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O6-甲基鸟嘌呤受体蛋白在不同类别的脊椎动物和无脊椎动物组织中的存在情况。

Presence of O6-methylguanine acceptor protein in the tissues of different classes of vertebrates and invertebrates.

作者信息

Woodhead A D, Grist E, Carlson C, White T E, Waldstein E, Cao E H

出版信息

Comp Biochem Physiol B. 1986;85(1):125-30. doi: 10.1016/0305-0491(86)90232-4.

Abstract

We have measured the ability of extracts of tissues from several species of mammals, birds, reptiles, amphibia and fish to demethylate adducts of O6-methylguanine in exogenous DNA by transfer of the methyl group to an acceptor protein. Our study also encompassed tissues from a smaller number of invertebrates, from arthropods, molluscs and annelids. The vertebrate tissues used were liver, brain, spleen and kidney. In the case of the invertebrates we sampled liver, neural tissue, gonads, digestive tract and hepatopancreas. There was no consistent change in the amount of acceptor activity per unit of protein or DNA going from cold-blooded to warm-blooded vertebrates. Liver invariably had the highest amount; this finding was not unexpected since metabolic processes in the liver are high, and good cellular protective mechanism important. Inter-class comparisons within the vertebrates are highly speculative, and hindered by the fact that there is little information on carcinogenesis in animals other than rodents and humans. O6-methylguanine acceptor activity was found in all the invertebrate tissues tested. The amounts were variable, 0.003-0.0051 fmol/micrograms cellular DNA, but the values fell within the range of those found in the tissues of vertebrates.

摘要

我们已测定了几种哺乳动物、鸟类、爬行动物、两栖动物和鱼类的组织提取物通过将甲基转移至一种受体蛋白来使外源DNA中O6-甲基鸟嘌呤加合物去甲基化的能力。我们的研究还涵盖了数量较少的无脊椎动物的组织,这些无脊椎动物来自节肢动物、软体动物和环节动物。所使用的脊椎动物组织为肝脏、大脑、脾脏和肾脏。对于无脊椎动物,我们采集了肝脏、神经组织、性腺、消化道和肝胰腺的样本。从冷血脊椎动物到温血脊椎动物,每单位蛋白质或DNA的受体活性量没有一致的变化。肝脏的受体活性量始终最高;这一发现并不意外,因为肝脏中的代谢过程活跃,且良好的细胞保护机制很重要。脊椎动物类群之间的比较极具推测性,并且由于除啮齿动物和人类之外的动物的致癌作用信息很少而受到阻碍。在所测试的所有无脊椎动物组织中均发现了O6-甲基鸟嘌呤受体活性。其含量各不相同,为0.003 - 0.0051 fmol/微克细胞DNA,但这些值落在脊椎动物组织中所发现的值的范围内。

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