Autor: |
Saxena RK; International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Hyderabad, India. r.saxena@cgiar.org., Patel K; International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Hyderabad, India., Sameer Kumar CV; International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Hyderabad, India., Tyagi K; Krishidhan Seeds Pvt. Ltd., Hyderabad, India., Saxena KB; International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Hyderabad, India., Varshney RK; International Crops Research Institute for the Semi-Arid Tropics (ICRISAT), Hyderabad, India. r.k.varshney@cgiar.org.; School of Plant Biology and Institute of Agriculture, The University of Western Australia, Crawley, WA, Australia. r.k.varshney@cgiar.org. |
Abstrakt: |
Key Message: We report molecular mapping and inheritance of restoration of fertility (Rf) in A4 hybrid system in pigeonpea. We have also developed PCR-based markers amenable to low-cost genotyping to identify fertility restorer lines. Commercial hybrids in pigeonpea are based on A4 cytoplasmic male sterility (CMS) system, and their fertility restoration is one of the key prerequisites for breeding. In this context, an effort has been made to understand the genetics and identify quantitative trait loci (QTL) associated with restoration of fertility (Rf). One F 2 population was developed by crossing CMS line (ICPA 2039) with fertility restorer line (ICPL 87119). Genetic analysis has shown involvement of two dominant genes in regulation of restoration of fertility. In parallel, the genotyping-by-sequencing (GBS) approach has generated ~ 33 Gb data on the F 2 population. GBS data have provided 2457 single nucleotide polymorphism (SNPs) segregating across the mapping population. Based on these genotyping data, a genetic map has been developed with 306 SNPs covering a total length 981.9 cM. Further QTL analysis has provided the region flanked by S8_7664779 and S8_6474381 on CcLG08 harboured major QTL explained up to 28.5% phenotypic variation. Subsequently, sequence information within the major QTLs was compared between the maintainer and the restorer lines. From this sequence information, we have developed two PCR-based markers for identification of restorer lines from non-restorer lines and validated them on parental lines of hybrids as well as on another F 2 mapping population. The results obtained in this study are expected to enhance the efficiency of selection for the identification of restorer lines in hybrid breeding and may reduce traditional time-consuming phenotyping activities. |