Tsukagoshi Hironaka, Saijo Takanori, Shibata Daisuke, Morikami Atsushi, Nakamura Kenzo
Laboratory of Biochemistry, Graduate School of Bioagricultural Science, Nagoya University, Chikusa, Nagoya 464-8601, Japan.
Plant Physiol. 2005 Jun;138(2):675-85. doi: 10.1104/pp.104.057752. Epub 2005 May 13.
A recessive mutation hsi2 of Arabidopsis (Arabidopsis thaliana) expressing luciferase (LUC) under control of a short promoter derived from a sweet potato (Ipomoea batatas) sporamin gene (Spo(min)LUC) caused enhanced LUC expression under both low- and high-sugar conditions, which was not due to increased level of abscisic acid. The hsi2 mutant contained a nonsense mutation in a gene encoding a protein with B3 DNA-binding domain. HSI2 and two other Arabidopsis proteins appear to constitute a novel subfamily of B3 domain proteins distinct from ABI3, FUS3, and LEC2, which are transcription activators involved in seed development. The C-terminal part of HSI2 subfamily proteins contained a sequence similar to the ERF-associated amphiphilic repression (EAR) motif. Deletion of the C-terminal portion of HSI2 lost in the hsi2 mutant caused reduced nuclear targeting of HSI2. Null allele of HSI2 showed even higher Spo(min)LUC expression than the hsi2 mutant, whereas overexpression of HSI2 reduced the LUC expression. Transient coexpression of 35SHSI2 with Spo(min)LUC in protoplasts repressed the expression of LUC activity, and deletion or mutation of the EAR motif significantly reduced the repression activity of HSI2. These results indicate that HSI2 and related proteins are B3 domain-EAR motif active transcription repressors.
拟南芥(Arabidopsis thaliana)的一个隐性突变体hsi2,其在源自甘薯(Ipomoea batatas)sporamin基因(Spo(min)LUC)的短启动子控制下表达荧光素酶(LUC),在低糖和高糖条件下均导致LUC表达增强,这并非由于脱落酸水平升高所致。hsi2突变体在一个编码具有B3 DNA结合结构域蛋白的基因中存在无义突变。HSI2和另外两种拟南芥蛋白似乎构成了一个与ABI3、FUS3和LEC2不同的B3结构域蛋白新亚家族,ABI3、FUS3和LEC2是参与种子发育的转录激活因子。HSI2亚家族蛋白的C末端部分包含一个与ERF相关两亲性抑制(EAR)基序相似的序列。hsi2突变体中缺失HSI2的C末端部分导致HSI2的核定位减少。HSI2的无效等位基因显示出比hsi2突变体更高的Spo(min)LUC表达,而HSI2的过表达则降低了LUC表达。在原生质体中35SHSI2与Spo(min)LUC瞬时共表达抑制了LUC活性的表达,EAR基序的缺失或突变显著降低了HSI2的抑制活性。这些结果表明,HSI2及相关蛋白是B3结构域-EAR基序活性转录抑制因子。