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361por Langewisch, Tiffany, Zhang, Hongxin, Vincent, Ryan, Joshi, Trupti, Xu, Dong, Bilyeu, Kristin“…For this study, we utilized two available soybean genomic datasets for a total of 72 soybean genotypes encompassing cultivars, landraces, and the wild species Glycine soja. The major soybean maturity genes E1, E2, E3, and E4 along with the Dt1 gene for plant growth architecture were analyzed in an effort to determine the number of major haplotypes for each gene, to evaluate the consistency of the haplotypes with characterized variant alleles, and to identify evidence of artificial selection. …”
Publicado 2014
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362“…Novel strain OO99(T) elicits effective nodules on Glycine max, Glycine soja and Macroptilium atropurpureum, partially effective nodules on Desmodium canadense and Vigna unguiculata, and ineffective nodules on Amphicarpaea bracteata and Phaseolus vulgaris. …”
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363por Manavalan, Lakshmi P., Prince, Silvas J., Musket, Theresa A., Chaky, Julian, Deshmukh, Rupesh, Vuong, Tri D., Song, Li, Cregan, Perry B., Nelson, James C., Shannon, J. Grover, Specht, James E., Nguyen, Henry T.“…Dunbar (PI 552538) and wild G. soja (PI 326582A) exhibited significant differences in root architecture and root-related traits. …”
Publicado 2015
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364por Jang, Seong-Jin, Sato, Masako, Sato, Kei, Jitsuyama, Yutaka, Fujino, Kaien, Mori, Haruhide, Takahashi, Ryoji, Benitez, Eduardo R., Liu, Baohui, Yamada, Tetsuya, Abe, Jun“…To dissect the molecular basis of qHS1, a quantitative trait locus for hard seededness in soybean (Glycine max (L) Merr.), we developed a near-isogenic line (NIL) of a permeable (soft-seeded) cultivar, Tachinagaha, containing a hard-seed allele from wild soybean (G. soja) introduced by successive backcrossings. The hard-seed allele made the seed coat of Tachinagaha more rigid by increasing the amount of β-1,4-glucans in the outer layer of palisade cells of the seed coat on the dorsal side of seeds, known to be a point of entrance of water. …”
Publicado 2015
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365por Xu, Zhaolong, Ali, Zulfiqar, Xu, Ling, He, Xiaolan, Huang, Yihong, Yi, Jinxin, Shao, Hongbo, Ma, Hongxiang, Zhang, Dayong“…Previously, our lab generated digital gene expression profiling (DGEP) data to identify differentially expressed genes in a salt-tolerant genotype of Glycine soja (STGoGS) and a salt-sensitive genotype of Glycine max (SSGoGM). …”
Publicado 2016
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366“…By contrast, the 4-amino acid deletion is absent in the VQ22 protein from wild soybean species (Glycine soja). Overexpression of wild soybean VQ22 in cultivated soybean inhibited growth, particularly after cold treatment. …”
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367por Jia, Qi, Sun, Song, Kong, Defeng, Song, Junliang, Wu, Lumei, Yan, Zhen, Zuo, Lin, Yang, Yingjie, Liang, Kangjing, Lin, Wenxiong, Huang, Jinwen“…In this study, we identified a novel 5PTase gene, Gs5PTase8, from the salt-tolerance locus of chromosome 3 in wild soybean (Glycine soja). Gs5PTase8 is highly up-regulated under salt treatment. …”
Publicado 2020
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368por Zhang, Xiao, Li, Lu, Yang, Ce, Cheng, Yanbo, Han, Zhenzhen, Cai, Zhandong, Nian, Hai, Ma, Qibin“…The GsMAS1 from the wild soybean BW69 line encodes a MADS-box transcription factor in Glycine soja by bioinformatics analysis. The putative GsMAS1 protein was localized in the nucleus. …”
Publicado 2020
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369por Roy, Neha Samir, Ban, Yong-Wook, Yoo, Hana, Ramekar, Rahul Vasudeo, Cheong, Eun Ju, Park, Nam-Il, Na, Jong Kuk, Park, Kyong-Cheul, Choi, Ik-Young“…Here, we report DNA variations between the normal and dwarf members of four lines harvested from a single seed parent in an F6 RIL population derived from a cross between Glycine max var. Peking and Glycine soja IT182936. Whole genome sequencing was carried out, and the DNA variations in the whole genome were compared between the normal and dwarf samples. …”
Publicado 2021
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370por Nisar, Tayyaba, Tahir, Muhammad Hammad Nadeem, Iqbal, Shahid, Sajjad, Muhammad, Nadeem, Muhammad Azhar, Qanmber, Ghulam, Baig, Ayesha, Khan, Zulqurnain, Zhao, Zhengyun, Geng, Zhide, Ur Rehman, Shoaib“…Sequence logos analyses between G. max and G. soja amino acid residues exhibited high conservation. …”
