Transcription of bxd noncoding RNAs promoted by trithorax represses Ubx in cis by transcriptional interference

被引:222
作者
Petruk, Svetlana
Sedkov, Yurii
Riley, Kristen M.
Hodgson, Jacob
Schweisguth, Francois
Hirose, Susumu
Jaynes, James B.
Brock, Hugh W.
Mazo, Alexander [1 ]
机构
[1] Thomas Jefferson Univ, Dept Biochem, Philadelphia, PA 19107 USA
[2] Univ British Columbia, Dept Zool, Vancouver, BC V6T 1Z4, Canada
[3] Ecole Normale Super, CNRS, UMR 8542, Paris, France
[4] Natl Inst Genet, Dept Dev Genet, Mishima, Shizuoka 4118540, Japan
[5] Grad Univ Adv Studies, Mishima, Shizuoka 4118540, Japan
关键词
D O I
10.1016/j.cell.2006.10.039
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
Much of the genome is transcribed into long noncoding RNAs (ncRNAs). Previous data suggested that bithoraxoid (bxd) ncRNAs of the Drosophila bithorax complex (BX-C) prevent silencing of Ultrabithorax (Ubx) and recruit activating proteins of the trithorax group (trxG) to their maintenance elements (MEs). We found that, surprisingly, Ubx and several bxd ncRNAs are expressed in nonoverlapping patterns in both embryos and imaginal discs, suggesting that transcription of these ncRNAs is associated with repression, not activation, of Ubx. Our data rule out siRNA or miRNA-based mechanisms for repression by bxd ncRNAs. Rather, ncRNA transcription itself, acting in cis, represses Ubx. The Trithorax complex TAC1 binds the Ubx coding region in nuclei expressing Ubx, and the bxd region in nuclei not expressing Ubx. We propose that TAC1 promotes the mosaic pattern of Ubx expression by facilitating transcriptional elongation of bxd ncRNAs, which represses Ubx transcription.
引用
收藏
页码:1209 / 1221
页数:13
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