The step-wise assembly of a functional nucleolus in preimplantation mouse embryos involves the Cajal (coiled) body

被引:81
作者
Zatsepina, O
Baly, C
Chebrout, M
Debey, P
机构
[1] Inst Biol Physicochim, IFR 63, MNHN, INRA UC 806,EA 2703, F-75005 Paris, France
[2] Moscow MV Lomonosov State Univ, AN Belozersky Inst Physicochem Biol, Moscow 119992, Russia
关键词
Cajal body; development; mouse preimplantation embryos; nucleologenesis; nucleolus precursor body; polymerase I;
D O I
10.1006/dbio.2002.0865
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
After fertilization, ribosomal RNA synthesis is silenced during a period which depends on the species. Data concerning the reassembly of a functional nucleolus remain scarce. We have examined by immunocytochemistry, Western blots, and BrUTP microinjection the dynamics of major nucleolar proteins during the first cycles of mouse embryogenesis, in relation to rDNA transcription sites and coilin, a marker of Cajal bodies. We show that: (1) the reinitiation of rDNA transcription occurs at the two-cell stage, 44-45 h after hCG injection (hphCG), at the surface of the nucleolar precursor bodies (NPBs), where the RNA polymerase I (pol I) transcription complex is recruited 4-5 h before; (2) the NPBs are not equal in their ability to support recruitment of pol I and rDNA transcription; (3) maternally inherited fibrillarin undergoes a dynamic redistribution during the second cell stage, together with coilin, leading to the assembly of the Cajal body around 40 hphCG; and (4) the pol I complex is first recruited to the Cajal body before reaching its rDNA template. We also find that fibrillarin and B23 are both directly assembled around NPBs prior to ongoing pre-rRNA synthesis. Altogether, our results reveal a role of the Cajal bodies in the building of a functional nucleolus. (C) 2003 Elsevier Science (USA).
引用
收藏
页码:66 / 83
页数:18
相关论文
共 91 条
[41]   NUCLEOLOGENESIS - U3 SNRNA-CONTAINING PRENUCLEOLAR BODIES MOVE TO SITES OF ACTIVE PRE-RIBOSOMAL-RNA TRANSCRIPTION AFTER MITOSIS [J].
JIMENEZGARCIA, LF ;
SEGURAVALDEZ, MD ;
OCHS, RL ;
ROTHBLUM, LI ;
HANNAN, R ;
SPECTOR, DL .
MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (09) :955-966
[42]   THE TIMING OF EARLY DEVELOPMENTAL EVENTS IN XENOPUS [J].
KIRSCHNER, M ;
NEWPORT, J ;
GERHART, J .
TRENDS IN GENETICS, 1985, 1 (02) :41-47
[43]  
KNOWLAND J, 1972, J EMBRYOL EXP MORPH, V27, P167
[44]   Non-isotopic detection of nucleolar transcription in pre-implantation mouse embryos [J].
Koberna, K ;
Landa, V ;
Kanka, J ;
Pliss, A ;
Eltsov, M ;
Stanek, D ;
Raska, I .
REPRODUCTION NUTRITION DEVELOPMENT, 1998, 38 (01) :117-126
[45]  
Kopecny V, 1996, CHROMOSOMA, V104, P561, DOI 10.1007/BF00352296
[46]   LOCALIZATION OF NUCLEIC-ACIDS IN THE NUCLEOLI OF OOCYTES AND EARLY EMBRYOS OF MOUSE AND HAMSTER - AN AUTORADIOGRAPHIC STUDY [J].
KOPECNY, V ;
LANDA, V ;
PAVLOK, A .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1995, 41 (04) :449-458
[47]  
Latham KE, 1999, INT REV CYTOL, V193, P71
[48]   Inhibition of protein dephosphorylation results in the accumulation of splicing snRNPs and coiled bodies within the nucleolus [J].
Lyon, CE ;
Bohmann, K ;
Sleeman, J ;
Lamond, AI .
EXPERIMENTAL CELL RESEARCH, 1997, 230 (01) :84-93
[49]   The SURF-6 protein is a component of the nucleolar matrix and has a high binding capacity for nucleic acids in vitro [J].
Magoulas, C ;
Zatsepina, OV ;
Jordan, PWH ;
Jordan, EG ;
Fried, M .
EUROPEAN JOURNAL OF CELL BIOLOGY, 1998, 75 (02) :174-183
[50]  
Moore GD, 1996, MOL REPROD DEV, V45, P264, DOI 10.1002/(SICI)1098-2795(199611)45:3&lt