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1
Presence of queuine in Drosophila melanogaster: correlation of free pool with queuosine content of tRNA and effect of mutations in pteridine metabolism.黑腹果蝇中喹啉的存在:游离库与tRNA中喹喔啉含量的相关性以及蝶啶代谢突变的影响。
Nucleic Acids Res. 1981 May 25;9(10):2351-66. doi: 10.1093/nar/9.10.2351.
2
Transfer ribonucleic acid guanine transglycosylase isolated from rat liver.从大鼠肝脏中分离出的转移核糖核酸鸟嘌呤转糖基酶。
Biochemistry. 1980 Jan 22;19(2):395-400. doi: 10.1021/bi00543a023.
3
Substrate and inhibitor specificity of tRNA-guanine ribosyltransferase.tRNA-鸟嘌呤核糖基转移酶的底物和抑制剂特异性
Biochim Biophys Acta. 1984 Feb 24;781(1-2):64-75. doi: 10.1016/0167-4781(84)90124-6.
4
Queuine metabolism and cadmium toxicity in Drosophila melanogaster.黑腹果蝇中的喹啉代谢与镉毒性
Biofactors. 1991 Jan;3(1):41-7.
5
Differential turnover of tRNAs of the queuosine family in Dictyostelium discoideum and its possible role in regulation.盘基网柄菌中 queuosine 家族 tRNA 的差异周转及其在调控中的可能作用。
Biol Chem Hoppe Seyler. 1985 Jan;366(1):69-76. doi: 10.1515/bchm3.1985.366.1.69.
6
Queuine-containing isoacceptor of tyrosine tRNA in Drosophila melanogaster. Alteration of levels by divalent cations.果蝇中含Q( queuine)的酪氨酸tRNA同工受体。二价阳离子对其水平的影响
Biochim Biophys Acta. 1982 Oct 29;699(1):40-8. doi: 10.1016/0167-4781(82)90169-5.
7
Administration of exogenous queuine is essential for the biosynthesis of the queuosine-containing transfer RNAs in the mouse.外源性 queuine 的给药对于小鼠中含 queuosine 的转运 RNA 的生物合成至关重要。
J Biol Chem. 1981 Nov 25;256(22):11591-4.
8
A factor in serum and amniotic fluid is a substrate for the tRNA-modifying enzyme tRNA-guanine transferase.血清和羊水中的一种因子是tRNA修饰酶tRNA-鸟嘌呤转移酶的底物。
Proc Natl Acad Sci U S A. 1979 Jul;76(7):3271-5. doi: 10.1073/pnas.76.7.3271.
9
Purification and properties of guanine, queuine-tRNA transglycosylase from wheat germ.小麦胚芽鸟嘌呤、反密码子-转运核糖核酸转糖基酶的纯化及性质
J Biol Chem. 1982 Nov 25;257(22):13218-22.
10
tRNA-guanine transglycosylase from Escherichia coli: recognition of full-length 'queuine-cognate' tRNAs.来自大肠杆菌的tRNA-鸟嘌呤转糖基酶:对全长“喹啉同源”tRNA的识别
FEBS Lett. 1998 Jul 24;431(3):427-32. doi: 10.1016/s0014-5793(98)00801-1.

