Research Articles

MOLECULAR ADAPTATION THROUGH DIVERSITY OF RETROTRANSPOSONS AND TRANSCRIPTIONAL FACTORS IN POPULATIONS OF WILD SOYBEAN (GLYCINE SOJA)

Expand
  • Institute of Botany, Chinese Academy of Sciences, Beijing 100093, China

Received date: 2006-04-03

  Accepted date: 2006-09-13

  Online published: 2007-09-30

Abstract

Aims Elucidation of the molecular mechanism of local adaptation to changing environments represents a central goal in evolutionary biology and ecology. Formation of adaptive populations probably involves activation or repression of pre-existing tolerant genes by transcription factors (TFs) and retrotransposons under stress. Research in this area can lead toward to a unified theory of evolution.

Methods The consensus sequence of drought responsive element binding protein (DREB) from the wild soybean (Glycine soja) in Yellow River delta has been cloned, sequenced, and called GsDREB1. An integrase gene of Gypsy-like retrotransposon called GsINT was also cloned from G. soja. Southern hybridization indicated that GsINT consisted of multiple copies and showed restriction fragment length polymorphism among individuals in salinity populations. From both sequences of GsINT and GsDREB1, other pairs of primers were designed for amplification of 5'upstream of GsDREB1 in order to see if partial sequence of GsINT was inserted. Results indicated multiple copies of space sequence between INT and DREB and its diversity among individuals of plants within each population. Gene cloning and sequencing of amplified products showed possible existence of GsINT sequence in 5' upstream of GsDREB1.

Important findings Results led to a hypothesis on the origin of tolerant populations, i.e., a molecular mechanism on adaptive evolution of plants. In normal conditions, plant populations mainly contain non-tolerant individuals. Under stress conditions, retrotransposons increase their frequency of transposition. Most mutants are neutral without phenotypical change. Few insertions located into 5' upstream of transcriptional factors will change intensity of TFs' expression. Then a series of pre-existed stress responsive genes controlled by TFs will simultaneously change their rates of gene expression, resulting in formation of more tolerant or sensitive individuals. Individuals with high stress tolerance may appear by accumulation of several tolerant inserts step by step. As a result of complicated interaction among genes, plants with different levels of stress tolerance occur quickly under stress. By means of natural selection, stress-sensitive plants are lost under stress conditions; however, stress itself continuously creates new sensitive individuals. Few of them with a short life cycle may survive by using a short period time of weakened stress. This hypothesis explains that tolerant populations quickly form because transposition frequency under stress becomes very high. It also explains why tolerant populations contain higher genetic diversity and why a few stress-sensitive individuals exist under stress conditions.

Cite this article

HU Zhi-Ang, JIANG Guo-Qiang, DENG Xin, WANG Hong-Xin . MOLECULAR ADAPTATION THROUGH DIVERSITY OF RETROTRANSPOSONS AND TRANSCRIPTIONAL FACTORS IN POPULATIONS OF WILD SOYBEAN (GLYCINE SOJA)[J]. Chinese Journal of Plant Ecology, 2007 , 31(5) : 952 -959 . DOI: 10.17521/cjpe.2007.0121

