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果蝇中甘油-3-磷酸脱氢酶合成的发育调控

Developmental regulation of glycerol-3-phosphate dehydrogenase synthesis in Drosophila.

作者信息

Sullivan D T, Donovan F A, Skuse G

出版信息

Biochem Genet. 1983 Feb;21(1-2):49-62. doi: 10.1007/BF02395391.

DOI:10.1007/BF02395391
PMID:6404247
Abstract

Methods have been developed to measure the synthesis of glycerol-3-phosphate dehydrogenase (GPDH) during the development of Drosophila melanogaster. In emerged adult flies, GPDH is a principal component of protein synthesis, comprising between 1 and 2% of the protein synthetic effort. This high relative rate of protein synthesis continues throughout adult life during a period of stable enzyme concentration. Therefore, it is evident that GPDH undergoes continual turnover. Analysis of GPDH synthesis in the adult segments reveals that this enzyme is synthesized in head, thorax, and abdomen. In 5-day-old flies, the relative rates of GPDH synthesis in the thorax and abdomen are similar. However, the concentration of GPDH in the thorax greatly exceeds that found in the abdomen. Therefore, it appears that the turnover rate of GPDH in the abdomen must be greater than the turnover rate of GPDH in the GPDH-containing cells (flight muscle) of the thorax. GPDH represents between 0.5 and 0.9% of the protein synthetic effort of larvae. The principle GPDH-containing tissue of larvae is fat body. The turnover of GPDH in larvae is similar to that in adult abdomen. This may be related to the concurrent presence of GPDH isozyme-3 in both tissues. Our studies indicate that the cell type-specific control of GPDH occurs at several levels.

摘要

已开发出方法来测量黑腹果蝇发育过程中甘油-3-磷酸脱氢酶(GPDH)的合成。在羽化后的成年果蝇中,GPDH是蛋白质合成的主要成分,占蛋白质合成量的1%至2%。在酶浓度稳定的成年期,这种较高的蛋白质合成相对速率会持续存在。因此,很明显GPDH会持续更新。对成年果蝇各体段中GPDH合成的分析表明,这种酶在头部、胸部和腹部均有合成。在5日龄的果蝇中,胸部和腹部GPDH的合成相对速率相似。然而,胸部GPDH的浓度大大超过腹部。因此,似乎腹部GPDH的更新速率必定大于胸部含GPDH细胞(飞行肌)中GPDH的更新速率。GPDH占幼虫蛋白质合成量的0.5%至0.9%。幼虫含GPDH的主要组织是脂肪体。幼虫中GPDH的更新与成年腹部相似。这可能与两种组织中同时存在GPDH同工酶-3有关。我们的研究表明,GPDH的细胞类型特异性控制发生在多个水平。

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本文引用的文献

1
Genetics of Catalase in DROSOPHILA MELANOGASTER: Rates of Synthesis and Degradation of the Enzyme in Flies Aneuploid and Euploid for the Structural Gene.黑腹果蝇过氧化氢酶的遗传学:结构基因单体型和二倍体型果蝇中酶的合成和降解速率。
Genetics. 1979 Apr;91(4):723-42. doi: 10.1093/genetics/91.4.723.
2
Structural analysis of adult and larval isozymes of sn-glycerol-3-phosphate dehydrogenase of Drosophila melanogaster.黑腹果蝇sn-甘油-3-磷酸脱氢酶成虫和幼虫同工酶的结构分析。
J Biol Chem. 1982 Jan 25;257(2):979-83.
3
A method for determining the in vivo stability of Drosophila alcohol dehydrogenase (E.C.1.1.1.1.).
果蝇飞行肌肉功能需要糖酵解酶的共定位。
Mol Biol Cell. 1997 Sep;8(9):1665-75. doi: 10.1091/mbc.8.9.1665.
4
Molecular heterogeneity of naturally occurring sn-glycerol-3-phosphate dehydrogenase low-activity variants in Drosophila melanogaster.黑腹果蝇中天然存在的sn-甘油-3-磷酸脱氢酶低活性变体的分子异质性
Biochem Genet. 1994 Jun;32(5-6):161-79. doi: 10.1007/BF00554620.
5
Biochemical and molecular analysis of naturally occurring Adh variants in Drosophila melanogaster.黑腹果蝇中天然存在的乙醇脱氢酶变体的生化与分子分析
Proc Natl Acad Sci U S A. 1983 Aug;80(15):4798-802. doi: 10.1073/pnas.80.15.4798.
6
Developmentally regulated alternate modes of expression of the Gpdh locus of Drosophila.果蝇Gpdh基因座发育调控的交替表达模式
EMBO J. 1985 Sep;4(9):2275-80. doi: 10.1002/j.1460-2075.1985.tb03926.x.
7
Structural characterization of the alpha-glycerol-3-phosphate dehydrogenase-encoding gene of Drosophila melanogaster.黑腹果蝇3-磷酸甘油脱氢酶编码基因的结构特征
Proc Natl Acad Sci U S A. 1989 Jul;86(13):5020-4. doi: 10.1073/pnas.86.13.5020.
一种测定果蝇乙醇脱氢酶(E.C.1.1.1.1.)体内稳定性的方法。
Biochem Genet. 1981 Apr;19(3-4):411-9. doi: 10.1007/BF00504284.
4
Purification and structural analysis of the soluble sn-glycerol-3-phosphate dehydrogenase isozymes in Drosophila melanogaster.黑腹果蝇中可溶性甘油-3-磷酸脱氢酶同工酶的纯化与结构分析。
J Biol Chem. 1980 May 10;255(9):4073-80.
5
Regulation of amylase activity in Drosophila melanogaster: variation in the number of enzyme molecules produced by different amylase genotypes.黑腹果蝇中淀粉酶活性的调控:不同淀粉酶基因型产生的酶分子数量的变化。
Biochem Genet. 1981 Aug;19(7-8):783-96. doi: 10.1007/BF00484009.
6
Drosophila lactate dehydrogenase and alpha-glycerolphosphate dehydrogenase: distribution and change in activity during development.果蝇乳酸脱氢酶和α-甘油磷酸脱氢酶:发育过程中的分布及活性变化
J Insect Physiol. 1970 Jun;16(6):1179-92. doi: 10.1016/0022-1910(70)90208-8.
7
Cleavage of structural proteins during the assembly of the head of bacteriophage T4.在噬菌体T4头部组装过程中结构蛋白的切割
Nature. 1970 Aug 15;227(5259):680-5. doi: 10.1038/227680a0.
8
Quantitative measurement of ovalbumin messenger ribonucleic acid activity. Localization in polysomes, induction by estrogen, and effect of actinomycin D.卵清蛋白信使核糖核酸活性的定量测定。在多核糖体中的定位、雌激素诱导作用及放线菌素D的影响。
J Biol Chem. 1973 Mar 25;248(6):2031-9.
9
The -glycerophosphate in Drosophila melanogaster. II. Genetic aspects.果蝇中的甘油磷酸。II. 遗传学方面。
Genetics. 1972 May;71(1):127-38. doi: 10.1093/genetics/71.1.127.
10
Control of enzyme levels in animal tissues.动物组织中酶水平的调控
Annu Rev Biochem. 1970;39:929-76. doi: 10.1146/annurev.bi.39.070170.004433.