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Published online 20 May 2008
Published in Crop Sci 48:1098-1106 (2008)
© 2008 Crop Science Society of America
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Development and Characterization of Microsatellite Markers for the Grain Amaranths

Melanie A. Mallorya, Rozaura V. Halla, Andrea R. McNabba, Donald B. Prattb, Eric N. Jellena and Peter J. Maughana,*

a Dep. of Plant and Animal Sci., Brigham Young University, Dep. of Plant & Animal Sciences, Provo, UT 84602
b Dep. of Biology, Stephen F. Austin State Univ., Nacogdoches, TX 75962

* Corresponding author (Jeff_Maughan{at}byu.edu).

The grain amaranths (Amaranthus hypochondriacus L., A. cruentus L., and A. caudatus L.) are important pseudo-cereals native to the Americas. The objective of this project was to produce and characterize a set of highly informative, reproducible microsatellite markers for the grain amaranths. A total of 1457 clones were sequenced from three microsatellite-enriched libraries. Of these, 353 contained unique microsatellites. An additional 29 microsatellite loci were identified from 728 bacterial artificial chromosome–end sequences. A total of 179 microsatellites were polymorphic across accessions from the three grain amaranths. Among these polymorphic microsatellite loci, a total of 731 alleles were identified with an average of four alleles per locus. Heterozygosity values ranged from 0.14 to 0.83, with a mean value of 0.62. Thirty-seven (21%) of the markers were polymorphic between the parents of a segregating population. Phylogenetic analysis using the marker data placed A. hybridus L. accessions into two of the three grain amaranth clades, suggesting the polyphyletic evolution of the three cultivated species from different A. hybridus ancestors. The transferability of these markers to A. hybridus, A. powellii S. Wats., and A. retroflexus L. is reported and suggests that these markers may be useful in studying other species within the genus Amaranthus, including several economically important weeds and ornamentals.

Abbreviations: AFLP, amplified fragment length polymorphism • BAC, bacterial artificial chromosome • BES, BAC-end sequence • H, heterozygosity • MAX, longest tandem repeat excluding half-repeats • ONA, observed number of alleles • PCR, polymerase chain reaction • SSR, simple sequence repeat


This research was funded by a Stephen F. Austin State University faculty research grant, as well as grants from the Ezra Taft Benson Agriculture and Food Institute and the Holmes Family Foundation. We gratefully acknowledge Dr. David McClellan (BYU) for his assistance with phylogenetic analyses. We also express our appreciation to Jimena Alvarez Soto and Mary N. Karanu for technical assistance in developing the microsatellite protocols.

All rights reserved. No part of this periodical may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any information storage and retrieval system, without permission in writing from the publisher. Permission for printing and for reprinting the material contained herein has been obtained by the publisher.

Received for publication August 16, 2007.





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