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PCF1和PCF2特异性结合水稻增殖细胞核抗原基因中的顺式元件。

PCF1 and PCF2 specifically bind to cis elements in the rice proliferating cell nuclear antigen gene.

作者信息

Kosugi S, Ohashi Y

机构信息

National Institute of Agrobiological Resources, Ibaraki, Japan.

出版信息

Plant Cell. 1997 Sep;9(9):1607-19. doi: 10.1105/tpc.9.9.1607.

Abstract

We have previously defined the promoter elements, sites IIa and IIb, in the rice proliferating cell nuclear antigen (PCNA) gene that are essential for meristematic tissue-specific expression. In this study, we isolated and characterized cDNAs encoding proteins that specifically bind to sites IIa and IIb. The two DNA binding proteins, designated PCF1 and PCF2, share > 70% homology in common conserved sequences at the N-terminal regions. The conserved regions are responsible for DNA binding and homodimer and heterodimer formation, and they contain a putative basic helix-loop-helix (bHLH) motif. The structure and DNA binding specificity of the bHLH motif are distinguishable from those of other known bHLH proteins that bind to the E-box. The motif is > 70% homologous to several expressed sequence tags from Arabidopsis and rice, suggesting that PCF1 and PCF2 are members of a novel family of proteins that are conserved in monocotyledons and dicotyledons. A supershift assay using an anti-PCF2 antibody showed the involvement of PCF2 in site IIa (site IIb) binding activities in rice nuclear extracts, particularly in meristematic tissues. PCF1 and PCF2 were also more likely to form heterodimers than homodimers. Our results suggest that PCF1 and PCF2 are involved in meristematic tissue-specific expression of the rice PCNA gene through binding to sites IIa and IIb and formation of homodimers or heterodimers.

摘要

我们之前已确定水稻增殖细胞核抗原(PCNA)基因中的启动子元件IIa和IIb位点,它们对于分生组织特异性表达至关重要。在本研究中,我们分离并鉴定了编码特异性结合IIa和IIb位点的蛋白质的cDNA。这两种DNA结合蛋白,命名为PCF1和PCF2,在N端区域的共同保守序列中具有超过70%的同源性。这些保守区域负责DNA结合以及同二聚体和异二聚体的形成,并且它们包含一个假定的碱性螺旋-环-螺旋(bHLH)基序。bHLH基序的结构和DNA结合特异性与其他已知的结合E-box的bHLH蛋白不同。该基序与来自拟南芥和水稻的几个表达序列标签具有超过70%的同源性,表明PCF1和PCF2是在单子叶植物和双子叶植物中保守的新型蛋白质家族的成员。使用抗PCF2抗体的超迁移分析表明PCF2参与水稻核提取物中IIa(IIb)位点的结合活性,特别是在分生组织中。PCF1和PCF2也比同二聚体更倾向于形成异二聚体。我们的结果表明,PCF1和PCF2通过结合IIa和IIb位点以及形成同二聚体或异二聚体参与水稻PCNA基因的分生组织特异性表达。

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