Title page for ETD etd-08182004-104543


Type of Document Dissertation
Author Mammadov, Jafar
Author's Email Address jmammado@vt.edu
URN etd-08182004-104543
Title Towards Cloning the Leaf Rust Resistance Gene Rph5
Degree PhD
Department Crop and Soil Environmental Sciences
Advisory Committee
Advisor Name Title
Maroof, M. A. Saghai Committee Chair
Buss, Glenn R. Committee Member
Esen, Asim Committee Member
Griffey, Carl A. Committee Member
Jelesko, John G. Committee Member
Keywords
  • Expressed Sequence Tag (EST)
  • high resolution map
  • Rph5
  • contig
  • barley
  • Bacterial Artificial Chromosome (BAC)
  • leaf rust
  • synteny
  • comparative mapping
  • molecular mapping
  • marker-assisted selection
  • gene pyramiding
  • Resistance Gene Analog (RGA)
  • rice
  • physical mapping
Date of Defense 2004-08-02
Availability unrestricted
Abstract
Leaf rust caused by Puccinia hordei is an important disease of barley (Hordeum vulgare) in many regions of the world. Yield losses up to 62% have been reported in susceptible cultivars. The Rph5 gene confers resistance to the most prevalent races (8 and 30) of barley leaf rust in the United States. Therefore, the molecular mapping of Rph5 is of great interest. Genetic studies were performed by analysis of 93 and 91 F2 plants derived from the crosses 'Bowman' (rph5) x 'Magnif 102' (Rph5) and 'Moore' (rph5) x Virginia 92-42-46 (Rph5), respectively. Linkage analysis positioned the Rph5 locus to the extreme telomeric region of the short arm of barley chromosome 3H at 0.2 cM proximal to RFLP marker VT1 and 0.5 cM distal from RFLP marker C970 in the Bowman x Magnif 102 population. Synteny between rice chromosome 1 and barley chromosome 3 was employed to saturate the region within the sub-centimorgan region around Rph5 using sequence-tagged site (STS) markers that were developed based on barley expressed sequence tags (ESTs) syntenic to the phage (P1)-derived artificial chromosome (PAC) clones comprising distal region of the rice chromosome 1S. Five rice PAC clones were used as queries to blastn 370,258 barley ESTs. Ninety four non-redundant EST sequences were identified from the EST database and used as templates to design 174 pairs of primer combinations. As a result, 10 EST-based STS markers were incorporated into the 'Bowman' x 'Magnif 102' high-resolution map of the Rph5 region. More importantly, six markers, including five EST-derived STS sequences, co-segregate with Rph5. Genes, represented by these markers, are putative candidates for Rph5. Results of this study demonstrate the usefulness of rice genomic resources for efficient deployment of barley EST resources for marker saturation of targeted barley genomic region.
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