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前B细胞中的继发性基因组重排事件:LINE-1序列取代VHDJH以及定向类别转换。

Secondary genomic rearrangement events in pre-B cells: VHDJH replacement by a LINE-1 sequence and directed class switching.

作者信息

Yancopoulos G D, DePinho R A, Zimmerman K A, Lutzker S G, Rosenberg N, Alt F W

出版信息

EMBO J. 1986 Dec 1;5(12):3259-66. doi: 10.1002/j.1460-2075.1986.tb04637.x.

DOI:10.1002/j.1460-2075.1986.tb04637.x
PMID:3028778
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1167320/
Abstract

We describe rearrangement events which alter expression from a productive VHDJH rearrangement in an Abelson murine leukemia virus-transformed pre-B cell line. One such rearrangement results in replacement of the initially expressed variable region gene by a site-specific join between the open reading frame of a LINE-1 repetitive element and a remaining JH segment. We discuss this event in the context of the 'accessibility' model of recombinase control, and with respect to similar rearrangements involved in oncogene activation. In another subclone of the same pre-B cell line, altered heavy chain expression resulted from a mu to gamma 2b class switch recombination which occurred by a recombination-deletion mechanism but involved a complex inversion. We provide evidence that the germline gamma 2b region is specifically expressed in pre-B cell lines and early in normal development. We propose that the predisposition of pre-B cell lines to switch to gamma 2b production may reflect a normal physiological phenomenon in which the switch event is directed by an increased 'accessibility' of the germline gamma 2b locus to switch-recombination enzymatic machinery. Our findings support the hypothesis that the apparently distinct recombination systems involved in variable region gene assembly and heavy chain class switching are both directed by the accessibility of their substrate gene segments.

摘要

我们描述了在阿贝尔逊鼠白血病病毒转化的前B细胞系中改变有功能的VHDJH重排所产生的表达的重排事件。其中一种重排导致最初表达的可变区基因被LINE-1重复元件的开放阅读框与剩余的JH片段之间的位点特异性连接所取代。我们在重组酶控制的“可及性”模型背景下以及与癌基因激活中涉及的类似重排相关的方面讨论了这一事件。在同一前B细胞系的另一个亚克隆中,重链表达的改变是由μ到γ2b类转换重组导致的,该重组通过重组缺失机制发生,但涉及一个复杂的倒位。我们提供证据表明,种系γ2b区域在前B细胞系和正常发育早期特异性表达。我们提出,前B细胞系倾向于转换为γ2b产生可能反映了一种正常的生理现象,即转换事件由种系γ2b基因座对转换重组酶机制的“可及性”增加所引导。我们的发现支持这样一种假设,即参与可变区基因组装和重链类转换的明显不同的重组系统均由其底物基因片段的可及性所引导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ed/1167320/f51d3ef7b460/emboj00175-0194-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ed/1167320/2c9ad2a2c66a/emboj00175-0192-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ed/1167320/f51d3ef7b460/emboj00175-0194-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ed/1167320/2c9ad2a2c66a/emboj00175-0192-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ed/1167320/f51d3ef7b460/emboj00175-0194-a.jpg

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