Spatial regulation of microRNA gene expression in the Drosophila embryo

被引:64
作者
Biemar, F
Zinzen, R
Ronshaugen, M
Sementchenko, V
Manak, JR
Levine, MS [1 ]
机构
[1] Univ Calif Berkeley, Div Genet & Dev, Dept Mol Cell Biol, Ctr Integrat Gen, Santa Clara, CA 95051 USA
[2] Affymetrix Inc, Santa Clara, CA 95051 USA
关键词
development; enhancer; transcription;
D O I
10.1073/pnas.0507817102
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
MicroRNAs (miRNAs) regulate posttranscriptional gene activity by binding to specific sequences in the 3' UTRs of target mRNAs. A number of metazoan miRNAs have been shown to exhibit tissue-specific patterns of expression. Here, we investigate the possibility that localized expression is mediated by tissue-specific enhancers, comparable to those seen for protein-coding genes. Two miRNA loci in Drosophila melanogaster are investigated, the mir-309-6 polycistron (8-miR) and the mir-1 gene. The 8-miR locus contains a cluster of eight distinct miRNAs that are transcribed in a common precursor RNA. The 8-miR primary transcript displays a dynamic pattern of expression in early embryos, including repression at the anterior and posterior poles. An 800-by 5' enhancer was identified that recapitulates this complex pattern when attached to a RNA polymerase 11 core promoter fused to a lacZ-reporter gene. The miR-1 locus is specifically expressed in the mesoderm of gastrulating embryos. Bioinformatics methods were used to identify a mesoderm-specific enhancer located approximate to 5 kb 5' of the miR-1 transcription unit. Evidence is presented that the 8-miR enhancer is regulated by the localized Huckebein repressor, whereas miR-1 is activated by Dorsal and Twist. These results provide evidence that restricted activities of the 8-miR and miR-1 miRNAs are mediated by classical tissue-specific enhancers.
引用
收藏
页码:15907 / 15911
页数:5
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