Molesini Barbara, Mennella Giuseppe, Martini Flavio, Francese Gianluca, Pandolfini Tiziana
Department of Biotechnology, University of Verona, Strada Le Grazie 15, 37134 Verona, Italy.
Consiglio per la Ricerca e la Sperimentazione in Agricoltura, CRA-ORT Centro di Ricerca per l'Orticoltura, via Cavalleggeri 25, 84098 Pontecagnano-Faiano (Salerno), Italy.
Plant Cell Physiol. 2015 Jun;56(6):1084-96. doi: 10.1093/pcp/pcv030. Epub 2015 Feb 23.
In eukaryotic cells, the non-proteinogenic amino acid ornithine is the precursor of arginine and polyamines (PAs). The final step of ornithine biosynthesis occurs in plants via a cyclic pathway catalyzed by N(2)-acetylornithine:N-acetylglutamate acetyltransferase (NAOGAcT). An alternative route for ornithine formation, the linear pathway, has been reported for enteric bacteria and a few other organisms; the acetyl group of N(2)-acetylornithine is released as acetate by N(2)-acetylornithine deacetylase (NAOD). NAOD activity has never been demonstrated in plants, although many putative NAOD-like genes have been identified. In this investigation, we examined the effect of down-regulation of the putative Arabidopsis thaliana NAOD gene by using AtNAOD-silenced (sil#17) and T-DNA insertional mutant (atnaod) plants. The ornithine content was consistently reduced in sil#17 and atnaod plants compared with wild-type plants, suggesting that in addition to NAOGAcT action, AtNAOD contributes to the regulation of ornithine levels in plant cells. Ornithine depletion was associated with altered levels of putrescine and spermine. Reduced AtNAOD expression resulted in alterations at the reproductive level, causing early flowering and impaired fruit setting. In this regard, the highest level of AtNAOD expression was observed in unfertilized ovules. Our findings suggest that AtNAOD acts as a positive regulator of fruit setting and agree with those obtained in tomato auxin-synthesizing parthenocarpic plants, where induction of SlNAOD was associated with the onset of ovary growth. Thus, here we have uncovered the first hints of the functions of AtNAOD by connecting its role in flower and fruit development with the regulation of ornithine and PA levels.
在真核细胞中,非蛋白质ogenic氨基酸鸟氨酸是精氨酸和多胺(PAs)的前体。鸟氨酸生物合成的最后一步发生在植物中,通过由N(2)-乙酰鸟氨酸:N-乙酰谷氨酸乙酰转移酶(NAOGAcT)催化的循环途径。已经报道了一种鸟氨酸形成的替代途径,即线性途径,存在于肠道细菌和其他一些生物体中;N(2)-乙酰鸟氨酸的乙酰基由N(2)-乙酰鸟氨酸脱乙酰酶(NAOD)作为乙酸盐释放。尽管已经鉴定出许多推定的NAOD样基因,但NAOD活性从未在植物中得到证实。在本研究中,我们通过使用AtNAOD沉默(sil#17)和T-DNA插入突变体(atnaod)植物来研究推定的拟南芥NAOD基因下调的影响。与野生型植物相比,sil#17和atnaod植物中的鸟氨酸含量持续降低,这表明除了NAOGAcT的作用外,AtNAOD有助于调节植物细胞中鸟氨酸的水平。鸟氨酸的消耗与腐胺和精胺水平的改变有关。AtNAOD表达的降低导致生殖水平的改变,导致早花和坐果受损。在这方面,未受精胚珠中观察到AtNAOD表达的最高水平。我们的研究结果表明,AtNAOD作为坐果的正调节因子,这与在番茄生长素合成单性结实植物中获得的结果一致,在那里SlNAOD的诱导与子房生长的开始有关。因此,在这里我们通过将其在花和果实发育中的作用与鸟氨酸和PA水平的调节联系起来,首次揭示了AtNAOD的功能线索。