Rice plants that form ventilated tissues, such as aerenchyma in the leaves, stems, and roots, allow for growth in waterlogged conditions (paddy fields), but they cannot breathe and drown in flooded environments where the whole plant body is submerged. However, deepwater rice plants grown in flood-prone areas of Southeast Asia survive in prolonged flooded environments by taking in air through an elongated stem (internode) and leaves that emerge above the water surface, even if the water level is several meters high and flooding continues for several months. Although it has been known that plant hormones, such as ethylene and gibberellins, promote internode elongation in deepwater rice plants, the genes that control rapid internode elongation during submergence have not been identified. We recently identified several genes responsible for the quantitative trait loci involved in internode elongation in deepwater rice. Identification of the the genes revealed a molecular gene network from ethylene to gibberellins in which internode elongation is promoted by novel ethylene-responsive factors and enhances gibberellin responsiveness at the internode. In addition, elucidation of the molecular mechanism of internode elongation in deepwater rice will help our understanding of the internode elongation mechanism in normal paddy rice and contribute to improving crops through the regulation of internode elongation.
{"title":"Molecular mechanism of internode elongation in rice.","authors":"Keisuke Nagai, Motoyuki Ashikari","doi":"10.1270/jsbbs.22086","DOIUrl":"https://doi.org/10.1270/jsbbs.22086","url":null,"abstract":"<p><p>Rice plants that form ventilated tissues, such as aerenchyma in the leaves, stems, and roots, allow for growth in waterlogged conditions (paddy fields), but they cannot breathe and drown in flooded environments where the whole plant body is submerged. However, deepwater rice plants grown in flood-prone areas of Southeast Asia survive in prolonged flooded environments by taking in air through an elongated stem (internode) and leaves that emerge above the water surface, even if the water level is several meters high and flooding continues for several months. Although it has been known that plant hormones, such as ethylene and gibberellins, promote internode elongation in deepwater rice plants, the genes that control rapid internode elongation during submergence have not been identified. We recently identified several genes responsible for the quantitative trait loci involved in internode elongation in deepwater rice. Identification of the the genes revealed a molecular gene network from ethylene to gibberellins in which internode elongation is promoted by novel ethylene-responsive factors and enhances gibberellin responsiveness at the internode. In addition, elucidation of the molecular mechanism of internode elongation in deepwater rice will help our understanding of the internode elongation mechanism in normal paddy rice and contribute to improving crops through the regulation of internode elongation.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"108-116"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316307/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10178167","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sexuality is the main strategy for maintaining genetic diversity within a species. In flowering plants (angiosperms), sexuality is derived from ancestral hermaphroditism and multiple sexualities can be expressed in an individual. The mechanisms conferring chromosomal sex determination in plants (or dioecy) have been studied for over a century by both biologists and agricultural scientists, given the importance of this field for crop cultivation and breeding. Despite extensive research, the sex determining gene(s) in plants had not been identified until recently. In this review, we dissect plant sex evolution and determining systems, with a focus on crop species. We introduced classic studies with theoretical, genetic, and cytogenic approaches, as well as more recent research using advanced molecular and genomic techniques. Plants have undergone very frequent transitions into, and out of, dioecy. Although only a few sex determinants have been identified in plants, an integrative viewpoint on their evolutionary trends suggests that recurrent neofunctionalization events are potentially common, in a "scrap and (re)build" cycle. We also discuss the potential association between crop domestication and transitions in sexual systems. We focus on the contribution of duplication events, which are particularly frequent in plant taxa, as a trigger for the creation of new sexual systems.
