Background: Glyoxalase pathway is a reactive carbonyl species (RCS) scavenging mechanism involved in the detoxification of methylglyoxal (MG), which is a reactive α-ketoaldehyde. In plants under abiotic stress, the cellular toxicity is reduced through glyoxalase pathway genes, i.e. Glyoxalase I (Gly I), Glyoxalase II (Gly II) and Glyoxalase III (Gly III). Salinity and water deficit stresses produce higher amounts of endogenous MG resulting in severe tissue damage. Thus, characterizing glyoxalase pathway genes that govern the MG metabolism should provide new insights on abiotic stress tolerance in Erianthus arundinaceus, a wild relative of sugarcane and commercial sugarcane hybrid (Co 86032).
Plant nuclear factor (NF-Y) is a transcriptional activating factor composed of three subfamilies: NF-YA, NF-YB, and NF-YC. These transcriptional factors are reported to function as activators, suppressors, and regulators under different developmental and stress conditions in plants. However, there is a lack of systematic research on the NF-Y gene subfamily in sugarcane. In this study, 51 NF-Y genes (ShNF-Y), composed of 9 NF-YA, 18 NF-YB, and 24 NF-YC genes, were identified in sugarcane (Saccharum spp.). Chromosomal distribution analysis of ShNF-Ys in a Saccharum hybrid located the NF-Y genes on all 10 chromosomes. Multiple sequence alignment (MSA) of ShNF-Y proteins revealed conservation of core functional domains. Sixteen orthologous gene pairs were identified between sugarcane and sorghum. Phylogenetic analysis of NF-Y subunits of sugarcane, sorghum, and Arabidopsis showed that ShNF-YA subunits were equidistant while ShNF-YB and ShNF-YC subunits clustered distinctly, forming closely related and divergent groups. Expression profiling under drought treatment showed that NF-Y gene members were involved in drought tolerance in a Saccharum hybrid and its drought-tolerant wild relative, Erianthus arundinaceus. ShNF-YA5 and ShNF-YB2 genes had significantly higher expression in the root and leaf tissues of both plant species. Similarly, ShNF-YC9 had elevated expression in the leaf and root of E. arundinaceus and in the leaf of a Saccharum hybrid. These results provide valuable genetic resources for further sugarcane crop improvement programs.
A total of sixteen accessions of Tripidium arundinaceum (Retz.) Welker, Voronts. & E.A. Kellogg (previously known as Erianthus arundinaceus (Retz.) Jeswiet) were evaluated for salinity tolerance at the bud germination stage by irrigating with 175 mM salinized Hoagland solution in perlite-sand hydroponics. Six accessions, IND99-907, IND01-1134, IND01-1136, IK76-48, and Bethuadahari, were germinated with healthy roots as compared to other accessions. These six accessions were further evaluated for morphological, physiological, and root anatomical parameters for different levels of salinity stress at the formative phase. Young leaf elongation was ceased after the fourth and twelfth day in Co 97010 and Co 86032, respectively, at 175 mM of salinity stress. The growth of young leaves in Co 97010 and Co 86032 was observed up to 25 mM of salinity stress only, whereas in T. arundinaceum accessions viz., IND99-907 and Bethuadahari, growth was recorded even at 175 mM. Lignification of cell walls, thickening of protoxylems, and vacuolization of cortex regions were observed in Co 97010, Co 86032, Bethuadahari, and IND01-1134 as compared to the normal anatomical structures in IND99-907. The accession IND99-907 recorded the lowest Na/K ratio, followed by IND99-1136 at 175 mM of salinity stress. The accession IND99-907 was identified as a salinity-tolerant genotype and suitable for utilization in the sugarcane crop improvement programmes.
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