DNA markers for Typhula resistance in timothy (Phleum pratense L.)

The objective of the study was to find DNA markers associated with resistance to Typhula ishikariensis in timothy (Phleum pratense L.) using bulked-segregant analysis. A progeny of 161 F1 individuals was created by crossing the Finnish resistant cultivar Tammisto II with the Japanese susceptible cu...

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Main Authors: Pirjo Tanhuanpää, Mika Isolahti, Nissinen Oiva, Outi Manninen
Format: Article
Language:English
Published: Scientific Agricultural Society of Finland 2016-11-01
Series:Agricultural and Food Science
Subjects:
Online Access:https://journal.fi/afs/article/view/58477
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spelling doaj-fe3ffbe0805a47c5b0059355a7081b342020-11-25T02:45:41ZengScientific Agricultural Society of FinlandAgricultural and Food Science1459-60671795-18952016-11-0125310.23986/afsci.58477DNA markers for Typhula resistance in timothy (Phleum pratense L.)Pirjo Tanhuanpää0Mika Isolahti1Nissinen Oiva2Outi Manninen3Green Technology, Natural Resources Institute Finland (Luke), Myllytie 1, FI-31600 Jokioinen, FinlandBoreal Plant Breeding Ltd, Myllytie 10, FI-31600 Jokioinen, FinlandFormerly at: MTT Agrifood Research Finland, Eteläranta 55, 96300 Rovaniemi, FinlandBoreal Plant Breeding Ltd, Myllytie 10, FI-31600 Jokioinen, Finland The objective of the study was to find DNA markers associated with resistance to Typhula ishikariensis in timothy (Phleum pratense L.) using bulked-segregant analysis. A progeny of 161 F1 individuals was created by crossing the Finnish resistant cultivar Tammisto II with the Japanese susceptible cultivar Nosappu. Six to ten clones of each F1 individual were tested for resistance in the greenhouse, and a survival index, which was based both on survival and the ability of plants to recover, was calculated for each F1 to describe resistance. Resistant and susceptible bulks of eight individuals in each were screened with a total of 292 primer combinations. Six DNA markers were found to be associated with resistance, together explaining 15% of phenotypic variation in Typhula resistance. Four of the markers formed one linkage group, which contained a QTL explaining 7% of the variation in Typhula resistance. https://journal.fi/afs/article/view/58477bulked segregant analysis (BSA)DNA markersdisease resistancePhleum pratensetimothyTyphula ishikariensis
collection DOAJ
language English
format Article
sources DOAJ
author Pirjo Tanhuanpää
Mika Isolahti
Nissinen Oiva
Outi Manninen
spellingShingle Pirjo Tanhuanpää
Mika Isolahti
Nissinen Oiva
Outi Manninen
DNA markers for Typhula resistance in timothy (Phleum pratense L.)
Agricultural and Food Science
bulked segregant analysis (BSA)
DNA markers
disease resistance
Phleum pratense
timothy
Typhula ishikariensis
author_facet Pirjo Tanhuanpää
Mika Isolahti
Nissinen Oiva
Outi Manninen
author_sort Pirjo Tanhuanpää
title DNA markers for Typhula resistance in timothy (Phleum pratense L.)
title_short DNA markers for Typhula resistance in timothy (Phleum pratense L.)
title_full DNA markers for Typhula resistance in timothy (Phleum pratense L.)
title_fullStr DNA markers for Typhula resistance in timothy (Phleum pratense L.)
title_full_unstemmed DNA markers for Typhula resistance in timothy (Phleum pratense L.)
title_sort dna markers for typhula resistance in timothy (phleum pratense l.)
publisher Scientific Agricultural Society of Finland
series Agricultural and Food Science
issn 1459-6067
1795-1895
publishDate 2016-11-01
description The objective of the study was to find DNA markers associated with resistance to Typhula ishikariensis in timothy (Phleum pratense L.) using bulked-segregant analysis. A progeny of 161 F1 individuals was created by crossing the Finnish resistant cultivar Tammisto II with the Japanese susceptible cultivar Nosappu. Six to ten clones of each F1 individual were tested for resistance in the greenhouse, and a survival index, which was based both on survival and the ability of plants to recover, was calculated for each F1 to describe resistance. Resistant and susceptible bulks of eight individuals in each were screened with a total of 292 primer combinations. Six DNA markers were found to be associated with resistance, together explaining 15% of phenotypic variation in Typhula resistance. Four of the markers formed one linkage group, which contained a QTL explaining 7% of the variation in Typhula resistance.
topic bulked segregant analysis (BSA)
DNA markers
disease resistance
Phleum pratense
timothy
Typhula ishikariensis
url https://journal.fi/afs/article/view/58477
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