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B细胞发育过程中控制膜结合型和分泌型免疫球蛋白产生的机制。

Mechanisms controlling production of membrane and secreted immunoglobulin during B cell development.

作者信息

Peterson Martha L

机构信息

Department of Microbiology, Immunology & Molecular Genetics, University of Kentucky College of Medicine, 800 Rose Street, Lexington, KY 40536, USA.

出版信息

Immunol Res. 2007;37(1):33-46. doi: 10.1007/BF02686094.

Abstract

The immunoglobulin gene which encodes both membrane-associated and secreted proteins through alternative RNA processing reactions has been a model system used for over 25 yr to better understand the regulatory mechanisms governing alternative RNA processing. This gene contains competing cleavage-polyadenylation and RNA splicing reactions and the relative use of the two pathways is differentially regulated between B cells and plasma cells. General cleavage-polyadenylation and RNA splicing reactions are both altered during B cell maturation to affect immunoglobulin expression. However, the specific factors involved in this regulation have yet to be identified clearly. As transcriptional regulators stimulate the developmental RNA processing switch, microarray analysis is a promising approach to identify candidate regulators of this complex RNA processing mechanism.

摘要

免疫球蛋白基因通过可变RNA加工反应编码膜相关蛋白和分泌蛋白,在过去25年多的时间里,它一直是一个模型系统,用于更好地理解调控可变RNA加工的机制。该基因包含相互竞争的切割-聚腺苷酸化和RNA剪接反应,并且这两条途径的相对使用在B细胞和浆细胞之间受到差异调节。在B细胞成熟过程中,一般的切割-聚腺苷酸化和RNA剪接反应都会发生改变,以影响免疫球蛋白的表达。然而,参与这种调节的具体因子尚未被明确鉴定。由于转录调节因子刺激发育性RNA加工转换,微阵列分析是鉴定这种复杂RNA加工机制候选调节因子的一种有前途的方法。

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