assessment of the genetic diversity within a collection of Saccharum spontaneum L. with RAPD-PCR

A local collection of 33 Saccharum spontaneum L. clones and two sugarcane cultivars (LCP 82-89 and LCP 85-384) were assessed for genetic variability using random amplified polymorphic DNA (RAPD)-PCR. A total of 157 polymorphic RAPD-PCR bands were scored with 17 primers. The number of RAPD-PCR produc...

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Veröffentlicht in:Genetic resources and crop evolution 2004-12, Vol.51 (8), p.895-903
Hauptverfasser: Pan, Y.B, Burner, D.M, Legendre, B.L, Grisham, M.P, White, W.H
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container_end_page 903
container_issue 8
container_start_page 895
container_title Genetic resources and crop evolution
container_volume 51
creator Pan, Y.B
Burner, D.M
Legendre, B.L
Grisham, M.P
White, W.H
description A local collection of 33 Saccharum spontaneum L. clones and two sugarcane cultivars (LCP 82-89 and LCP 85-384) were assessed for genetic variability using random amplified polymorphic DNA (RAPD)-PCR. A total of 157 polymorphic RAPD-PCR bands were scored with 17 primers. The number of RAPD-PCR products per primer ranged from four to 16. The data were analyzed with two multivariate analysis software programs, NTSYSpc and DNAMAN. Although these two programs yielded similar results, a bootstrapped phylogenetic tree could only be generated with the DNAMAN software. A substantial degree of genetic diversity was found within the local S. spontaneum collection. Pairwise genetic homology coefficients ranged from 65% (SES, 196/Tainan 2n = 96) to 88.5% (IND 81-80/IND 81-144). LCP 82-89 and LCP 85-384 shared a greater similarity (82%) than either was to any clone of S. spontaneum (ranging from 60.5 to 75.2%). The 33 S. spontaneum clones were assigned to eight groups independent of their geographic origin or morphology, while the two sugarcane cultivars were assigned to the ninth group. All but two pairs of S. spontaneum clones could be distinguished by a single RAPD primer OPBB-02. The use of a second primer, either OPBE-04 or Primer 262, separated all S. spontaneum clones. One amplification product from the RAPD primer OPA-11, OPA-11-336, proved to be cultivar-specific and has been adopted for use in our breeding program. Information from this study would help conserve the genetic diversity of S. spontaneum.
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A total of 157 polymorphic RAPD-PCR bands were scored with 17 primers. The number of RAPD-PCR products per primer ranged from four to 16. The data were analyzed with two multivariate analysis software programs, NTSYSpc and DNAMAN. Although these two programs yielded similar results, a bootstrapped phylogenetic tree could only be generated with the DNAMAN software. A substantial degree of genetic diversity was found within the local S. spontaneum collection. Pairwise genetic homology coefficients ranged from 65% (SES, 196/Tainan 2n = 96) to 88.5% (IND 81-80/IND 81-144). LCP 82-89 and LCP 85-384 shared a greater similarity (82%) than either was to any clone of S. spontaneum (ranging from 60.5 to 75.2%). The 33 S. spontaneum clones were assigned to eight groups independent of their geographic origin or morphology, while the two sugarcane cultivars were assigned to the ninth group. All but two pairs of S. spontaneum clones could be distinguished by a single RAPD primer OPBB-02. The use of a second primer, either OPBE-04 or Primer 262, separated all S. spontaneum clones. One amplification product from the RAPD primer OPA-11, OPA-11-336, proved to be cultivar-specific and has been adopted for use in our breeding program. 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subjects clones
cultivars
DNA primers
genetic variation
germplasm
plant genetic resources
polymerase chain reaction
random amplified polymorphic DNA technique
Saccharum spontaneum
sugarcane
title assessment of the genetic diversity within a collection of Saccharum spontaneum L. with RAPD-PCR
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