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Molecular Breeding

, 39:17 | Cite as

Identification of a new GmSACPD-C allele in high stearic acid mutant Hfa180 derived from gamma-ray irradiation

  • Sang Hun Kim
  • Jaihyunk Ryu
  • Woon Ji Kim
  • Ryulyi Kang
  • Eunju Seo
  • Gyutae Kim
  • Si-Yong Kang
  • Jeong-Dong Lee
  • Bo-Keun HaEmail author
Article
  • 12 Downloads

Abstract

Stearic acid is the most important saturated fatty acid compound in soybean oil. A typical soybean cultivar has 2–3% stearic acid content of total oil. Recently, a new high stearic acid mutant Hfa180 was developed from gamma-ray irradiation with “Ilmikong.” The objectives of this study were to identify the mutant gene associated with high stearic acid content in Hfa180 and to develop a Kompetitive Allele-Specific PCR (KASP) assay for selection of soybeans with elevated levels of stearic acid in seeds. Target sequencing of the whole GmSACPD-C gene encoding D9-stearoyl-ACP-desaturase revealed that Hfa180 contained a three-base-pair deletion (GAG) at genomic positions 190 to 192 of the 1st exon of GmSACPD-C. The three-base deletion caused a variant with a single amino acid (glutamine) deletion at position 64 in the predicted GmSACPD-C amino acid in Hfa180, as well as an average 60% reduction in GmSACPD-C gene expression in Hfa180 compared to that of the wild type. Genetic linkage analysis using the F2 population derived from a crossing between Hfa180 and the wild-type “Deapung” confirmed that the mutation allele of GmSACPD-C was perfectly correlated with elevation of seed stearic acid content. In addition, a KASP marker was developed to identify the mutation allele on the GmSACPD-C gene, which was successfully applied to select high stearic acid soybean lines. The identification of the mutant gene of the high stearic acid mutant Hfa180 and development of the KASP marker could be useful for improving stearic acid content in soybean oil.

Keywords

Soybean High stearic acid Mutation Gamma ray Fatty acid 

Notes

Author contribution

Sang Hun Kim and Jaihyunk Ryu conducted experiments and data analysis, and wrote the manuscript. Woon Ji Kim contributed to the development of the F2 mapping population. Ryulyi Kang and Eunju Seo contributed to the KASP genotyping assay. Gyutae Kim contributed to the RT-PCR assay. Si-Yong Kang contributed to the gamma-ray irradiated population. Jeong-Dong Lee contributed to the fatty-acid determination. Bo-Keun Ha designed the study and reviewed and edited the manuscript. All authors read and approved the final manuscript.

Funding information

This work was carried out with the support of the “Cooperative Research Program for Agriculture Science and Technology Development (Project No. PJ012214)” Rural Development Administration and the National Research Foundation of Korea (NRF) (NRF-2018M2A2A6A05057264), Republic of Korea.

Compliance with ethical standards

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

This study does not include human or animal subjects.

Supplementary material

11032_2019_928_MOESM1_ESM.docx (1.9 mb)
ESM 1 (DOCX 1970 kb)

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Copyright information

© Springer Nature B.V. 2019

Authors and Affiliations

  1. 1.Division of Plant BiotechnologyChonnam National UniversityGwangjuRepublic of Korea
  2. 2.Advanced Radiation Technology InstituteKorea Atomic Energy Research InstituteJeongeupRepublic of Korea
  3. 3.School of Applied BiosciencesKyungpook National UniversityDaeguRepublic of Korea

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