PHYSIOLOGICALLY INACTIVE NUCLEOLI CONTAIN NUCLEOPLASMIC RIBONUCLEOPROTEINS - IMMUNOELECTRON MICROSCOPY OF MOUSE SPERMATIDS AND EARLY EMBRYOS

被引:43
作者
BIGGIOGERA, M
MARTIN, TE
GORDON, J
AMALRIC, F
FAKAN, S
机构
[1] UNIV LAUSANNE, CTR ELECTRON MICROSCOPY, CH-1005 LAUSANNE, SWITZERLAND
[2] UNIV CHICAGO, DEPT MOLEC GENET & CELL BIOL, CHICAGO, IL 60637 USA
[3] ABBOTT LABS, N CHICAGO, IL 60064 USA
[4] CNRS, CTR RECH BIOCHIM & GENET CELLULAIRES, F-31062 TOULOUSE, FRANCE
关键词
D O I
10.1006/excr.1994.1172
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Physiologically inactivating or reactivating nucleoli represent a good model to investigate modifications of the nucleolar activity, which influence to a great extent the morphology of this organelle. We have studied the nucleoli of mouse spermatids during gradual inactivation, as well as those of early mouse preimplantation embryos, which undergo reactivation. In the 2-cell systems, inactive nucleoli are represented by homogeneously, finely fibrillar spherical bodies. With the aim of clarifying the composition of these nucleoli, we have analyzed them by means of immunoelectron microscopy using specific antibodies directed against nucleoplasmic snRNPs, hnRNPs, ribosomal proteins, or fibrillarin as well as by cytochemical methods for visualizing DNA and RNA. Our results indicate that RNA is present in zygote and 2-cell nucleolus precursor bodies (NPBs) as well as in 4- to 8-cell or more advanced embryo nucleoli, but not in inactive spermatid nucleoli. DNA is absent from inactive spermatid nucleoli and NPBs but is present within the nucleolus-associated chromatin and the nucleolonema of active nucleoli. The dense masses constituting the NPBs of the zygote and 2-cell embryos contain ribosomal proteins and fibrillarin but also hnRNPs and nucleoplasmic snRNPs. Of these, only fibrillarin is present in the spermatid residual nucleoli. (C) 1994 Academic Press, Inc.
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页码:55 / 63
页数:9
相关论文
共 42 条
[1]   ULTRASTRUCTURAL AND CYTOCHEMICAL STUDIES ON EXTRANUCLEOLAR BODIES IN RAT OOCYTES AT THE PREOVULATORY FOLLICLE STAGE [J].
ANTOINE, N ;
THIRY, M ;
GOESSENS, G .
BIOLOGY OF THE CELL, 1989, 65 (01) :61-66
[2]  
BIGGIOGERA M, 1990, DEVELOPMENT, V110, P1263
[3]   ETHIDIUM BROMIDE-PTA AND PROPIDIUM IODIDE-PTA STAINING OF NUCLEIC-ACIDS AT THE ELECTRON-MICROSCOPIC LEVEL [J].
BIGGIOGERA, M ;
BIGGIOGERA, FF .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1989, 37 (07) :1161-1166
[4]   IMMUNOELECTRON MICROSCOPICAL VISUALIZATION OF RIBONUCLEOPROTEINS IN THE CHROMATOID BODY OF MOUSE SPERMATIDS [J].
BIGGIOGERA, M ;
FAKAN, S ;
LESER, G ;
MARTIN, TE ;
GORDON, J .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1990, 26 (02) :150-158
[5]   IMMUNOELECTRON MICROSCOPE LOCALIZATION OF SNRNP, HNRNP, AND RIBOSOMAL-PROTEINS IN MOUSE SPERMATOGENESIS [J].
BIGGIOGERA, M ;
VONSCHACK, ML ;
MARTIN, TE ;
GORDON, J ;
MULLER, M ;
FAKAN, S .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1993, 35 (03) :261-271
[6]   DISTRIBUTION OF NUCLEOLAR PROTEINS B23 AND NUCLEOLIN DURING MOUSE SPERMATOGENESIS [J].
BIGGIOGERA, M ;
KAUFMANN, SH ;
SHAPER, JH ;
GAS, N ;
AMALRIC, F ;
FAKAN, S .
CHROMOSOMA, 1991, 100 (03) :162-172
[7]   RESIN DEVELOPMENT FOR ELECTRON-MICROSCOPY AND AN ANALYSIS OF EMBEDDING AT LOW-TEMPERATURE [J].
CARLEMALM, E ;
GARAVITO, RM ;
VILLIGER, W .
JOURNAL OF MICROSCOPY-OXFORD, 1982, 126 (MAY) :123-143
[8]   POLY(A)LENGTH, CYTOPLASMIC ADENYLATION AND SYNTHESIS OF POLY(A)+ RNA IN EARLY MOUSE EMBRYOS [J].
CLEGG, KB ;
PIKO, L .
DEVELOPMENTAL BIOLOGY, 1983, 95 (02) :331-341
[9]  
COGLIATI R, 1973, CR ACAD SCI D NAT, V276, P3041
[10]   A CYTOCHEMICAL AND IMMUNOCYTOCHEMICAL STUDY OF DNA DISTRIBUTION IN SPERMATID NUCLEI OF MOUSE, RABBIT, AND BULL [J].
COURTENS, JL ;
BIGGIOGERA, M ;
FAKAN, S .
CELL AND TISSUE RESEARCH, 1991, 265 (03) :517-525