Graduate Program in Neuroscience, University of Illinois at Chicago
Abstract
The Caenorhabditis elegans UNC-62 homothorax/Meis/TALE homeodomain protein functions sequentially to regulate general identity of the AWC olfactory neuron pair and the stochastic choice of asymmetric AWC subtypes during embryogenesis. Here we analyze the expression pattern of unc-62 during AWC development using an integrated unc-62::GFP fosmid rescuing transgene. UNC-62::GFP was not detected in AWC neurons in early or late embryos. These results are consistent with previous single-cell RNA sequencing data and also suggest an undetectable level of unc-62 expression and/or low stability of UNC-62 protein in AWC neurons during embryogenesis.
Description
The UNC-62 homeodomain protein regulates AWC general identity and subsequently plays a cell autonomous role, determined by mosaic analysis, in AWC asymmetry during embryogenesis (Hsieh et al., 2021). An integrated unc-62::GFP fosmid transgene, in which all UNC-62 protein isoforms are tagged with GFP at the C- terminus (Van Nostrand et al., 2013) (Figure 1A), rescued unc-62(lf) mutant phenotypes of AWC general identity, determined by odr-1p::DsRed expression, and AWC asymmetry, determined by str-2p::GFP expression (Hsieh et al., 2021). These results suggest that UNC-62::GFP fusion protein expressed from the unc-62::GFP fosmid transgene is functional for AWC development. It has been shown that this integrated unc-62::GFP fosmid transgene is expressed in sensory neurons, touch neurons, interneurons, ventral nerve cord motor neurons, and head motor neurons, but it is not expressed in AWC in late-stage larvae or young-stage adult worms using the multicolor transgene NeuroPAL (Reilly et al., 2020).
The AWC neurons are born near the end of gastrulation; AWC asymmetry is established around the 1.5-fold and 3-fold embryonic stage (Sulston et al., 1983; Chuang and Bargmann, 2005). To determine whether unc-62 is expressed in AWC neurons at the embryonic stages of AWC development, the expression pattern of the integrated unc-62::GFP fosmid transgene (Van Nostrand et al., 2013) (Figure 1A), was analyzed with integrated hlh-16::H1-wCherry or odr-1p::TagRFP transgene, early or late AWC marker, respectively. UNC-62::GFP was not detected in AWC neurons at the end of gastrulation, 1.5-fold, or 3-fold embryos (Figure 1B-D). Consistent with our results, single-cell RNA sequencing data revealed a very low expression level of unc-62 in AWC during early embryogenesis as well as an undetectable level of unc-62 in AWC in the later embryonic stage and second-larval stage (Cao et al., 2017; Packer et al., 2019). Together, these results suggest that unc-62 may be expressed at an undetectable level and/or UNC-62 protein may have a very short half-life in embryonic AWC neurons.
Reagents
Strain | Genotype | Source |
SD1871 | wgIs600 [unc-62::GFP fosmid (derived from unc-62 fosmid clone WRM061dC01); unc-119(+)] | Van Nostrand et al., 2013 |
RW10588 | unc-119(ed3); zuIs178 [his-72(1kb 5′ UTR)::his-72::SRPVAT::GFP::his-72 (1KB 3′ UTR) + 5.7 kb XbaI – HindIII unc-119(+)]; stIs10544 [hlh-16::H1-wCherry::let-858 3′ UTR] | Murray et al., 2012 |
IX5658 | wgIs600; stIs10544 | This study |
IX3577 | wgIs600; vyIs56[odr-1p::TagRFP] III (Cochella et al., 2014) | This study |
Acknowledgments
We thank Drs. Eric L. Van Nostrand and Stuart Kim for the SD1871 strain. The RW10588 strain was provided by the Caenorhadbitis Genetics Center (CGC), which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440).
References
Funding
This work was funded by a grant, R01GM098026 awarded to CFC, from the National Institute of General Medical Sciences of the National Institutes of Health.
Reviewed By
Paschalis Kratsios and Filipe Goncalves MarquesHistory
Received: January 15, 2022Revision received: February 10, 2022
Accepted: February 11, 2022
Published: February 18, 2022
Copyright
© 2022 by the authors. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (CC BY 4.0) License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.Citation
Hsieh, YW; Chuang, CF (2022). Analysis of unc-62 expression pattern in C. elegans embryonic AWC neurons. microPublication Biology. 10.17912/micropub.biology.000530.Download: RIS BibTeX