IN-SITU CHARACTERIZATION OF THE LATE VACUOLATE MICROSPORE AS A CONVENIENT STAGE TO INDUCE EMBRYOGENESIS IN CAPSICUM

被引:34
作者
GONZALEZMELENDI, P
TESTILLANO, PS
AHMADIAN, P
FADON, B
VICENTE, O
RISUENO, MC
机构
[1] CSIC, BIOL RES CTR, NUCL ORG PLANT DEV LAB, E-28006 MADRID, SPAIN
[2] UNIV ALCALA DE HENARES, FAC MED, DEPT MORPHOL & SURG, ALCALA DE HENARES, SPAIN
[3] UNIV TEHRAN, FAC AGR, DEPT PLANT BREEDING, TEHRAN, IRAN
[4] UNIV VIENNA, INST MICROBIOL & GENET, A-1090 VIENNA, AUSTRIA
关键词
CAPSICUM ANNUUM; IN SITU METHODS; LATE VACUOLATE MICROSPORE; NUCLEAR ANTIGENS; NUCLEAR ORGANIZATION; POLLEN EMBRYOGENESIS;
D O I
10.1007/BF01280233
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Pollen embryogenesis has been induced in Capsicum annuum L., selecting the late vacuolate microspore as the suitable developmental stage for the induction. Various modem in situ methods including cytochemistry, immunocytochemistry, and in situ hybridization have been used to characterize the functional organization of the microspore nucleus at this specific stage of development in which the change to the sporophytic program can be induced. The results on the chromatin pattern, interchromatin structures and nucleolar subcompartments reveal a transcriptionally very active nucleus in the late vacuolate microspore and define characteristic cellular features of this specific period. The first stages of the microspore derived embryos have also been studied identifying the main ultrastructural features exhibited by the nuclei of two-cell and multicellular pollen grains. The approach used, providing information on the subcellular location and expression time of key molecules involved in gene expression, presents a high potential for studying the complex process of pollen embryogenesis induction.
引用
收藏
页码:60 / 71
页数:12
相关论文
共 63 条
[1]  
Bajaj Y.P.S., In vitro production of haploids, Handbook of plant cell culture. Techniques for propagation and breeding, pp. 228-287, (1983)
[2]  
Benito Moreno R.M., Macke F., Hauser M-T, Alwen A., Heberle-Bors E., Sporophytes and male gametophytes from in vivo cultured, immature tobacco pollen, Sexual reproduction in higher plants, pp. 137-142, (1988)
[3]  
Bernhard W., A new staining procedure for electron microscopical cytology, J Cell Sci, 27, pp. 250-265, (1969)
[4]  
Billings P.B., Barton J.R., Hoch S.O., A murine monoclonal antibody recognizes the 13,000 molecular weight polypeptide of the Sm small nuclear ribonucleoprotein complex, J Immunol, 135, pp. 428-432, (1985)
[5]  
Christensen M.E., Moloo J., Swischuk J., Schelling M.E., Characterization of the nucleolar protein, B-36 using monoclonal antibodies, Exp Cell Res, 166, pp. 77-93, (1986)
[6]  
Chuong P.V., Beversdorf W.D., High frequency embryogenesis through isolated microspore culture in Brassica napus L. and B. carinata Braun, Plant Sci, 39, pp. 219-226, (1985)
[7]  
Cook P.R., RNA polymerase: structural determinant of the chromatin loop and the chromosome, BioEssays, 16, pp. 425-430, (1994)
[8]  
Cortezon T., Sanchez-Pina M.A., Testillano P.S., Risueno M.C., Desarrollo de la célula generativa del grano de polen de Scilla peruviana al microscopio óptico y microscopio electronico de transmisión, Polen, esporas y sus aplicaciones, pp. 87-94, (1990)
[9]  
De la Torre C., Sacristan-Garate A., Navarrete M.M., Structural changes in chromatin during interphase, Chromosoma, 51, pp. 183-198, (1975)
[10]  
Delseny M., Cooke R., Penon P., Sequence heterogeneity in radish nuclear ribosomal RNA genes, Plant Sci Lett, 30, pp. 107-119, (1983)