{"title":"Evolution of sex in crops: recurrent scrap and rebuild.","authors":"Kanae Masuda, Takashi Akagi","doi":"10.1270/jsbbs.22082","DOIUrl":"https://doi.org/10.1270/jsbbs.22082","url":null,"abstract":"<p><p>Sexuality is the main strategy for maintaining genetic diversity within a species. In flowering plants (angiosperms), sexuality is derived from ancestral hermaphroditism and multiple sexualities can be expressed in an individual. The mechanisms conferring chromosomal sex determination in plants (or dioecy) have been studied for over a century by both biologists and agricultural scientists, given the importance of this field for crop cultivation and breeding. Despite extensive research, the sex determining gene(s) in plants had not been identified until recently. In this review, we dissect plant sex evolution and determining systems, with a focus on crop species. We introduced classic studies with theoretical, genetic, and cytogenic approaches, as well as more recent research using advanced molecular and genomic techniques. Plants have undergone very frequent transitions into, and out of, dioecy. Although only a few sex determinants have been identified in plants, an integrative viewpoint on their evolutionary trends suggests that recurrent neofunctionalization events are potentially common, in a \"scrap and (re)build\" cycle. We also discuss the potential association between crop domestication and transitions in sexual systems. We focus on the contribution of duplication events, which are particularly frequent in plant taxa, as a trigger for the creation of new sexual systems.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"95-107"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316312/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10178168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Mari Sugiyama, Miyu Norizuki, Shinji Kikuchi, Yasuo Yasui, Katsuhiro Matsui
Common buckwheat (Fagopyrum esculentum) is an annual self-incompatible plant that is widely grown. The genus Fagopyrum comprises more than 20 species, including F. cymosum, a perennial that, unlike common buckwheat, is highly resistant to excess water. In this study, we developed interspecific hybrids between F. esculentum and F. cymosum via embryo rescue, to improve undesirable traits of common buckwheat, such as low tolerance to excess water. The interspecific hybrids were confirmed by genomic in situ hybridization (GISH). We also developed DNA markers to confirm the identity of the hybrids and if genes derived from each genome were inherited by the next generation. Observations of pollen indicated that the interspecific hybrids were essentially sterile. Unpaired chromosomes and abnormal segregation during meiosis were likely responsible for the pollen sterility of the hybrids. These findings could facilitate buckwheat breeding to produce lines that can withstand harsh environments with wild or related species in the genus Fagopyrum.
{"title":"Development and chromosomal characterization of interspecific hybrids between common buckwheat (<i>Fagopyrum esculentum</i>) and a related perennial species (<i>F. cymosum</i>).","authors":"Mari Sugiyama, Miyu Norizuki, Shinji Kikuchi, Yasuo Yasui, Katsuhiro Matsui","doi":"10.1270/jsbbs.22063","DOIUrl":"https://doi.org/10.1270/jsbbs.22063","url":null,"abstract":"<p><p>Common buckwheat (<i>Fagopyrum esculentum</i>) is an annual self-incompatible plant that is widely grown. The genus <i>Fagopyrum</i> comprises more than 20 species, including <i>F. cymosum</i>, a perennial that, unlike common buckwheat, is highly resistant to excess water. In this study, we developed interspecific hybrids between <i>F. esculentum</i> and <i>F. cymosum</i> via embryo rescue, to improve undesirable traits of common buckwheat, such as low tolerance to excess water. The interspecific hybrids were confirmed by genomic <i>in situ</i> hybridization (GISH). We also developed DNA markers to confirm the identity of the hybrids and if genes derived from each genome were inherited by the next generation. Observations of pollen indicated that the interspecific hybrids were essentially sterile. Unpaired chromosomes and abnormal segregation during meiosis were likely responsible for the pollen sterility of the hybrids. These findings could facilitate buckwheat breeding to produce lines that can withstand harsh environments with wild or related species in the genus <i>Fagopyrum</i>.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"230-236"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316306/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10178169","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Hyungjun Park, Tomoko Abe, Hisato Kunitake, Tomonari Hirano
Sweet potato is a widely cultivated crop with storage roots. Although many studies have been conducted on the mechanism of its storage root formation, the details have not been fully elucidated. We screened mutant lines with inhibition of storage root formation to clarify parts of the mechanism. In this study, the process of storage root formation in one of the mutant lines, C20-8-1, was investigated. The inhibition of storage root formation was observed during the early stages of growth. The roots in C20-8-1 did not show histological differences compared to those in wild type. The transition from fibrous roots to pencil roots, which are the developmental stages prior to mature storage root formation, was delayed or inhibited in C20-8-1. The upregulation of starch biosynthesis-related genes and downregulation of lignin biosynthesis genes with storage root swelling were not confirmed in the root of C20-8-1 during the developmental transition stage, suggesting that most of the roots in C20-8-1 are in the pre-transition state toward the storage root swelling. C20-8-1 showed a mutant phenotype during the critical period of storage root swelling initiation, and further clarification of this mutation is expected to provide new insights into storage root formation.