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Dinucleotide preferences underlie apparent codon preference reversals in the lineage.二核苷酸偏好是该谱系中明显的密码子偏好逆转的基础。
Proc Natl Acad Sci U S A. 2025 May 27;122(21):e2419696122. doi: 10.1073/pnas.2419696122. Epub 2025 May 22.
2
Queuine Micronutrient Deficiency Promotes Warburg Metabolism and Reversal of the Mitochondrial ATP Synthase in Hela Cells.Queuine 微量营养素缺乏促进了 HeLa 细胞的瓦博格代谢和线粒体 ATP 合酶的逆转。
Nutrients. 2020 Mar 24;12(3):871. doi: 10.3390/nu12030871.
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Discovery of novel bacterial queuine salvage enzymes and pathways in human pathogens.发现人类病原体中新的细菌 Queuine 回收酶和途径。
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Cross-Talk between Dnmt2-Dependent tRNA Methylation and Queuosine Modification.依赖Dnmt2的tRNA甲基化与Queuosine修饰之间的相互作用
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The queuine micronutrient: charting a course from microbe to man.夸昆微量营养素:从微生物到人类的探索之旅。
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A nutrient-driven tRNA modification alters translational fidelity and genome-wide protein coding across an animal genus.一种由营养驱动的tRNA修饰改变了整个动物属的翻译保真度和全基因组蛋白质编码。
PLoS Biol. 2014 Dec 9;12(12):e1002015. doi: 10.1371/journal.pbio.1002015. eCollection 2014 Dec.
8
Queuine in plants and plant tRNAs: Differences between embryonic tissue and mature leaves.植物和植物 tRNA 中的 Queuine:胚胎组织与成熟叶片之间的差异。
Plant Mol Biol. 1987 Jul;8(4):345-53. doi: 10.1007/BF00021314.
9
Differential heterocyclic substrate recognition by, and pteridine inhibition of E. coli and human tRNA-guanine transglycosylases.大肠杆菌和人 tRNA 鸟嘌呤转糖基酶对差异杂环碱基底物的识别及喋呤抑制作用。
Biochem Biophys Res Commun. 2011 Jun 24;410(1):34-9. doi: 10.1016/j.bbrc.2011.05.100. Epub 2011 May 24.
10
Guanosine triphosphate cyclohydrolase activity in rat tissues.大鼠组织中的鸟苷三磷酸环化水解酶活性
Biochem J. 1984 Jan 1;217(1):59-65. doi: 10.1042/bj2170059.

本文引用的文献

1
Pteridines and Gene Homologies in the Eye Color Mutants of DROSOPHILA HYDEI and DROSOPHILA MELANOGASTER.海德果蝇和黑腹果蝇眼色突变体中的蝶啶与基因同源性
Genetics. 1965 Nov;52(5):1023-34. doi: 10.1093/genetics/52.5.1023.
2
Structure of an amniotic fluid component, 7-(4,5-cis-dihydroxy-1-cyclopenten-3-ylaminomethyl)-7-deazaguanine (queuine), a substrate for tRNA: guanine transglycosylase.羊水成分7-(4,5-顺式二羟基-1-环戊烯-3-基氨甲基)-7-脱氮鸟嘌呤(queuine)的结构,tRNA:鸟嘌呤转糖基酶的一种底物
J Biol Chem. 1980 Sep 25;255(18):8405-7.
3
Administration of queuine to mice relieves modified nucleoside queuosine deficiency in Ehrlich ascites tumor tRNA.给小鼠施用喹啉可缓解艾氏腹水瘤tRNA中修饰核苷queuosine的缺乏。
Biochem Biophys Res Commun. 1980 Sep 16;96(1):313-9. doi: 10.1016/0006-291x(80)91216-4.
4
Effect of diet on the queuosine family of tRNAs of germ-free mice.饮食对无菌小鼠tRNA中queuosine家族的影响。
J Biol Chem. 1980 Jul 25;255(14):6832-5.
5
Changes in rat liver transfer RNA following growth hormone administration and in regenerating liver.生长激素给药后及再生肝脏中大鼠肝脏转移核糖核酸的变化。
Biochim Biophys Acta. 1970 Sep 17;217(1):64-71. doi: 10.1016/0005-2787(70)90123-1.
6
Guanylation of transfer ribonucleic acid by a cell-free lysate of rabbit reticulocytes.兔网织红细胞无细胞裂解物对转运核糖核酸的鸟苷酸化作用。
J Biol Chem. 1973 Nov 25;248(22):7780-5.
7
Guanylation of transfer RNA by rabbit reticulocytes.兔网织红细胞对转运RNA的鸟苷酸化作用。
Biochim Biophys Acta. 1970 Jul 16;213(1):77-89. doi: 10.1016/0005-2787(70)90009-2.
8
The biosynthesis of folic acid. 8. Purification and properties of the enzyme that catalyzes the production of formate from carbon atom 8 of guanosine triphosphate.叶酸的生物合成。8. 催化从三磷酸鸟苷的第8位碳原子生成甲酸的酶的纯化及性质。
J Biol Chem. 1968 May 10;243(9):2349-58.
9
Activity of a transfer RNA modifying enzyme during the development of Drosophila and its relationship to the su(s) locus.果蝇发育过程中一种转运RNA修饰酶的活性及其与su(s)基因座的关系。
J Mol Biol. 1973 Mar 15;74(4):635-51. doi: 10.1016/0022-2836(73)90054-5.
10
Biosynthesis of the modified nucleoside Q in transfer RNA.转运核糖核酸中修饰核苷Q的生物合成
Nucleic Acids Res. 1976 Feb;3(2):393-8. doi: 10.1093/nar/3.2.393.

