Marker assisted selection reveal SNP deletion mutation in gene associated with cytoplasmic male sterility in Solanum villosum

Abstract

Male sterility (MS) is powerful tool for improvement of various traits of economic importance. MS has not been characterized in Solanum villosum, and molecular mechanism underlying mutation change have not yet been studied. In this study, Sanger sequence platform was employed to amplify the MS genic region using mt ATPase marker. The molecular mechanism governing sterility was studied, and the results detected the amplification region at 1150bp. The sequence query was 97 % identical with atp subunit 6 gene loci. Significance mutation detected in this study was deletion GG (delGG) and deletion C (delC) occurring between 536bp and 542bp position in atp6 gene transcript. The mutation score was 16 for delGG and 17 for delC, with a 90 % mutation confidence interval. The study observed that SNP changes due to base deletions in the atp6 gene region were the main cause of male sterility in the studied mutants due to anticipated frameshifts of the open reading frame (ORF) of the mitochondrial atp6 gene, this is regarded as cytoplasmic male sterility type (CMS). Deformed and low pollen count was morphological changes confirmed this study that associated with sterility. Disruption of the ATP synthesis in mitochondria, limits the energy supply for pollen grain formation and anticipated pollen sterility however, mitochondria nuclear gene interaction governing the CMS should be further studied in case of S.villosum. These findings shed-light on molecular mechanism underlying the CMS and can be utilized as a molecular marker for agronomic traits improvement of S.villosum.