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首页> 外文期刊>Plant Molecular Biology >Abundance of mRNAs encoding HMG1/HMG2 class high-mobility-group DNA-binding proteins are differentially regulated in cotyledons of Pharbitis nil
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Abundance of mRNAs encoding HMG1/HMG2 class high-mobility-group DNA-binding proteins are differentially regulated in cotyledons of Pharbitis nil

机译:编码HMG1 / HMG2类高迁移率组DNA结合蛋白的mRNA的丰度在无性子炎的子叶中有不同的调控。

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The abundance of an mRNA encoding an HMG1/2 protein from Pharbitis nil (HMG1) has been previously shown to be regulated by light and an endogenous rhythm in cotyledons. A second Pharbitis nil HMG cDNA (HMG2) was characterized. The sequence of HMG2 was 82% and 86% identical to HMG1 at the nucleotide and amino acid levels, respectively. As with HMG1, HMG2 mRNA was detected in all vegetative tissues and was most abundant in roots. However, unlike HMG1, HMG2 mRNA abundance did not increase upon transfer of cotyledons to darkness and did not exhibit regulation by an endogenous circadian rhythm when maintained in continuous darkness over a 68 h period. Similarly, while the abundance of HMG1 mRNA during a dark period that induced photoperiodically controlled flowering was markedly affected by brief light exposure (night break), this treatment had no effect on HMG2 mRNA abundance. Collectively, these data are consistent with a role of HMG1 in contributing to the circadian-regulated and/or dark-regulatedgene expression with constitutive expression of HMG2 playing a housekeeping role in the general regulation of gene expression in Pharbitis nil cotyledons. Nucleotide sequence data have been submitted to the EMBL/GenBank/DDBJ databases under the accessionnumber U39747.
机译:先前已显示,编码无鞭毛杆菌(HMG1)的HMG1 / 2蛋白的mRNA的丰度受子叶中光和内源性节奏的调节。鉴定了第二个无咽炎HMG cDNA(HMG2)。 HMG2的序列在核苷酸和氨基酸水平上分别与HMG1相同,分别为82%和86%。与HMG1一样,在所有营养组织中均检测到HMG2 mRNA,并且在根中含量最高。但是,与HMG1不同,当子叶转移到黑暗中时,HMG2 mRNA的丰度不会增加,并且在连续黑暗中维持68小时后,其内源性昼夜节律也不会表现出调控作用。类似地,虽然短暂的光照(夜间休息)显着影响了在黑暗时期诱导光周期控制开花的HMG1 mRNA的丰度,但这种处理对HMG2 mRNA的丰度没有影响。总的来说,这些数据与HMG1在昼夜调节的和/或黑暗调节的基因表达中的作用相一致,而HMG2的组成型表达在无子夜蛾子叶的基因表达的一般调节中起管家作用。核苷酸序列数据已以登录号U39747提交至EMBL / GenBank / DDBJ数据库。

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