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免疫球蛋白信使核糖核酸的稳定性在B淋巴细胞分化过程中会发生变化。

Immunoglobulin mRNA stability varies during B lymphocyte differentiation.

作者信息

Jäck H M, Wabl M

机构信息

Laboratory of Radiobiology and Environmental Health, University of California, San Francisco 94143-0750.

出版信息

EMBO J. 1988 Apr;7(4):1041-6. doi: 10.1002/j.1460-2075.1988.tb02911.x.

Abstract

During differentiation of B lymphocytes, the change in the amount of immunoglobulin heavy chain produced is reflected by a change in the steady state level of heavy chain mRNA. At the pre-B cell stage, the earliest stage at which immunoglobulin chain is produced, and later at the small resting B cell stage, there is a low steady state level of heavy chain mRNA. After the small B cell has differentiated to become a plasma cell, the steady state level of heavy chain mRNA is much higher. We confirm that the transcription rate at the immunoglobulin mu heavy chain gene does not change during differentiation from the pre-B cell to the plasma cell stage. In contrast, we show here that differences in the stability of mu mRNA are sufficient to account for the differences in the steady state level at the various differentiation stages.

摘要

在B淋巴细胞分化过程中,重链mRNA稳态水平的变化反映了所产生的免疫球蛋白重链量的变化。在前B细胞阶段,即产生免疫球蛋白链的最早阶段,以及之后的小静止B细胞阶段,重链mRNA的稳态水平较低。小B细胞分化为浆细胞后,重链mRNA的稳态水平要高得多。我们证实,从pre-B细胞到浆细胞阶段的分化过程中,免疫球蛋白μ重链基因的转录速率没有变化。相比之下,我们在此表明,μ mRNA稳定性的差异足以解释不同分化阶段稳态水平的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b2b/454432/bbd5831138a1/emboj00141-0163-a.jpg

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