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维甲酸诱导F9细胞分化后,RBP-Jκ转录因子免疫染色缺失。

Loss of immunostaining of the RBP-J kappa transcription factor upon F9 cell differentiation induced by retinoic acid.

作者信息

Sakai T, Furukawa T, Iwanari H, Oka C, Nakano T, Kawaichi M, Honjo T

机构信息

Department of Medical Chemistry, Kyoto University Faculty of Medicine.

出版信息

J Biochem. 1995 Sep;118(3):621-8. doi: 10.1093/oxfordjournals.jbchem.a124955.

Abstract

RBP-Jkappa is a novel type of transcriptional regulatory protein that does not contain any known DNA-binding motif. We raised anti-RBP-Jkappa monoclonal antibodies (K0043 and T6709) to investigate the roles of RBP-Jkappa in cell differentiation. These antibodies stained nuclei of undifferentiated embryonic stem cells and F9 cells but not those of the other differentiated cell lines tested so far although the RBP-Jkappa protein is expressed at similar levels. Interestingly, differentiated F9 cells lost the immunostaining reaction with the anti-RBP-Jkappa monoclonal antibodies. Biochemical subcellular fractionation study showed that the majority of RBP-Jkappa was localized in nuclei of F9 cells and that there are at least two forms of the RBP-Jkapppa protein in the nuclei of undifferentiated F9 cells, a free form and a chromatin-bound form. Upon induction of F9 cell differentiation, free nuclear RBP-Jkappa disappeared concomitantly with the loss of immunostaining, suggesting that the anti-RBP-Jkapppa antibodies cannot recognize chromatin-bound RBP-Jkappa. Since there is no evidence to indicate covalent modification of RBP-Jkappa, we assume that chromatin-bound RBP-Jkappa interacts with a large number of proteins which block the exposure of RBP-Jkappa epitopes to the monoclonal antibodies.

摘要

RBP-Jκ是一种新型转录调节蛋白,不包含任何已知的DNA结合基序。我们制备了抗RBP-Jκ单克隆抗体(K0043和T6709),以研究RBP-Jκ在细胞分化中的作用。尽管RBP-Jκ蛋白以相似水平表达,但这些抗体对未分化的胚胎干细胞和F9细胞的细胞核进行了染色,而对目前测试的其他分化细胞系的细胞核未染色。有趣的是,分化的F9细胞失去了与抗RBP-Jκ单克隆抗体的免疫染色反应。生化亚细胞分级分离研究表明,大多数RBP-Jκ定位于F9细胞的细胞核中,并且在未分化的F9细胞核中至少有两种形式的RBP-Jκ蛋白,一种游离形式和一种与染色质结合的形式。在诱导F9细胞分化时,游离的核RBP-Jκ随着免疫染色的丧失而消失,这表明抗RBP-Jκ抗体不能识别与染色质结合的RBP-Jκ。由于没有证据表明RBP-Jκ发生了共价修饰,我们推测与染色质结合的RBP-Jκ与大量蛋白质相互作用,这些蛋白质阻碍了RBP-Jκ表位与单克隆抗体的接触。

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