Anthracnose, caused by the fungus Colletotrichum lindemuthianum, is one of the devastating disease affecting common bean production and productivity worldwide. Several quantitative trait loci (QTLs) for anthracnose resistance have been identified. In order to make use of these QTLs in common bean breeding programs, a detailed meta-QTL (MQTL) analysis has been conducted. For the MQTL analysis, 92 QTLs related to anthracnose disease reported in 18 different earlier studies involving 16 mapping populations were compiled and projected on to the consensus map. This meta-analysis led to the identification of 11 MQTLs (each involving QTLs from at least two different studies) on 06 bean chromosomes and 10 QTL hotspots each involving multiple QTLs from an individual study on 07 chromosomes. The confidence interval (CI) of the identified MQTLs was found 3.51 times lower than the CI of initial QTLs. Marker-trait associations (MTAs) reported in published genome-wide association studies (GWAS) were used to validate nine of the 11 identified MQTLs, with MQTL4.1 overlapping with as many as 40 MTAs. Functional annotation of the 11 MQTL regions revealed 1,251 genes including several R genes (such as those encoding for NBS-LRR domain-containing proteins, protein kinases, etc.) and other defense related genes. The MQTLs, QTL hotspots and the potential candidate genes identified during the present study will prove useful in common bean marker-assisted breeding programs and in basic studies involving fine mapping and cloning of genomic regions associated with anthracnose resistance in common beans.
Cuttage propagation of Aesculus indica was tested by treatments with different concentrations of indole-3-acetic acid (IAA) @ 2000, 4000 (ppm), indolebutyric acid (IBA) @ 2000, 4000 (ppm) and naphthlcetic acid (NAA) @ 2000, 4000 (ppm) in dry formulation in the Forest Nursery, Faculty of Forestry, SKUAST-K, Shalimar. The cuttings treated with IBA @ 4000 ppm and IBA @ 2000 ppm had asprouting rate of 75% and 50%, respectively, which was significantly higher than that of control and other treatments. The highest rooting rate (50%) was recorded in the cuttings with the application of IBA @ 4000 ppm. The cuttings treated with IBA @ 2000 ppm had 25% rooting rate. All other treatments along with control (talc powder) failed to induce rooting. It was concluded that IBA @ 4000 ppm was a better-applied concentration for vegetative propagation of A. indica under Kashmir conditions.
Human population growth in combination with changing patterns of global food consumption under climate change is posing formidable challenge to attaining sustainable global food security. Besides being economically viable sources of plant based protein for human consumption, pulses are also beneficial for the environment owing to their inherent capacity of nitrogen fixation. Hence, further development of pulses has become imperative in the vigorously transitional global scenario where flourishing anthropogenic activities are triggering irreplaceable depletion of natural resources. During past years, considerable attention has been given on the use of next generation sequencing for enriching the genomic resources in pulse crops including high-throughput DNA markers, candidate gene(s) and QTLs for predicting plant phenotypes, and whole genome sequences. With refinements in DNA sequencing technologies and computational analytical tools, the rapidly grown numbers of sequenced pulse genomes offer novel insights on crop evolution and breeding history.Integration of new-generation genomic and phenomic tools with generation acceleration procedures like genomic selection and speed breeding could greatly accelerate progress in pulses genetic improvement. The present review discusses current status and future scope of using next-generation breeding approaches in pulses that will cause not only an increase in the rate of developing climateresilient superior cultivars but also help to reach to goal of global food security.
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