2019
DOI: 10.1007/s00497-019-00377-6
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Molecular mapping of a novel male-sterile gene msNJ in soybean [Glycine max (L.) Merr.]

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Cited by 17 publications
(18 citation statements)
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“…Plant male sterile mutants are important materials for studying the anther development mechanisms and crucial tools for crop hybrid breeding. So far, 13 genetic loci in soybean have been reported to condition male sterile phenotype independently when they are mutated, including ms1-ms9, msp, msMOS, mst-M, and ms NJ (Yang et al 2014;Zhao et al 2019;Nie et al 2019;Thu et al 2019), but only ms4 has been molecularly identi ed, which encodes a PHD-nger protein and is involved in the meiosis process of microsporocyte (Thu et al, 2019). Amongst these mutants, two ms6 mutants identi ed decades ago exhibit no-pollen phenotypes (Fig.…”
Section: Discussionmentioning
confidence: 99%
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“…Plant male sterile mutants are important materials for studying the anther development mechanisms and crucial tools for crop hybrid breeding. So far, 13 genetic loci in soybean have been reported to condition male sterile phenotype independently when they are mutated, including ms1-ms9, msp, msMOS, mst-M, and ms NJ (Yang et al 2014;Zhao et al 2019;Nie et al 2019;Thu et al 2019), but only ms4 has been molecularly identi ed, which encodes a PHD-nger protein and is involved in the meiosis process of microsporocyte (Thu et al, 2019). Amongst these mutants, two ms6 mutants identi ed decades ago exhibit no-pollen phenotypes (Fig.…”
Section: Discussionmentioning
confidence: 99%
“…However, it has not been applied in soybean as lack of cloned GMS gene. So far, 13 non-allelic genic loci distributed on 7 different chromosomes have been reported to condition anther development in soybean, including ms1-ms9, msp, msMOS, mst-M, and ms NJ (Yang et al 2014;Zhao et al 2019;Nie et al 2019;Thu et al 2019). Mutations at these loci all confer recessive sporophytic male-sterile phenotype.…”
Section: Introductionmentioning
confidence: 99%
“…It is a tool initially developed for allogamous crops; however, application in autogamous plants, such as wheat, oats, rice, and common bean have increased in recent years. In the case of soybean, there are reports of the use of recurrent selection outside of Brazil for grain protein content (Patil et al 2017, Rialch andSharma 2019) and grain yield (Sumarno and Fehr 1982, Posadas et al 2014, Vello and Nazato 2017, Nie et al 2019, Hegstad et al 2019. However, it should be highlighted that for the purpose of expanding the genetic variability of the base population of the recurrent selection program, the authors used exotic germplasm, i.e., germplasm with low adaptability and, likewise, lower frequency of favorable alleles.…”
Section: Discussionmentioning
confidence: 99%
“…With the aim of maximizing resources, as well as efficient use of the time necessary for identification of superior genotypes for recombination, recurrent selection is a useful strategy. Although this strategy has been promoted for breeding of allogamous plants, its use is reported in the literature in autogamous IO Soares et al plants like common bean (Pereira et al 2017a, Anjos et al 2018, Melo et al 2019) and soybean (Posadas et al 2014, Vello and Nazato 2017, Nie et al 2019. The use of this technique for the purpose of increasing grain yield in Brazil has not been reported in the literature.…”
Section: Introductionmentioning
confidence: 99%
“…The morphology of anthers from opened flowers of soybean and Arabidopsis was observed under an Olympus CX31 microscope (Japan). Pollen viability of soybean and Arabidopsis was analyzed by I 2 -KI staining (Nie et al, 2019) and Alexander's staining (Ding et al, 2020), respectively. The stamen and pistil length of Arabidopsis was measured with the cellSens software (Olympus, Japan).…”
Section: Gus Staining and Plant Trait Investigationmentioning
confidence: 99%