Cereal Crops Research Site Logo
ARS Home About Us Helptop nav spacerContact Us En Espanoltop nav spacer
Printable VersionPrintable Version     E-mail this pageE-mail this page
Agricultural Research Service United States Department of Agriculture
Search
  Advanced Search
 
Programs and Projects
Subjects of Investigation
 

Title: TECHNIQUE FOR RAPID IDENTIFICATION OF PLANTS HETEROZYGOUS FOR THE PH1 DELETION IN WHEAT.

Authors
item Jauhar, Prem
item Peterson, Terrance
item Bergh, Lisa - PLNT SCI, NDSU, FARGO, ND

Submitted to: Agronomy Abstracts
Publication Type: Abstract Only
Publication Acceptance Date: September 1, 2001
Publication Date: October 25, 2001
Citation: Jauhar, P.P., Peterson, T.S., Bergh, L.L. 2001. Technique for rapid identification of plants heterozygous for the ph1 deletion in wheat. Agronomy Abstracts.

Technical Abstract: The Ph1 gene located in the long arm of chromosome 5B controls diploid-like pairing in both bread wheat and durum wheat. Manipulation of this gene helps incorporate alien genes from related species into wheat via sexual hybridization. Maintaining and detecting the ph1b mutant in the heterozygous (Ph1 ph1b) condition usually requires crossing the mutant with rye, followed by scoring of chromosome pairing in the progeny, which is time-consuming. By combining the existing PCR protocols with FISH (fluorescent in situ hybridization) we are attempting to detect the heterozygous state of ph1b or ph1c in wheat mutants or the presence of chromosome 5B in the durum 5D(5B) substitution line before planting the seed. Using the primers, PSR128 and PSR574, which are specific to a region on the long arm of chromosome 5B but are absent in the ph1b (or ph1c) deletion region, we generated a biotin-labeled FISH probe. Somatic chromosome preparations (obtained from root-tips of germinated seed) were then hybridized with the FISH probe specific for the deletion region. The homozygous dominant (Ph1Ph1), the heterozygous (Ph1ph1), or the homozygous recessive (ph1ph1) state of the gene in a seed is shown, respectively, by the presence of a fluorescent band in both chromosomes, one chromosome, or its total absence. Preliminary results are promising and we plan to use a larger fragment for detecting specific sites and obtaining higher visual consistency. We plan to use the same technique to identify a specific wheat chromosome (or even chromosome arm) in our hybrid derivatives and thereby localize alien chromatin integration in it.

   
 
 
Last Modified: 05/21/2013
ARS Home | USDA.gov | Site Map | Policies and Links 
FOIA | Accessibility Statement | Privacy Policy | Nondiscrimination Statement | Information Quality | USA.gov | White House