A PCR assay for detection of a 2RL.2BS wheat-rye chromosome translocation

被引:15
作者
Lee, JH
Graybosch, RA
Kaeppler, SM
Sears, RG
机构
[1] UNIV NEBRASKA,DEPT AGRON,USDA,ARS,LINCOLN,NE 68583
[2] KANSAS STATE UNIV,DEPT AGRON,MANHATTAN,KS 66506
关键词
2RL.2BS wheat-rye chromosome translocation; polymerase chain reaction; detection;
D O I
10.1139/g96-076
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A 2RL.2BS wheat-rye translocation, present in the wheat germplasm line Hamlet, carries a gene for resistance to Hessian fly biotype L, one of the most virulent biotypes presently encountered in wheat production environments. Unlike several other wheat-rye chromosome translocations common in wheat breeding programs, 2RL lacks genes encoding storage proteins or other easily selected markers. Oligonucleotide primers synthesized from published sequences derived from the R173 family of moderately repetitive rye DNA were used in the DNA polymerase chain reaction (PCR) to identify specific markers for 2RL. The same primers, when used with DNA extracted from additional wheat-rye translocation lines of importance to the wheat breeding community, gave distinctive PCR products for each genotype. The single primer pair, PAWS5 and PAWS6, may, therefore, have wide applicability for the identification of wheat-rye chromosomal translocations presently encountered in wheat breeding populations.
引用
收藏
页码:605 / 608
页数:4
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