WsMAGO2 a duplicated protein in Withania through interactions with MPF2-like proteins affects male fertility by producing fewer flowers and aborted non-viable pollens/seeds regulated by anther-specific GAATTTGTGA motif. The MAGO NASHIs are highly conserved genes that encode proteins known to be involved in RNA physiology and many other developmental processes including germ cell differentiation in animals. However, their structural and functional implications in plants as fertility function proteins remained fragmented. MAGO (shorter name of MAGO NASHI) proteins form heterodimers with MPF2-like MADS-box proteins which are recruited in calyx identity and male fertility in Solanaceous plants. Four MAGO genes namely WsMAGO1 and WsMAGO2 and TaMAGO1 and TaMAGO2 were isolated from Withania somnifera and Tubocapsicum anomalum, respectively. These genes have duplicated probably due to whole genome duplication event. Dysfunction of WsMAGO2 through double-stranded RNAi in Withania revealed suppression of RNA transcripts, non-viable pollens, fewer flowers and aborted non-viable seeds in the developing berry suggesting a role of this protein in many traits particularly male fertility. WsMAGO2 flaunted stronger yeast 2-hybrid interactions with MPF2-like proteins WSA206, WSB206 and TAB201 than other MAGO counterparts. The native transcripts of WsMAGO2 culminated in stamens and seed-bearing berries though other MAGO orthologs also exhibited expression albeit at lower level. Coding sequences of the two orthologs are highly conserved, but they differ substantially in their upstream promoter regions. Remarkably, WsMAGO2 promoter is enriched with many anther-specific cis-motifs common in fertility function genes promoters. Among them, disruption of GAATTTGTGA abolished YFP/GUS gene expression in anthers alluding towards its involvement in regulating expression of MAGO in anther. Our findings support a possible recruitment of WsMAGO2 in fertility trait in Withania. These genes have practical application in hybrid production through cytoplasmic male sterility maintenance for enhancement in crops yield.
Background: Rice is the staple food for more than half of the world's population. Rice cultivation needs expansion to meet the increasing food demands across the globe. Genetic diversity is desired for crop breeding because it serves as the backbone for improving cultivars. The process of domestication and modern plant breeding technologies applied to rice has contributed to the erosion of genetic diversity. Current breeding programs have extensively shaped the genetic diversity of elite rice cultivars to no small extent. Results: We explored the genetic diversity of traditional landraces and improved cultivars by inspecting the whole genome SNP markers of 20 rice accessions. We found a higher number of genetic variations (76.70%) and observed heterozygosity (0.024) in landraces than improved cultivars. The principal component analysis also revealed the higher genetic diversity among the landraces. While population structure based on the phylogenetic tree suggested the population's structure according to rice subspecies. The genetic diversity parameter, FST, was applied to estimate the genetic differentiation of rice, which revealed week genetic differentiation (0.121) and nucleotide diversity (0.314) in modern rice cultivars. Genome-wide genetic differentiation (FST) analysis identified the two domesticated genes: Kala4 (pericarp color) and Ghd7 (heading date), and eight improvement genes: Sd1, Ghd8, GW2, NRT1.1b, GW6a, and Hd3a, that coincide with the candidate selective sweeps. Inbreeding depression (0.68617) among the modern cultivars suggests no genetic gain in future breeding efforts and compels exotic material utilization in the breeding programs. Conclusion: These findings demonstrate that modern cultivars have a narrow genetic base compared to landraces. Therefore, exploring the genome of landraces at a large scale to identify the genes responsible for stability and adaptation to abiotic stresses can help design varieties that can survive vulnerable climates.
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