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小鼠6号染色体上免疫球蛋白可变κ链基因的组织

The organization of immunoglobulin variable kappa chain genes on mouse chromosome 6.

作者信息

D'Hoostelaere L A, Gibson D M

出版信息

Immunogenetics. 1986;23(4):260-5. doi: 10.1007/BF00373021.

DOI:10.1007/BF00373021
PMID:3084380
Abstract

One mouse with a known recombination (NAK) at the Igk locus on chromosome 6 and two new recombinants [B6.PL (75NS) and B6.PL (85NS)] were examined using a series of probes, each of which is specific for a set of immunoglobulin (Ig) Vk genes. Under high stringency conditions, each probe detects from 1 to 19 Bam HI restriction endonuclease fragments (REFs) in genomic DNA by Southern transfer hybridization techniques. Analysis of the REF patterns indicate that the NAK recombination event occurred within the variable region of Igk. The REF patterns of the two B6.PL congenic mice provided two additional recombination events which could be examined. Although some of the REFs had shared mobility among the parental strains, at least 1 and up to 13 polymorphic REFs were present for a given probe among the NZB and AKR parental strains. The results from the NAK mouse indicate that at least some members of Vk4, Vk8, Vk10, and Vk21 were on one side of the recombination event linked to the Lyt-2 alpha and Igk-Ef1 alpha alleles of AKR, while the Vk9, Vk11, and Vk24 REF patterns came from the NZB parental strain linked to the Igk-Ef2 beta (Vk1) allele. The two B6.PL congenics produced a refined map on the Lyt-2, Lyt-3 side of the Vk region. The B6.PL (85NS) mice retained the Vk21 REF pattern of the Lyt-2 alpha, Lyt-3 alpha donor strain PL/J, while displaying the C57BL/6 REF pattern for the other Vk gene groups tested. The B6.PL (75NS) mice retained the REF patterns of PL/J for Vk21 and Ef-1, indicating a third recombination. This indicates the Vk gene order is (Lyt-2; Vk21); Ef-1; (Vk4; Vk8; Vk10); and (Vk9; Vk11; Vk24; Ef-2).

摘要

对一只在6号染色体上的Igk基因座具有已知重组(NAK)的小鼠以及两个新的重组体[B6.PL(75NS)和B6.PL(85NS)]使用一系列探针进行了检测,每个探针都对一组免疫球蛋白(Ig)Vk基因具有特异性。在高严格条件下,通过Southern转移杂交技术,每个探针在基因组DNA中检测到1至19个Bam HI限制性内切酶片段(REFs)。对REF模式的分析表明,NAK重组事件发生在Igk的可变区内。两只B6.PL同源小鼠的REF模式提供了另外两个可检测的重组事件。尽管一些REFs在亲本菌株之间具有共同的迁移率,但在NZB和AKR亲本菌株中,对于给定的探针,至少存在1个且最多有13个多态性REFs。来自NAK小鼠的结果表明,Vk4、Vk8、Vk10和Vk21的至少一些成员位于与AKR的Lyt-2α和Igk-Ef1α等位基因连锁的重组事件的一侧,而Vk9、Vk11和Vk24的REF模式来自与Igk-Ef2β(Vk1)等位基因连锁的NZB亲本菌株。这两只B6.PL同源小鼠在Vk区域的Lyt-2、Lyt-3一侧产生了一个精细的图谱。B6.PL(85NS)小鼠保留了Lyt-2α、Lyt-3α供体菌株PL/J的Vk21 REF模式,同时对于所测试的其他Vk基因组显示出C57BL/6的REF模式。B6.PL(75NS)小鼠保留了PL/J对于Vk21和Ef-1的REF模式,表明发生了第三次重组。这表明Vk基因顺序为(Lyt-2;Vk21);Ef-1;(Vk4;Vk8;Vk10);以及(Vk9;Vk11;Vk24;Ef-2)。

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引用本文的文献

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2
The organization of the mouse Igh-V locus. Dispersion, interspersion, and the evolution of VH gene family clusters.小鼠Igh-V基因座的组织。VH基因家族簇的分散、散布及进化。
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本文引用的文献

1
Classification of mouse VK groups based on the partial amino acid sequence to the first invariant tryptophan: impact of 14 new sequences from IgG myeloma proteins.基于至首个不变色氨酸的部分氨基酸序列对小鼠VK基因群的分类:来自IgG骨髓瘤蛋白的14条新序列的影响
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Mapping of the Ly-4 (L3T4) T-cell differentiation antigen on mouse chromosome 6 by the use of RFLPs in an interspecific cross.利用种间杂交中的限制性片段长度多态性(RFLP)将小鼠Ly-4(L3T4)T细胞分化抗原定位到6号染色体上。
Immunogenetics. 1988;27(5):396-8. doi: 10.1007/BF00395138.
7
A mouse homeo box gene, Hox-1.5, and the morphological locus, Hd, map to within 1 cM on chromosome 6.一个小鼠同源异型盒基因Hox-1.5和形态学位点Hd,定位于6号染色体上1厘摩(cM)范围内。
Genetics. 1987 Aug;116(4):607-12. doi: 10.1093/genetics/116.4.607.
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Mapping of Igk-V genes using backcrossed laboratory and wild mice.利用回交的实验室小鼠和野生小鼠对Igk-V基因进行定位。
Immunogenetics. 1988;28(4):233-9. doi: 10.1007/BF00345499.
9
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Immunogenetics. 1989;29(2):65-74. doi: 10.1007/BF00395853.
10
The mouse immunoglobulin kappa light-chain genes are located in early- and late-replicating regions of chromosome 6.小鼠免疫球蛋白κ轻链基因位于6号染色体的早期和晚期复制区域。
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免疫球蛋白轻链可变区基因的体细胞突变
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Proc Natl Acad Sci U S A. 1980 Oct;77(10):6022-6. doi: 10.1073/pnas.77.10.6022.
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Immunogenetics. 1984;20(5):493-501. doi: 10.1007/BF00364352.
7
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Nature. 1983;306(5938):77-9. doi: 10.1038/306077a0.
10
Recombination between kappa chain genetic markers and the Lyt-3 locus.κ链遗传标记与Lyt-3基因座之间的重组。
Immunogenetics. 1983;18(2):111-6. doi: 10.1007/BF00368538.