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      QTL Mapping and Candidate Gene Analysis for Pod Shattering Tolerance in Soybean ( Glycine max)

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          Abstract

          Pod shattering is an important reproductive process in many wild species. However, pod shattering at the maturing stage can result in severe yield loss. The objectives of this study were to discover quantitative trait loci (QTLs) for pod shattering using two recombinant inbred line (RIL) populations derived from an elite cultivar having pod shattering tolerance, namely “Daewonkong”, and to predict novel candidate QTL/genes involved in pod shattering based on their allele patterns. We found several QTLs with more than 10% phenotypic variance explained (PVE) on seven different chromosomes and found a novel candidate QTL on chromosome 16 ( qPS-DS16-1) from the allele patterns in the QTL region. Out of the 41 annotated genes in the QTL region, six were found to contain SNP (single-nucleotide polymorphism)/indel variations in the coding sequence of the parents compared to the soybean reference genome. Among the six potential candidate genes, Glyma.16g076600, one of the genes with known function, showed a highly differential expression levels between the tolerant and susceptible parents in the growth stages R3 to R6. Further, Glyma.16g076600 is a homolog of AT4G19230 in Arabidopsis, whose function is related to abscisic acid catabolism. The results provide useful information to understand the genetic mechanism of pod shattering and could be used for improving the efficiency of marker-assisted selection for developing varieties of soybeans tolerant to pod shattering.

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          Most cited references45

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          Stage of Development Descriptions for Soybeans, Glycine Max (L.) Merrill1

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            QTL IciMapping: Integrated software for genetic linkage map construction and quantitative trait locus mapping in biparental populations

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              Arabidopsis CYP707As encode (+)-abscisic acid 8'-hydroxylase, a key enzyme in the oxidative catabolism of abscisic acid.

              Abscisic acid (ABA) is involved in a number of critical processes in normal growth and development as well as in adaptive responses to environmental stresses. For correct and accurate actions, a physiologically active ABA level is controlled through fine-tuning of de novo biosynthesis and catabolism. The hydroxylation at the 8'-position of ABA is known as the key step of ABA catabolism, and this reaction is catalyzed by ABA 8'-hydroxylase, a cytochrome P450. Here, we demonstrate CYP707As as the P450 responsible for the 8'-hydroxylation of (+)-ABA. First, all four CYP707A cDNAs were cloned from Arabidopsis and used for the production of the recombinant proteins in insect cells using a baculovirus system. The insect cells expressing CYP707A3 efficiently metabolized (+)-ABA to yield phaseic acid, the isomerized form of 8'-hydroxy-ABA. The microsomes from the insect cells exhibited very strong activity of 8'-hydroxylation of (+)-ABA (K(m) = 1.3 microm and k(cat) = 15 min(-1)). The solubilized CYP707A3 protein bound (+)-ABA with the binding constant K(s) = 3.5 microm, but did not bind (-)-ABA. Detailed analyses of the reaction products confirmed that CYP707A3 does not have the isomerization activity of 8'-hydroxy-ABA to phaseic acid. Further experiments revealed that Arabidopsis CYP707A1 and CYP707A4 also encode ABA 8'-hydroxylase. The transcripts of the CYP707A genes increased in response to salt, osmotic, and dehydration stresses as well as ABA. These results establish that the CYP707A family plays a key role in regulating the ABA level through the 8'-hydroxylation of (+)-ABA.
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                Author and article information

                Journal
                Plants (Basel)
                Plants (Basel)
                plants
                Plants
                MDPI
                2223-7747
                08 September 2020
                September 2020
                : 9
                : 9
                : 1163
                Affiliations
                [1 ]National Institute of Crop Science, Rural Development Administration, Jeonju 55365, Korea; next0501@ 123456korea.kr (J.-H.S.); hellobk01@ 123456korea.kr (B.-K.K.); sanjeev@ 123456korea.kr (S.K.D.); mschoi73@ 123456korea.kr (M.-S.C.); heeya91@ 123456korea.kr (J.-H.P.); shinso32@ 123456korea.kr (S.-O.S.); kimhongs@ 123456korea.kr (H.-S.K.); baekiy@ 123456korea.kr (I.-Y.B.); sjs31@ 123456korea.kr (J.-S.S.); jung100@ 123456korea.kr (C.-S.J.)
                [2 ]National Institute of Agricultural Sciences, Rural Development Administration, Jeonju 55365, Korea; jhoh8288@ 123456korea.kr
                [3 ]FarmHannong, Ltd., Daejeon 34115, Korea; leehan26@ 123456snu.ac.kr
                [4 ]Department of Plant Bioscience, Pusan National University, Miryang 50463, Korea
                [5 ]Life and Industry Convergence Research Institute, Pusan National University, Miryang 50463, Korea
                Author notes
                [* ]Correspondence: thjun76@ 123456pusan.ac.kr
                Author information
                https://orcid.org/0000-0002-2495-9078
                https://orcid.org/0000-0003-1100-6953
                https://orcid.org/0000-0002-8502-2238
                Article
                plants-09-01163
                10.3390/plants9091163
                7569788
                32911865
                e09de06f-81ac-4152-a13c-f96c9e3bb149
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 11 August 2020
                : 07 September 2020
                Categories
                Article

                soybean,pod shattering,quantitative trait loci,candidate gene,abscisic acid

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