TY - JOUR
T1 - Comparison of the utility of barley retrotransposon families for genetic analysis by molecular marker techniques
AU - Leigh, F.
AU - Kalendar, R.
AU - Lea, V.
AU - Lee, D.
AU - Donini, P.
AU - Schulman, A. H.
N1 - Funding Information:
Acknowledgements This work was funded by the European Union FP5 initiative projects QLRT-1999-PL1499 and QLK5-CT-2000-01502. DNA was kindly provided by Keygene NV (Wageningen, The Netherlands). The authors wish to thank the two anonymous referees and the Communicating Editor for helpful comments on the manuscript.
Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.
PY - 2003/7/1
Y1 - 2003/7/1
N2 - The Sequence-Specific Amplification Polymorphism (S-SAP) method, and the related molecular marker techniques IRAP (inter-retrotransposon amplified polymorphism) and REMAP (retrotransposon-microsatellite amplified polymorphism), are based on retrotransposon activity, and are increasingly widely used. However, there have been no systematic analyses of the parameters of these methods or of the utility of different retrotransposon families in producing polymorphic, scorable fingerprints. We have generated S-SAP, IRAP, and REMAP data for three barley (Hordeum vulgare L.) varieties using primers based on sequences from six retrotransposon families (BARE-1, BAGY-1, BAGY-2, Sabrina, Nikita and Sukkula). The effect of the number of selective bases on the S-SAP profiles has been examined and the profiles obtained with eight MseI+3 selective primers compared for all the elements. Polymorphisms detected in the insertion pattern of all the families show that each can be used for S-SAP. The uniqueness of each transposition event and differences in the historic activity of each family suggest that the use of multiple retrotransposon families for genetic analysis will find applications in mapping, fingerprinting, and marker-assisted selection and evolutionary studies, not only in barley and other Hordeum species and related taxa, but also more generally.
AB - The Sequence-Specific Amplification Polymorphism (S-SAP) method, and the related molecular marker techniques IRAP (inter-retrotransposon amplified polymorphism) and REMAP (retrotransposon-microsatellite amplified polymorphism), are based on retrotransposon activity, and are increasingly widely used. However, there have been no systematic analyses of the parameters of these methods or of the utility of different retrotransposon families in producing polymorphic, scorable fingerprints. We have generated S-SAP, IRAP, and REMAP data for three barley (Hordeum vulgare L.) varieties using primers based on sequences from six retrotransposon families (BARE-1, BAGY-1, BAGY-2, Sabrina, Nikita and Sukkula). The effect of the number of selective bases on the S-SAP profiles has been examined and the profiles obtained with eight MseI+3 selective primers compared for all the elements. Polymorphisms detected in the insertion pattern of all the families show that each can be used for S-SAP. The uniqueness of each transposition event and differences in the historic activity of each family suggest that the use of multiple retrotransposon families for genetic analysis will find applications in mapping, fingerprinting, and marker-assisted selection and evolutionary studies, not only in barley and other Hordeum species and related taxa, but also more generally.
KW - Barley DNA fingerprinting Inter-retrotransposon amplified polymorphism (IRAP)
KW - Retrotransposon insertional polymorphism
KW - Retrotransposon-microsatellite amplified polymorphism (REMAP)
KW - Sequence-specific amplified polymorphism (S-SAP) markers
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U2 - 10.1007/s00438-003-0850-2
DO - 10.1007/s00438-003-0850-2
M3 - Article
C2 - 12768410
AN - SCOPUS:0043124416
SN - 1617-4615
VL - 269
SP - 464
EP - 474
JO - Molecular Genetics and Genomics
JF - Molecular Genetics and Genomics
IS - 4
ER -