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位于小鼠免疫球蛋白λ基因座3'端的增强子序列可使转基因小鼠B细胞中的免疫球蛋白λ基因实现高水平表达。

Enhancer sequences located 3' of the mouse immunoglobulin lambda locus specify high-level expression of an immunoglobulin lambda gene in B cells of transgenic mice.

作者信息

Eccles S, Sarner N, Vidal M, Cox A, Grosveld F

机构信息

MRC Collaborative Centre, London, UK.

出版信息

New Biol. 1990 Sep;2(9):801-11.

PMID:2126202
Abstract

In contrast to the mouse immunoglobulin heavy chain and kappa light chain genes, very little is known about the regulation of expression of the immunoglobulin lambda light chain locus. To identify elements responsible for lambda gene regulation we mapped DNaseI hypersensitive sites associated with a functionally rearranged lambda 1 gene in nuclei from the myeloma cell line J558L. Tissue-specific hypersensitive sites were identified 2.3 to 2.5 kb upstream of the CAP site of both the lambda 1 gene and the unrearranged variable (V) lambda 2 gene segments. DNA sequences flanking the lambda 1 gene were isolated and tested for their influence on expression of the lambda 1 gene after transfection into myeloma cells and after injection into fertilized mouse eggs. Two enhancer elements were identified downstream of the lambda 1 gene. A proximal element (located 4 to 10 kb 3' of the gene) enhanced expression of a lambda 1 gene in stable myeloma cell transfectants but had no effect on the expression of a heterologous reporter gene in transient assays. A second, distal element, located approximately 30 kb 3' of the gene, enhanced heterologous expression in J558L cells expressing a lambda gene but not in a non-lambda myeloma cell line (SP2/0-Ag14). Co-injection of cosmids containing the lambda 1 gene and both the proximal and distal downstream elements into fertilized mouse eggs resulted in high-level expression of the lambda 1 transgene in B cells of transgenic mice. The identification of these lambda regulatory elements, in addition to contributing to an understanding of lambda gene regulation per se, will facilitate the study of the regulation of differential expression of kappa and lambda light chain genes in the immune system.

摘要

与小鼠免疫球蛋白重链和κ轻链基因不同,人们对免疫球蛋白λ轻链基因座表达调控的了解甚少。为了鉴定负责λ基因调控的元件,我们绘制了与骨髓瘤细胞系J558L细胞核中功能重排的λ1基因相关的DNaseI超敏位点。在λ1基因和未重排的可变(V)λ2基因片段的CAP位点上游2.3至2.5 kb处鉴定到组织特异性超敏位点。分离了λ1基因侧翼的DNA序列,并在转染到骨髓瘤细胞中以及注射到受精小鼠卵中后,测试它们对λ1基因表达的影响。在λ1基因下游鉴定到两个增强子元件。一个近端元件(位于基因3'端4至10 kb处)增强了稳定的骨髓瘤细胞转染子中λ1基因的表达,但在瞬时分析中对异源报告基因的表达没有影响。第二个远端元件位于基因3'端约30 kb处,在表达λ基因的J558L细胞中增强异源表达,但在非λ骨髓瘤细胞系(SP2/0-Ag14)中则不然。将含有λ1基因以及近端和远端下游元件的黏粒共注射到受精小鼠卵中,导致转基因小鼠B细胞中λ1转基因的高水平表达。这些λ调控元件的鉴定,除了有助于本身对λ基因调控的理解外,还将促进对免疫系统中κ和λ轻链基因差异表达调控的研究。

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