Pearce Stephen, Tabbita Facundo, Cantu Dario, Buffalo Vince, Avni Raz, Vazquez-Gross Hans, Zhao Rongrong, Conley Christopher J, Distelfeld Assaf, Dubcovksy Jorge
BMC Plant Biol. 2014 Dec 19;14:368. doi: 10.1186/s12870-014-0368-2.
During wheat senescence, leaf components are degraded in a coordinated manner, releasing amino acids and micronutrients which are subsequently transported to the developing grain. We have previously shown that the simultaneous downregulation of Grain Protein Content (GPC) transcription factors, GPC1 and GPC2, greatly delays senescence and disrupts nutrient remobilization, and therefore provide a valuable entry point to identify genes involved in micronutrient transport to the wheat grain.
We generated loss-of-function mutations for GPC1 and GPC2 in tetraploid wheat and showed in field trials that gpc1 mutants exhibit significant delays in senescence and reductions in grain Zn and Fe content, but that mutations in GPC2 had no significant effect on these traits. An RNA-seq study of these mutants at different time points showed a larger proportion of senescence-regulated genes among the GPC1 (64%) than among the GPC2 (37%) regulated genes. Combined, the two GPC genes regulate a subset (21.2%) of the senescence-regulated genes, 76.1% of which are upregulated at 12 days after anthesis, before the appearance of any visible signs of senescence. Taken together, these results demonstrate that GPC1 is a key regulator of nutrient remobilization which acts predominantly during the early stages of senescence. Genes upregulated at this stage include transporters from the ZIP and YSL gene families, which facilitate Zn and Fe export from the cytoplasm to the phloem, and genes involved in the biosynthesis of chelators that facilitate the phloem-based transport of these nutrients to the grains.
This study provides an overview of the transport mechanisms activated in the wheat flag leaf during monocarpic senescence. It also identifies promising targets to improve nutrient remobilization to the wheat grain, which can help mitigate Zn and Fe deficiencies that afflict many regions of the developing world.
在小麦衰老过程中,叶片成分以协调的方式降解,释放出氨基酸和微量营养素,随后这些物质被转运到发育中的籽粒中。我们之前已经表明,同时下调籽粒蛋白质含量(GPC)转录因子GPC1和GPC2会极大地延迟衰老并破坏养分再转运,因此为鉴定参与向小麦籽粒转运微量营养素的基因提供了一个有价值的切入点。
我们在四倍体小麦中产生了GPC1和GPC2的功能缺失突变,并在田间试验中表明,gpc1突变体的衰老显著延迟,籽粒锌和铁含量降低,但GPC2突变对这些性状没有显著影响。对这些突变体在不同时间点进行的RNA测序研究表明,GPC1调控的基因中衰老调控基因的比例(64%)高于GPC2调控的基因(37%)。综合来看,这两个GPC基因调控了衰老调控基因的一个子集(21.2%),其中76.1%在开花后12天上调,此时尚未出现任何明显的衰老迹象。综上所述,这些结果表明GPC1是养分再转运的关键调节因子,主要在衰老早期发挥作用。在这个阶段上调的基因包括来自ZIP和YSL基因家族的转运蛋白,它们促进锌和铁从细胞质输出到韧皮部,以及参与螯合剂生物合成的基因,这些螯合剂有助于将这些养分通过韧皮部转运到籽粒中。
本研究概述了单花衰老过程中小麦旗叶中激活的转运机制。它还确定了改善向小麦籽粒养分再转运的有前景的靶点,这有助于缓解困扰发展中世界许多地区的锌和铁缺乏问题。