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RESEARCH ARTICLE

Assessment of genetic diversity in Australian canola (Brassica napus L.) cultivars using SSR markers

J. Wang A , S. Kaur B , N. O. I. Cogan B , M. P. Dobrowolski A , P. A. Salisbury B D , W. A. Burton B , R. Baillie B , M. Hand B , C. Hopkins B , J. W. Forster B C , K. F. Smith B C and G. Spangenberg B C E
+ Author Affiliations
- Author Affiliations

A Department of Primary Industries, Biosciences Research Division, Hamilton Centre, Mount Napier Road, Hamilton, Vic. 3300, Australia.

B Department of Primary Industries, Biosciences Research Division, Victorian AgriBiosciences Centre, La Trobe University Research and Development Park, Bundoora, Vic. 3083, Australia.

C Department of Life Sciences, La Trobe University, Bundoora, Vic. 3083, Australia.

D Melbourne School of Land and Environment, The University of Melbourne, Parkville, Vic. 3010, Australia.

E Corresponding author. Email: german.spangenberg@dpi.vic.gov.au

Crop and Pasture Science 60(12) 1193-1201 https://doi.org/10.1071/CP09165
Submitted: 9 June 2009  Accepted: 25 August 2009   Published: 23 November 2009

Abstract

Australian canola (Brassica napus L.) has been relatively isolated from the global gene pool and limited knowledge is available for genetic variability based on DNA profiling. In the present study, genetic diversity of recent Australian canola cultivars was determined by simple sequence repeat (SSR) marker analysis. In total, 405 individuals from 48 varieties were genotyped with 18 primer pairs, resulting in 112 polymorphic features. The number of polymorphic features amplified by each SSR primer pair varied from 3 to 16. Analysis of molecular variance (AMOVA) detected 53.7% and 46.3% within- and between-cultivar variation, respectively. Intra-cultivar genetic variability differed according to cultivar. The number of polymorphic features per cultivar varied from 35 (Ag-Spectrum) to 72 (Ag-Insignia), while mean sum of squares (MSS) varied from 6.29 (Tornado TT) to 24.76 (Ag-Emblem). Genetic differentiation of cultivars generally reflected pedigree structure and origin by breeding organisation. Clustering and principal coordinate analysis (PCoA) indicated that the individuals were separated into 4 major groups. The genetic diversity information from this study will be useful for future Australian canola breeding programs.

Additional keywords: AMOVA, cluster, PCA, rapeseed.


Acknowledgments

The authors thank the following DPI staff for their input during data collection and analysis: K. Lawless, E. vanZijl de Jong, A. Keniry, and H. Mountford.


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