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Analysis of genetic variation within and among Ulva pertusa (Ulvaceae, Chlorophyta) populations using ISSR markers

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  • Hydrobiology
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Chinese Science Bulletin

Abstract

Ulva pertusa is a native species to Asia along the western coast of Pacific Ocean, with new occurrence records in the eastern coast of Pacific, the northwest coast of Atlantic and the Mediterranean Sea. However, little is known about its population genetic structure. In this study, twelve U. pertusa populations from 3 coastal areas of China: Qingdao, Yantai and Dalian, were applied to ISSR analysis. The selected 4 ISSR primers amplified 120 polymorphic bands totally. Nei’s gene diversity (H) ranged from 0.0729 to 0.1496, and Shannon’s information index (I) ranged from 0.1072 to 0.2196. Genetic diversity was greater within Qingdao populations (H = 0.2069, I = 0.3232). Analysis of molecular variance (AMOVA) showed the greatest variance within populations (68.57%), much less variance among populations (22.63%) and among areas (8.79%). Unweighted pair-group mean analysis (UPGMA) indicated that clustering of U. pertusa individuals mainly relates to their populations and geographic distances separating those populations. Genetic differentiation and limited gene flow among U. pertusa populations were indicated by ISSR analysis.

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References

  1. Tseng, C K, Zhang D R, Zhang J F, et al. Manual of Chinese economic seaweeds (in Chinese). Beijing: Science Press, 1962. 43–50

    Google Scholar 

  2. Aguilar-Rosas R, Aguilar-Rosas L E, Shimada S. First record of Ulva pertusa Kjellman (Ulvales, Chlorophyta) in the Pacific coast of Mexico. Algae, 2008, 23: 201–207

    Article  Google Scholar 

  3. López S B, Fernández I B, Lozano R B, et al. Is the cryptic alien seaweed Ulva pertusa (Ulvales, Chlorophyta) widely distributed along European Atlantic coasts? Bot Mar, 2007, 50: 267–274

    Article  Google Scholar 

  4. Verlaque M, Belsher T, Deslous-Paoli J M. Morphology and reproduction of Asiatic Ulva pertusa (Ulvales, Chlorophyta) in Thau Lagoon (France, Mediterranean Sea). Cryptogamie Algol, 2002, 23: 301–310

    Google Scholar 

  5. Su X R, Li T W, Chang S J. A study on nutrition of Ulva pertusa Kjellm (in Chinese). Chinese J Mar Drugs, 1997, 61: 33–35

    Google Scholar 

  6. Yu P Z, Li N, Liu X G, et al. Antihyperlipidemic effects of different molecular weights sulfated-polysaccharides from Ulva pertusa. Pharmacol Res, 2003, 48: 543–549

    Article  Google Scholar 

  7. Shimada S, Hiraoka M, Nabataet S, et al. Molecular phylogenetic analyses of the Japanese Ulva and Enteromorpha (Ulvales, Ulvophyceae), with special reference to the free-floating Ulva. Phycol Res, 2003, 51: 99–108

    Article  Google Scholar 

  8. Slatkin M. Gene flow and the geographic structure of populations. Science, 1987, 236: 787–792

    Article  Google Scholar 

  9. Ji J M, Ma J H, Li Y H, et al. Isomorphic alternation of generations of Ulva pertusa (in Chinese). Fishery Modernization, 2008, 35: 32–35

    Google Scholar 

  10. Hiraoka, M, Shimada S, Ohno M, et al. Asexual life history by quadriflagellate swarmers of Ulva spinulosa (Ulvales, Ulvophyceae). Phycol Res, 2003, 51: 29–34

    Article  Google Scholar 

  11. Callow M E, Callow J A, et al. Primary adhesion of Enteromorpha (Chlorophyta, Ulvales) propagules: Quantitative settlement studies and video microscopy. J Phycol, 1997, 33: 938–947

    Article  Google Scholar 

  12. Innes D J. Genetic structure of asexually reproducing Enteromorpha linza (Ulvales, Chlorophyta) in Long Island Sound. Mar Biol, 1987, 94: 459–467

    Article  Google Scholar 

  13. Innes D J. Genetic differentiation in the intertidal zone in populations of the alga Enteromorpha Linza (Ulvales, Chlorophyta). Mar Biol, 1988, 97: 9–16