黑腹果蝇中喹啉的存在:游离库与tRNA中喹喔啉含量的相关性以及蝶啶代谢突变的影响。

Presence of queuine in Drosophila melanogaster: correlation of free pool with queuosine content of tRNA and effect of mutations in pteridine metabolism.

作者信息

Jacobson K B, Farkas W R, Katze J R

出版信息

Nucleic Acids Res. 1981 May 25;9(10):2351-66. doi: 10.1093/nar/9.10.2351.

DOI:10.1093/nar/9.10.2351
PMID:6789305
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC326850/
Abstract

Queuine, a modified form of 7-deazaguanine present in certain transfer RNAs, is shown to occur in Drosophila melanogaster adults in a free form and its concentration varies as a function of age, nutrition and genotype. In several, but not all mutant strains, the concentrations of queuine and the Q(+) (queuine-containing) form of tRNATyr are correlated. The bioassay employs L-M cells which respond to the presence of queuine by an increase in their Q(+)tRNAAsp that is accompanied by a decrease in the Q(-)tRNAAsp isoacceptors. The increase in Q(+)tRNATyr in Drosophila that occurs on a yeast diet is accompanied by an increase in queuine. Similarly the increase of Q(+)tRNAs with age also is accompanied by an increase in free queuine. In two mutants, brown and sepia, these correlations were either diminished or failed to occur. Indeed, the extract of both mutants inhibited the response of the L-M cells to authentic queuine. When the pteridines that occur at abnormally high levels in sepia were used at 1 x 10(-6)M, the inhibition of the L-M cell assay occurred in the order biopterin greater than pterin greater than sepiapterin. These pteridines were also inhibitory for the purified guanine:tRNA transglycosylase from rabbit but the relative effectiveness then was pterin greater than biopterin greater than sepiapterin. Pterin was competitive with guanine in the enzyme reaction with Ki = 0.9 x 10(-7)M. Also when an extract of sepia was chromatographed on Sephadex G-50, the pteridine-containing fractions only were inhibitory toward the L-M cell assay or the enzyme assay. These results indicate that free queuine occurs in Drosophila but also that certain pteridines may interfere with the incorporation of queuine into RNA.

摘要

喹啉是某些转运RNA中存在的7-脱氮鸟嘌呤的一种修饰形式,已证实在黑腹果蝇成虫中以游离形式存在,其浓度随年龄、营养和基因型而变化。在一些但并非所有突变株中,喹啉浓度与tRNATyr的Q(+)(含喹啉)形式相关。生物测定采用L-M细胞,喹啉的存在会使其Q(+)tRNAAsp增加,同时Q(-)tRNAAsp同工受体减少。果蝇在酵母饮食条件下Q(+)tRNATyr的增加伴随着喹啉的增加。同样,随着年龄增长Q(+)tRNAs的增加也伴随着游离喹啉的增加。在棕色和乌棕色这两个突变体中,这些相关性要么减弱,要么不存在。实际上,这两个突变体的提取物均抑制L-M细胞对纯喹啉的反应。当乌棕色中异常高水平存在的蝶啶以1×10(-6)M使用时,对L-M细胞测定的抑制作用顺序为:生物蝶呤>蝶呤>异蝶呤。这些蝶啶对兔纯化的鸟嘌呤:tRNA转糖基酶也有抑制作用,但相对效力顺序为:蝶呤>生物蝶呤>异蝶呤。在酶反应中,蝶呤与鸟嘌呤竞争,Ki = 0.9×10(-7)M。此外,当乌棕色的提取物在Sephadex G-50上进行色谱分析时,仅含蝶啶的级分对L-M细胞测定或酶测定有抑制作用。这些结果表明,游离喹啉存在于果蝇中,但某些蝶啶可能会干扰喹啉掺入RNA。