2013
DOI: 10.2135/cropsci2012.07.0446
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Validation of Molecular Markers for New Stem Rust Resistance Genes in U.S. Hard Winter Wheat

Abstract: Stem rust, caused by Puccinia graminis f. sp. tritici (Pgt), is one of the most serious diseases of wheat (Triticum aestivum L.) worldwide. The discovery of new Pgt races in Africa, Ug99 and its variants, brings a new threat to global wheat production. Pyramiding several stem rust resistance genes into adapted varieties as opposed to breeding varieties with a single resistance gene is considered a more effective method to combat new races, but the success of gene pyramiding depends on the availability of molec… Show more

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Cited by 24 publications
(21 citation statements)
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References 40 publications
(53 reference statements)
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“…A set of 174 advanced winter wheat breeding lines from the USDA‐ARS‐coordinated Southern Regional Performance Nursery (SRPN) from 2008 to 2012 were screened with markers linked to various genes at the USDA‐ARS Central Small Grain Genotyping Laboratory, Manhattan, KS, following the protocol from Bernardo et al (2013) (Supplemental Table S3; Supplemental Fig. S2).…”
Section: Arthropod and Virus Resistancementioning
confidence: 99%
“…A set of 174 advanced winter wheat breeding lines from the USDA‐ARS‐coordinated Southern Regional Performance Nursery (SRPN) from 2008 to 2012 were screened with markers linked to various genes at the USDA‐ARS Central Small Grain Genotyping Laboratory, Manhattan, KS, following the protocol from Bernardo et al (2013) (Supplemental Table S3; Supplemental Fig. S2).…”
Section: Arthropod and Virus Resistancementioning
confidence: 99%
“…Polymerase chain reaction was performed in a PTC‐200 thermal cycler (Bio‐Rad Labs, Hercules, CA) using a touchdown program starting at 96°C for 5 min; followed by 5 cycles of 1 min at 96°C, 5 min at 68°C minus 2°C per cycle, and 1 min at 72°C; 5 cycles of 1 min at 96°C, 2 min at 58°C minus 2°C per cycle, and 1 min at 72°C; 25 cycles of 1 min at 96°C, 1 min at 50°C, and 1 min at 72°C; and a final extension of 5 min at 72°C. Primers labeled with FAM, VIC, NED, or PET (Life Technologies, Grand Island, NY) were run as described by Bernardo et al (2013). Fluorescent dye‐labeled PCR products were visualized on an ABI3730 sequencer (Life Technologies) and were scored using GeneMarker V1.5 (SoftGenetics, State College, PA).…”
Section: Methodsmentioning
confidence: 99%
“…н.) (Dundas et al, 2007;Bernardo et al, 2013). Результаты анализа продуктов ПЦР по обо-им маркерам совпали.…”
Section: идентификация генов Sr с использованием молекулярных маркеровunclassified
“…Оба маркера идентифицировали Sr32 у контрольных линий C77.19.SR32 и CnsSr32AS, несущих транслокацию от Ae. speltoides в хромосоме 2B (McIntosh et al, 1995;Bernardo et al, 2013), а также у ана-лизируемых линий 119/4-06rw, 9/00w и сорта Донская полукарликовая.…”
Section: идентификация генов Sr с использованием молекулярных маркеровunclassified
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