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利用核糖核酸和脱氧寡聚物引物,通过三磷酸腺苷由玉米多聚核苷酸外切转移酶合成聚腺苷酸。

Utilization of ribonucleic acid and deoxyoligomer primers for polyadenylic acid synthesis by adenosine triphosphate: polynucleotidylexotransferase from maize.

作者信息

Mans R J, Huff N J

出版信息

J Biol Chem. 1975 May 25;250(10):3672-8.

PMID:1168636
Abstract

The ATP:polynucleotidylexotransferase isolated and purified from maize seedlings catalyzes the synthesis of polyadenylic acid by the sequential addition of 80 to 200 AMP moieties from ATP to the 3'-hydroxyl terminus of either ribo- or deoxyoligomers. Copurification of the RNA and DNA-primed activities, identical metal cofactor and reaction requirements for either primer and identical heat inactivation curves with either primer strongly suggest that both primers are utilized by the same enzyme.

摘要

从玉米幼苗中分离纯化得到的ATP:多核苷酸外切转移酶,通过将ATP中的80至200个AMP基团依次添加到核糖或脱氧寡聚物的3'-羟基末端,催化聚腺苷酸的合成。RNA和DNA引发活性的共纯化、相同的金属辅因子以及对两种引物相同的反应要求,以及两种引物相同的热失活曲线,都强烈表明两种引物被同一种酶所利用。

相似文献

1
Utilization of ribonucleic acid and deoxyoligomer primers for polyadenylic acid synthesis by adenosine triphosphate: polynucleotidylexotransferase from maize.利用核糖核酸和脱氧寡聚物引物,通过三磷酸腺苷由玉米多聚核苷酸外切转移酶合成聚腺苷酸。
J Biol Chem. 1975 May 25;250(10):3672-8.
2
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Biochim Biophys Acta. 1970 Sep 17;217(1):72-82.
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Transfer RNA-primed oligoadenylate synthesis in maize seedlings. II. Primer, substrate and metal specificities and size of product.玉米幼苗中转移RNA引发的寡腺苷酸合成。II. 引物、底物、金属特异性及产物大小。
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引用本文的文献

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A rapid technique for the estimation of polynucleotide adenylyltransferase and ribonucleic Acid polymerase in plant tissues.一种快速估算植物组织中多核苷酸腺苷酸转移酶和核糖核酸聚合酶的技术。
Plant Physiol. 1975 Dec;56(6):821-5. doi: 10.1104/pp.56.6.821.
2
Molecular cloning and characterization of potato spindle tuber viroid cDNA sequences.马铃薯纺锤块茎类病毒 cDNA 序列的分子克隆与特性分析。
Proc Natl Acad Sci U S A. 1980 Sep;77(9):5302-6. doi: 10.1073/pnas.77.9.5302.
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Plant Mol Biol. 1996 Oct;32(1-2):43-61. doi: 10.1007/BF00039376.
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Organization of human histone genes.人类组蛋白基因的组织
Proc Natl Acad Sci U S A. 1982 Mar;79(6):1795-9. doi: 10.1073/pnas.79.6.1795.
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Purification of cDNA complementary to sea urchin histone mRNA.与海胆组蛋白mRNA互补的cDNA的纯化。
Nucleic Acids Res. 1977 Sep;4(9):3187-98. doi: 10.1093/nar/4.9.3187.
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Reassessment of histone gene expression during cell cycle in human cells by using homologous H4 histone cDNA.利用同源H4组蛋白cDNA对人类细胞周期中组蛋白基因表达进行重新评估。
Proc Natl Acad Sci U S A. 1979 Oct;76(10):4995-9. doi: 10.1073/pnas.76.10.4995.
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Proc Natl Acad Sci U S A. 1977 Jan;74(1):173-7. doi: 10.1073/pnas.74.1.173.
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