4.4 Article

Analysis and mapping quantitative trait loci for histidine content in barley (Hordeum vulgare L.) using microsatellite markers

期刊

GENETIC RESOURCES AND CROP EVOLUTION
卷 68, 期 5, 页码 2107-2118

出版社

SPRINGER
DOI: 10.1007/s10722-021-01121-8

关键词

Barley; Histidine (HIS); Recombinant inbred lines (RILs); QTL mapping; Simple sequence repeat (SSR) markers

资金

  1. China Agriculture Research System [CARS-05-01A04]
  2. National Natural Science Foundation of China [31260326]
  3. International Cooperation Project of Yunnan [2019IB011]
  4. Key R&D Plan of Yunnan [2018BB013]
  5. Science and Technology Benefiting People Program of Yunnan [2016RA032]
  6. R&D Funding Input Subsidy Project of Yunnan and Three-year Plan for Yunnan [2018DS004]

向作者/读者索取更多资源

The study successfully identified QTLs of histidine content in barley grains located on chromosomes 2H, 4H, and 7H, providing a reference for further fine mapping, cloning, and transformation of this gene.
Mining the gene of histidine content in barley grain helps with the breeding of functional barley varieties. The study constructed a recombinant inbred lines (RILs) containing 193 families derived from the cross between Ziguangmangluoerling (ZGMLEL) (female) and Schooner No.3 (male). The histidine (HIS) content in the grain of the mapping population and its parents were determined by an automatic amino acid analyzer. The HIS content of ZGMLEL was 0.53 mg/g. The grain HIS content of Schooner No. 3 was 0.21 mg/g, and the grain HIS content of population ranged from 0.23 to 0.54. Genetic linkage maps, including those of seven chromosomes of barley, were constructed by using 180 pairs of simple sequence repeat (SSR) markers, with a total genetic distance of 2671.03 cM and average marker spacing of 14.84 cM. Quantitative trait locus (QTL) IciMappingV3.3 was used to analyze QTL of HIS content in barley grains, and three QTLs were detected. Mapping results showed that the three loci were located on chromosomes 2H, 4H, and 7H, respectively. The major QTL with a contribution rate of 10.11% was located on barley chromosome 4H (HVBAMMGB84-BMAG0808). The additive effect is positive (0.025). Thus, it comes from the high-value parent ZGMLEL. Another major QTL with a contribution rate of 13.75% was located on barley chromosome 7H (GBM1303-GMS056). The minor QTL with a contribution rate of 6.01% was located on chromosome 2H (Scssr03381-Scssr07759). The additive effects of 4H and 7H QTLs were negative (- 0.02 and - 0.033). So, they came from the male parent Schooner. The results provided a reference for further fine mapping, cloning, and transformation of HIS genes in barley grains.

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