between young and targeted replacement mice in a sex-dependent manner.骨骼肌蛋白质组在年轻小鼠和靶向替换小鼠之间存在性别依赖性差异。
Front Aging Neurosci. 2024 Nov 20;16:1486762. doi: 10.3389/fnagi.2024.1486762. eCollection 2024.
3
Pregnancy Disorders: A Potential Role for Mitochondrial Altered Homeostasis.
妊娠疾病:线粒体稳态改变的潜在作用
Antioxidants (Basel). 2024 Aug 13;13(8):979. doi: 10.3390/antiox13080979.
4
Cytoplasmic Endonuclease G promotes nonalcoholic fatty liver disease via mTORC2-AKT-ACLY and endoplasmic reticulum stress.细胞质核酸内切酶 G 通过 mTORC2-AKT-ACLY 和内质网应激促进非酒精性脂肪性肝病。
Nat Commun. 2023 Oct 4;14(1):6201. doi: 10.1038/s41467-023-41757-x.
5
Maternal mosaicism in SSBP1 causing optic atrophy with retinal degeneration: implications for genetic counseling.SSBP1 所致视神经萎缩伴视网膜变性的母源性嵌合体:遗传咨询的意义。
Orphanet J Rare Dis. 2023 May 31;18(1):131. doi: 10.1186/s13023-023-02748-9.
6
Maternal Mosaicism in SSBP1 Causing Optic Atrophy with Retinal Degeneration: Implications for Genetic Counseling.SSBP1基因的母体镶嵌现象导致视神经萎缩伴视网膜变性:对遗传咨询的启示
Res Sq. 2023 Mar 15:rs.3.rs-2554402. doi: 10.21203/rs.3.rs-2554402/v1.
7
Photoreceptor Manifestations of Primary Mitochondrial Optic Nerve Disorders.原发性线粒体视神经病变的光感受器表现。
Invest Ophthalmol Vis Sci. 2022 May 2;63(5):5. doi: 10.1167/iovs.63.5.5.
8
Identification and Characterization of a Double-Stranded RNA Degrading Nuclease Influencing RNAi Efficiency in the Rice Leaf Folder .影响稻纵卷叶螟RNA干扰效率的双链RNA降解核酸酶的鉴定与特性分析
Int J Mol Sci. 2022 Apr 2;23(7):3961. doi: 10.3390/ijms23073961.
9
New Insights into Molecular Mechanisms Mediating Adaptation to Exercise; A Review Focusing on Mitochondrial Biogenesis, Mitochondrial Function, Mitophagy and Autophagy.运动适应的分子机制新见解:一篇聚焦于线粒体生物发生、线粒体功能、线粒体自噬和自噬的综述。
Cells. 2021 Oct 2;10(10):2639. doi: 10.3390/cells10102639.
10
Co-expression analysis identifies neuro-inflammation as a driver of sensory neuron aging in Aplysia californica.共表达分析将神经炎症确定为加利福尼亚海兔感觉神经元衰老的驱动因素。
PLoS One. 2021 Jun 11;16(6):e0252647. doi: 10.1371/journal.pone.0252647. eCollection 2021.