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在免疫球蛋白增强子或启动子存在的情况下被激活的基因受到一种T淋巴瘤细胞系的负调控。

Genes activated in the presence of an immunoglobulin enhancer or promoter are negatively regulated by a T-lymphoma cell line.

作者信息

Zaller D M, Yu H, Eckhardt L A

机构信息

Department of Biological Sciences, Columbia University, New York, New York 10027.

出版信息

Mol Cell Biol. 1988 May;8(5):1932-9. doi: 10.1128/mcb.8.5.1932-1939.1988.

Abstract

The tissue-specific expression of immunoglobulin genes can be partially explained by a requirement for activating factors found only in B lymphocytes and their derivatives. However, loss of immunoglobulin expression upon fusion of an immunoglobulin-producing myeloma cell with a T lymphoma cell (BW5147) or fibroblast (L cell) suggests that negatively acting factors also play a role in the tissue specificity of immunoglobulin genes. Expression of a cloned immunoglobulin heavy-chain gene introduced into myeloma cells was suppressed after fusion of the myeloma transformants with BW5147. The presence of either the immunoglobulin heavy-chain enhancer or promoter conferred suppression, under similar conditions, upon a heterologous gene that is normally expressed in both B and T lymphocytes. These immunoglobulin heavy-chain gene control regions, or gene modifications induced by them, are subject to negative control by T-lymphocyte-derived factors.

摘要

免疫球蛋白基因的组织特异性表达,部分原因可能是只有在B淋巴细胞及其衍生物中才存在激活因子。然而,产生免疫球蛋白的骨髓瘤细胞与T淋巴瘤细胞(BW5147)或成纤维细胞(L细胞)融合后免疫球蛋白表达丧失,这表明负性作用因子在免疫球蛋白基因的组织特异性中也发挥作用。将克隆的免疫球蛋白重链基因导入骨髓瘤细胞后,骨髓瘤转化体与BW5147融合后,该基因的表达受到抑制。在类似条件下,免疫球蛋白重链增强子或启动子的存在会使通常在B淋巴细胞和T淋巴细胞中均表达的异源基因受到抑制。这些免疫球蛋白重链基因控制区或由它们诱导的基因修饰,受到T淋巴细胞衍生因子的负调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/391f/363371/b81ef4bb185e/molcellb00065-0084-a.jpg

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