<p>The allelic variations of high-molecular-weight glutenin subunit locus in common wheat (<i>Triticum aestivum</i> L.) markedly influence grain end-use quality. <i>GLU</i>-<i>A1</i>, <i>GLU</i>-<i>B1</i>, and <i>GLU</i>-<i>D1</i>, which encode high-molecular-weight glutenin subunits, are located on the long arms of chromosomes 1A, 1B, and 1D, respectively. However, existing markers for distinguishing alleles at the <i>GLU-A1</i> and <i>GLU-D1</i> are limited with regard to both number and resolution. In the present study, we enhanced the utility of PCR-based allele detection by developing seven new agarose gel-based markers capable of differentiating four <i>Glu</i>-<i>A1x</i>, four <i>Glu</i>-<i>D1x</i>, and two <i>Glu</i>-<i>D1y</i> alleles. These new markers, in combination with previously published PCR markers, were used to successfully identify the <i>Glu</i>-<i>A1 × 1</i>, <i>Glu</i>-<i>A1 x 2</i>*, <i>Glu</i>-<i>A1 x 2.1</i>*, and <i>Glu</i>-<i>A1x-null</i> alleles and the <i>Glu</i>-<i>D1 x 5</i>, <i>Glu</i>-<i>D1 x 2</i>, <i>Glu</i>-<i>D1 x 2.1</i>, and <i>Glu</i>-<i>D1 x 2.2</i> alleles across 25 wheat resources. Additionally, we developed a novel marker that enables us to distinguish between the <i>Glu</i>-<i>D1y10</i> and <i>Glu</i>-<i>D1y12</i> alleles more clearly than conventional markers. These improved PCR markers represent a reliable and efficient tool for detecting allelic variations at the <i>GLU-A1</i> and <i>GLU-D1</i> loci. They are expected to serve as valuable resources for marker-assisted selection and marker-assisted backcrossing aimed at improving the processing quality of wheat.</p>

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Development of PCR-based markers for the identification of wheat HMW glutenin subunit alleles at the GLU-A1 and GLU-D1 loci

  • Myoung Hui Lee,
  • Chon-Sik Kang,
  • Myoung-Goo Choi,
  • Jun-Seok Choi,
  • Min-Ju Kim,
  • Mira Yoon,
  • Kyeong-Min Kim,
  • Changhyun Choi

摘要

The allelic variations of high-molecular-weight glutenin subunit locus in common wheat (Triticum aestivum L.) markedly influence grain end-use quality. GLU-A1, GLU-B1, and GLU-D1, which encode high-molecular-weight glutenin subunits, are located on the long arms of chromosomes 1A, 1B, and 1D, respectively. However, existing markers for distinguishing alleles at the GLU-A1 and GLU-D1 are limited with regard to both number and resolution. In the present study, we enhanced the utility of PCR-based allele detection by developing seven new agarose gel-based markers capable of differentiating four Glu-A1x, four Glu-D1x, and two Glu-D1y alleles. These new markers, in combination with previously published PCR markers, were used to successfully identify the Glu-A1 × 1, Glu-A1 x 2*, Glu-A1 x 2.1*, and Glu-A1x-null alleles and the Glu-D1 x 5, Glu-D1 x 2, Glu-D1 x 2.1, and Glu-D1 x 2.2 alleles across 25 wheat resources. Additionally, we developed a novel marker that enables us to distinguish between the Glu-D1y10 and Glu-D1y12 alleles more clearly than conventional markers. These improved PCR markers represent a reliable and efficient tool for detecting allelic variations at the GLU-A1 and GLU-D1 loci. They are expected to serve as valuable resources for marker-assisted selection and marker-assisted backcrossing aimed at improving the processing quality of wheat.