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运用血清学和Southern印迹分析对非人类灵长类动物及其他物种的人类Rh血型系统进行研究。

Investigation of the human Rh blood group system in nonhuman primates and other species with serologic and Southern blot analysis.

作者信息

Westhoff C M, Wylie D E

机构信息

School of Biological Sciences, University of Nebraska, Lincoln 68588.

出版信息

J Mol Evol. 1994 Jul;39(1):87-92. doi: 10.1007/BF00178253.

Abstract

To investigate the evolution of the Rh blood-group system in anthropoid apes, New and Old World monkeys, and nonprimate animals, serologic typing of erythrocytes from these species with antibodies specific for the human Rh blood-group antigens was performed. In addition, genomic DNA from these animals was analyzed on Southern blots with a human Rh-specific cDNA. Consistent with earlier reports, serologic results showed that gorilla and chimpanzee erythrocytes had epitopes recognized by human Rh D and c antisera, and gibbon erythrocytes were recognized by the c antisera. Surprisingly, some Old and New World monkeys also expressed a Rh c epitope on their erythrocytes. No erythrocytes from the nonprimate animals reacted specifically with any of the human Rh antisera. Southern blot analysis with a human Rh-specific cDNA probe detected Rh-related sequences in anthropoid apes, all New and Old World monkeys, and in most nonprimate animals tested. Although some Rh-related restriction fragments were conserved across species lines in primates, the Rh locus was more polymorphic in chimpanzees and gorillas than in humans. In addition, restriction fragments segregating with the presence of the D antigen in humans were present in the primate species that expressed the D antigen.

摘要

为了研究类人猿、新旧世界猴以及非灵长类动物中Rh血型系统的进化情况,我们使用针对人类Rh血型抗原的特异性抗体对这些物种的红细胞进行了血清学分型。此外,我们还使用人类Rh特异性cDNA对这些动物的基因组DNA进行了Southern印迹分析。与早期报告一致,血清学结果显示,大猩猩和黑猩猩的红细胞具有人类Rh D和c抗血清所识别的表位,长臂猿的红细胞被c抗血清所识别。令人惊讶的是,一些新旧世界猴的红细胞也表达了Rh c表位。非灵长类动物的红细胞均未与任何一种人类Rh抗血清发生特异性反应。使用人类Rh特异性cDNA探针进行的Southern印迹分析在类人猿、所有新旧世界猴以及大多数受试非灵长类动物中检测到了Rh相关序列。尽管在灵长类动物中,一些Rh相关的限制性片段在物种间是保守的,但Rh基因座在黑猩猩和大猩猩中比在人类中具有更高的多态性。此外,在表达D抗原的灵长类物种中存在与人类D抗原存在相关的限制性片段。

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