The CCCTC-Binding Factor (CTCF) of Drosophila Contributes to the Regulation of the Ribosomal DNA and Nucleolar Stability

被引:37
作者
Guerrero, Paola A. [1 ]
Maggert, Keith A. [2 ]
机构
[1] Texas A&M Univ, Dept Biochem Biophys, College Stn, TX 77843 USA
[2] Texas A&M Univ, Dept Biol, College Stn, TX 77843 USA
来源
PLOS ONE | 2011年 / 6卷 / 01期
基金
美国国家卫生研究院;
关键词
POSITION-EFFECT VARIEGATION; CHROMATIN-STRUCTURE; RNA GENES; EPIGENETIC REGULATION; GENOME ORGANIZATION; ENHANCER BLOCKING; POLYMERASE PARP; RDNA; MELANOGASTER; INSULATOR;
D O I
10.1371/journal.pone.0016401
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the repeat array of ribosomal DNA (rDNA), only about half of the genes are actively transcribed while the others are silenced. In arthropods, transposable elements interrupt a subset of genes, often inactivating transcription of those genes. Little is known about the establishment or separation of juxtaposed active and inactive chromatin domains, or preferential inactivation of transposable element interrupted genes, despite identity in promoter sequences. CTCF is a sequence-specific DNA binding protein which is thought to act as a transcriptional repressor, block enhancer-promoter communication, and delimit juxtaposed domains of active and inactive chromatin; one or more of these activities might contribute to the regulation of this repeated gene cluster. In support of this hypothesis, we show that the Drosophila nucleolus contains CTCF, which is bound to transposable element sequences within the rDNA. Reduction in CTCF gene activity results in nucleolar fragmentation and reduced rDNA silencing, as does disruption of poly-ADP-ribosylation thought to be necessary for CTCF nucleolar localization. Our data establish a role for CTCF as a component necessary for proper control of transposable element-laden rDNA transcription and nucleolar stability.
引用
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页数:11
相关论文
共 59 条
[1]  
ANGSHUMAN S, 2007, COLD SPRING HARB PRO
[2]  
ASHBURNER M., 2005, Drosophila: A laboratory handbook, VSeconde, P1409
[3]   CTCFBSDB: a CTCF-binding site database for characterization of vertebrate genomic insulators [J].
Bao, Lei ;
Zhou, Mi ;
Cui, Yan .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D83-D87
[4]   PML regulates p53 stability by sequestering Mdm2 to the nucleolus [J].
Bernardi, R ;
Scaglioni, PP ;
Bergmann, S ;
Horn, HF ;
Vousden, KH ;
Pandolfi, PP .
NATURE CELL BIOLOGY, 2004, 6 (07) :665-672
[5]  
Bogart K., 2006, Extraction of Total RNA from Drosophila
[6]   SITE SPECIFIC INSERTION OF A TYPE-I RDNA ELEMENT INTO A UNIQUE SEQUENCE IN THE DROSOPHILA-MELANOGASTER GENOME [J].
BROWNE, MJ ;
READ, CA ;
ROIHA, H ;
GLOVER, DM .
NUCLEIC ACIDS RESEARCH, 1984, 12 (23) :9111-9122
[7]   Negative protein 1, which is required for function of the chicken lysozyme gene silencer in conjunction with hormone receptors, is identical to the multivalent zinc finger repressor CTCF [J].
Burcin, M ;
Arnold, R ;
Lutz, M ;
Kaiser, B ;
Runge, D ;
Lottspeich, F ;
Filippova, GN ;
Lobanenkov, VV ;
Renkawitz, R .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1281-1288
[8]   Extrachromosomal circular DNA of tandemly repeated genomic sequences in Drosophila [J].
Cohen, S ;
Yacobi, K ;
Segal, D .
GENOME RESEARCH, 2003, 13 (06) :1133-1145
[9]   2 DIFFERENT CHROMATIN STRUCTURES COEXIST IN RIBOSOMAL-RNA GENES THROUGHOUT THE CELL-CYCLE [J].
CONCONI, A ;
WIDMER, RM ;
KOLLER, T ;
SOGO, JM .
CELL, 1989, 57 (05) :753-761
[10]   Identification of a Ctcf cofactor, Yy1, for the X chromosome binary switch [J].
Donohoe, Mary E. ;
Zhang, Li-Feng ;
Xu, Na ;
Shi, Yang ;
Lee, Jeannie T. .
MOLECULAR CELL, 2007, 25 (01) :43-56