首页> 外文期刊>The Plant Cell >Arabidopsis cuticular wax biosynthesis is negatively regulated by the DEWAX gene encoding an AP2/ERF-type transcription factor.
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Arabidopsis cuticular wax biosynthesis is negatively regulated by the DEWAX gene encoding an AP2/ERF-type transcription factor.

机译:拟南芥表皮蜡的生物合成受到编码AP2 / ERF型转录因子的DEWAX基因的负调控。

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摘要

The aerial parts of plants are protected from desiccation and other stress by surface cuticular waxes. The total cuticular wax loads and the expression of wax biosynthetic genes are significantly downregulated in Arabidopsis thaliana under dark conditions. We isolated Decrease Wax Biosynthesis (DEWAX), which encodes an AP2/ERF-type transcription factor that is preferentially expressed in the epidermis and induced by darkness. Disruption of DEWAX leads to an increase in total leaf and stem wax loads, and the excess wax phenotype of dewax was restored to wild type levels in complementation lines. Moreover, overexpression of DEWAX resulted in a reduction in total wax loads in leaves and stems compared with the wild type and altered the ultrastructure of cuticular layers. DEWAX negatively regulates the expression of alkane-forming enzyme, long-chain acyl-CoA synthetase, ATP citrate lyase A subunit, enoyl-CoA reductase, and fatty acyl-CoA reductase, and chromatin immunoprecipitation analysis suggested that DEWAX directly interacts with the promoters of wax biosynthesis genes. Cuticular wax biosynthesis is negatively regulated twice a day by the expression of DEWAX, throughout the night and at stomata closing. Significantly higher levels (10- to 100-fold) of DEWAX transcripts were found in leaves than in stems, suggesting that DEWAX-mediated transcriptional repression may be an additional mechanism contributing to the different total wax loads in leaves and stems.
机译:植物的地上部分受到表皮蜡的保护,免受干燥和其他压力。在黑暗条件下,拟南芥中的总表皮蜡负荷和蜡生物合成基因的表达显着下调。我们分离了减少蜡的生物合成(DEWAX),它编码优先在表皮中表达并由黑暗诱导的AP2 / ERF型转录因子。破坏DEWAX会导致总的叶子和茎蜡含量增加,并且多余的蜡表型在互补系中恢复到野生型水平。此外,与野生型相比,DEWAX的过表达导致叶和茎中总蜡负荷的减少,并改变了表皮层的超微结构。 DEWAX负调节链烷形成酶,长链酰基辅酶A合成酶,ATP柠檬酸裂合酶A亚基,烯酰基辅酶A还原酶和脂肪酰基辅酶A还原酶的表达,染色质免疫沉淀分析表明DEWAX直接与SNP的启动子相互作用蜡生物合成基因。整个晚上和气孔关闭时,DEWAX的表达每天两次对表皮蜡的生物合成产生负调控。叶片中发现的DEWAX转录水平显着高于茎中(10至100倍),这表明DEWAX介导的转录抑制可能是导致叶片和茎中总蜡含量不同的另一种机制。

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