{"title":"Characterization of a novel mutant with inhibition of storage root formation in sweet potato.","authors":"Hyungjun Park, Tomoko Abe, Hisato Kunitake, Tomonari Hirano","doi":"10.1270/jsbbs.22090","DOIUrl":"https://doi.org/10.1270/jsbbs.22090","url":null,"abstract":"<p><p>Sweet potato is a widely cultivated crop with storage roots. Although many studies have been conducted on the mechanism of its storage root formation, the details have not been fully elucidated. We screened mutant lines with inhibition of storage root formation to clarify parts of the mechanism. In this study, the process of storage root formation in one of the mutant lines, C20-8-1, was investigated. The inhibition of storage root formation was observed during the early stages of growth. The roots in C20-8-1 did not show histological differences compared to those in wild type. The transition from fibrous roots to pencil roots, which are the developmental stages prior to mature storage root formation, was delayed or inhibited in C20-8-1. The upregulation of starch biosynthesis-related genes and downregulation of lignin biosynthesis genes with storage root swelling were not confirmed in the root of C20-8-1 during the developmental transition stage, suggesting that most of the roots in C20-8-1 are in the pre-transition state toward the storage root swelling. C20-8-1 showed a mutant phenotype during the critical period of storage root swelling initiation, and further clarification of this mutation is expected to provide new insights into storage root formation.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"212-218"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316310/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10178172","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Self-incompatibility is the system that inhibits pollen germination and pollen tube growth by self-pollen. This trait is important for the breeding of Brassica and Raphanus species. In these species, self-incompatibility is governed by the S locus, which contains three linked genes (a set called the S haplotype), i.e., S-locus receptor kinase, S-locus cysteine-rich protein/S-locus protein 11, and S-locus glycoprotein. A large number of S haplotypes have been identified in Brassica oleracea, B. rapa, and Raphanus sativus to date, and the nucleotide sequences of their many alleles have also been registered. In this state, it is important to avoid confusion between S haplotypes, i.e., an identical S haplotype with different names and a different S haplotype with an identical S haplotype number. To mitigate this issue, we herein constructed a list of S haplotypes that are easily accessible to the latest nucleotide sequences of S-haplotype genes, together with revisions to and an update of S haplotype information. Furthermore, the histories of the S-haplotype collection in the three species are reviewed, the importance of the collection of S haplotypes as a genetic resource is discussed, and the management of information on S haplotypes is proposed.
{"title":"<i>S</i> haplotype collection in Brassicaceae crops-an updated list of <i>S</i> haplotypes.","authors":"Masaya Yamamoto, Tomoko Ishii, Marina Ogura, Takashi Akanuma, Xing-Yu Zhu, Hiroyasu Kitashiba","doi":"10.1270/jsbbs.22091","DOIUrl":"https://doi.org/10.1270/jsbbs.22091","url":null,"abstract":"<p><p>Self-incompatibility is the system that inhibits pollen germination and pollen tube growth by self-pollen. This trait is important for the breeding of <i>Brassica</i> and <i>Raphanus</i> species. In these species, self-incompatibility is governed by the <i>S</i> locus, which contains three linked genes (a set called the <i>S</i> haplotype), i.e., <i>S</i>-locus receptor kinase, <i>S</i>-locus cysteine-rich protein/<i>S</i>-locus protein 11, and <i>S</i>-locus glycoprotein. A large number of <i>S</i> haplotypes have been identified in <i>Brassica oleracea</i>, <i>B. rapa</i>, and <i>Raphanus sativus</i> to date, and the nucleotide sequences of their many alleles have also been registered. In this state, it is important to avoid confusion between <i>S</i> haplotypes, i.e., an identical <i>S</i> haplotype with different names and a different <i>S</i> haplotype with an identical <i>S</i> haplotype number. To mitigate this issue, we herein constructed a list of <i>S</i> haplotypes that are easily accessible to the latest nucleotide sequences of <i>S</i>-haplotype genes, together with revisions to and an update of <i>S</i> haplotype information. Furthermore, the histories of the <i>S</i>-haplotype collection in the three species are reviewed, the importance of the collection of <i>S</i> haplotypes as a genetic resource is discussed, and the management of information on <i>S</i> haplotypes is proposed.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"132-145"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316313/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10178173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lijiao Fan, Dongshan Wei, Xingwang Yu, Fengqiang Yu, Jiameng Wang, Guirong Sun, Alatengsuhe, Li Zhang, Guosheng Zhang, Haifeng Yang
To identify the function of the SpsNAC042 gene and its response to salt and drought stress, the SpsNAC042 gene was transformed into Populus hopeiensis by the Agrobacterium-mediated leaf disc method, and the phenotypic, physiological changes and related genes expression of transgenic lines were analyzed. The results showed that the number and length of roots of transgenic lines increased significantly. The leaves of transgenic lines curled inward. Under salt and simulated drought stress, the transgenic lines showed improved tolerance to salt and drought. The activities of SOD, POD, CAT and proline content in the transgenic lines were significantly increased, and the reduction rates of total chlorophyll and MDA content were significantly decreased, which indicated that the transgenic lines showed strong physiological responses under stress. Meanwhile, the gene expression of MPK6, SOS1, HKT1 and P5CS1 were significantly upregulated, and the gene expression of PRODH1 was significantly downregulated, which preliminarily verified the stress regulation mechanism that SpsNAC042 might activate. The above results showed that the SpsNAC042 gene could promote root development, make leaf morphology curl, and enhance P. hopeiensis tolerance to stress.
