Homeotic Function of Drosophila Bithorax-Complex miRNAs Mediates Fertility by Restricting Multiple Hox Genes and TALE Cofactors in the CNS

被引:39
作者
Garaulet, Daniel L. [1 ,2 ]
Castellanos, Monica C. [3 ]
Bejarano, Fernando [1 ]
Sanfilippo, Piero [1 ,4 ]
Tyler, David M. [1 ]
Allan, Douglas W. [3 ]
Sanchez-Herrero, Ernesto [2 ]
Lai, Eric C. [1 ]
机构
[1] Sloan Kettering Inst, Dept Dev Biol, New York, NY 10065 USA
[2] Univ Autonoma Madrid, Ctr Biol Mol Severe Ochoa CSIC UAM, E-28049 Madrid, Spain
[3] Univ British Columbia, Life Sci Ctr 2401, Vancouver, BC V6T 1Z3, Canada
[4] Gerstner Sloan Kettering Grad Sch Biomed Sci, New York, NY 10065 USA
基金
加拿大健康研究院;
关键词
PHENOTYPIC SUPPRESSION; REGULATORY RNAS; MICRORNA; EXPRESSION; EXTRADENTICLE; SPECIFICITY; COMPETITION; HOMOTHORAX; UNDERLIES; EVOLUTION;
D O I
10.1016/j.devcel.2014.04.023
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Drosophila Bithorax complex (BX-C) Hox cluster contains a bidirectionally transcribed miRNA locus, and a deletion mutant (Delta mir) lays no eggs and is completely sterile. We show these miRNAs are expressed and active in distinct spatial registers along the anterior-posterior axis in the CNS. Delta mir larvae derepress a network of direct homeobox gene targets in the posterior ventral nerve cord (VNC), including BX-C genes and their TALE cofactors. These are phenotypically critical targets, because sterility of Delta mir mutants was substantially rescued by heterozygosity of these genes. The posterior VNC contains IIp7+ oviduct motoneurons, whose innervation and morphology are defective in Delta mir females, and substantially rescued by heterozygosity of Delta mir targets, especially within the BX-C. Collectively, we reveal (1) critical roles for Hox miRNAs that determine segment-specific expression of homeotic genes, which are not masked by transcriptional regulation; and (2) that BX-C miRNAs are essential for neural patterning and reproductive behavior.
引用
收藏
页码:635 / 648
页数:14
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