Global Identification of Myc Target Genes Reveals Its Direct Role in Mitochondrial Biogenesis and Its E-Box Usage In Vivo

被引:183
作者
Kim, Jonghwan [1 ]
Lee, Ji-hoon [1 ]
Iyer, Vishwanath R. [1 ]
机构
[1] Univ Texas Austin, Inst Cell & Mol Biol, Ctr Systems & Synthet Biol, Sect Mol Genet & Microbiol, Austin, TX USA
来源
PLOS ONE | 2008年 / 3卷 / 03期
关键词
D O I
10.1371/journal.pone.0001798
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
The Myc oncoprotein is a transcription factor involved in a variety of human cancers. Overexpression of Myc is associated with malignant transformation. In normal cells, Myc is induced by mitotic signals, and in turn, it regulates the expression of downstream target genes. Although diverse roles of Myc have been predicted from many previous studies, detailed functions of Myc targets are still unclear. By combining chromatin immunoprecipitation (ChIP) and promoter microarrays, we identified a total of 1469 Myc direct target genes, the majority of which are novel, in HeLa cells and human primary fibroblasts. We observed dramatic changes of Myc occupancy at its target promoters in foreskin fibroblasts in response to serum stimulation. Among the targets of Myc, 107 were nuclear encoded genes involved in mitochondrial biogenesis. Genes with important roles in mitochondrial replication and biogenesis, such as POLG, POLG2, and NRF1 were identified as direct targets of Myc, confirming a direct role for Myc in regulating mitochondrial biogenesis. Analysis of target promoter sequences revealed a strong preference for Myc occupancy at promoters containing one of several described consensus sequences, CACGTG, in vivo. This study thus sheds light on the transcriptional regulatory networks mediated by Myc in vivo.
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页数:11
相关论文
共 45 条
[1]   Transcriptional regulation and transformation by MYC proteins [J].
Adhikary, S ;
Eilers, M .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2005, 6 (08) :635-645
[2]   FatiGO:: a web tool for finding significant associations of Gene Ontology terms with groups of genes [J].
Al-Shahrour, F ;
Díaz-Uriarte, R ;
Dopazo, J .
BIOINFORMATICS, 2004, 20 (04) :578-580
[3]   MitoP2, an integrated database on mitochondrial proteins in yeast and man [J].
Andreoli, C ;
Prokisch, H ;
Hörtnagel, K ;
Mueller, JC ;
Münsterkötter, M ;
Scharfe, C ;
Meitinger, T .
NUCLEIC ACIDS RESEARCH, 2004, 32 :D459-D462
[4]   MAD - A HETERODIMERIC PARTNER FOR MAX THAT ANTAGONIZES MYC TRANSCRIPTIONAL ACTIVITY [J].
AYER, DE ;
KRETZNER, L ;
EISENMAN, RN .
CELL, 1993, 72 (02) :211-222
[5]   BINDING OF MYC PROTEINS TO CANONICAL AND NONCANONICAL DNA-SEQUENCES [J].
BLACKWELL, TK ;
HUANG, J ;
MA, A ;
KRETZNER, L ;
ALT, FW ;
EISENMAN, RN ;
WEINTRAUB, H .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (09) :5216-5224
[6]  
BLACKWOOD EM, 1991, COLD SPRING HARB SYM, V56, P109
[7]   MAX - A HELIX-LOOP-HELIX ZIPPER PROTEIN THAT FORMS A SEQUENCE-SPECIFIC DNA-BINDING COMPLEX WITH MYC [J].
BLACKWOOD, EM ;
EISENMAN, RN .
SCIENCE, 1991, 251 (4998) :1211-1217
[8]   Transcriptional interactions between yeast tRNA genes, flanking genes and Ty elements: A genomic point of view [J].
Bolton, EC ;
Boeke, JD .
GENOME RESEARCH, 2003, 13 (02) :254-263
[9]   Translocations involving c-myc and c-myc function [J].
Boxer, LM ;
Dang, CV .
ONCOGENE, 2001, 20 (40) :5595-5610
[10]   Expression analysis with oligonucleotide microarrays reveals that MYC regulates genes involved in growth, cell cycle, signaling, and adhesion [J].
Coller, HA ;
Grandori, C ;
Tamayo, P ;
Colbert, T ;
Lander, ES ;
Eisenman, RN ;
Golub, TR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3260-3265