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鸡免疫球蛋白轻链通过点突变实现体细胞多样化。

Somatic diversification of chicken immunoglobulin light chains by point mutations.

作者信息

Parvari R, Ziv E, Lantner F, Heller D, Schechter I

机构信息

Department of Chemical Immunology, Weizmann Institute of Science, Rehovot, Israel.

出版信息

Proc Natl Acad Sci U S A. 1990 Apr;87(8):3072-6. doi: 10.1073/pnas.87.8.3072.

Abstract

The light-chain locus of chicken has 1 functional V lambda 1 gene, 1 J gene, and 25 pseudo-V lambda-genes (where V = variable and J = joining). A major problem is which somatic mechanisms expand this extremely limited germ-line information to generate many different antibodies. Weill's group [Reynaud, C. A., Anquez, V., Grimal, H. & Weill, J. C. (1987) Cell 48, 379-388] has shown that the pseudo-V lambda-genes diversify the rearranged V lambda 1 by gene conversion. Here we demonstrate that chicken light chains are further diversified by somatic point mutations and by V lambda 1-J flexible joining. Somatic point mutations were identified in the J and 3' noncoding DNA of rearranged light-chain genes of chicken. These regions were analyzed because point mutations in V lambda 1 are obscured by gene conversion; the J and 3' noncoding DNA are presented in one copy per haploid genome and are not subject to gene conversion. In rodents point mutations occur as frequently in the V-J coding regions as in the adjacent flanking DNA. Therefore, we conclude that somatic point mutations diversify the V lambda 1 of chicken. The frequency (0-1%) and distribution of the mutations (decreasing in number with increased distance from the V lambda 1 segment) in chicken were as observed in rodents. Sequence variability at the V lambda 1-J junctions could be attributed to imprecise joining of the V lambda 1 and J genes. The modification by gene conversion of rearranged V lambda 1 genes in the bursa was similar in chicken aged 3 months (9.5%) or 3 weeks (9.1%)--i.e., gene conversion that generates the preimmune repertoire in the bursa seems to level off around 3 weeks of age. This preimmune repertoire can be further diversified by somatic point mutations that presumably lead to the formation of antibodies with increased affinity. A segment with structural features of a matrix association region [(A + T)-rich and four topoisomerase II binding sites] was identified in the middle of the J-C lambda intron (where C = constant).

摘要

鸡的轻链基因座有1个功能性Vλ1基因、1个J基因和25个假Vλ基因(其中V代表可变区,J代表连接区)。一个主要问题是哪些体细胞机制能扩展这种极其有限的种系信息,以产生许多不同的抗体。威尔小组[雷诺,C.A.,安奎兹,V.,格里马尔,H.和威尔,J.C.(1987年)《细胞》48卷,379 - 388页]已表明,假Vλ基因通过基因转换使重排的Vλ1多样化。在此我们证明,鸡的轻链通过体细胞点突变和Vλ1 - J灵活连接进一步多样化。在鸡重排轻链基因的J区和3'非编码DNA中鉴定出体细胞点突变。对这些区域进行分析是因为Vλ1中的点突变会被基因转换掩盖;每个单倍体基因组中J区和3'非编码DNA只呈现一份,且不受基因转换影响。在啮齿动物中,V - J编码区的点突变频率与相邻侧翼DNA中的相同。因此,我们得出结论,体细胞点突变使鸡的Vλ1多样化。鸡中突变的频率(0 - 1%)和分布(数量随与Vλ1区段距离增加而减少)与在啮齿动物中观察到的情况相同。Vλ1 - J连接处的序列变异性可归因于Vλ1和J基因的不精确连接。在3个月龄(9.5%)或3周龄(9.1%)的鸡中,法氏囊中重排的Vλ1基因经基因转换的修饰相似——即,在法氏囊中产生免疫前库的基因转换似乎在3周龄左右趋于稳定。这种免疫前库可通过体细胞点突变进一步多样化,这些点突变大概会导致形成亲和力增加的抗体。在J - Cλ内含子(其中C代表恒定区)中间鉴定出一个具有基质附着区结构特征(富含A + T且有四个拓扑异构酶II结合位点)的区段。

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