TY - JOUR
T1 - Isolation and Characterization of the Soybean Sg-3 Gene that is Involved in Genetic Variation in Sugar Chain Composition at the C-3 Position in Soyasaponins
AU - Yano, Ryoichi
AU - Takagi, Kyoko
AU - Tochigi, Saeko
AU - Fujisawa, Yukiko
AU - Nomura, Yuhta
AU - Tsuchinaga, Hiroki
AU - Takahashi, Yuya
AU - Takada, Yoshitake
AU - Kaga, Akito
AU - Anai, Toyoaki
AU - Tsukamoto, Chigen
AU - Seki, Hikaru
AU - Muranaka, Toshiya
AU - Ishimoto, Masao
N1 - Funding Information:
This work was supported by the Program for the Promotion of Basic and Applied Research for Innovations in the Bio-oriented Industry (BRAIN) [to H.S., T.M. and M.I.]; the Ministry of Agriculture, Forestry and Fisheries of Japan and the Scientific Technique Research Promotion Program for Agriculture, Forestry, Fisheries and Food Industry [to H.S., T.M. and M.I.]; Genomics-based Technology for Agricultural Improvement [to A.K., T.A. and M.I.]; and the National Institute of Agrobiological Sciences (NIAS) Strategic Research Fund [to A.K. and M.I].
Publisher Copyright:
© The Author(s) 2018. Published by Oxford University Press on behalf of Japanese Society of Plant Physiologists. All rights reserved.
PY - 2018/4/1
Y1 - 2018/4/1
N2 - Soyasaponins are specialized metabolites present in soybean seeds that affect the taste and quality of soy-based foods. The composition of the sugar chains attached to the aglycone moiety of soyasaponins is regulated by genetic loci such as sg-1, sg-3 and sg-4. Here, we report the cloning and characterization of the Sg-3 gene, which is responsible for conjugating the terminal (third) glucose (Glc) at the C-3 sugar chain of soyasaponins. The gene Glyma.10G104700 is disabled in the sg-3 cultivar, € Mikuriya-ao', due to the deletion of genomic DNA that results in the absence of a terminal Glc residue on the C-3 sugar chain. Sg-3 encodes a putative glycosyltransferase (UGT91H9), and its predicted protein sequence has a high homology with that of the product of GmSGT3 (Glyma.08G181000; UGT91H4), which conjugates rhamnose (Rha) to the third position of the C-3 sugar chain in vitro. A recombinant Glyma.10G104700 protein could utilize UDP-Glc as a substrate to conjugate the third Glc to the C-3 sugar chain, and introducing a functional Glyma.10G104700 transgene into the mutant complemented the sg-3 phenotype. Conversely, induction of a premature stop codon mutation in Glyma.10G104700 (W270∗) resulted in the sg-3 phenotype, suggesting that Glyma.10G104700 was Sg-3. The gmsgt3 (R339H) mutant failed to accumulate soyasaponins with the third Rha at the C-3 sugar chain, and the third Glc and Rha conjugations were both disabled in the sg-3 gmsgt3 double mutant. These results demonstrated that Sg-3 and GmSGT3 are non-redundantly involved in conjugation of the third Glc and Rha at the C-3 sugar chain of soyasaponins, respectively.
AB - Soyasaponins are specialized metabolites present in soybean seeds that affect the taste and quality of soy-based foods. The composition of the sugar chains attached to the aglycone moiety of soyasaponins is regulated by genetic loci such as sg-1, sg-3 and sg-4. Here, we report the cloning and characterization of the Sg-3 gene, which is responsible for conjugating the terminal (third) glucose (Glc) at the C-3 sugar chain of soyasaponins. The gene Glyma.10G104700 is disabled in the sg-3 cultivar, € Mikuriya-ao', due to the deletion of genomic DNA that results in the absence of a terminal Glc residue on the C-3 sugar chain. Sg-3 encodes a putative glycosyltransferase (UGT91H9), and its predicted protein sequence has a high homology with that of the product of GmSGT3 (Glyma.08G181000; UGT91H4), which conjugates rhamnose (Rha) to the third position of the C-3 sugar chain in vitro. A recombinant Glyma.10G104700 protein could utilize UDP-Glc as a substrate to conjugate the third Glc to the C-3 sugar chain, and introducing a functional Glyma.10G104700 transgene into the mutant complemented the sg-3 phenotype. Conversely, induction of a premature stop codon mutation in Glyma.10G104700 (W270∗) resulted in the sg-3 phenotype, suggesting that Glyma.10G104700 was Sg-3. The gmsgt3 (R339H) mutant failed to accumulate soyasaponins with the third Rha at the C-3 sugar chain, and the third Glc and Rha conjugations were both disabled in the sg-3 gmsgt3 double mutant. These results demonstrated that Sg-3 and GmSGT3 are non-redundantly involved in conjugation of the third Glc and Rha at the C-3 sugar chain of soyasaponins, respectively.
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U2 - 10.1093/pcp/pcy019
DO - 10.1093/pcp/pcy019
M3 - Article
C2 - 29401289
AN - SCOPUS:85045510406
SN - 0032-0781
VL - 59
SP - 792
EP - 805
JO - Plant and Cell Physiology
JF - Plant and Cell Physiology
IS - 4
ER -