{"title":"Effects of <i>SpsNAC042</i> transgenic <i>Populus hopeiensis</i> on root development, leaf morphology and stress resistance.","authors":"Lijiao Fan, Dongshan Wei, Xingwang Yu, Fengqiang Yu, Jiameng Wang, Guirong Sun, Alatengsuhe, Li Zhang, Guosheng Zhang, Haifeng Yang","doi":"10.1270/jsbbs.22079","DOIUrl":"https://doi.org/10.1270/jsbbs.22079","url":null,"abstract":"<p><p>To identify the function of the <i>SpsNAC042</i> gene and its response to salt and drought stress, the <i>SpsNAC042</i> gene was transformed into <i>Populus hopeiensis</i> by the Agrobacterium-mediated leaf disc method, and the phenotypic, physiological changes and related genes expression of transgenic lines were analyzed. The results showed that the number and length of roots of transgenic lines increased significantly. The leaves of transgenic lines curled inward. Under salt and simulated drought stress, the transgenic lines showed improved tolerance to salt and drought. The activities of SOD, POD, CAT and proline content in the transgenic lines were significantly increased, and the reduction rates of total chlorophyll and MDA content were significantly decreased, which indicated that the transgenic lines showed strong physiological responses under stress. Meanwhile, the gene expression of <i>MPK6</i>, <i>SOS1</i>, <i>HKT1</i> and <i>P5CS1</i> were significantly upregulated, and the gene expression of <i>PRODH1</i> was significantly downregulated, which preliminarily verified the stress regulation mechanism that <i>SpsNAC042</i> might activate. The above results showed that the <i>SpsNAC042</i> gene could promote root development, make leaf morphology curl, and enhance <i>P. hopeiensis</i> tolerance to stress.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"180-192"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316303/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10178170","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
To uncover population structure, phylogenetic relationship, and diversity in melons along the famous Silk Road, a seed size measurement and a phylogenetic analysis using five chloroplast genome markers, 17 RAPD markers and 11 SSR markers were conducted for 87 Kazakh melon accessions with reference accessions. Kazakh melon accessions had large seed with exception of two accessions of weedy melon, Group Agrestis, and consisted of three cytoplasm types, of which Ib-1/-2 and Ib-3 were dominant in Kazakhstan and nearby areas such as northwestern China, Central Asia and Russia. Molecular phylogeny showed that two unique genetic groups, STIa-2 with Ib-1/-2 cytoplasm and STIa-1 with Ib-3 cytoplasm, and one admixed group, STIAD combined with STIa and STIb, were prevalent across all Kazakh melon groups. STIAD melons that phylogenetically overlapped with STIa-1 and STIa-2 melons were frequent in the eastern Silk Road region, including Kazakhstan. Evidently, a small population contributed to melon development and variation in the eastern Silk Road. Conscious preservation of fruit traits specific to Kazakh melon groups is thought to play a role in the conservation of Kazakh melon genetic variation during melon production, where hybrid progenies were generated through open pollination.
