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酿酒酵母含有两个功能性柠檬酸合酶基因。

Saccharomyces cerevisiae contains two functional citrate synthase genes.

作者信息

Kim K S, Rosenkrantz M S, Guarente L

出版信息

Mol Cell Biol. 1986 Jun;6(6):1936-42. doi: 10.1128/mcb.6.6.1936-1942.1986.

DOI:10.1128/mcb.6.6.1936-1942.1986
PMID:3023912
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC367731/
Abstract

The tricarboxylic acid cycle occurs within the mitochondria of the yeast Saccharomyces cerevisiae. A nuclear gene encoding the tricarboxylic acid cycle enzyme citrate synthase has previously been isolated (M. Suissa, K. Suda, and G. Schatz, EMBO J. 3:1773-1781, 1984) and is referred to here as CIT1. We report here the isolation, by an immunological method, of a second nuclear gene encoding citrate synthase (CIT2). Disruption of both genes in the yeast genome was necessary to produce classical citrate synthase-deficient phenotypes: glutamate auxotrophy and poor growth on rich medium containing lactate, a nonfermentable carbon source. Therefore, the citrate synthase produced from either gene was sufficient for these metabolic roles. Transcription of both genes was maximally repressed in medium containing both glucose and glutamate. However, transcription of CIT1 but not of CIT2 was derepressed in medium containing a nonfermentable carbon source. The significance of the presence of two genes encoding citrate synthase in S. cerevisiae is discussed.

摘要

三羧酸循环发生在酿酒酵母的线粒体中。之前已分离出一个编码三羧酸循环酶柠檬酸合酶的核基因(M. 苏伊萨、K. 须田和G. 沙茨,《欧洲分子生物学组织杂志》3:1773 - 1781, 1984),本文中称之为CIT1。我们在此报告通过免疫学方法分离出的另一个编码柠檬酸合酶的核基因(CIT2)。要产生典型的柠檬酸合酶缺陷型表型,即谷氨酸营养缺陷型以及在含有乳酸(一种不可发酵碳源)的丰富培养基上生长不良,有必要破坏酵母基因组中的这两个基因。因此,由任一基因产生的柠檬酸合酶对于这些代谢功能来说都是足够的。在同时含有葡萄糖和谷氨酸的培养基中,这两个基因的转录均受到最大程度的抑制。然而,在含有不可发酵碳源的培养基中,CIT1的转录而非CIT2的转录被解除抑制。本文讨论了酿酒酵母中存在两个编码柠檬酸合酶基因的意义。

相似文献

1
Saccharomyces cerevisiae contains two functional citrate synthase genes.酿酒酵母含有两个功能性柠檬酸合酶基因。
Mol Cell Biol. 1986 Jun;6(6):1936-42. doi: 10.1128/mcb.6.6.1936-1942.1986.
2
Citrate synthase encoded by the CIT2 gene of Saccharomyces cerevisiae is peroxisomal.由酿酒酵母CIT2基因编码的柠檬酸合酶是过氧化物酶体的。
Mol Cell Biol. 1990 Apr;10(4):1399-405. doi: 10.1128/mcb.10.4.1399-1405.1990.
3
Mitochondrial and nonmitochondrial citrate synthases in Saccharomyces cerevisiae are encoded by distinct homologous genes.酿酒酵母中的线粒体和非线粒体柠檬酸合酶由不同的同源基因编码。
Mol Cell Biol. 1986 Dec;6(12):4509-15. doi: 10.1128/mcb.6.12.4509-4515.1986.
4
Extramitochondrial citrate synthase activity in bakers' yeast.面包酵母中的线粒体外柠檬酸合酶活性。
Mol Cell Biol. 1986 Feb;6(2):488-93. doi: 10.1128/mcb.6.2.488-493.1986.
5
Derepression of citrate synthase in Saccharomyces cerevisiae may occur at the level of transcription.酿酒酵母中柠檬酸合酶的去阻遏可能发生在转录水平。
Mol Cell Biol. 1984 Feb;4(2):247-53. doi: 10.1128/mcb.4.2.247-253.1984.
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Intramitochondrial functions regulate nonmitochondrial citrate synthase (CIT2) expression in Saccharomyces cerevisiae.线粒体内功能调节酿酒酵母中非线粒体柠檬酸合酶(CIT2)的表达。
Mol Cell Biol. 1991 Jan;11(1):38-46. doi: 10.1128/mcb.11.1.38-46.1991.
7
Mutations in the IDH2 gene encoding the catalytic subunit of the yeast NAD+-dependent isocitrate dehydrogenase can be suppressed by mutations in the CIT1 gene encoding citrate synthase and other genes of oxidative metabolism.编码酵母NAD⁺依赖性异柠檬酸脱氢酶催化亚基的IDH2基因突变可被编码柠檬酸合酶的CIT1基因及其他氧化代谢基因的突变所抑制。
Arch Biochem Biophys. 1997 Aug 1;344(1):139-49. doi: 10.1006/abbi.1997.0191.
8
Distinct upstream activation regions for glucose-repressed and derepressed expression of the yeast citrate synthase gene CIT1.酵母柠檬酸合酶基因CIT1葡萄糖抑制型和去抑制型表达的不同上游激活区域。
Curr Genet. 1994 Mar;25(3):185-95. doi: 10.1007/BF00357161.
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[Effect of the pho85 mutation on the catabolite repression of the CIT1 gene in yeasts Saccharomyces cerevisiae].[pho85突变对酿酒酵母中CIT1基因分解代谢阻遏的影响]
Genetika. 2003 Jun;39(6):732-8.
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Isolation of the nuclear yeast genes for citrate synthase and fifteen other mitochondrial proteins by a new screening method.通过一种新的筛选方法分离柠檬酸合酶及其他十五种线粒体蛋白的核酵母基因。
EMBO J. 1984 Aug;3(8):1773-81. doi: 10.1002/j.1460-2075.1984.tb02045.x.

