TY - JOUR
T1 - spe-43 is required for sperm activation in C. elegans
AU - Krauchunas, Amber R.
AU - Mendez, Ernesto
AU - Ni, Julie Zhouli
AU - Druzhinina, Marina
AU - Mulia, Amanda
AU - Parry, Jean
AU - Gu, Sam Guoping
AU - Stanfield, Gillian M.
AU - Singson, Andrew
N1 - Funding Information:
This work was supported by National Institutes of Health R01HD054681 to AS, R01GM087705 to GMS, and 1K12GM093854 that supported ARK. We thank the CGC (which is funded by NIH Office of Research Infrastructure Programs P40 OD010440) and WormBase. We also thank Matt Marcello for useful discussion regarding SPE-43 binding data and anonymous reviewers for their helpful comments.
Funding Information:
This work was supported by National Institutes of Health R01HD054681 to AS, R01GM087705 to GMS, and 1K12GM093854 that supported ARK. We thank the CGC (which is funded by NIH Office of Research Infrastructure Programs P40 OD010440 ) and WormBase. We also thank Matt Marcello for useful discussion regarding SPE-43 binding data and anonymous reviewers for their helpful comments.
Publisher Copyright:
© 2018 Elsevier Inc.
PY - 2018/4/15
Y1 - 2018/4/15
N2 - Successful fertilization requires that sperm are activated prior to contacting an oocyte. In C. elegans, this activation process, called spermiogenesis, transforms round immobile spermatids into motile, fertilization-competent spermatozoa. We describe the phenotypic and genetic characterization of spe-43, a new component of the spe-8 pathway, which is required for spermiogenesis in hermaphrodites; spe-43 hermaphrodites are self-sterile, while spe-43 males show wild-type fertility. When exposed to Pronase to activate sperm in vitro, spe-43 spermatids form long rigid spikes radiating outward from the cell periphery instead of forming a motile pseudopod, indicating that spermiogenesis initiates but is not completed. Using a combination of recombinant and deletion mapping and whole genome sequencing, we identified F09E8.1 as spe-43. SPE-43 is predicted to exist in two isoforms; one isoform appears to be a single-pass transmembrane protein while the other is predicted to be a secreted protein. SPE-43 can bind to other known sperm proteins, including SPE-4 and SPE-29, which are known to impact spermiogenesis. In summary, we have identified a membrane protein that is present in C. elegans sperm and is required for sperm activation via the hermaphrodite activation signal.
AB - Successful fertilization requires that sperm are activated prior to contacting an oocyte. In C. elegans, this activation process, called spermiogenesis, transforms round immobile spermatids into motile, fertilization-competent spermatozoa. We describe the phenotypic and genetic characterization of spe-43, a new component of the spe-8 pathway, which is required for spermiogenesis in hermaphrodites; spe-43 hermaphrodites are self-sterile, while spe-43 males show wild-type fertility. When exposed to Pronase to activate sperm in vitro, spe-43 spermatids form long rigid spikes radiating outward from the cell periphery instead of forming a motile pseudopod, indicating that spermiogenesis initiates but is not completed. Using a combination of recombinant and deletion mapping and whole genome sequencing, we identified F09E8.1 as spe-43. SPE-43 is predicted to exist in two isoforms; one isoform appears to be a single-pass transmembrane protein while the other is predicted to be a secreted protein. SPE-43 can bind to other known sperm proteins, including SPE-4 and SPE-29, which are known to impact spermiogenesis. In summary, we have identified a membrane protein that is present in C. elegans sperm and is required for sperm activation via the hermaphrodite activation signal.
KW - C. elegans
KW - Sperm
KW - Sperm activation
KW - Spermiogenesis
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U2 - 10.1016/j.ydbio.2018.02.013
DO - 10.1016/j.ydbio.2018.02.013
M3 - Article
C2 - 29477340
AN - SCOPUS:85043362916
VL - 436
SP - 75
EP - 83
JO - Developmental Biology
JF - Developmental Biology
SN - 0012-1606
IS - 2
ER -