High stability of nuclear microsatellite loci during the early stages of somatic embryogenesis in Norway spruce.

Somatic embryos of Norway spruce (Picea abies (L.) Karst.) differentiate from proembryogenic masses (PEMs), which are subject to autodestruction through programmed cell death. In PEMs, somatic embryo formation and activation of programmed cell death are interrelated processes. We sought to determine if activation of programmed cell death in PEMs is caused by genetic aberrations during somatic embryogenesis. Based on the finding that withdrawal of auxin and cytokinin induces programmed cell death in PEMs, 1-week-old cell suspensions were cultured in medium either with or without auxin and cytokinin and then transferred to maturation medium containing abscisic acid. We analyzed the stability of three nuclear simple sequence repeat (SSR) microsatellite markers at successive stages of somatic embryogenesis in two cell lines. There were no mutations at the SSR loci at any of the successive developmental stages from PEMs to cotyledonary embryos, irrespective of whether or not the proliferation medium in which cell suspensions had been cultured contained auxin or cytokinin. The morphologies of plants regenerated from the cultures were similar, although withdrawal of auxin and cytokinin significantly stimulated the yield of both embryos and plants. We conclude, therefore, that the high genetic stability of somatic embryos in Norway spruce is unaffected by the induction of programmed cell death caused by withdrawal of auxin and cytokinin.

[1]  P. Martínez-Gómez,et al.  Sexual polyembryony in almond , 2003, Sexual Plant Reproduction.

[2]  C. Plomion,et al.  Inheritance and diversity of simple sequence repeat (SSR) microsatellite markers in various families of Picea abies. , 2003, Hereditas.

[3]  P. Hussey,et al.  Re-organisation of the cytoskeleton during developmental programmed cell death in Picea abies embryos. , 2003, The Plant journal : for cell and molecular biology.

[4]  P. Bozhkov,et al.  Early selection improves clonal performance and reduces intraclonal variation of Norway spruce plants propagated by somatic embryogenesis. , 2003, Tree physiology.

[5]  P. Bozhkov,et al.  Programmed cell death eliminates all but one embryo in a polyembryonic plant seed , 2002, Cell Death and Differentiation.

[6]  P. Bozhkov,et al.  A key developmental switch during Norway spruce somatic embryogenesis is induced by withdrawal of growth regulators and is associated with cell death and extracellular acidification. , 2002, Biotechnology and bioengineering.

[7]  J. Trontin,et al.  Molecular evidence of true-to-type propagation of a 3-year-old Norway spruce through somatic embryogenesis , 2001, Planta.

[8]  P. Bozhkov,et al.  Critical Factors Affecting Ex Vitro Performance of Somatic Embryo Plants of Picea abies , 2001 .

[9]  B. Zhivotovsky,et al.  Two waves of programmed cell death occur during formation and development of somatic embryos in the gymnosperm, Norway spruce. , 2000, Journal of cell science.

[10]  J. Stark,et al.  From Cell Death to Embryo Arrest: Mathematical Models of Human Preimplantation Embryo Development , 2000 .

[11]  M. Qumsiyeh,et al.  Cytogenetics and mechanisms of spontaneous abortions: increased apoptosis and decreased cell proliferation in chromosomally abnormal villi , 2000, Cytogenetic and Genome Research.

[12]  P. Bozhkov,et al.  Developmental pathway of somatic embryogenesis in Picea abies as revealed by time-lapse tracking. , 2000, Journal of experimental botany.

[13]  S. Hahn,et al.  Current applications of single-cell PCR , 2000, Cellular and Molecular Life Sciences CMLS.

[14]  K. Hardy,et al.  Apoptosis in the human embryo. , 1999, Reviews of reproduction.

[15]  Y. Park,et al.  Somaclonal variation in cryopreserved embryogenic clones of white spruce [Picea glauca (Moench) Voss.] , 1999, Plant Cell Reports.

[16]  D. Spandidos,et al.  Microsatellite mutations in spontaneously aborted embryos. , 1998, Fertility and sterility.

[17]  P. Bozhkov,et al.  Polyethylene glycol promotes maturation but inhibits further development of Picea abies somatic embryos , 1998 .

[18]  S. Arnold,et al.  Integration of somatic embryogenesis in a tree breeding programme: a case study with Picea abies , 1998 .

[19]  M. Morgante,et al.  Identification and characterization of microsatellites in Norway spruce (Picea abies K.). , 1997, Genome.

[20]  F. Tremblay,et al.  OCCURRENCE OF SOMACLONAL VARIATION AMONG SOMATIC EMBRYO-DERIVED WHITE SPRUCES (PICEA GLAUCA, PINACEAE) , 1996 .

[21]  A. Møller Developmental stability of flowers, embryo abortion, and developmental selection in plants , 1996, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[22]  N. Freimer,et al.  Mutational processes of simple-sequence repeat loci in human populations. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[23]  P. Krogstrup,et al.  Variations in cryotolerance of embryogenic Picea abies cell lines and the association to genetic, morphological, and physiological factors , 1993 .

[24]  L. Jin,et al.  Genetic variation at five trimeric and tetrameric tandem repeat loci in four human population groups. , 1992, Genomics.

[25]  Clarice R. Weinberg,et al.  Incidence of early loss of pregnancy. , 1988, The New England journal of medicine.

[26]  D. Spandidos,et al.  Microsatellite instability in aborted embryos. , 1996, Molecular human reproduction.

[27]  B. Bentzer Strategies for Clonal Forestry with Norway Spruce , 1993 .

[28]  M. R. Ahuja,et al.  Conservation and application , 1993 .