4.7 Article

An approach for high-resolution genetic mapping of distant wild relatives of bread wheat: example of fine mapping of Lr57 and Yr40 genes

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THEORETICAL AND APPLIED GENETICS
卷 134, 期 8, 页码 2671-2686

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SPRINGER
DOI: 10.1007/s00122-021-03851-w

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  1. US Department of Agriculture-National Institute of Food and Agriculture [2020-67013-32558, 2020-67013-31460]
  2. US National Science Foundation [1943155]
  3. Division Of Integrative Organismal Systems
  4. Direct For Biological Sciences [1943155] Funding Source: National Science Foundation

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The article introduces a simple and powerful approach for high-resolution mapping of important genes from distant relatives of wheat, which can be used for eventual map-based cloning. By utilizing existing germplasm resources, this method opens up new possibilities for researchers to access and study important genes in tertiary gene pools of wheat.
Key message The article reports a powerful but simple approach for high-resolution mapping and eventual map-based cloning of agronomically important genes from distant relatives of wheat, using the already existing germplasm resources. Wild relatives of wheat are a rich reservoir of genetic diversity for its improvement. The effective utilization of distant wild relatives in isolation of agronomically important genes is hindered by the lack of recombination between the homoeologous chromosomes. In this study, we propose a simple yet powerful approach that can be applied for high-resolution mapping of a targeted gene from wheat's distant gene pool members. A wheat-Aegilops geniculata translocation line TA5602 with a small terminal segment from chromosome 5 M-g of Ae. geniculata translocated to 5D of wheat contains genes Lr57 and Yr40 for leaf rust and stripe rust resistance, respectively. To map these genes, TA5602 was crossed with a susceptible Ae. geniculata 5 M-g addition line. Chromosome pairing between the 5 M-g chromosomes of susceptible and resistant parents resulted in the development of a high-resolution mapping panel for the targeted genes. Next-generation-sequencing data from flow-sorted 5 M-g chromosome of Ae. geniculata allowed us to generate 5 M-g-specific markers. These markers were used to delineate Lr57 and Yr40 genes each to distinct similar to 1.5 Mb physical intervals flanked by gene markers on 5 M-g. The method presented here will allow researchers worldwide to utilize existing germplasm resources in genebanks and seed repositories toward routinely performing map-based cloning of important genes from tertiary gene pools of wheat.

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