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Ctp1 and Yhm2: Two Mitochondrial Citrate Transporters to Support Metabolic Flexibility of .Ctp1 和 Yhm2:两种线粒体柠檬酸转运蛋白,支持. 的代谢灵活性

本文引用的文献

1
Changes in the enzyme activities of Saccharomyces cerevisiae during aerobic growth on different carbon sources.酿酒酵母在不同碳源上有氧生长期间酶活性的变化。
Biochem J. 1965 Oct;97(1):284-97. doi: 10.1042/bj0970284.
2
Crystallographic refinement and atomic models of two different forms of citrate synthase at 2.7 and 1.7 A resolution.分辨率为2.7埃和1.7埃的两种不同形式柠檬酸合酶的晶体学精修及原子模型。
J Mol Biol. 1982 Jun 15;158(1):111-52. doi: 10.1016/0022-2836(82)90452-1.
3
In vitro translation of mRNA for yeast citrate synthase.
Int J Mol Sci. 2024 Feb 3;25(3):1870. doi: 10.3390/ijms25031870.
4
Transcriptional response of Saccharomyces cerevisiae to lactic acid enantiomers.酿酒酵母对乳酸对映异构体的转录反应。
Appl Microbiol Biotechnol. 2024 Dec;108(1):121. doi: 10.1007/s00253-023-12863-z. Epub 2024 Jan 13.
5
Sharing the wealth: The versatility of proteins targeted to peroxisomes and other organelles.共享财富:靶向过氧化物酶体及其他细胞器的蛋白质的多功能性
Front Cell Dev Biol. 2022 Sep 26;10:934331. doi: 10.3389/fcell.2022.934331. eCollection 2022.
6
Top-Down, Knowledge-Based Genetic Reduction of Yeast Central Carbon Metabolism.基于知识的自上而下的酵母中心碳代谢遗传缩减。
mBio. 2022 Oct 26;13(5):e0297021. doi: 10.1128/mbio.02970-21. Epub 2022 Sep 21.
7
Bacterial cell cycle control by citrate synthase independent of enzymatic activity.柠檬酸合酶非依赖于酶活性的细菌细胞周期调控。
Elife. 2020 Mar 9;9:e52272. doi: 10.7554/eLife.52272.
8
Filamentation Regulatory Pathways Control Adhesion-Dependent Surface Responses in Yeast.丝状调控途径控制酵母中黏附依赖性表面反应。
Genetics. 2019 Jul;212(3):667-690. doi: 10.1534/genetics.119.302004. Epub 2019 May 3.
9
Transcriptional profiling of Zygosaccharomyces bailii early response to acetic acid or copper stress mediated by ZbHaa1.毕赤酵母转录组分析 ZbHaa1 介导的对乙酸或铜胁迫的早期响应。
Sci Rep. 2018 Sep 20;8(1):14122. doi: 10.1038/s41598-018-32266-9.
10
Role of Mitochondrial Retrograde Pathway in Regulating Ethanol-Inducible Filamentous Growth in Yeast.线粒体逆行途径在调控酵母中乙醇诱导的丝状生长中的作用
Front Physiol. 2017 Mar 29;8:148. doi: 10.3389/fphys.2017.00148. eCollection 2017.
酵母柠檬酸合酶mRNA的体外翻译
J Biol Chem. 1982 Sep 25;257(18):11181-5.
4
A GAL10-CYC1 hybrid yeast promoter identifies the GAL4 regulatory region as an upstream site.一个GAL10-CYC1杂交酵母启动子将GAL4调控区域鉴定为一个上游位点。
Proc Natl Acad Sci U S A. 1982 Dec;79(23):7410-4. doi: 10.1073/pnas.79.23.7410.
5
Yeast RNA polymerase II genes: isolation with antibody probes.酵母RNA聚合酶II基因:用抗体探针分离
Science. 1983 Nov 18;222(4625):778-82. doi: 10.1126/science.6356359.
6
Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
J Bacteriol. 1983 Jan;153(1):163-8. doi: 10.1128/jb.153.1.163-168.1983.
7
Distinctly regulated tandem upstream activation sites mediate catabolite repression of the CYC1 gene of S. cerevisiae.明显受调控的串联上游激活位点介导酿酒酵母CYC1基因的分解代谢物阻遏。
Cell. 1984 Feb;36(2):503-11. doi: 10.1016/0092-8674(84)90243-5.
8
One-step gene disruption in yeast.酵母中的一步基因破坏
Methods Enzymol. 1983;101:202-11. doi: 10.1016/0076-6879(83)01015-0.
9
Yeast promoters and lacZ fusions designed to study expression of cloned genes in yeast.用于研究酵母中克隆基因表达的酵母启动子和乳糖操纵子Z融合体。
Methods Enzymol. 1983;101:181-91. doi: 10.1016/0076-6879(83)01013-7.
10
Heme regulates transcription of the CYC1 gene of S. cerevisiae via an upstream activation site.血红素通过一个上游激活位点调节酿酒酵母CYC1基因的转录。
Cell. 1983 Apr;32(4):1279-86. doi: 10.1016/0092-8674(83)90309-4.