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日本人群和美国人群纤溶酶原表型频率分布的差异:纤溶酶原变体检测的新方法。

Differences of frequency distributions of plasminogen phenotypes between Japanese and American populations: new methods for the detection of plasminogen variants.

作者信息

Aoki N, Tateno K, Sakata Y

出版信息

Biochem Genet. 1984 Oct;22(9-10):871-81. doi: 10.1007/BF00499478.

DOI:10.1007/BF00499478
PMID:6517852
Abstract

Frequency distributions of various plasminogen phenotypes in Japanese and American white populations were studied using electrofocusing in polyacrylamide gels followed by zymography and immunofixation. Using a synthetic substrate, tosyl-lysine-alpha-naphthyl ester, for zymography allowed zymography and immunofixation to be performed sequentially on the same gel plate. By this method, a nonfunctional abnormal plasminogen variant, plasminogen Tochigi, was readily detected in both plasma and serum. The gene frequency of this abnormal variant in a Japanese population was 0.018, whereas the abnormal variant was not detected in an American white population, suggesting the very rare occurrence of this variant in whites. Two common alleles, A and B, clearly identified in neuraminidase-treated samples, were observed at gene frequencies of 0.98 and 0.003, respectively, in the Japanese. These values are significantly different from the reported values in whites of 0.69 for A and 0.3 for B.

摘要

采用聚丙烯酰胺凝胶等电聚焦,随后进行酶谱分析和免疫固定,研究了日本人群和美国白人群体中各种纤溶酶原表型的频率分布。使用合成底物甲苯磺酰赖氨酸-α-萘酯进行酶谱分析,可在同一凝胶板上依次进行酶谱分析和免疫固定。通过这种方法,在血浆和血清中均很容易检测到一种无功能的异常纤溶酶原变体——富木纤溶酶原。该异常变体在日本人群中的基因频率为0.018,而在美国白人群体中未检测到这种异常变体,这表明该变体在白人中非常罕见。在经神经氨酸酶处理的样本中清晰鉴定出的两个常见等位基因A和B,在日本人中的基因频率分别为0.98和0.003。这些值与报道的白人中A为0.69、B为0.3的值有显著差异。

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本文引用的文献

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Genetic polymorphism of human plasminogen.人纤溶酶原的基因多态性
Am J Hum Genet. 1980 Sep;32(5):681-9.
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Plasminogen (PLG) polymorphism in northern Japanese: confirmation of PLG*M6 allele.日本北部人群纤溶酶原(PLG)多态性:PLG*M6等位基因的确认
Z Rechtsmed. 1989;103(1):43-5. doi: 10.1007/BF01255845.
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Two types of abnormal genes for plasminogen in families with a predisposition for thrombosis.在有血栓形成倾向的家族中发现的两种纤溶酶原异常基因。
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Genetic polymorphism of human plasminogen in a Japanese population.日本人群中人纤溶酶原的基因多态性。
Hum Hered. 1982;32(4):296-7. doi: 10.1159/000153311.
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Genetic polymorphism of human plasminogen in the Japanese population: new plasminogen variants and relationship between plasminogen phenotypes and their biological activities.日本人群中人类纤溶酶原的基因多态性:新型纤溶酶原变体以及纤溶酶原表型与其生物学活性之间的关系。
Hum Genet. 1982;60(1):57-9. doi: 10.1007/BF00281264.
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Genetic polymorphism of plasminogen: a new basic variant (PLG B) and population study in Japanese.纤溶酶原的基因多态性:一种新的基本变异型(PLG B)及日本人的群体研究
Vox Sang. 1981;40(6):422-5. doi: 10.1111/j.1423-0410.1981.tb00731.x.
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Molecular abnormality of plasminogen.纤溶酶原的分子异常
J Biol Chem. 1980 Jun 10;255(11):5442-7.
8
Plasminogen Tochigi: inactive plasmin resulting from replacement of alanine-600 by threonine in the active site.纤溶酶原栃木:活性位点上丙氨酸600被苏氨酸取代后产生的无活性纤溶酶。
Proc Natl Acad Sci U S A. 1982 Oct;79(20):6132-6. doi: 10.1073/pnas.79.20.6132.
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Abnormal plasminogen. A hereditary molecular abnormality found in a patient with recurrent thrombosis.异常纤溶酶原。在一名复发性血栓形成患者中发现的一种遗传性分子异常。
J Clin Invest. 1978 May;61(5):1186-95. doi: 10.1172/JCI109034.
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Genetic polymorphism of human plasminogen.人纤溶酶原的基因多态性
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