Promoters Recognized by Forkhead Proteins Exist for Individual 21U-RNAs

被引:64
作者
Cecere, Germano [1 ]
Zheng, Grace X. Y. [2 ]
Mansisidor, Andres R. [1 ]
Klymko, Katherine E. [1 ,3 ]
Grishok, Alla [1 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[2] MIT, Koch Inst Integrat Canc Res, Cambridge, MA 02139 USA
[3] Columbia Univ, Dept Biol, Columbia Coll, New York, NY 10027 USA
基金
美国国家卫生研究院;
关键词
SMALL RNAS; PIWI; GENES; EXPRESSION; MICRORNAS; PIRNAS; NUCLEOSOMES; PATHWAYS; REVEALS; BINDING;
D O I
10.1016/j.molcel.2012.06.021
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. elegans 21U-RNAs are equivalent to the piRNAs discovered in other metazoans and have important roles in gannetogenesis and transposon control. The biogenesis and molecular function of 21U-RNAs and piRNAs are poorly understood. Here, we demonstrate that transcription of each 21U-RNA is regulated separately through a conserved upstream DNA motif. We use genomic analysis to show that this motif is associated with low nucleosome occupancy, a characteristic of many promoters that drive expression of protein-coding genes, and that RNA polymerase II is localized to this nucleosome-depleted region. We establish that the most conserved 8-mer sequence in the upstream region of 21U-RNAs, CTGTTTCA, is absolutely required for their individual expression. Furthermore, we demonstrate that the 8-mer is specifically recognized by Forkhead family (FKH) transcription factors and that 21U-RNA expression is diminished in several FKH mutants. Our results suggest that thousands of small noncoding transcription units are regulated by FKH proteins.
引用
收藏
页码:734 / 745
页数:12
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