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编码葡萄糖-6-磷酸脱氢酶(G6PD)的管家基因的靶向破坏:G6PD对于戊糖合成并非必需,但对于抵御氧化应激至关重要。

Targeted disruption of the housekeeping gene encoding glucose 6-phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stress.

作者信息

Pandolfi P P, Sonati F, Rivi R, Mason P, Grosveld F, Luzzatto L

机构信息

Department of Haematology, Royal Postgraduate Medical School, London, UK.

出版信息

EMBO J. 1995 Nov 1;14(21):5209-15. doi: 10.1002/j.1460-2075.1995.tb00205.x.

DOI:10.1002/j.1460-2075.1995.tb00205.x
PMID:7489710
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC394630/
Abstract

Glucose 6-phosphate dehydrogenase (G6PD) is a housekeeping enzyme encoded in mammals by an X-linked gene. It has important functions in intermediary metabolism because it catalyzes the first step in the pentose phosphate pathway and provides reductive potential in the form of NADPH. In human populations, many mutant G6PD alleles (some present at polymorphic frequencies) cause a partial loss of G6PD activity and a variety of hemolytic anemias, which vary from mild to severe. All these mutants have some residual enzyme activity, and no large deletions in the G6PD gene have ever been found. To test which, if any, function of G6PD is essential, we have disrupted the G6PD gene in male mouse embryonic stem cells by targeted homologous recombination. We have isolated numerous clones, shown to be recombinant by Southern blot analysis, in which G6PD activity is undetectable. We have extensively characterized individual clones and found that they are extremely sensitive to H2O2 and to the sulfydryl group oxidizing agent, diamide. Their markedly impaired cloning efficiency is restored by reducing the oxygen tension. We conclude that G6PD activity is dispensable for pentose synthesis, but is essential to protect cells against even mild oxidative stress.

摘要

葡萄糖-6-磷酸脱氢酶(G6PD)是一种管家酶,在哺乳动物中由X连锁基因编码。它在中间代谢中具有重要功能,因为它催化磷酸戊糖途径的第一步,并以NADPH的形式提供还原电位。在人类群体中,许多突变的G6PD等位基因(有些以多态频率存在)会导致G6PD活性部分丧失以及各种溶血性贫血,其严重程度各不相同。所有这些突变体都有一些残余的酶活性,并且从未发现G6PD基因有大的缺失。为了测试G6PD的哪些功能(如果有的话)是必不可少的,我们通过靶向同源重组在雄性小鼠胚胎干细胞中破坏了G6PD基因。我们分离出了许多通过Southern印迹分析显示为重组体的克隆,其中G6PD活性无法检测到。我们对单个克隆进行了广泛的表征,发现它们对H2O2和巯基氧化剂二酰胺极其敏感。通过降低氧张力可以恢复它们明显受损的克隆效率。我们得出结论,G6PD活性对于戊糖合成是可有可无的,但对于保护细胞免受即使是轻度的氧化应激至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a569/394630/669938624d91/emboj00045-0077-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a569/394630/15a0866f689a/emboj00045-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a569/394630/dd9212d5e5d1/emboj00045-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a569/394630/669938624d91/emboj00045-0077-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a569/394630/15a0866f689a/emboj00045-0074-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a569/394630/dd9212d5e5d1/emboj00045-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a569/394630/669938624d91/emboj00045-0077-a.jpg

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本文引用的文献

1
GENERATION OF HYDROGEN PEROXIDE IN ERYTHROCYTES BY HEMOLYTIC AGENTS.溶血剂在红细胞中产生过氧化氢
Biochemistry. 1964 Jul;3:895-900. doi: 10.1021/bi00895a006.
2
A genetically defined animal model of anembryonic pregnancy.一种基因定义的胚胎妊娠缺失动物模型。
Hum Reprod. 1993 Aug;8(8):1316-23. doi: 10.1093/oxfordjournals.humrep.a138249.
3
Variants of glucose-6-phosphate dehydrogenase are due to missense mutations spread throughout the coding region of the gene.葡萄糖-6-磷酸脱氢酶的变体是由遍布该基因编码区域的错义突变引起的。
G6PD A型小鼠中性粒细胞HO生成增加及肺部清除能力增强
Res Sq. 2024 Mar 11:rs.3.rs-3931558. doi: 10.21203/rs.3.rs-3931558/v1.
4
Monogenic Disorders of ROS Production and the Primary Anti-Oxidative Defense.单基因氧化还原产物异常和主要抗氧化防御异常。
Biomolecules. 2024 Feb 9;14(2):206. doi: 10.3390/biom14020206.
5
mTOR-dependent loss of PON1 secretion and antiphospholipid autoantibody production underlie autoimmunity-mediated cirrhosis in transaldolase deficiency.转醛醇酶缺乏导致的自身免疫性疾病相关性肝硬化的发病机制与 mTOR 依赖性 PON1 分泌缺失和抗磷脂自身抗体产生有关。
J Autoimmun. 2023 Nov;140:103112. doi: 10.1016/j.jaut.2023.103112. Epub 2023 Sep 22.
6
Antimicrobial and studies of the triterpenoids of Dichapetalum albidum.白花毒鼠子的抗菌作用及三萜类化合物研究。
Heliyon. 2023 Jul 14;9(7):e18299. doi: 10.1016/j.heliyon.2023.e18299. eCollection 2023 Jul.
7
Cognitive dysfunction in diabetes: abnormal glucose metabolic regulation in the brain.糖尿病认知功能障碍:大脑中葡萄糖代谢调节异常。
Front Endocrinol (Lausanne). 2023 Jun 16;14:1192602. doi: 10.3389/fendo.2023.1192602. eCollection 2023.
8
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9
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10
Cytosolic aldose metabolism contributes to progression from cirrhosis to hepatocarcinogenesis.细胞质醛糖代谢促进肝硬化向肝癌发生的进展。
Nat Metab. 2023 Jan;5(1):41-60. doi: 10.1038/s42255-022-00711-9. Epub 2023 Jan 19.
Hum Mutat. 1993;2(3):159-67. doi: 10.1002/humu.1380020302.
4
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Curr Opin Genet Dev. 1993 Jun;3(3):484-90. doi: 10.1016/0959-437x(93)90124-8.
5
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FASEB J. 1994 Feb;8(2):174-81. doi: 10.1096/fasebj.8.2.8119488.
6
Molecular human genetics and the Duchenne/Becker muscular dystrophy gene.分子人类遗传学与杜兴/贝克型肌营养不良症基因
Mol Cell Biol Hum Dis Ser. 1993;3:1-11. doi: 10.1007/978-94-011-1528-5_1.
7
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8
Targeted disruption of the GATA3 gene causes severe abnormalities in the nervous system and in fetal liver haematopoiesis.GATA3基因的靶向破坏会导致神经系统和胎儿肝脏造血功能出现严重异常。
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9
Pentose phosphate pathway mutants of yeast.酵母的磷酸戊糖途径突变体
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10
Regulation of glucose 6-phosphate dehydrogenase expression in CHO-human fibroblast somatic cell hybrids.葡萄糖-6-磷酸脱氢酶在CHO-人成纤维体细胞杂种中的表达调控
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