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低丰度人类血浆蛋白的遗传学研究。V. 血浆中表达的第二个类粘蛋白结构基因座(ORM2)的证据。

Genetic studies of low-abundance human plasma proteins. V. Evidence for a second orosomucoid structural locus (ORM2) expressed in plasma.

作者信息

Escallon M H, Ferrell R E, Kamboh M I

出版信息

Am J Hum Genet. 1987 Sep;41(3):418-27.

Abstract

Orosomucoid (ORM) or alpha-1-acid glycoprotein is an acute-phase protein of human plasma whose function is suggested to be the competitive inhibition of cellular recognition by infective agents. Genetically determined variation in ORM has been reported, with two major alleles segregating in all populations studied to date. Isoelectric focusing-immunoblotting studies of ORM revealed the presence of isoprotein species that did not segregate with the predominant alleles at the ORM locus and suggested the expression of a second structural gene locus for orosomucoid (ORM2). Genetically independent variation consistent with expression of the ORM2 locus was observed in plasma samples from American blacks but was not observed in U.S. whites or sampled populations of North- and South-American Indians, Eskimos, Aleuts, or New Guinea Highlanders. The population allele frequencies for this locus were .958, .025, .006, and .011 for alleles ORM1, ORM22, ORM23, and ORM24, respectively. Family studies confirm the autosomal codominant inheritance of the observed phenotypes.

摘要

血清类黏蛋白(ORM)或α-1-酸性糖蛋白是人类血浆中的一种急性期蛋白,其功能被认为是竞争性抑制感染因子的细胞识别。已有报道称ORM存在基因决定的变异,在迄今为止研究的所有群体中,有两个主要等位基因在分离。对ORM的等电聚焦免疫印迹研究显示,存在一些同型蛋白,它们在ORM位点上并不与主要等位基因一起分离,这表明存在血清类黏蛋白的第二个结构基因位点(ORM2)。在美国黑人的血浆样本中观察到了与ORM2位点表达一致的基因独立变异,但在美国白人或北美和南美印第安人、爱斯基摩人、阿留申人或新几内亚高地人的抽样群体中未观察到。该位点的群体等位基因频率分别为:等位基因ORM1为0.958、ORM22为0.025、ORM23为0.006、ORM24为0.011。家系研究证实了所观察到的表型的常染色体共显性遗传。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb3c/1684184/1b0dd35ba039/ajhg00132-0095-a.jpg

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