Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition Line

Earlier, we produced a stable Fusarium head blight (FHB)-tolerant durum wheat ( L.) alien disomic addition line, DGE-1 (released in 2008), incorporating chromosome 1E of diploid wheatgrass [ (Host) Á. Löve; 2 = 2 = 14; EE]. For stable FHB resistance, the ultimate goal would be to transfer resistance...

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Main Authors: Prem P. Jauhar, Terrance S. Peterson
Format: Article
Language:English
Published: Wiley 2011-07-01
Series:The Plant Genome
Online Access:https://dl.sciencesocieties.org/publications/tpg/articles/4/2/102
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spelling doaj-aa91fe0cf09c4444818775b5609a81632020-11-25T03:06:26ZengWileyThe Plant Genome1940-33722011-07-014210210910.3835/plantgenome2011.01.0002102Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition LinePrem P. JauharTerrance S. PetersonEarlier, we produced a stable Fusarium head blight (FHB)-tolerant durum wheat ( L.) alien disomic addition line, DGE-1 (released in 2008), incorporating chromosome 1E of diploid wheatgrass [ (Host) Á. Löve; 2 = 2 = 14; EE]. For stable FHB resistance, the ultimate goal would be to transfer resistance from 1E into the durum chromosome 1A or 1B. Such transfer is more likely to occur when these target chromosomes are in a single dose. Therefore, we crossed DGE-1 with ‘Langdon’ substitution lines 1D(1A) and 1D(1B) and produced hybrid derivatives with chromosomes 1A, 1B, 1D, and 1E in a single dose. As an important first step, we standardized a method to readily identify these group-1 chromosomes. Multicolor fluorescent genomic in situ hybridization that we standardized earlier is useful for such identification but is tedious and expensive. To identify these chromosomes more expeditiously and economically in a large plant population, we also used chromosome-specific molecular markers and identified each of the group-1 chromosomes. We used marker to identify chromosome 1A, for 1B, for 1D, and for 1E. , which profiles chromosome 1E, also generated two characteristic bands for chromosome 1D and may therefore be useful in identifying both chromosomes simultaneously.https://dl.sciencesocieties.org/publications/tpg/articles/4/2/102
collection DOAJ
language English
format Article
sources DOAJ
author Prem P. Jauhar
Terrance S. Peterson
spellingShingle Prem P. Jauhar
Terrance S. Peterson
Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition Line
The Plant Genome
author_facet Prem P. Jauhar
Terrance S. Peterson
author_sort Prem P. Jauhar
title Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition Line
title_short Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition Line
title_full Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition Line
title_fullStr Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition Line
title_full_unstemmed Cytological and Molecular Characterization of Homoeologous Group-1 Chromosomes in Hybrid Derivatives of a Durum Disomic Alien Addition Line
title_sort cytological and molecular characterization of homoeologous group-1 chromosomes in hybrid derivatives of a durum disomic alien addition line
publisher Wiley
series The Plant Genome
issn 1940-3372
publishDate 2011-07-01
description Earlier, we produced a stable Fusarium head blight (FHB)-tolerant durum wheat ( L.) alien disomic addition line, DGE-1 (released in 2008), incorporating chromosome 1E of diploid wheatgrass [ (Host) Á. Löve; 2 = 2 = 14; EE]. For stable FHB resistance, the ultimate goal would be to transfer resistance from 1E into the durum chromosome 1A or 1B. Such transfer is more likely to occur when these target chromosomes are in a single dose. Therefore, we crossed DGE-1 with ‘Langdon’ substitution lines 1D(1A) and 1D(1B) and produced hybrid derivatives with chromosomes 1A, 1B, 1D, and 1E in a single dose. As an important first step, we standardized a method to readily identify these group-1 chromosomes. Multicolor fluorescent genomic in situ hybridization that we standardized earlier is useful for such identification but is tedious and expensive. To identify these chromosomes more expeditiously and economically in a large plant population, we also used chromosome-specific molecular markers and identified each of the group-1 chromosomes. We used marker to identify chromosome 1A, for 1B, for 1D, and for 1E. , which profiles chromosome 1E, also generated two characteristic bands for chromosome 1D and may therefore be useful in identifying both chromosomes simultaneously.
url https://dl.sciencesocieties.org/publications/tpg/articles/4/2/102
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AT terrancespeterson cytologicalandmolecularcharacterizationofhomoeologousgroup1chromosomesinhybridderivativesofadurumdisomicalienadditionline
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