Panicle architecture and grain weight, both of which are influenced by genetic and environmental factors, have significant effects on grain yield potential. Here, we used a recombinant inbred line population (RIL) of 333 lines, which were grown in 13 trials with varying environmental conditions, to identify quantitative trait loci (QTL) that control differences in 9 agronomic traits related to panicle architecture and grain yield. We find that panicle weight, grain weight per panicle, panicle length, panicle diameter, and panicle exsertion length varied across different geographical locations. QTL mapping revealed 159 QTL for nine traits, of these, 34 QTL were identified in 2 to 12 environments, suggesting that the genetic control of panicle architecture in foxtail millet is sensitive to photoperiod or other environmental factors. 88 QTL controlling different traits formed 34 co-located QTL clusters, including the triple QTL cluster qPD9.2/qPL9.5/qPEL9.3, the genomic region of which was detected by 23 times in 13 environments. Several candidate genes were identified in the genomic intervals of multi-environmental QTL or co-located QTL clusters, including Seita.2G388700, Seita.3G136000, Seita.4G185300, Seita.5G241500, Seita.5G243100, Seita.9G281300, and Seita.9G342700. Among these, Seita.9G342700 was the candidate gene of qPD9.2/qPL9.5/qPEL9.3 QTL cluster, it is homologous to rice OsMADS56, which encodes a putative MADS-box transcription factor that determines inflorescence architecture in rice. These results not only provided a basis for further fine mapping, functional studies and marker-assisted selection of panicle architecture related traits in foxtail millet, but also benefited comparative genomics of cereal crops.

Figure 1

Figure 2
This is a list of supplementary files associated with this preprint. Click to download.
Figure S1. Phenotypic distribution and correlations of nine panicle architecture related parameters in 13 environments. The plots on the diagonal show the phenotypic distribution of each trail. The values above the diagonal are pairwise correlation coefficients between traits, and the plots below the diagonal are scatter plots of compared traits. Figure S2. Co-locations of QTL for multiple traits. qC2-1~qC2-17 were double co-located QTL clusters, qC3-1~qC3-14 were triple co-located QTL cluster, qC4 was a quadruple co-located QTL cluster, qC5-1 and qC5-2 were quintuple co-located QTL clusters.
Table S1. Phenotypic variations of the RIL population and parental lines among different envrionments.
Table S2. QTLs identified in this study
Table S3. QTL clulsters identified for different traits.
Loading...
Posted 16 Feb, 2021
On 16 Feb, 2021
On 21 Jan, 2021
Posted 16 Feb, 2021
On 16 Feb, 2021
On 21 Jan, 2021
Panicle architecture and grain weight, both of which are influenced by genetic and environmental factors, have significant effects on grain yield potential. Here, we used a recombinant inbred line population (RIL) of 333 lines, which were grown in 13 trials with varying environmental conditions, to identify quantitative trait loci (QTL) that control differences in 9 agronomic traits related to panicle architecture and grain yield. We find that panicle weight, grain weight per panicle, panicle length, panicle diameter, and panicle exsertion length varied across different geographical locations. QTL mapping revealed 159 QTL for nine traits, of these, 34 QTL were identified in 2 to 12 environments, suggesting that the genetic control of panicle architecture in foxtail millet is sensitive to photoperiod or other environmental factors. 88 QTL controlling different traits formed 34 co-located QTL clusters, including the triple QTL cluster qPD9.2/qPL9.5/qPEL9.3, the genomic region of which was detected by 23 times in 13 environments. Several candidate genes were identified in the genomic intervals of multi-environmental QTL or co-located QTL clusters, including Seita.2G388700, Seita.3G136000, Seita.4G185300, Seita.5G241500, Seita.5G243100, Seita.9G281300, and Seita.9G342700. Among these, Seita.9G342700 was the candidate gene of qPD9.2/qPL9.5/qPEL9.3 QTL cluster, it is homologous to rice OsMADS56, which encodes a putative MADS-box transcription factor that determines inflorescence architecture in rice. These results not only provided a basis for further fine mapping, functional studies and marker-assisted selection of panicle architecture related traits in foxtail millet, but also benefited comparative genomics of cereal crops.

Figure 1

Figure 2
This is a list of supplementary files associated with this preprint. Click to download.
Figure S1. Phenotypic distribution and correlations of nine panicle architecture related parameters in 13 environments. The plots on the diagonal show the phenotypic distribution of each trail. The values above the diagonal are pairwise correlation coefficients between traits, and the plots below the diagonal are scatter plots of compared traits. Figure S2. Co-locations of QTL for multiple traits. qC2-1~qC2-17 were double co-located QTL clusters, qC3-1~qC3-14 were triple co-located QTL cluster, qC4 was a quadruple co-located QTL cluster, qC5-1 and qC5-2 were quintuple co-located QTL clusters.
Table S1. Phenotypic variations of the RIL population and parental lines among different envrionments.
Table S2. QTLs identified in this study
Table S3. QTL clulsters identified for different traits.
Loading...