MicroRNAs act sequentially and asymmetrically to control chemosensory laterality in the nematode

Sarah Chang, Robert J. Johnston, Christian Frøkjær-Jensen, Shawn Lockery and Oliver Hobert ()
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Sarah Chang: Center for Neurobiology and Behavior, Columbia University Medical Center
Robert J. Johnston: Center for Neurobiology and Behavior, Columbia University Medical Center
Christian Frøkjær-Jensen: University of Oregon
Shawn Lockery: University of Oregon
Oliver Hobert: Center for Neurobiology and Behavior, Columbia University Medical Center

Nature, 2004, vol. 430, issue 7001, 785-789

Abstract: Abstract Animal microRNAs (miRNAs) are gene regulatory factors that prevent the expression of specific messenger RNA targets by binding to their 3′ untranslated region1,2,3. The Caenorhabditis elegans lsy-6 miRNA (for lateral symmetry defective) is required for the left/right asymmetric expression of guanyl cyclase (gcy) genes in two chemosensory neurons termed ASE left (ASEL) and ASE right (ASER)4,5. The asymmetric expression of these putative chemoreceptors in turn correlates with the functional lateralization of the ASE neurons6. Here we find that a mutation in the die-1 zinc-finger transcription factor disrupts both the chemosensory laterality and left/right asymmetric expression of chemoreceptor genes in the ASE neurons. die-1 controls chemosensory laterality by activating the expression of lsy-6 specifically in ASEL, but not in ASER, where die-1 expression is downregulated through two sites in its 3′ untranslated region. These two sites are complementary to mir-273, a previously uncharacterized miRNA, whose expression is strongly biased towards ASER. Forced bilateral expression of mir-273 in ASEL and ASER causes a loss of asymmetric die-1 expression and ASE laterality. Thus, an inverse distribution of two sequentially acting miRNAs in two bilaterally symmetric neurons controls laterality of the nematode chemosensory system.

Date: 2004
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DOI: 10.1038/nature02752

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