References

[1] Ab-Shukor NA, Kay QON, Stevens DP, Skibinski DOF (1988). Salt tolerance in natural populations of Trifolium repens L. New Phytologist, 109,483-490.
[2] Bennetzen JL (2000). Transposable element contributions to plant gene and genome evolution. Plant Molecular Biology, 42,251-269.
[3] Bradshaw AD (1952). Populations of Agrostis tenuis resistant to lead and zinc poisoning. Nature, 169,1098.
[4] Bult CJ, Kiang YT (1992). Electrophoretic and morphological variation within and among natural populations of the wild soybean, Glycine soja Sieb & Zucc. Botanical Bulletin of Academia Sinica, 33,111-122.
[5] Burke T (1999). Editorial. Molecular Ecology, 8, i-ii.
[6] Burke T, Seidler R, Smith H (1992). Editorial. Molecular Ecology, 1,1.
[7] Chinnusamy V, Jagendorf A, Zhu JK (2005). Understanding and improving salt tolerance in plants. Crop Science, 45,437-448.
[8] Clark RM, Wagler TN, Quijada P, Doebley J (2006). A distant upstream enhancer at the maize domestication gene tb1 has pleiotropic effects on plant and inflorescent architecture. Nature Genetics, 38,594-597.
[9] DeBarry JD, Ganko EW, McCarthy EM, McDonald JF (2006). The contribution of LTR retrotransposon sequences to gene evolution in Mus musculus. Molecular Biology and Evolution, 23,479-481.
[10] Doebley J (2006). Unfallen grains: how ancient farmers turned weeds into crops. Science, 312,1318-1319.
[11] Gartside DW, McNeilly T (1974). The potential for evolution of heavy metal tolerance in plants. II. Copper tolerance in normal population of different plant species. Heredity, 32,335-348.
[12] Grandbastien MA (1998). Activation of plant retrotransposons under stress conditions. Trends in Plant Science, 3,181-187.
[13] Hannon N, Bradshaw AD (1968). Evolution of salt tolerance in two coexisting species of grass. Nature, 220,1342-1343.
[14] Hirochika H, Sugimoto K, Otsuki Y, Tsugawa H, Kanda M (1996). Retrotransposons of rice involved in mutations induced by tissue culture. Proceedings of the National Academy of Sciences of the United States of America, 93,7783-7788.
[15] Hu ZA (胡志昂), Wang HX (王洪新) (1983). An improved method to detect allozymes of Sp1 and Ti loci in soybean seed proteins. Acta Botanica Sinica (植物学报), 25,532-536. (in Chinese with English abstract)
[16] Hu ZA (胡志昂), Wang HX (王洪新) (1985). Genetic structure of natural populations of wild soybean (Glycine soja) in Beijing region. Acta Botanica Sinica (植物学报), 27,599-604. (in Chinese with English abstract)
[17] Hu ZA (胡志昂), Wang HX (王洪新), Yan LF (阎龙飞) (1983). Biochemical systematics of gymnosperm. I. Peroxidases of Pinaceae. Acta Phytotaxonomica Sinica (植物分类学报), 21,423-432. (in Chinese with English abstract)
[18] Hu ZA (胡志昂), Yun R (恽锐), Zhong M (钟敏), Dong FG (董夫贵), Wang HX (王洪新), Qian YQ (钱迎倩) (1997). Comparison and improvement of polymorphism amplification methods used for detecting DNA diversity of plants. Acta Botanica Sinica (植物学报), 39,144-148. (in Chinese with English abstract)
[19] Hu ZA (胡志昂), Zhang YP (张亚平) (1997). Genetic Diversity of Animals and Plants in China (中国动植物的遗传多样性). Zhejiang Science and Technology Press, Hangzhou. (in Chinese with English abstract)
[20] Jacob F, Monod J (1961). On the regulation of gene activity. Cold Spring Harbor Symposium on Quantitative Biology, 26,193-211.
[21] Kasuga M, Liu Q, Miura S, Yamaguchi-Shinozaki K, Shinozaki K (1999). Improving plant drought, salt, and freezing tolerance by gene transfer of a single stress-inducible transcription factor. Nature Biotechnology, 17,287-291.
[22] Kimura M (1968). Evolutionary rate at the molecular level. Nature, 217,624-626.
[23] Liu Q, Kasuga M, Sakuma Y, Abe H, Miura S, Yamaguchi-Shinozaki K, Shinozaki K (1998). Two transcription factors, DREB1 and DREB2, with an EREBP/AP2 DNA binding domain separate two cellular signal transduction pathways in drought- and low-temperature-responsive gene expression, respectively, in Arabidopsis. Plant Cell, 10,1391-1406.
