Laboratorio de Bioquímica Ecológica. Centro de Investigación y Estudios Avanzados del IPN. CP 36821 , Irapuato Guanajuato , México ; Grupo de Desarrollo Reproductivo y Apomixis. Departamento de Ingeniería Genética de Plantas y Laboratorio Nacional de Genómica para la Biodiversidad , Centro de Investigación y Estudios Avanzados, CP 36821, Irapuato Guanajuato , México.
Braz J Microbiol. 2012 Apr;43(2):716-38. doi: 10.1590/S1517-83822012000200037. Epub 2012 Jun 1.
To explore the molecular mechanisms that prevail during the establishment of the arbuscular mycorrhiza symbiosis involving the genus Glomus, we transcriptionally analysed spores of Glomus intraradices BE3 during early hyphal growth. Among 458 transcripts initially identified as being expressed at presymbiotic stages, 20% of sequences had homology to previously characterized eukaryotic genes, 30% were homologous to fungal coding sequences, and 9% showed homology to previously characterized bacterial genes. Among them, GintPbr1a encodes a homolog to Phenazine Biosynthesis Regulator (Pbr) of Burkholderia cenocepacia, an pleiotropic regulatory protein that activates phenazine production through transcriptional activation of the protein D isochorismatase biosynthetic enzyme phzD (Ramos et al., 2010). Whereas GintPbr1a is expressed during the presymbiotic phase, the G. intraradices BE3 homolog of phzD (BGintphzD) is transcriptionally active at the time of the establishment of the arbuscular mycorrhizal symbiosis. DNA from isolated bacterial cultures found in spores of G. intraradices BE3 confirmed that both BGintPbr1a and BGintphzD are present in the genome of its potential endosymbionts. Taken together, our results indicate that spores of G. intraradices BE3 express bacterial phenazine biosynthetic genes at the onset of the fungal-plant symbiotic interaction.
为了探索在丛枝菌根共生体形成过程中起主导作用的分子机制,我们对 Glomus intraradices BE3 孢子在早期菌丝生长阶段进行了转录分析。在最初鉴定为在共生前阶段表达的 458 个转录本中,20%的序列与先前鉴定的真核基因具有同源性,30%与真菌编码序列具有同源性,9%与先前鉴定的细菌基因具有同源性。其中,GintPbr1a 编码 Burkholderia cenocepacia 中 Phenazine Biosynthesis Regulator(Pbr)的同源物,Pbr 是一种多效调节蛋白,通过转录激活蛋白 D 异胡豆醇合成酶的生物合成酶 phzD 来激活吩嗪的产生(Ramos 等人,2010)。虽然 GintPbr1a 在共生前阶段表达,但在丛枝菌根共生体建立时,G. intraradices BE3 的 phzD 同源物(BGintphzD)转录活跃。从 G. intraradices BE3 孢子中分离出的细菌培养物的 DNA 证实,BGintPbr1a 和 BGintphzD 都存在于其潜在内共生体的基因组中。综上所述,我们的研究结果表明,G. intraradices BE3 孢子在真菌-植物共生相互作用开始时表达细菌吩嗪生物合成基因。