4.7 Article

The development of sequence-tagged sites (STSs) in Lolium perenne L.:: the application of primer sets derived from other genera

Journal

THEORETICAL AND APPLIED GENETICS
Volume 103, Issue 4, Pages 648-658

Publisher

SPRINGER-VERLAG
DOI: 10.1007/PL00002920

Keywords

sequence tagged sites; PCR; homology; wheat; barley; Lolium; forage grasses

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Genetic analysis, particularly the development of genetic linkage maps in forage grass species, lags well behind other members of the Poaceae. Comparative mapping within this family has revealed extensive conservation in gene and marker synteny among chromosomes of diverse genera. Recently, the ability to transfer mapped STS markers between barley and wheat has been demonstrated. The transfer of mapped STS markers between cereals and forage grasses could provide PCR-based markers for comparative mapping in these species providing they amplify homologous sequences. In this study, primers derived from three barley genes of defined function and a gene from Phalaris coerulescens were used to amplify homologous fragments in Lolium perenne. Primers derived from two barley and two oat cDNA clones were also tested along with eight barley and two Triticum tauchii STS markers. Twenty one primer pairs derived from 18 loci were tested. Eleven primer pairs (52%) amplified homologous sequences in L. perenne from ten (55%) of the loci targetted. Thirteen new STS markers were generated in L. perenne, of which ten have been mapped in barley or rye and amplify homologous sequences in L. perenne.

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