c-Myc induces changes in higher order rDNA structure on stimulation of quiescent cells

被引:58
作者
Shiue, C-N [1 ]
Berkson, R. G. [1 ]
Wright, A. P. H. [1 ]
机构
[1] Karolinska Inst, Sch Life Sci, Sodertorns Hogskola & Dept Biosci & Nutr, SE-14189 Huddinge, Sweden
关键词
c-Myc; nucleolus; transcription; ribosome biogenesis; RNA polymerase I; RNA-POLYMERASE-I; RIBOSOMAL DNA; SPATIAL-ORGANIZATION; NUCLEAR-MATRIX; TRANSCRIPTION; GENES; VIVO; NUCLEOLAR; UBF; TUMORIGENESIS;
D O I
10.1038/onc.2009.21
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
c-Myc is an oncogenic transcription factor capable of activating transcription by all three nuclear RNA polymerases, thus acting as a high-level coordinator of protein synthesis capacity and cell growth rate. c-Myc recruits RNA polymerase I-related transcription factors to the rDNA when quiescent cells are stimulated to re-enter the cell cycle. Using a model system of cell lines with variable c-Myc status, we show that on stimulation c-Myc rapidly induces gene loop structures in rDNA chromatin that juxtapose upstream and downstream rDNA sequences. c-Myc activation is both necessary and sufficient for this change in rDNA chromatin conformation. c-Myc activation induces association of TTF-1 with the rDNA, and c-Myc is physically associated with induced rDNA gene loops. The origins of two or more rDNA gene loops are closely juxtaposed, suggesting the possibility that c-Myc induces nucleolar chromatin hubs. Induction of rDNA gene loops may be an early step in the reprogramming of quiescent cells as they re-enter the growth cycle.
引用
收藏
页码:1833 / 1842
页数:10
相关论文
共 36 条
[1]   A role for the CPF 3′-end processing machinery in RNAP II-dependent gene looping [J].
Ansari, A ;
Hampsey, M .
GENES & DEVELOPMENT, 2005, 19 (24) :2969-2978
[2]   c-Myc associates with ribosomal DNA and activates RNA polymerase I transcription [J].
Arabi, A ;
Wu, SQ ;
Ridderstråle, K ;
Bierhoff, H ;
Shiue, C ;
Fatyol, K ;
Fahlén, S ;
Hydbring, P ;
Söderberg, O ;
Grummt, I ;
Larsson, LG ;
Wright, APH .
NATURE CELL BIOLOGY, 2005, 7 (03) :303-310
[3]   Modified method of AgNOR staining for tissue and interpretation in histopathology [J].
Bukhari, Mulazim Hussain ;
Niazi, Shahida ;
Khan, Saeed Akhter ;
Hashmi, Ihsanulla ;
Perveen, Shahida ;
Qureshi, Shahzad Shafqat ;
Chaudhry, Naseer Ahmed ;
Qureshi, G. R. ;
Hasan, Mumtaz .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2007, 88 (01) :47-53
[4]   ADDITIONAL RNA POLYMERASE-I INITIATION SITE WITHIN THE NONTRANSCRIBED SPACER REGION OF THE RAT RIBOSOMAL-RNA GENE [J].
CASSIDY, BG ;
YANGYEN, HF ;
ROTHBLUM, LI .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (07) :2388-2396
[5]   THE TATA-BINDING PROTEIN AND ASSOCIATED FACTORS ARE INTEGRAL COMPONENTS OF THE RNA POLYMERASE-I TRANSCRIPTION FACTOR, SL1 [J].
COMAI, L ;
TANESE, N ;
TJIAN, R .
CELL, 1992, 68 (05) :965-976
[6]   Spatial organization of gene expression: the active chromatin hub [J].
de Laat, W ;
Grosveld, F .
CHROMOSOME RESEARCH, 2003, 11 (05) :447-459
[7]  
DEAN M, 1986, J BIOL CHEM, V261, P9161
[8]   Molecular aspects of diagnostic nucleolar and nuclear envelope changes in prostate cancer [J].
Fischer, AH ;
Bardarov, S ;
Jiang, Z .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 91 (01) :170-184
[9]   TBP-TAF complex SL1 directs RNA polymerase I pre-initiation complex formation and stabilizes upstream binding factor at the rDNA promoter [J].
Friedrich, JK ;
Panov, KI ;
Cabart, P ;
Russell, J ;
Zomerdijk, JCBM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (33) :29551-29558
[10]   Activation by c-Myc of transcription by RNA polymerases I, II and III [J].
Gomez-Roman, N ;
Felton-Edkins, ZA ;
Kenneth, NS ;
Goodfellow, SJ ;
Athineos, D ;
Zhang, JX ;
Ramsbottom, BA ;
Innes, F ;
Kantidakis, T ;
Kerr, ER ;
Brodie, J ;
Grandori, C ;
White, RJ .
TRANSCRIPTION, 2006, 73 :141-154