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Human fetal G gamma- and A gamma-globin genes: complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes.人类胎儿Gγ-和Aγ-珠蛋白基因:完整的核苷酸序列表明,这些重复基因之间可发生DNA交换。
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Multiple amino acid substitutions between murine gamma 2a heavy chain Fc regions of Ig1a and Ig1b allotypic forms.Ig1a和Ig1b同种异型形式的小鼠γ2a重链Fc区域之间存在多个氨基酸替换。
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Heavy chain variable region contribution to the NPb family of antibodies: somatic mutation evident in a gamma 2a variable region.重链可变区对NPb抗体家族的贡献:γ2a可变区中明显的体细胞突变。
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Structure of the constant and 3' untranslated regions of the murine Balb/c gamma 2a heavy chain messenger RNA.小鼠Balb/cγ2a重链信使核糖核酸的恒定区和3'非翻译区的结构
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小鼠IgG2aa和IgG2ab等位基因的核酸序列之间存在多种差异。

Multiple differences between the nucleic acid sequences of the IgG2aa and IgG2ab alleles of the mouse.

作者信息

Schreier P H, Bothwell A L, Mueller-Hill B, Baltimore D

出版信息

Proc Natl Acad Sci U S A. 1981 Jul;78(7):4495-9. doi: 10.1073/pnas.78.7.4495.

DOI:10.1073/pnas.78.7.4495
PMID:6170065
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC319818/
Abstract

To compare the structure of IgG2a alleles we have determined the complete DNA sequence of the constant region, coding sequence, and 3' untranslated region of a cDNA clone, pAB gamma 2a-1, which was derived from the C57BL/6 mouse strain (b allotype). This sequence was compared with the corresponding IgG2a DNA sequence of BALB/c origin (a allotype). The DNA sequences showed 10% differences, and the deduced protein sequences differed by about 15%. These differences were not evenly distributed: most differences were in the hinge region, the CH3 domain and the 3' untranslated region. It is evident that many alterations in the IgG2a alleles have occurred since the a and b haplotypes were separated--some of these changes were point mutations but some appear to have resulted from gene conversion of the IgG2ab allele by the IgG2bb allele.

摘要

为了比较IgG2a等位基因的结构,我们测定了一个cDNA克隆pABγ2a - 1恒定区、编码序列和3'非翻译区的完整DNA序列,该克隆源自C57BL/6小鼠品系(b同种异型)。将此序列与源自BALB/c(a同种异型)的相应IgG2a DNA序列进行比较。DNA序列显示出10%的差异,推导的蛋白质序列差异约为15%。这些差异分布不均:大多数差异存在于铰链区、CH3结构域和3'非翻译区。显然,自a和b单倍型分离以来,IgG2a等位基因发生了许多改变——其中一些变化是点突变,但有些似乎是由IgG2bb等位基因对IgG2ab等位基因的基因转换导致的。