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The research was conducted at ICARDA, Rabat. Twenty-four accessions were obtained from LCRI for marker analysis. Wizard Genomic DNA Purification Kit was used for DNA extraction. DNA was extracted by CTAB method and quantified using 1.0 % (w/v) agarose gels. Total of 12 loci, 5 functional and 7 linked random DNA markers to the traits of interest were used. PowerMarker and DARwin software were used to calculate the No. of alleles and values of genetic diversity, PIC, genetic distance, and NJ dendrogram. The total No. of detected alleles was 39; and mean No. of alleles was 3.25. No. of alleles range from 1 (Dreb-B1) to 9 (Xgwm577). Genetic diversity index ranged from 0.0000 in Dreb-B1 to 0.8471 in Xgwm577. The PIC value was also varied from 0.0000 (Dreb-B1) to 0.8296 (Xgwm577). The frequency of biotic resistance linked random DNA marker allele at Xgwm144 and Xwmc44, associated with yellow and leaf rust gene was 25% each. Marker alleles Xgwm577 and Xgwm533 linked to Stb2 and Stb8 at 150 and 120bp have frequencies of 21 and 4%. The frequency of abiotic resistance showed 50% of accessions had 1R segment (1BL.1RS translocation) and 58% of accessions showed presence of 120bp allele of Xwmc89, associated with QTL for drought tolerant. Functional marker alleles of Dreb-B1 associated with drought tolerant genes showed alleles frequency in all accessions. Linked marker allele Xgwm111 linked to heat tolerant gene showed 17% allele frequency at 220bp. Rht1 and Rht2, the allele frequencies were 92 and 4%. 92% of the cultivars had photoperiod insensitive allele at Ppd-D1 locus. VrnA1a and VrnA1c primer pair amplified at 965, 876, and 484bp, allele frequency of 13 and 87%. Cluster analysis had grouped the accessions into 5 at a genetic distance level 0.15.
L-myo-inositol phosphate synthase (MIPS; EC 188.8.131.52) have been involved in abiotic stress tolerance and its disruption leads to spontaneous cell death and enhanced tolerance to pathogen. However, its molecular mechanism underlying role of MIPS in growth, immunity and abiotic stress tolerance remains unknown. To delve deeper into the conserved molecular mechanism of MIPS action during growth and stress condition, we characterized the overexpression transgenic of TaMIPS and mutant lines of AtMIPS1. Subsequent, transcriptome analysis revealed the activation of ET/JA dependent immune response in transgenic and SA defense response in mutant. Pull-down analysis revealed the interaction of TaMIPS2 with ethylene synthesis (ACO) and signaling protein (CTR1) component. Due to the established role of ethylene during the skotomorphogenesis, we investigated the effect of myo-inositol phosphate synthase role in ethylene response during hook formation. Our results thus suggest the requirement of MIPS for ethylene response and regulating the growth and immunity.