Drosophila mir-9a regulates wing development via fine-tuning expression of the LIM only factor, dLMO

被引:64
作者
Biryukova, Inna [1 ]
Asmar, Joelle [1 ]
Abdesselem, Houari [1 ]
Heitzler, Pascal [1 ]
机构
[1] IGBMC, Dept Cell & Dev Biol, Illkirch Graffenstaden, France
关键词
miRNAs; dLMO; 3 ' UTR; Drosophila; Wing development; HOMEODOMAIN ACTIVITY; GENE-EXPRESSION; VENTRAL CELLS; NOTCH LIGAND; MICRORNA; FRINGE; BOUNDARY; DORSAL; GLYCOSYLTRANSFERASE; ACTIVATION;
D O I
10.1016/j.ydbio.2008.12.036
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
MicroRNAs are short non-coding endogenous RNAs that are implicated in regulating various aspects of plants and animal development, however their functions in organogenesis are largely unknown, Here we report that mir-9a belonging to the mir-9 family, regulates Drosophila wing development through a functional target site in the 3' untranslated region of the Drosophila LIM only protein, dLMO. dLMO is a transcription cofactor, that directly inhibits the activity of Apterous, the LIM-HD factor required for the proper dorsal identity of the wings. Deletions of the 3' untranslated region, including the mir-9a site, generate gain-of-function dLMO mutants (Beadex) associated with high levels of dLMO mRNA and protein. Beadex mutants lack wing margins, a phenotype also observed in null mir-9a mutants. We found that mir-9a and dLMO are co-expressed in wing discs and interact genetically for controlling wing development. Lack of mir-9a results in overexpression of dLMO, while gain-of-function mir-9a mutant suppresses dLMO expression. These data indicate that a function of mir-9a is to ensure the appropriate stoichiometry of dLMO during Drosophila wing development. The mir-9a binding site is conserved in the human counterpart LMO2, the T-cell acute leukemia oncogene, suggesting that mir-9 might apply a similar strategy to maintain LMO2 expression under a detrimental threshold. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:487 / 496
页数:10
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