12
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Genetic diversity of male and female Chinese bayberry ( Myrica rubra) populations and identification of sex-associated markers

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Background

          Chinese bayberry ( Myrica rubra Sieb. & Zucc.) is an important subtropical evergreen fruit tree in southern China. Generally dioecious, the female plants are cultivated for fruit and have been studied extensively, but male plants have received very little attention. Knowledge of males may have a major impact on conservation and genetic improvement as well as on breeding. Using 84 polymorphic SSRs, we genotyped 213  M. rubra individuals (99 male individuals, 113 female varieties and 1 monoecious) and compared the difference in genetic diversity between the female and the male populations.

          Results

          Neighbour-joining cluster analysis separated M. rubra from three related species, and the male from female populations within M. rubra. By structure analysis, 178  M. rubra accessions were assigned to two subpopulations: Male dominated (98) and Female dominated (80). The well-known cultivars ‘Biqi’ and ‘Dongkui’, and the landraces ‘Fenhong’ are derived from three different gene pools. Female population had a slightly higher values of genetic diversity parameters (such as number of alleles and heterozygosity) than the male population, but not significantly different. The SSR loci ZJU062 and ZJU130 showed an empirical Fst value of 0.455 and 0.333, respectively, which are significantly above the 95 % confidence level, indicating that they are outlier loci related to sex separation.

          Conclusion

          The male and female populations of Chinese bayberry have similar genetic diversity in terms of average number of alleles and level of heterozygosity, but were clearly separated by genetic structure analysis due to two markers associated with sex type, ZJU062 and ZJU130. Zhejiang Province China could be the centre of diversity of M. rubra in China, with wide genetic diversity coverage; and the two representative cultivars ‘Biqi’ and ‘Dongkui’, and one landrace ‘Fenhong’ in three female subpopulations. This research provides genetic information on male and female Chinese bayberry and will act as a reference for breeding programs.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12864-015-1602-5) contains supplementary material, which is available to authorized users.

          Related collections

          Most cited references36

          • Record: found
          • Abstract: found
          • Article: found
          Is Open Access

          ADZE: a rarefaction approach for counting alleles private to combinations of populations

          Motivation: Analysis of the distribution of alleles across populations is a useful tool for examining population diversity and relationships. However, sample sizes often differ across populations, sometimes making it difficult to assess allelic distributions across groups. Results: We introduce a generalized rarefaction approach for counting alleles private to combinations of populations. Our method evaluates the number of alleles found in each of a set of populations but absent in all remaining populations, considering equal-sized subsamples from each population. Applying this method to a worldwide human microsatellite dataset, we observe a high number of alleles private to the combination of African and Oceanian populations. This result supports the possibility of a migration out of Africa into Oceania separate from the migrations responsible for the majority of the ancestry of the modern populations of Asia, and it highlights the utility of our approach to sample size correction in evaluating hypotheses about population history. Availability: We have implemented our method in the computer pro-gram ADZE, which is available for download at http://rosenberglab.bioinformatics.med.umich.edu/adze.html. Contact: szpiechz@umich.edu
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Sequencing papaya X and Yh chromosomes reveals molecular basis of incipient sex chromosome evolution.

            Sex determination in papaya is controlled by a recently evolved XY chromosome pair, with two slightly different Y chromosomes controlling the development of males (Y) and hermaphrodites (Y(h)). To study the events of early sex chromosome evolution, we sequenced the hermaphrodite-specific region of the Y(h) chromosome (HSY) and its X counterpart, yielding an 8.1-megabase (Mb) HSY pseudomolecule, and a 3.5-Mb sequence for the corresponding X region. The HSY is larger than the X region, mostly due to retrotransposon insertions. The papaya HSY differs from the X region by two large-scale inversions, the first of which likely caused the recombination suppression between the X and Y(h) chromosomes, followed by numerous additional chromosomal rearrangements. Altogether, including the X and/or HSY regions, 124 transcription units were annotated, including 50 functional pairs present in both the X and HSY. Ten HSY genes had functional homologs elsewhere in the papaya autosomal regions, suggesting movement of genes onto the HSY, whereas the X region had none. Sequence divergence between 70 transcripts shared by the X and HSY revealed two evolutionary strata in the X chromosome, corresponding to the two inversions on the HSY, the older of which evolved about 7.0 million years ago. Gene content differences between the HSY and X are greatest in the older stratum, whereas the gene content and order of the collinear regions are identical. Our findings support theoretical models of early sex chromosome evolution.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Plant sex determination and sex chromosomes.

              Sex determination systems in plants have evolved many times from hermaphroditic ancestors (including monoecious plants with separate male and female flowers on the same individual), and sex chromosome systems have arisen several times in flowering plant evolution. Consistent with theoretical models for the evolutionary transition from hermaphroditism to monoecy, multiple sex determining genes are involved, including male-sterility and female-sterility factors. The requirement that recombination should be rare between these different loci is probably the chief reason for the genetic degeneration of Y chromosomes. Theories for Y chromosome degeneration are reviewed in the light of recent results from genes on plant sex chromosomes.
                Bookmark

                Author and article information

                Contributors
                jiahuimin1988@163.com
                jydyx@163.com
                517614074@qq.com
                liyinghui@caas.cn
                jiahuijuan@zju.edu.cn
                whx1106@163.com
                cxccy@sina.com
                justdx@126.com
                ypguo@nwsuaf.edu.cn
                lpzhang8263@163.com
                qkgao@zju.edu.cn
                carchen110@163.com
                ljsong@163.com
                eric.vandeweg@wur.nl
                gaozhongshan@zju.edu.cn
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                19 May 2015
                19 May 2015
                2015
                : 16
                : 1
                : 394
                Affiliations
                [ ]Department of Horticulture, College of Agriculture and Biotechnology, Zhejiang University, 310058 Hangzhou, Zhejiang China
                [ ]Fruit Research Institute, 315400 Yuyao, Ningbo PR China
                [ ]The National Key Facility for Crop Gene Resources and Genetic Improvement (NFCRI)/Key Lab of Germplasm Utilization (MOA), Chinese Academy of Agricultural Sciences, Institute of Crop Science, 100081 Beijing, China
                [ ]Forestry Technology Extension Center, 315300 Cixi, Ningbo China
                [ ]Bio-Macromolecules Analysis Lab, Analysis Center of Agrobiology, Environmental Sciences of Zhejiang University, 310058 Hangzhou, China
                [ ]Zhejiang Institute of Subtropical Crops, Wenzhou, 325005 China
                [ ]Wenzhou Vocational and Technical College, 325035 Wenzhou, China
                [ ]Plant Breeding-Wageningen University and Research Centre, P.O. Box 16, 6700 AA Wageningen, The Netherlands
                Article
                1602
                10.1186/s12864-015-1602-5
                4436740
                25986380
                cd1d398b-8c8b-49d0-9bea-10ff34a76983
                © Jia et al.; licensee BioMed Central. 2015

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 21 October 2014
                : 1 May 2015
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2015

                Genetics
                Genetics

                Comments

                Comment on this article