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Copulation in C. elegans males requires a nuclear hormone receptor
In Caenorhabditis elegans, uncoordinated (unc)-55 encodes a nuclear hormone receptor that is necessary for coordinated movement and male mating. An unc-55 reporter gene revealed a sexually dimorphic pattern: early in post-embryonic motor neurons in both sexes; and later in a subset of male-specific...
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Published in: | Developmental biology 2008-10, Vol.322 (1), p.11-20 |
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Main Authors: | , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | In
Caenorhabditis elegans,
uncoordinated (unc)-55 encodes a nuclear hormone receptor that is necessary for coordinated movement and male mating. An
unc-55 reporter gene revealed a sexually dimorphic pattern: early in post-embryonic motor neurons in both sexes; and later in a subset of male-specific cells that included an interneuron and eight muscle cells. A behavioral analysis coupled with RNA interference (RNAi) revealed that males require UNC-55 to execute copulatory motor programs. Two mRNA isoforms (
unc-55a and
unc-55b) were detected throughout post-embryonic development in males, whereas only one,
unc-55a, was detected in hermaphrodites. In
unc-55 mutant males isoform
a rescued the locomotion and mating defect, whereas isoform
b rescued the mating defect only. Isoform
b represents the first report of male-specific splicing in
C. elegans. In addition, isoform
b extended the number of days that transgenic
unc-55 mutant males mated when compared to males rescued with isoform
a, suggesting an anabolic role for the nuclear hormone receptor. The male-specific expression and splicing is part of a regulatory hierarchy that includes two key genes,
male abnormal (mab)-5 and
mab-9, required for the generation and differentiation of male-specific cells. We suggest that UNC-55 acts as an interface between genes involved in male tail pattern formation and those responsible for function. |
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ISSN: | 0012-1606 1095-564X |
DOI: | 10.1016/j.ydbio.2008.06.034 |