首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >R2R3-type MYB transcription factor, CmMYB1, is a central nitrogen assimilation regulator in Cyanidioschyzon merolae
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R2R3-type MYB transcription factor, CmMYB1, is a central nitrogen assimilation regulator in Cyanidioschyzon merolae

机译:R2R3型MYB转录因子CmMYB1是Cyanidioschyzon merolae中的中央氮同化调节剂

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摘要

Plant cells sense environmental nitrogen levels and alter their gene expression accordingly to survive; however, the underlying regulatory mechanisms still remains to be elucidated. Here, we identified and characterized a transcription factor that is responsible for expression of nitrogen assimilation genes in a unicellular red alga Cyanidioschyzon merolae. DNA microarray and Northern blot analyses revealed that transcript of the gene encoding CmMYB1, an R2R3-type MYB transcription factor, increased 1 h after nitrogen depletion. The CmMYBI protein started to accumulate after 2 h and reached a peak after 4 h after nitrogen depletion, correlating with the expression of key nitrogen assimilation genes, such as CmNRT, CmNAR, CmNIR, CmAMT. and CmGS. Although the transcripts of these nitrogen assimilation genes were detected in nitrate-grown cells, they disappeared upon the addition of preferred nitrogen source such as ammonium or glutamine, suggesting the presence of a nitrogen catabolite repression (NCR) mechanism. The nitrogen depletion-induced gene expression disappeared in a CmMYB1-null mutant, and the mutant showed decreased cell viability after exposure to the nitrogen-depleted conditions compared with the parental strain. Chromatin immunoprecipitation analysis demonstrated that CmMYBI specifically occupied these nitrogen-responsive promoter regions only under nitrogen-depleted conditions, and electrophoretic mobility shift assays using crude cell extract revealed specific binding of CmMYB1, or a complex containing CmMYB1, to these promoters. Thus, the presented results indicated that CmMYB1 is a central nitrogen regulator in C. merolae.
机译:植物细胞感知环境中的氮水平,并相应地改变其基因表达以存活。然而,潜在的监管机制仍有待阐明。在这里,我们确定并表征了一个转录因子,该转录因子负责单细胞红藻Cyanidioschyzon merolae中氮同化基因的表达。 DNA芯片和Northern印迹分析表明,氮耗竭后1小时,R2R3型MYB转录因子CmMYB1编码基因的转录本增加。氮耗竭后2 h,CmMYBI蛋白开始积累,并在4 h后达到峰值,这与关键的氮同化基因,如CmNRT,CmNAR,CmNIR,CmAMT的表达有关。和CmGS。尽管这些氮同化基因的转录本在硝酸盐生长的细胞中被检测到,但它们在添加优选的氮源(如铵或谷氨酰胺)后消失了,这表明存在氮分解代谢物阻遏(NCR)机制。氮耗竭诱导的基因表达在CmMYB1-null突变体中消失,并且与亲本菌株相比,该突变体在暴露于贫氮条件后显示出降低的细胞活力。染色质的免疫沉淀分析表明,CmMYBI仅在贫氮条件下专门占据了这些氮响应性启动子区域,使用粗细胞提取物的电泳迁移率变动分析表明,CmMYB1或含有CmMYB1的复合物与这些启动子具有特异性结合。因此,提出的结果表明CmMYB1是C. merolae中的中央氮调节剂。

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    Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan;

    Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan;

    Department of Life Science, College of Science, Rikkyo (St. Paul's) University, Nishi-ikebukuro, Toshima-ku, Tokyo 171-8501, Japan;

    Department of Life Science, College of Science, Rikkyo (St. Paul's) University, Nishi-ikebukuro, Toshima-ku, Tokyo 171-8501, Japan;

    Department of Life Science, College of Science, Rikkyo (St. Paul's) University, Nishi-ikebukuro, Toshima-ku, Tokyo 171-8501, Japan;

    Department of Life Science, College of Science, Rikkyo (St. Paul's) University, Nishi-ikebukuro, Toshima-ku, Tokyo 171-8501, Japan;

    Department of Life Science, College of Science, Rikkyo (St. Paul's) University, Nishi-ikebukuro, Toshima-ku, Tokyo 171-8501, Japan;

    Institute of Molecular and Cellular Biosciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-0032, Japan Graduate School of Horticulture, Chiba University, 648 Matsudo, Matsudo, Chiba 271-8510, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 入库时间 2022-08-18 00:42:03

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