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同基因抗独特型反应的分子基础。

Molecular basis of an isogeneic anti-idiotypic response.

作者信息

Sablitzky F, Rajewsky K

出版信息

EMBO J. 1984 Dec 1;3(12):3005-12. doi: 10.1002/j.1460-2075.1984.tb02247.x.

Abstract

The nucleotide sequences of the variable region genes expressed in the heavy and light chains of six isogeneic anti-idiotope antibodies recognizing idiotopes on two closely related antibodies with specificity for the hapten (4-hydroxy-3-nitrophenyl)acetyl (NP) were determined. In two independently derived anti-idiotope cell lines the same or strongly homologous V kappa, VH and D region genes had originally been rearranged. The two lines express long and partly homologous N sequences (presumed to be not of germ line origin) at the border of D, resulting in CDR3s of unusual length. An unusually long CDR3, partly encoded by N sequences, is also present in the heavy chain of a third anti-idiotope antibody. The VH regions of the three remaining anti-idiotope antibodies originate from a single VH gene which belongs to the same VH group as the VH genes expressed in the other anti-idiotopes. Two of these antibodies, expressing similar V, D and J elements, had been isolated from the same mouse and appear to have diverged from the same B cell precursor by at least two rounds of somatic mutation. Somatic point mutations have occurred in most, if not all anti-idiotope V region sequences. In two instances somatic mutations in J increase the structural homology between anti-idiotopes. The anti-idiotypic response in this system is thus genetically restricted and may depend upon the selection of non-germ line sequences, suggesting an explanation for the low frequency at which anti-idiotope antibodies are expressed in this system.

摘要

测定了六种同基因抗独特型抗体重链和轻链中表达的可变区基因的核苷酸序列,这些抗体识别两种对半抗原(4-羟基-3-硝基苯基)乙酰基(NP)具有特异性的密切相关抗体上的独特型。在两个独立衍生的抗独特型细胞系中,相同或高度同源的Vκ、VH和D区基因最初发生了重排。这两个细胞系在D区边界表达长的且部分同源的N序列(推测不是种系起源),导致CDR3长度异常。第三种抗独特型抗体的重链中也存在部分由N序列编码的异常长的CDR3。其余三种抗独特型抗体的VH区源自单个VH基因,该基因与其他抗独特型中表达的VH基因属于同一VH组。其中两种抗体表达相似的V、D和J元件,是从同一只小鼠中分离出来的,似乎通过至少两轮体细胞突变从同一个B细胞前体分化而来。大多数(如果不是全部)抗独特型V区序列中都发生了体细胞点突变。在两个实例中,J区的体细胞突变增加了抗独特型之间的结构同源性。因此,该系统中的抗独特型反应在遗传上受到限制,可能取决于非种系序列的选择,这为该系统中抗独特型抗体表达频率低提供了解释。

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Molecular basis of an isogeneic anti-idiotypic response.同基因抗独特型反应的分子基础。
EMBO J. 1984 Dec 1;3(12):3005-12. doi: 10.1002/j.1460-2075.1984.tb02247.x.

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