Aleksza Dávid, Horváth Gábor V, Sándor Györgyi, Szabados László
Institute of Plant Biology, Biological Research Centre, 6726-Szeged, Hungary.
Institute of Plant Biology, Biological Research Centre, 6726-Szeged, Hungary
Plant Physiol. 2017 Sep;175(1):555-567. doi: 10.1104/pp.17.00791. Epub 2017 Aug 1.
Pro accumulation in plants is a well-documented physiological response to osmotic stress caused by drought or salinity. In Arabidopsis (), the stress and ABA-induced Δ1-PYRROLINE-5-CARBOXYLATE SYNTHETASE1 () gene was previously shown to control Pro biosynthesis in such adverse conditions. To identify regulatory factors that control the transcription of , Y1H screens were performed with a genomic fragment of , containing 1.2-kB promoter and 0.8-kb transcribed regions. The myeloblastosis (MYB)-type transcription factors PHOSPHATE STARVATION RESPONSE1 (PHR1) and PHR1-LIKE1 (PHL1) were identified to bind to regulatory sequences in the first intron, which carries a conserved PHR1-binding site (P1BS) motif. Binding of PHR1 and PHL1 factors to P1BS was confirmed by Y1H, electrophoretic mobility assay and chromatin immunoprecipitation. Phosphate starvation led to gradual increase in Pro content in wild-type Arabidopsis plants as well as transcriptional activation of and PRO DEHYDROGENASE2 genes. Induction of transcription and Pro accumulation during phosphate deficiency was considerably reduced by and mutations and was impaired in the ABA-deficient and ABA-insensitive mutants. Growth and viability of double mutant was significantly reduced in phosphate-depleted medium, while growth was only marginally affected in the mutants, suggesting that ABA is implicated in growth retardation in such nutritional stress. Our results reveal a previously unknown link between Pro metabolism and phosphate nutrition and show that Pro biosynthesis is target of cross talk between ABA signaling and regulation of phosphate homeostasis through PHR1- and PHL1-mediated transcriptional activation of the gene.
脯氨酸在植物中的积累是对干旱或盐度引起的渗透胁迫的一种有充分记录的生理反应。在拟南芥中,应激和脱落酸诱导的Δ1-吡咯啉-5-羧酸合成酶1(P5CS1)基因先前已被证明在这种不利条件下控制脯氨酸的生物合成。为了鉴定控制P5CS1转录的调控因子,利用包含1.2-kB启动子和0.8-kB转录区域的P5CS1基因组片段进行了酵母单杂交(Y1H)筛选。发现成髓细胞白血病(MYB)型转录因子磷饥饿反应1(PHR1)和类PHR1(PHL1)与第一个内含子中的P5CS1调控序列结合,该内含子带有一个保守的PHR1结合位点(P1BS)基序。通过Y1H、电泳迁移率分析和染色质免疫沉淀证实了PHR1和PHL1因子与P1BS的结合。磷饥饿导致野生型拟南芥植株中脯氨酸含量逐渐增加,以及P5CS1和脯氨酸脱氢酶2基因的转录激活。在磷缺乏期间,P5CS1转录和脯氨酸积累的诱导在phr1和phl1突变体中显著降低,并且在脱落酸缺陷型aba2和脱落酸不敏感型abi1突变体中受到损害。phr1phl1双突变体在缺磷培养基中的生长和活力显著降低,而在phr1或phl1突变体中生长仅受到轻微影响,这表明脱落酸与这种营养胁迫下的生长迟缓有关。我们的结果揭示了脯氨酸代谢与磷营养之间以前未知的联系,并表明脯氨酸生物合成是脱落酸信号传导与通过PHR1和PHL1介导的P5CS1基因转录激活来调节磷稳态之间相互作用的靶点。