    Article  Google Scholar 

  14. Wang X L, Zhao F J, Hu Z M, et al. Inter-simple sequence repeat (ISSR) analysis of genetic variation of Chondrus crispus populations from North Atlantic. Aquat Bot, 2008, 88: 154–159

    Article  Google Scholar 

  15. Leskinen E, Pamilo P. Evolution of the ITS sequences of ribosomal DNA in Enteromorpha (Chlorophyceae). Hereditas, 1997, 126: 17–23

    Article  Google Scholar 

  16. Ballard H E, Sytsma K J, Kowal R R. Shrinking the violets: Phylogenetic relationships of infrageneric groups in Viola (Violaceae) based on internal transcribed spacer DNA sequences. Syst Bot, 1998, 23: 439–458

    Article  Google Scholar 

  17. Drets M E. BANDSCAN-a computer program for on-line linear scanning of human banded chromosomes. Comput Programs Biomed, 1978, 8: 283–294

    Article  Google Scholar 

  18. Wolfe A D, Liston A. Contributions of PCR-based methods to plant systematics and evolutionary biology. In: Soltis D E, Soltis P S, Doyle J J, eds. Plant Molecular Systematics. Boston: Kluwer Academic Press, 1998. 43–86

    Google Scholar 

  19. Yeh F C, Yang R C, Boyle T. Popgene, version 1.32. Microsoft Window-based freeware for population genetic analysis. University of Alberta and Center for International Forestry Research, 1999

  20. Nei M. Estimation of average heterozygosity and genetic distance from a small number of individuals. Genetics, 1978, 89: 583–590

    Google Scholar 

  21. Miller M P. AMOVA-PREP 1.01: A program for the preparation of AMOVA input files from dominant-markers raw data. Computer software distributed by author. 1998

  22. Huff D R, Peakall R, Smouse P E. RAPD variation within and among natural-populations of outcrossing buffalograss [Buchloë dactyloides (Nutt.) Engelm.]. Theor Appl Genet, 1993, 86: 927–934

    Article  Google Scholar 

  23. Excoffier L, Smouse P E, Quattro J M. Analysis of molecular variance inferred from metric distances among DNA haplotypes: application to human mitochondrial DNA restriction data. Genetics, 1992, 131: 479–491

    Google Scholar 

  24. Meekins J F, Ballard H E, McCarthy B C. Genetic variation and molecular biogeography of a North American invasive plant species (Alliaria petiolata, Brassicaceae). Int J Plant Sci, 2001, 162: 161–169

    Article  Google Scholar 

  25. Rohlf F J. NTSYS-pc: numerical taxonomy and multivariate analysis system, version 2.1. New York: Exeter Software. 2000

    Google Scholar 

  26. Salimath S S, Deoliveira A C, Godwin I D, et al. Assessment of genome origins and genetic diversity in the genus Eleusine with DNA markers. Genome, 1995, 38: 757–763

    Article  Google Scholar 

  27. Nei M, Li W H. Mathematical model for studying genetic variation in terms of restriction endonucleases. Proc Nati Acad Sci USA, 1979, 76: 5269–5273

    Article  Google Scholar 

  28. Rice W R. Analyzing tables of statistical tests. Evolution, 1989, 43: 223–225

    Article  Google Scholar 

  29. Kostamo K, Blomster J, Korpelainen H, et al. New microsatellite markers for Ulva intestinalis (Chlorophyta) and the transferability of markers across species of Ulvaceae. Phycologia, 2008, 47: 580–587

    Article  Google Scholar 

  30. Zhao F J, Liu F L, Liu J D, et al. Genetic structure analysis of natural Sargassum muticum (Fucales, Phaeophyta) populations using RAPD and ISSR markers. J Appl Phycol, 2008, 20: 191–198

    Article  Google Scholar 

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Correspondence to Peng Jiang or Song Qin.

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Zhao, J., Jiang, P., Li, N. et al. Analysis of genetic variation within and among Ulva pertusa (Ulvaceae, Chlorophyta) populations using ISSR markers. Chin. Sci. Bull. 55, 705–711 (2010). https://doi.org/10.1007/s11434-009-0715-0

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  • DOI: https://doi.org/10.1007/s11434-009-0715-0

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