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Brassica rapa NGATHA1 (BrNGA1) encodes a B3-type

机译:甘蓝型油菜NGATHA1(BrNGA1)编码为B3型

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Brassica rapa NGATHA1 (BrNGA1) encodes a B3-type transcription factor. By analyzing Arabidopsis overexpressors of BrNGA1 (BrNGA1ox), we have previously demonstrated that BrNGA1 may be involved in negative regulation of cell proliferation during lateral organ and root growth. In the present study, we have found that BrNGA1ox seedlings grown in the dark display de-etiolation phenotypes, such as short hypocotyls, open and elongated cotyledons, and developing true leaves. BrNGA1ox seedlings as well as adult plants and calli are also resistant specifically to exogenous cytokinins. These data raise the possibility that the de-etiolation phenotypes of BrNGA1ox seedlings may result from an alteration in cytokinin response. We set out to test whether the de-etiolation phenotype is due to cytokinin overproduction or constitutively activated cytokinin response. First, BrNGA1ox was crossed to the CKX2ox plant, an overexpression line of CYTOKIN OXIDASE 2, which is responsible for degradation of active cytokinins. We found, however, no difference in the de-etiolation and shoot growth phenotypes between BrNGA1ox and BrNGA1ox CKX2ox plants. Next, we measured the transcripts level of ARR5 and ARR7, frequently employed as molecular markers for cytokinin signaling and yet found no difference in their transcripts levels of the wild-type and BrNGA1ox seedlings and shoots. These data indicate that biological role of BrNGA1 involved in de-etiolation seems to be associated with neither cytokinin overproduction nor its altered signaling. Possible molecular mechanisms by which BrNGA1 may interfere with cytokinin responses and etiolation are discussed.
机译:甘蓝型油菜NGATHA1(BrNGA1)编码B3型转录因子。通过分析BrNGA1(BrNGA1ox)的拟南芥过表达,我们以前已经证明BrNGA1可能参与了侧器官和根生长过程中细胞增殖的负调控。在本研究中,我们发现在黑暗中生长的BrNGA1ox幼苗表现出去异位表型,例如短下胚轴,开放和延长的子叶,并发育出真叶。 BrNGA1ox幼苗以及成年植物和愈伤组织也对外源细胞分裂素具有特异性抗性。这些数据增加了BrNGA1ox幼苗的去异位表型可能是由于细胞分裂素反应改变的结果。我们着手测试去异位表型是由于细胞分裂素的过量生产还是组成性激活的细胞分裂素应答。首先,将BrNGA1ox与CKX2ox植物杂交,后者是CYTOKIN OXIDASE 2的过度表达株,负责活性细胞分裂素的降解。但是,我们发现,BrNGA1ox和BrNGA1ox CKX2ox植物之间的去开环和芽生长表型没有差异。接下来,我们测量了经常用作细胞分裂素信号转导分子标记的ARR5和ARR7的转录水平,但发现野生型和BrNGA1ox幼苗和新芽的转录水平没有差异。这些数据表明,BrNGA1参与去开环的生物学作用似乎与细胞分裂素的过量生产及其信号传导均无关。讨论了BrNGA1可能干扰细胞分裂素反应和黄化的可能分子机制。

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