Molecular characterization and validation of sunflower (Helianthus annuus L.) hybrids through SSR markers

• Published in: PloS one Vol. 17; no. 5; p. e0267383
• Main Authors: Ahmed, Hafiz Ghulam Muhu-Din, Rizwan, Muhammad, Naeem, Muhammad, Khan, Muhammad Ahsan, Baloch, Faheem Shehzad, Sun, Sangmi, Chung, Gyuhwa
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 19.05.2022; Public Library of Science (PLoS)
• Subjects: Alleles; Amplification; Analysis; Bayesian analysis; Biology and Life Sciences; Carbon monoxide; Cluster analysis; Computer and Information Sciences; Corn; Deoxyribonucleic acid; DNA; Engineering and Technology; Females; Fertility; Genetic aspects; Genetic diversity; Genetic polymorphisms; Germplasm; Helianthus annuus; Hybrids; Identification; Males; Markers; Nucleotide sequence; Polymorphism; Purity; Research and Analysis Methods; Seeds; Sunflowers; Pakistan
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0267383

Genetic purity is a prerequisite for exploiting the potential of hybrids in cross-pollinated crops, such as sunflower. In this regard DNA-based study was conducted using 110 simple sequence repeat (SSR) markers to check the genetic purity of 23 parents and their 60 hybrids in sunflower. The polymorphism was shown in 92 markers with value 83.63%. The SSR markers ORS-453 and CO-306 showed the highest PIC values of 0.76 and 0.74, respectively. The primer ORS-453 amplified allele size of 310 base pairs (bp) for female parent L6 and 320 bp for L11, while for male parents, T1 and T2 had allele size 350 bp and 340 bp, respectively. The hybrids from these parents showed a similar size of alleles with parents, including hybrids L6×T1 (310 bp and 350 bp), L6×T2 (310 bp and 340 bp), and L11×T2 (320 bp and 340 bp). Similarly, the primer CO-306 amplified allele size 350 bp and 330 bp for female parents L6 and L11, respectively, while, allele size 300 bp and 310 bp for male parents T1 and T2, respectively. The hybrids' allele size was like the parents viz., L6×T1 (350 bp and 300 bp), L6×T2 (350 bp and 310 bp), and L11×T2 (330 bp and 310 bp). All 60 hybrids and their 23 parents were grouped into three main clusters (A, B and C) based upon DARWIN v.6.0 and STRUCTURE v.2.3 Bayesian analyses using genotypic data. Further, each main cluster was divided into two sub-divisions. Each sub-division showed the relatedness of parents and their hybrids, thus authenticating the genetic purity of hybrids. In conclusion, this study provides useful for accurate and effective identification of hybrids, which will help to improve seed genetic purity testing globally.