{"title":"Melon diversity on the Silk Road by molecular phylogenetic analysis in Kazakhstan melons.","authors":"Katsunori Tanaka, Mitsuhiro Sugiyama, Gentaro Shigita, Ryoma Murakami, Thanh-Thuy Duong, Yasheng Aierken, Anna M Artemyeva, Zharas Mamypbelov, Ryuji Ishikawa, Hidetaka Nishida, Kenji Kato","doi":"10.1270/jsbbs.22030","DOIUrl":"10.1270/jsbbs.22030","url":null,"abstract":"<p><p>To uncover population structure, phylogenetic relationship, and diversity in melons along the famous Silk Road, a seed size measurement and a phylogenetic analysis using five chloroplast genome markers, 17 RAPD markers and 11 SSR markers were conducted for 87 Kazakh melon accessions with reference accessions. Kazakh melon accessions had large seed with exception of two accessions of weedy melon, Group Agrestis, and consisted of three cytoplasm types, of which Ib-1/-2 and Ib-3 were dominant in Kazakhstan and nearby areas such as northwestern China, Central Asia and Russia. Molecular phylogeny showed that two unique genetic groups, <sup>ST</sup>Ia-2 with Ib-1/-2 cytoplasm and <sup>ST</sup>Ia-1 with Ib-3 cytoplasm, and one admixed group, <sup>ST</sup>I<sub>AD</sub> combined with <sup>ST</sup>Ia and <sup>ST</sup>Ib, were prevalent across all Kazakh melon groups. <sup>ST</sup>I<sub>AD</sub> melons that phylogenetically overlapped with <sup>ST</sup>Ia-1 and <sup>ST</sup>Ia-2 melons were frequent in the eastern Silk Road region, including Kazakhstan. Evidently, a small population contributed to melon development and variation in the eastern Silk Road. Conscious preservation of fruit traits specific to Kazakh melon groups is thought to play a role in the conservation of Kazakh melon genetic variation during melon production, where hybrid progenies were generated through open pollination.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"219-229"},"PeriodicalIF":2.0,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316308/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9801023","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Domestication of azuki bean and soybean has enabled them to acquire non-dormant seeds, non-shattering pods, and larger seed size. Seed remains of the Jomon period recently discovered at archeological sites in the Central Highlands of Japan (6,000-4,000 BP) suggest that the use of azuki bean and soybean and their increase in seed size began earlier in Japan than in China and Korea; molecular phylogenetic studies indicate that azuki bean and soybean originated in Japan. Recent identification of domestication genes indicate that the domestication traits of azuki bean and soybean were established by different mechanisms. Analyses of domestication related genes using DNA extracted from the seed remains would reveal further details about their domestication processes.
{"title":"Domestication of azuki bean and soybean in Japan: From the insight of archeological and molecular evidence.","authors":"Yu Takahashi, Hiroo Nasu, Seiji Nakayama, Norihiko Tomooka","doi":"10.1270/jsbbs.22074","DOIUrl":"https://doi.org/10.1270/jsbbs.22074","url":null,"abstract":"<p><p>Domestication of azuki bean and soybean has enabled them to acquire non-dormant seeds, non-shattering pods, and larger seed size. Seed remains of the Jomon period recently discovered at archeological sites in the Central Highlands of Japan (6,000-4,000 BP) suggest that the use of azuki bean and soybean and their increase in seed size began earlier in Japan than in China and Korea; molecular phylogenetic studies indicate that azuki bean and soybean originated in Japan. Recent identification of domestication genes indicate that the domestication traits of azuki bean and soybean were established by different mechanisms. Analyses of domestication related genes using DNA extracted from the seed remains would reveal further details about their domestication processes.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"117-131"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316305/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9801025","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ngoc B Nguyen, Nguyet T M Nguyen, Nhai T Nguyen, Linh H Le, Nghia T La, Thuy T T Nguyen, Mary Jeany Yanoria, Nagao Hayashi, Hiroki Saito, Mitsuhiro Obara, Tadashi Sato, Yoshimichi Fukuta
A unique genetic variation with respect to blast resistance was clarified in 201 rice accessions from Vietnam. These accessions were classified into three clusters-A, B1, and B2-based on their reactions to 26 standard differential blast isolates selected in Vietnam. Cluster A was the dominant cultivar group in Vietnam and the most susceptible of the three clusters. Cluster B1 was the smallest group and the most resistant. Cluster B2 was the second-most dominant group and of intermediate resistance between clusters A and B1. The percentages of accessions comprising each cluster varied by region and area. Accessions in cluster A were distributed widely throughout Vietnam and had the highest frequencies in both the Central and North regions. Accessions in cluster B2 were found with highest frequencies in the mountainous and intermediate areas of the North region. Accessions in cluster B1 were found with highest frequencies in the Central region and Red River Delta area (North region). These results suggest that rice accessions in Vietnam were basically susceptible (cluster A) or of intermediate resistance (cluster B2), and that high-resistance cultivars were mainly distributed in the low altitude areas, such as the Red River Delta area and Central region.