[24] Liviero L, Maestri E, Gulli M, Nevo E, Marmiroli N (2002). Ecogeographic adaptation and genetic variation in wild barley, application of molecular markers targeted to environmentally regulated genes. Genetic Resources and Crop Evolution, 49,133-144.
[25] McClintock B (1984). The significance of responses of the genome to challenge. Science, 226,792-801.
[26] Mitton JB (1998). Molecular markers and natural selection. In: Carvalho GRed. Advances in Molecular Ecology. IOS Press, Amsterdam,225-241.
[27] Nevo E (2001). Evolution of genome-phenome diversity under environmental stress. Proceedings of the National Academy of Sciences of the United States of America, 98,6233-6240.
[28] Novillo F, Alonso JM, Ecker JR, Salinas J (2004). CBF2/DREB1C is a negative regulator of CBF1/DREB1B and CBF3/DREB1A expression and plays a central role in stress tolerance in Arabidopsis. Proceedings of the National Academy of Sciences of the United States of America, 101,3985-3990.
[29] Owuor ED, Beharav A, Fahima T, Kirzhner VM, Korol AB, Nevo E (2003). Microscale ecological stress causes RAPD molecular selection in wild barley, Neve Yaar microsite, Israel. Genetic Resources and Crop Evolution, 50,213-224.
[30] Sambrook J, Fritsch EF, Maniatis T (1993). Molecular Cloning: A Laboratory Manual 2nd edn. Cold Spring Harbor Laboratory Press, New York.
[31] Schulman AH, Kalendar R (2005). A movable feast: diverse retrotransposons and their contribution to barley genome dynamics. Cytogenetic and Genome Research, 110,598-605.
[32] Singh RJ, Kollipara KP, Hymowitz T (1992). Genomic relationships among diploid wild perennial species of the genus Glycine Willd. subgenus Glycine revealed by crossability, meiotic chromosome pairing and seed protein electrophoresis. Theoretical and Applied Genetics, 85,276-282.
[33] Storz JF (2005). Using genome scans of DNA polymorphism to infer adaptive population divergence. Molecular Ecology, 14,671-688.
[34] Turpeinen T, Tenhola T, Manninen O, Nevo E, Nissil? E (2001). Microsatellite diversity associated with ecological factors in Hordeum spontaneum populations in Israel. Molecular Ecology, 10,1577-1591.
[35] Wang HX (王洪新), Hu ZA (胡志昂), Zhong M (钟敏), Lu WJ (陆文静), Wei W (魏伟), Yun R (恽锐), Qian YQ (钱迎倩) (1997). Genetic differentiation and physiological adaptation of wild soybean (Glycine soja) populations under saline conditions: isozymatic and random amplified polymorphic DNA study. Acta Botanica Sinica (植物学报), 39,34-42. (in Chinese with English abstract)
[36] Wang RL, Stec A, Hey J, Lukens L, Doebly J (1999). The limits of selection during maize domestication. Nature, 398,236-239.
[37] Weaver KR, Caetano-Anollés G, Gresshoff PM, Callahan LM (1994). Isolation and cloning of DNA amplification products from silver-stained polyacrylamide gels. BioTechniques, 16,226-227.
[38] Wessler SR (1996). Plant retrotransposons: turned on by stress. Current Biology, 6,959-961.
[39] Wilson AC, Carlson SS, White TJ (1977). Biochemical evolution. Annual Review of Biochemistry, 46,573-639.
[40] Wu L, Bradshaw AD, Thurman DA (1975). The potential for evolution of heavy metal tolerance in plants. III. The rapid evolution of copper tolerance in Agrostis stolonifera. Heredity, 34,165-187.
[41] Yamaguchi-Shinozaki K, Shinozaki K (1994). A novel cis-acting element in an Arabidopsis gene is involved in responsiveness to drought, low-temperature, or high-salt stress. Plant Cell, 6,251-264.
[42] Yamaguchi-Shinozaki K, Shinozaki K (2005). Organization of cis-acting regulatory elements in osmotic- and cold-stress responsive promoters. Trends in Plant Science, 10,1360-1385.
[43] Yu H, Kiang YT (1993). Genetic variation in South Korean natural populations of wild soybean (Glycine soja). Euphytica, 68,213-221.
[44] Zhang Q, Wang HX, Hu ZA (1999). RAPD markers associated with salt tolerance in wild soybean populations. Soybean Genetics Newsletter, 26,10.
[45] Zhou S, Zhao KF (2003). Discussion on the problem of salt gland of Glycine soja. Acta Botanica Sinica (植物学报), 45,574-580.
Outlines

/