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Mapping the expression of the sex determining factor Doublesex1 in Daphnia magna using a knock-in reporter
Sexually dimorphic traits are common and widespread among animals. The expression of the Doublesex-/Mab-3-domain (DM-domain) gene family has been widely studied in model organisms and has been proven to be essential for the development and maintenance of sex-specific traits. However, little is known...
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Published in: | Scientific reports 2017-11, Vol.7 (1), p.13521-13, Article 13521 |
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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: | Sexually dimorphic traits are common and widespread among animals. The expression of the Doublesex-/Mab-3-domain (DM-domain) gene family has been widely studied in model organisms and has been proven to be essential for the development and maintenance of sex-specific traits. However, little is known about the detailed expression patterns in non-model organisms. In the present study, we demonstrated the spatiotemporal expression of the DM-domain gene,
doublesex1
(
dsx1
), in the crustacean
Daphnia magna
, which parthenogenetically produces males in response to environmental cues. We developed a
dsx1
reporter strain to track
dsx1
activity
in vivo
by inserting the
mCherry
gene into the
dsx1
locus using the TALEN-mediated knock-in approach. After confirming
dsx1
expression in male-specific traits in juveniles and adults, we performed time-lapse imaging of embryogenesis. Shortly after gastrulation stage, a presumptive primary organiser, named cumulus, first showed male-specific
dsx1
expression. This cell mass moved to the posterior growth zone that distributes
dsx1-
expressing progenitor cells across the body during axial elongation, before embryos start male-specific
dsx1
expression in sexually dimorphic structures. The present study demonstrated the sex-specific
dsx1
expression in cell populations involved in basal body formation. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/s41598-017-13730-4 |