The Journal of Neuroscience, August 27, 2003, 23(21):7854-7862
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Differential Roles of Engrailed Paralogs in Determining Sensory Axon Guidance and Synaptic Target Recognition
Bruno Marie1 and
Jonathan M. Blagburn1,2
1Institute of Neurobiology and
2Department of Physiology, Medical Sciences Campus,
University of Puerto Rico, San Juan, Puerto Rico 00901
The transcription factor Engrailed (En) controls axon pathfinding and
synaptic target choice in an identified neuron (6m) of the cockroach cercal
sensory system. Knock-out of En using double-stranded RNA interference
(dsRNAi) transforms 6m so that it resembles a neighboring neuron that normally
does not express the en gene, has a different arbor anatomy, and
makes different connections. Like many animals, the cockroach has two En
paralogs, Pa-En1 and Pa-En2. In this study we tested the hypothesis that the
paralogs have different effects on axon guidance and synaptic target
recognition, using RNAi to knock out each one individually. Using dye
injections into 6m and intracellular recordings from target interneurons, we
obtained evidence that both Pa-En1 and Pa-En2 determine the axonal
arborization, but only Pa-En1 controls synaptic connections. However, because
immunocytochemical quantification of En protein in 6m after RNAi showed that
Pa-En1 represents 65% of the total En activity and Pa-En2 only 35%, our
results could be caused by dosage effects. We measured the effects of diluting
the mixture of both dsRNAs on the amounts of En protein. From this
dose-response curve, we calculated the appropriate dilutions of the dsRNA
mixture that would titrate total En protein to levels equivalent to knock-out
of either paralog. RNAi using these dilutions showed that Pa-En1 and Pa-En2
both contribute toward the control of axonal guidance and confirmed that
Pa-En1 has the paralog-specific function of controlling synaptic target
recognition.
Key words: Engrailed; RNA interference; homeodomain; synaptic specificity; axon guidance; evolution
Received May 6, 2003;
revised June 12, 2003;
accepted June 17, 2003.
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