{"title":"A unique genetic variation with respect to blast (<i>Pyricularia oryzae</i> Cavara) resistance in rice (<i>Oryza sativa</i> L.) varieties in Vietnam.","authors":"Ngoc B Nguyen, Nguyet T M Nguyen, Nhai T Nguyen, Linh H Le, Nghia T La, Thuy T T Nguyen, Mary Jeany Yanoria, Nagao Hayashi, Hiroki Saito, Mitsuhiro Obara, Tadashi Sato, Yoshimichi Fukuta","doi":"10.1270/jsbbs.22073","DOIUrl":"https://doi.org/10.1270/jsbbs.22073","url":null,"abstract":"<p><p>A unique genetic variation with respect to blast resistance was clarified in 201 rice accessions from Vietnam. These accessions were classified into three clusters-A, B1, and B2-based on their reactions to 26 standard differential blast isolates selected in Vietnam. Cluster A was the dominant cultivar group in Vietnam and the most susceptible of the three clusters. Cluster B1 was the smallest group and the most resistant. Cluster B2 was the second-most dominant group and of intermediate resistance between clusters A and B1. The percentages of accessions comprising each cluster varied by region and area. Accessions in cluster A were distributed widely throughout Vietnam and had the highest frequencies in both the Central and North regions. Accessions in cluster B2 were found with highest frequencies in the mountainous and intermediate areas of the North region. Accessions in cluster B1 were found with highest frequencies in the Central region and Red River Delta area (North region). These results suggest that rice accessions in Vietnam were basically susceptible (cluster A) or of intermediate resistance (cluster B2), and that high-resistance cultivars were mainly distributed in the low altitude areas, such as the Red River Delta area and Central region.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"193-203"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316314/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9792240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The isolation of disease resistance genes introduced from wild or related cultivated species is essential for understanding their mechanisms, spectrum and risk of breakdown. To identify target genes not included in reference genomes, genomic sequences with the target locus must be reconstructed. However, de novo assembly approaches of the entire genome, such as those used for constructing reference genomes, are complicated in higher plants. Moreover, in the autotetraploid potato, the heterozygous regions and repetitive structures located around disease resistance gene clusters fragment the genomes into short contigs, making it challenging to identify resistance genes. In this study, we report that a de novo assembly approach of a target gene-specific homozygous dihaploid developed through haploid induction was suitable for gene isolation in potatoes using the potato virus Y resistance gene Rychc as a model. The assembled contig containing Rychc-linked markers was 3.3 Mb in length and could be joined with gene location information from the fine mapping analysis. Rychc was successfully identified in a repeated island located on the distal end of the long arm of chromosome 9 as a Toll/interleukin-1 receptor-nucleotide-binding site-leucine rich repeat (TIR-NBS-LRR) type resistance gene. This approach will be practical for other gene isolation projects in potatoes.
{"title":"<i>De novo</i> genome assembly of the partial homozygous dihaploid potato identified PVY resistance gene (<i>Ry<sub>chc</sub></i>) derived from <i>Solanum chacoense</i>.","authors":"Kotaro Akai, Kenji Asano, Chika Suzuki, Etsuo Shimosaka, Seiji Tamiya, Takako Suzuki, Toru Takeuchi, Takehiro Ohki","doi":"10.1270/jsbbs.22078","DOIUrl":"https://doi.org/10.1270/jsbbs.22078","url":null,"abstract":"<p><p>The isolation of disease resistance genes introduced from wild or related cultivated species is essential for understanding their mechanisms, spectrum and risk of breakdown. To identify target genes not included in reference genomes, genomic sequences with the target locus must be reconstructed. However, <i>de novo</i> assembly approaches of the entire genome, such as those used for constructing reference genomes, are complicated in higher plants. Moreover, in the autotetraploid potato, the heterozygous regions and repetitive structures located around disease resistance gene clusters fragment the genomes into short contigs, making it challenging to identify resistance genes. In this study, we report that a <i>de novo</i> assembly approach of a target gene-specific homozygous dihaploid developed through haploid induction was suitable for gene isolation in potatoes using the potato virus Y resistance gene <i>Ry<sub>chc</sub></i> as a model. The assembled contig containing <i>Ry<sub>chc</sub></i>-linked markers was 3.3 Mb in length and could be joined with gene location information from the fine mapping analysis. <i>Ry<sub>chc</sub></i> was successfully identified in a repeated island located on the distal end of the long arm of chromosome 9 as a Toll/interleukin-1 receptor-nucleotide-binding site-leucine rich repeat (TIR-NBS-LRR) type resistance gene. This approach will be practical for other gene isolation projects in potatoes.</p>","PeriodicalId":9258,"journal":{"name":"Breeding Science","volume":"73 2","pages":"168-179"},"PeriodicalIF":2.4,"publicationDate":"2023-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10316315/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9801024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}