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首页> 外文期刊>Transfusion: The Journal of the American Association of Blood Banks >The low-incidence MNS antigens M(v), s(D), and Mit arise from single amino acid substitutions on GPB.
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The low-incidence MNS antigens M(v), s(D), and Mit arise from single amino acid substitutions on GPB.

机译:低发病率MNS抗原M(v),s(D)和Mit来自GPB上的单个氨基酸取代。

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摘要

BACKGROUND: GPB carries 'N' at its N:-terminus and S and s, determined by a polymorphism at amino acid position 29 (Met29Thr). The low-incidence antigens M(v), s(D), and Mit are associated with weakened expression of S and/or s, and the purpose of this study was to define their molecular bases. METHODS: The GPB gene (GYPB) was sequenced after RT-PCR of RNA from four samples: two M(v)+, one s(D)+, and one Mit+. The point mutations observed were confirmed by sequencing of genomic DNA from these and other examples of s(D)+ and Mit+ samples. RESULTS: A point mutation of 65C>G observed in the M(v)+ samples predicted a change of Thr3Ser. A mutation of C>G at nucleotide 173 of the GYPB coding sequence, observed in two s(D)+ samples, predicted a change of Pro39Arg. Three Mit+ samples showed a nucleotide substitution of 161G>A, which predicted a change of Arg35His. Altered expression of S or s was confirmed by serologic tests. CONCLUSION: These results confirm that Arg35 is important for full expression of S. Pro39 and, surprisingly, Thr3 are also important for full expression of s. Furthermore, Thr3 must be essential for expression of 'N,' as M(v)+ RBCs lack 'N.'
机译:背景:GPB在其N:端和S和s带有“ N”,这是由第29位氨基酸(Met29Thr)的多态性决定的。低发病率抗原M(v),s(D)和Mit与S和/或s的表达减弱有关,本研究的目的是确定其分子碱基。方法:对来自四个样本的RNA进行RT-PCR后,对GPB基因(GYPB)进行了测序:两个M(v)+,一个s(D)+和一个Mit +。通过对来自s(D)+和Mit +样品的这些以及其他实例的基因组DNA进行测序,可以确认观察到的点突变。结果:在M(v)+样品中观察到65C> G的点突变可预测Thr3Ser的变化。在两个s(D)+样品中观察到的GYPB编码序列的核苷酸173处C> G突变预测Pro39Arg发生变化。三个Mit +样品显示161G> A的核苷酸取代,预测Arg35His的变化。通过血清学检查证实了S或s的表达改变。结论:这些结果证实Arg35对于S.Pro39的完整表达很重要,并且令人惊讶的是,Thr3对于s的完整表达也很重要。此外,Thr3对于表达“ N”必不可少,因为M(v)+ RBC缺少“ N”。

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