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白种人群中D(C)(e)单倍型的分子背景。

Molecular background of D(C)(e) haplotypes within the white population.

作者信息

Noizat-Pirenne France, Le Pennec Pierre-Yves, Mouro Isabelle, Rouzaud Anne-Marie, Juszczak Geneviève, Roussel Michèle, Lauroua Pierre, Krause Claire, Rouger Philippe, Cartron Jean-Pierre, Ansart-Pirenne Hélène

机构信息

Blood Group National Reference Center, Paris, France.

出版信息

Transfusion. 2002 May;42(5):627-33. doi: 10.1046/j.1537-2995.2002.00097.x.

Abstract

BACKGROUND

D(C)(e) and D(C)e haplotypes may be encountered in the white population. Few data are available on the molecular backgrounds responsible for depressed expression of C and e.

STUDY DESIGN AND METHODS

Individuals of white origin carrying a D(C)(e) genotype resulting in depressed expression of C or both C and e were subdivided into two categories based on the RBC reactivity with the human sera Mol and Hor, which contain antibodies against low-frequency antigens of the Rh (RH) system and other non-Rh low-frequency antigens. Neither Hor+, Mol+ nor Hor+, Mol- RBCs expressed the V (RH10), VS (RH20), and/or Rh32 (RH32) low-frequency antigens. These results suggested that Hor+, Mol+ variants expressed Rh33 (RH33 or Har) and FPTT (RH50), whereas Hor+, Mol- variants might express an undefined low-frequency antigen. Further serologic and molecular analyses were performed.

RESULTS

Molecular analysis of Hor+, Mol+ variants revealed a hybrid gene structure RHCe-D(5)-Ce, in which exon 5 of RHCE (RHCe allele) was replaced by exon 5 of RHD (the so-called RHCeVA allele). The presence of exon 5RHD resulted in several amino acid alterations predicted in the external loop 4 of the CeVA polypeptide. Molecular analysis of Hor+, Mol- variants revealed the presence of a new RHCe allele characterized by a single point mutation C340T within exon 3 (the so-called RHCeMA allele), resulting in a R114W substitution predicted on the external loop 2 of the CeMA polypeptide. A serologic study showed a different pattern of reactivity with C and e MoAbs.

CONCLUSION

Two types of mutations resulted in amino acid substitutions predicted in external loops 4 and 2, respectively, which altered both the C and e reactivity, and indicated conformation changes or defective interaction between nonadjacent loops of the Ce polypeptide. Serologic analysis showed that together with Hor and Mol sera testing, the use of different C and e MoAbs could help to identify these variants within the white population.

摘要

背景

在白种人群中可能会遇到D(C)(e)和D(C)e单倍型。关于导致C和e表达降低的分子背景,可用数据很少。

研究设计与方法

携带D(C)(e)基因型导致C表达降低或C和e表达均降低的白种人个体,根据红细胞与人类血清Mol和Hor的反应性分为两类,这两种血清含有针对Rh(RH)系统低频抗原和其他非Rh低频抗原的抗体。Hor +、Mol +和Hor +、Mol -红细胞均不表达V(RH10)、VS(RH20)和/或Rh32(RH32)低频抗原。这些结果表明,Hor +、Mol +变体表达Rh33(RH33或Har)和FPTT(RH50),而Hor +、Mol -变体可能表达一种未明确的低频抗原。进行了进一步的血清学和分子分析。

结果

对Hor +、Mol +变体的分子分析揭示了一种杂合基因结构RHCe - D(5) - Ce,其中RHCE(RHCe等位基因)的外显子5被RHD的外显子5取代(所谓的RHCeVA等位基因)。外显子5RHD的存在导致CeVA多肽外环4中预测有几个氨基酸改变。对Hor +、Mol -变体的分子分析揭示了一种新的RHCe等位基因,其特征是外显子3内的单点突变C340T(所谓的RHCeMA等位基因),导致CeMA多肽外环2上预测有R114W取代。血清学研究显示与C和e单克隆抗体的反应模式不同。

结论

两种类型的突变分别导致外环4和外环2中预测的氨基酸取代,这改变了C和e的反应性,并表明Ce多肽非相邻环之间的构象变化或相互作用缺陷。血清学分析表明,与Hor和Mol血清检测一起,使用不同的C和e单克隆抗体有助于在白种人群中识别这些变体。

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