posted on 2016-02-18, 19:06authored byTie-Mei Li, Jie Chen, Xiangke Li, Xiao-Jun Ding, Yao Wu, Li-Feng Zhao, She Chen, Xiaoguang Lei, Meng-Qiu Dong
Under
favorable conditions, Caenorhabditis elegans larvae
grow into reproductive adults after a series of molting cycles.
When environmental conditions are harsh, they arrest as dauer larvae.
Dafachronic acid (DA), a C. elegans steroid hormone,
is required for reproductive development. Here, we report a mass spectrometry
(MS) method for absolute quantitation of DA in C. elegans. The extraction of DA from C. elegans was optimized
to achieve a recovery rate of greater than 83%. The MS sensitivity
to DA increased 100-fold after carboxyl group derivatization with
2-picolylamine. High-resolution selected ion monitoring (HR-SIM) on
a Q-Orbitrap mass spectrometer Q Exactive outperformed targeted-MS2
on the same instrument and selected reaction monitoring (SRM) on a
triple-quadrupole mass spectrometer TSQ Quantum Discovery. With a
limit of quantification as low as 1 pg of DA, the HR-SIM method enables
absolute quantification of endogenous DA during the reproductive development
of C. elegans. We found that in wild-type (WT) worms,
DA increases from 0.04 ± 0.02 ng/mg protein in the L1 larval
stage to 1.21 ± 0.67 ng/mg protein in the L2 larval stage and
decreases again after the L3 stage. In comparison, four genetic mutants
that have a constitutive dauer-formation phenotype due to disrupted
insulin, TGF-β, or cGMP signaling all have a very low DA level
in the L2 stage (below 15% of the WT). These mutants are able to escape
the dauer fate and most of them grow into fertile adults when supplied
with exogenous DA. Therefore, a DA spike in the L2 stage is critical
for the reproductive development of C. elegans.