Publicado 2022
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371“…Merr.) into farming systems raises great concern that transgenes may flow to endemic wild soybeans (Glycine soja Sieb. et Zucc.) via pollen, which may increase the ecological risks by increasing the fitness of hybrids under certain conditions and threaten the genetic diversity of wild soybean populations. …”
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372por Liu, Baohui, Fujita, Toshiro, Yan, Ze-Hong, Sakamoto, Shinichi, Xu, Donghe, Abe, Jun“…METHODS: A population of 96 recombinant inbred lines derived from a cultivated (ssp. max) × wild (ssp. soja) cross was used for mapping and QTL analysis. …”
Publicado 2007
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373por Yuan, Cui-Ping, Li, Ying-Hui, Liu, Zhang-Xiong, Guan, Rong-Xia, Chang, Ru-Zhen, Qiu, Li-Juan“…A domestication bottleneck was found because of lower sequence diversity and 58% unique SNPs loss in landraces compared with Glycine soja. Intensive selection increased the sequence diversity of cultivars, which had higher diversity and more unique SNPs than landraces. …”
Publicado 2012
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374por Sun, Mingzhe, Sun, Xiaoli, Zhao, Yang, Zhao, Chaoyue, DuanMu, Huizi, Yu, Yang, Ji, Wei, Zhu, Yanming“…In previous studies, we constructed a Glycine soja transcriptional profile, and identified three PPCK genes (GsPPCK1, GsPPCK2 and GsPPCK3) as potential alkali stress responsive genes. …”
Publicado 2014
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375por Sundaramoorthy, Jagadeesh, Park, Gyu Tae, Chang, Jeong Ho, Lee, Jeong-Dong, Kim, Jeong Hoe, Seo, Hak Soo, Chung, Gyuhwa, Song, Jong Tae“…In this study, we searched for new genetic components responsible for the production of white flowers in soybean and isolated four white-flowered mutant lines, i.e., two Glycine soja accessions (CW12700 and CW13381) and two EMS-induced mutants of Glycine max (PE1837 and PE636). …”
Publicado 2016
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376por Sundaramoorthy, Jagadeesh, Park, Gyu Tae, Mukaiyama, Kyosuke, Tsukamoto, Chigen, Chang, Jeong Ho, Lee, Jeong-Dong, Kim, Jeong Hoe, Seo, Hak Soo, Song, Jong Tae“…In this study, we elucidated the molecular identity of a novel mutant of Glycine soja, ′CWS5095′. Phenotypic analysis using TLC and LC-PDA/MS/MS showed that the mutant ′CWS5095′ did not produce any group A saponins. …”
Publicado 2018
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377por Zhang, Xiaoli, Wang, Wubin, Guo, Na, Zhang, Youyi, Bu, Yuanpeng, Zhao, Jinming, Xing, Han“…RESULTS: In this study, we used a mapping population derived from a cross between a chromosome segment substitution line CSSL3228 (donor N24852 (G. Soja), a receptor NN1138–2 (G. max)) and NN1138–2 to fine map a wild soybean allele of greater PH by QTL-seq and linkage mapping. …”
Publicado 2018
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378“…RESULTS: We investigate the genomic landscape and evolution of putative crop-wild-relative introgression by analyzing the nuclear and chloroplast genomes from a panel of wild (Glycine soja) and domesticated (Glycine max) soybeans. Our data suggest that naturally occurring introgression between wild and domesticated soybeans was widespread and that introgressed variation in both wild and domesticated soybeans was selected against throughout the genomes and preferentially removed from the genomic regions underlying selective sweeps and domestication quantitative trait locus (QTL). …”
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379por Han, Jianan, Han, Dezhi, Guo, Yong, Yan, Hongrui, Wei, Zhongyan, Tian, Yu, Qiu, Lijuan“…ABSTRACT: Pod dehiscence is necessary for propagation in wild soybean (Glycine soja). It is a major component causing yield losses in cultivated soybean, however, and thus, cultivated soybean varieties have been artificially selected for resistance to pod dehiscence. …”
Publicado 2019
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380por Prince, Silvas J., Vuong, Tri D., Wu, Xiaolei, Bai, Yonghe, Lu, Fang, Kumpatla, Siva P., Valliyodan, Babu, Shannon, J. Grover, Nguyen, Henry T.“…Wild soybean species (Glycine soja Siebold & Zucc.) comprise a unique resource to widen the genetic base of cultivated soybean [Glycine max (L.) …”
Publicado 2020
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