SNF-10 connects male-derived signals to the onset of sperm motility in C. elegans

References

• Suarez S. Regulation of sperm storage and movement in the mammalian oviduct. Int J Dev Biol 2008; 52:455-62; PMID:18649258; http://dx.doi.org/10.1387/ijdb.072527ss
   PubMed Web of Science ®Google Scholar
• Urner F, Sakkas D. Protein phosphorylation in mammalian spermatozoa. Reproduction 2003; 125:17-26; PMID:12622692; http://dx.doi.org/10.1530/rep.0.1250017
   PubMed Web of Science ®Google Scholar
• Shakes D, Ward S. Initiation of spermiogenesis in C. elegans: a pharmacological and genetic analysis. Dev Biol 1989; 134:189-200; PMID:2731646; http://dx.doi.org/10.1016/0012-1606(89)90088-2
   PubMed Web of Science ®Google Scholar
• Nelson G, Roberts T, Ward S. C. elegans spermatozoan locomotion: amoeboid movement with almost no actin. J Cell Biol 1982; 92:212-131; PMID:7199049; http://dx.doi.org/10.1083/jcb.92.1.121
   PubMedGoogle Scholar
• Ward S, Argon Y, Nelson G. Sperm morphogenesis in wild-type and fertilization-defective mutants of C. elegans. J Cell Biol 1981; PMID:7298721
   PubMedGoogle Scholar
• Xu X, Sternberg P. A C. elegans sperm TRP protein required for sperm-egg interactions during fertilization. Cell 2003; 114:285-97; PMID:12914694; http://dx.doi.org/10.1016/S0092-8674(03)00565-8
   PubMed Web of Science ®Google Scholar
• Washington N, Ward S. FER-1 regulates Ca2+-mediated membrane fusion during C. elegans spermatogenesis. J Cell Sci 2006; 119:2552-62; PMID:16735442; http://dx.doi.org/10.1242/jcs.02980
   PubMedGoogle Scholar
• de Lamirande E, Leclerc, P, Gagnon C. Capacitation as a regulatory event that primes spermatozoa for the acrosome reaction and fertilization. Mol Hum Reprod 1997; 3:175-94; PMID:9237244; http://dx.doi.org/10.1093/molehr/3.3.175
   PubMed Web of Science ®Google Scholar
• Inoue N, Ikawa M, Isotani A, Okabe M. The immunoglobulin superfamily protein Izumo is required for sperm to fuse with eggs. Nature 2005; 434:234-8; PMID:15759005; http://dx.doi.org/10.1038/nature03362
   PubMed Web of Science ®Google Scholar
• L'Hernault, S. Spermatogenesis (February 20, 2006), WormBook, ed. The C. elegans Research Community, http://dx.doi.org/10.1895/wormbook.1.85.1, http://www.wormbook.org
   Google Scholar
• L'Hernault S, Shakes D, Ward S. Developmental genetics of chromosome I spermatogenesis-defective mutants in the nematode C. elegans. Genetics 1988; 120:435-52; PMID:3197956
   PubMed Web of Science ®Google Scholar
• Geldziler B, Chatterjee I, Singson A. The genetic and molecular analysis of spe-19, a gene required for sperm activation in C. elegans. Dev Biol 2005; 283:424-36; PMID:15939418; http://dx.doi.org/10.1016/j.ydbio.2005.04.036
   PubMedGoogle Scholar
• Liu Z, Chen L, Shang Y, Huang P, Miao L. The micronutrient element zinc modulates sperm activation through the SPE-8 pathway in C. elegans. Development 2013; 140:2103-7; PMID:23578924; http://dx.doi.org/10.1242/dev.091025
   PubMedGoogle Scholar
• Stanfield G, Villeneuve A. Regulation of sperm activation by SWM-1 is required for reproductive success of C. elegans males. Curr Biol 2006; 16:252-63; PMID:16461278; http://dx.doi.org/10.1016/j.cub.2005.12.041
   PubMed Web of Science ®Google Scholar
• Argon Y, Ward S. C. elegans fertilization-defective mutants with abnormal sperm. Genetics 1980; 96:413-33; PMID:7196361
   PubMed Web of Science ®Google Scholar
• Smith J, Stanfield G. TRY-5 is a sperm-activating protease in C. elegans seminal fluid. PLoS Genetics 2011; 7:e1002375; PMID:22125495; http://dx.doi.org/10.1371/journal.pgen.1002375
   PubMedGoogle Scholar
