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佛波酯诱导人白血病细胞分化过程中发育调控的NFI基因家族的表达改变。

Altered expression of the developmentally regulated NFI gene family during phorbol ester-induced differentiation of human leukemic cells.

作者信息

Kulkarni S, Gronostajski R M

机构信息

Department of Cancer Biology, Cleveland Clinic Foundation, Ohio 44195, USA.

出版信息

Cell Growth Differ. 1996 Apr;7(4):501-10.

PMID:9052991
Abstract

The nuclear factor I (NFI) family of transcription/replication proteins is required for the cell type-specific expression of a number of cellular and viral genes. There are four evolutionarily conserved NFI genes (NFI-A, -B, -C and -X) that encode DNA-binding proteins of similar or identical DNA-binding specificity. To address the role of this family of highly conserved transcription/replication proteins in cell differentiation and development, we have assessed the expression of NFI proteins (by DNA binding) and mRNAs of each of the four NFI genes during the in vitro differentiation of several human leukemic cell lines. These cell lines differ in their pattern of differentiation upon exposure to the phorbol ester 12-0-tetradecanoylphorbol-13-acetate (TPA). In K562 and OCI/AML-3 cells, the levels of the four NFI mRNAs and the mobility of NFI-DNA complexes present in nuclear extracts changed during treatment with TPA. The TPA-induced change in mobility of NFI-DNA complexes in OCI/AML-3 cells was blocked by an inhibitor of protein synthesis, cycloheximide. These changes in NFI protein and mRNA expression appear to be cell type-or lineage-specific since no changes were seen during the TPA-induced differentiation of HL-60 or U937 cells. These studies indicate that although their DNA-binding specificities are similar, the proteins encoded by the four NFI genes may differ in their biological functions and play distinct roles in hematopoietic development.

摘要

转录/复制蛋白的核因子I(NFI)家族是许多细胞和病毒基因细胞类型特异性表达所必需的。有四个进化上保守的NFI基因(NFI-A、-B、-C和-X),它们编码具有相似或相同DNA结合特异性的DNA结合蛋白。为了研究这个高度保守的转录/复制蛋白家族在细胞分化和发育中的作用,我们评估了几种人类白血病细胞系体外分化过程中NFI蛋白(通过DNA结合)和四个NFI基因各自的mRNA的表达。这些细胞系在暴露于佛波酯12-0-十四烷酰佛波醇-13-乙酸酯(TPA)后,其分化模式有所不同。在K562和OCI/AML-3细胞中,用TPA处理期间,四个NFI mRNA的水平以及核提取物中存在的NFI-DNA复合物的迁移率发生了变化。OCI/AML-3细胞中TPA诱导的NFI-DNA复合物迁移率变化被蛋白质合成抑制剂环己酰亚胺阻断。NFI蛋白和mRNA表达的这些变化似乎是细胞类型或谱系特异性的,因为在TPA诱导的HL-60或U937细胞分化过程中未观察到变化。这些研究表明,尽管四个NFI基因编码的蛋白具有相似的DNA结合特异性,但它们在生物学功能上可能存在差异,并且在造血发育中发挥不同的作用。

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