Partially processed pre-rRNA is preserved in association with processing components in nucleolus-derived foci during mitosis

被引:74
作者
Dundr, M [1 ]
Olson, MOJ [1 ]
机构
[1] Univ Mississippi, Med Ctr, Dept Biochem, Jackson, MS 39216 USA
关键词
D O I
10.1091/mbc.9.9.2407
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Previous studies showed that components implicated in pre-rRNA processing, including U3 small nucleolar (sno)RNA, fibrillarin, nucleolin, and proteins B23 and p52, accumulate in perichromosomal regions and in numerous mitotic cytoplasmic particles, termed nucleolus-derived foci (NDF) between early anaphase and late telophase. The latter structures were analyzed for the presence of pre-rRNA by fluorescence in situ hybridization using probes for segments of pre-rRNA with known half-lives. The NDF did not contain the short-lived 5'-external transcribed spacer (ETS) leader segment upstream from the primary processing site in 47S pre-rRNA. However, the NDF contained sequences from the 5'-ETS core, 18S, internal transcribed spacer 1 (ITS1), and 28S segments and also had detectable, but significantly reduced, levels of the 3'-ETS sequence. Northern analyses showed that in mitotic cells, the latter sequences were present predominantly in 45S-46S pre-rRNAs, indicating that high-molecular weight processing intermediates are preserved during mitosis. Two additional essential processing components were also found in the NDF: U8 snoRNA and hPop1 (a protein component of RNase MRP and RNase P). Thus, the NDF appear to be large complexes containing partially processed pre-rRNA associated with processing components in which processing has been significantly suppressed. The NDF may facilitate coordinated assembly of postmitotic nucleoli.
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页码:2407 / 2422
页数:16
相关论文
共 68 条
[1]   BASE-PAIRING BETWEEN U3 AND THE PRE-RIBOSOMAL-RNA IS REQUIRED FOR 18S RIBOSOMAL-RNA SYNTHESIS [J].
BELTRAME, M ;
TOLLERVEY, D .
EMBO JOURNAL, 1995, 14 (17) :4350-4356
[2]  
Beven AF, 1996, J CELL SCI, V109, P1241
[3]   STUDIES ON SYNCHRONOUS DIVISION OF TISSUE CULTURE CELLS INITIATED BY EXCESS THYMIDINE [J].
BOOTSMA, D ;
VOS, O ;
BUDKE, L .
EXPERIMENTAL CELL RESEARCH, 1964, 33 (1-2) :301-&
[4]   An RNase P RNA subunit mutation affects ribosomal RNA processing [J].
Chamberlain, JR ;
PaganRamos, E ;
Kindelberger, DW ;
Engelke, DR .
NUCLEIC ACIDS RESEARCH, 1996, 24 (16) :3158-3166
[5]   THE RNA OF RNASE MRP IS REQUIRED FOR NORMAL PROCESSING OF RIBOSOMAL-RNA [J].
CHU, S ;
ARCHER, RH ;
ZENGEL, JM ;
LINDAHL, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (02) :659-663
[6]   Mpp10p, a U3 small nucleolar ribonucleoprotein component required for pre-18S rRNA processing in yeast [J].
Dunbar, DA ;
Wormsley, S ;
Agentis, TM ;
Baserga, SJ .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (10) :5803-5812
[7]  
Dundr M, 1996, J CELL SCI, V109, P2239
[8]   A class of nonribosomal nucleolar components is located in chromosome periphery and in nucleolus-derived foci during anaphase and telophase [J].
Dundr, M ;
Meier, UT ;
Lewis, N ;
Rekosh, D ;
Hammarskjold, ML ;
Olson, MOJ .
CHROMOSOMA, 1997, 105 (7-8) :407-417
[9]   A TBP-CONTAINING MULTIPROTEIN COMPLEX (TIF-IB) MEDIATES TRANSCRIPTION SPECIFICITY OF MURINE RNA POLYMERASE-I [J].
EBERHARD, D ;
TORA, L ;
EGLY, JM ;
GRUMMT, I .
NUCLEIC ACIDS RESEARCH, 1993, 21 (18) :4180-4186
[10]  
EICHLER DC, 1994, PROG NUCLEIC ACID RE, V49, P197