|
|
||||||||
Dep. of Crop and Soil Science, Oregon State Univ., Corvalis, OR 97331-3002
* Corresponding author (knapps{at}css.orst.edu).
Cultivated sunflower (Helianthus annuus L.) seems to have originated from a small number of ancestral germplasm sources. The number of key ancestors and how much each ancestor has contributed to the genetic diversity of public inbred lines is not known. We used coancestry analysis to assess this. The pedigrees of publicly released inbred lines were traced as far back as possible. Coancestries were estimated among 106 oilseed and 50 confectionery inbred lines and 157 ancestral germplasm sources. Cluster and principal component analyses of the coancestry matrix separated lines into broad market (oilseed versus confectionery) and fertility restorer (restorer versus maintainer) classes. There were four subgroups among oilseed maintainer lines (B-lines) and three subgroups among oilseed restorer lines (R-lines); however, the R-line subgroups were heterogeneous and the boundaries between them were not sharp. These B and R subgroups may constitute heterotic groups. Sixty-eight percent of oilseed R-line diversity traced to seven germplasm sources, while 73% of oilseed B-line diversity traced to eight germplasm sources. Seventy-three percent of confectionery R-line diversity traced to two germplasm sources, while 65% of confectionery B-line diversity traced to four germplasm sources. The mean coancestry between oilseed R-lines was 0.25, between oilseed B-lines was 0.10, between confectionery Rlines was 0.31, and between confectionery B-lines was 0.25; thus, the genetic diversity among oilseed B-lines seems to be wider than among lines within other groups. Pedigree analysis created a nearly complete framework of heterotic groups for public germplasm developed in the USA, even though some lines could not be assigned to heterotic groups because of incomplete pedigree data. By combining pedigree and DNA fingerprint data, a more comprehensive picture of heterotic groups should emerge for cultivated sunflower.
Received for publication July 7, 1997.
This article has been cited by other articles:
![]() |
B. Yue, X. Cai, B. A. Vick, and J. Hu Genetic Diversity and Relationships among 177 Public Sunflower Inbred Lines Assessed by TRAP Markers Crop Sci., June 26, 2009; 49(4): 1242 - 1249. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. M. Kolkman, S. T. Berry, A. J. Leon, M. B. Slabaugh, S. Tang, W. Gao, D. K. Shintani, J. M. Burke, and S. J. Knapp Single Nucleotide Polymorphisms and Linkage Disequilibrium in Sunflower Genetics, September 1, 2007; 177(1): 457 - 468. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Tang, A. Leon, W. C. Bridges, and S. J. Knapp Quantitative Trait Loci for Genetically Correlated Seed Traits are Tightly Linked to Branching and Pericarp Pigment Loci in Sunflower Crop Sci., February 24, 2006; 46(2): 721 - 734. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. S. C. Smith, D. N. Duvick, O. S. Smith, M. Cooper, and L. Feng Changes in Pedigree Backgrounds of Pioneer Brand Maize Hybrids Widely Grown from 1930 to 1999 Crop Sci., November 1, 2004; 44(6): 1935 - 1946. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. C. Meyer, O. Torjek, M. Becher, and T. Altmann Heterosis of Biomass Production in Arabidopsis. Establishment during Early Development Plant Physiology, April 1, 2004; 134(4): 1813 - 1823. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. T. Cheres, J. F. Miller, and S. J. Knapp Donor Inbred Lines for Enhancing the Performance of Single-Cross Sunflower Hybrids Crop Sci., September 1, 1999; 39(5): 1325 - 1331. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| The SCI Journals | Agronomy Journal | Vadose Zone Journal | |||
| Journal of Natural Resources and Life Sciences Education |
Soil Science Society of America Journal | ||||
| Journal of Plant Registrations | Journal of Environmental Quality |
The Plant Genome | |||