• Fenker K, Hansen A, Chong C, Jud M, Duffy B, Norton J, Hansen J, Stanfield G. SLC6 family transporter SNF-10 is required for protease-mediated activation of sperm motility in C. elegans. Dev Biol 2014; 393:171-82; PMID:24929237; http://dx.doi.org/10.1016/j.ydbio.2014.06.001
   PubMedGoogle Scholar
• Bröer S, Gether U. The solute carrier 6 family of transporters. Br J Pharmacol 2012; 167:256-78; PMID:22519513; http://dx.doi.org/10.1111/j.1476-5381.2012.01975.x
   PubMed Web of Science ®Google Scholar
• Kristensen A, Andersen J, Jørgensen T, Sørensen L, Eriksen J, Loland C, Strømgaard K, Gether U. SLC6 neurotransmitter transporters: structure, function, and regulation. Pharmacol Rev 2011; 63:585-640; PMID:21752877; http://dx.doi.org/10.1124/pr.108.000869
   PubMed Web of Science ®Google Scholar
• Chatterjee I, Richmond A, Putiri E, Shakes DC, Singson A. The C. elegans spe-38 gene encodes a novel four-pass integral membrane protein required for sperm function at fertilization. Development 2005; 132:2795-808; PMID:15930110; http://dx.doi.org/10.1242/dev.01868
   PubMedGoogle Scholar
• Zannoni S, L'Hernault S, Singson A. Dynamic localization of SPE-9 in sperm: a protein required for sperm-oocyte interactions in C. elegans. BMC Dev Biol 2003; 3:10; PMID:14653860; http://dx.doi.org/10.1186/1471-213X-3-10
   PubMedGoogle Scholar
• Rawls A, Schultz S, Mitra R, Wolff T. Bedraggled, a putative transporter, influences the tissue polarity complex during the R3/R4 fate decision in the Drosophila eye. Genetics 2007; 177:313-28; PMID:17890365; http://dx.doi.org/10.1534/genetics.107.075945
   PubMedGoogle Scholar
• Golub T, Wacha S, Caroni P. Spatial and temporal control of signaling through lipid rafts. Curr Opin Neurobiol 2004; 14:542-50; PMID:15464886; http://dx.doi.org/10.1016/j.conb.2004.08.003
   PubMedGoogle Scholar
• Rudnick G, Kramer R, Blakely R, Murphy D, Verrey F. The SLC6 transporters: perspectives on structure, functions, regulation, and models for transporter dysfunction. Eur J Physiol 2014; 466:25-42; http://dx.doi.org/10.1007/s00424-013-1410-1
   PubMed Web of Science ®Google Scholar
• Khan S, Ahmad N, Ahmad F, Kumar R. Naturally occurring organic osmolytes: from cell physiology to disease prevention. IUBMB Life 2010; 62:891-5; PMID:21190292; http://dx.doi.org/10.1002/iub.406
   PubMed Web of Science ®Google Scholar
• Abbas M, Foor W. Ascaris suum: free amino acids and proteins in the pseudocoelom, seminal vesicle, and glandular vas deferens. Exp Parasitol 1978; 45:263-73; PMID:680082; http://dx.doi.org/10.1016/0014-4894(78)90068-1
   PubMedGoogle Scholar
• DeFelice L, Goswami T. Transporters as channels. Ann Rev Physiol 2007; 69:87-112; PMID:17059369; http://dx.doi.org/10.1146/annurev.physiol.69.031905.164816
   PubMed Web of Science ®Google Scholar
• Shukla K, Mahdi A, Rajender S. Ion channels in sperm physiology and male fertility and infertility. J Androl 2012; 33:777-88; PMID:22441763; http://dx.doi.org/10.2164/jandrol.111.015552
   PubMed Web of Science ®Google Scholar
• Ward S, Hogan, E, Nelson GA. The initiation of spermiogenesis in the nematode C. elegans. Dev Biol 1983; 98:70-9; PMID:6345236
   PubMed Web of Science ®Google Scholar
• Machaca K, DeFelice L, L'Hernault S. A novel chloride channel localizes to C. elegans spermatids and chloride channel blockers induce spermatid differentiation. Dev Biol 1996; 176:1-16; PMID:8654886; http://dx.doi.org/10.1006/dbio.1996.9999
   PubMedGoogle Scholar
• Nelson G, Roberts T, Ward S. Vesicle fusion, pseudopod extension and amoeboid motility are induced in nematode spermatids by the ionophore monensin. Cell 1980; 19:457-64; PMID:7357613; http://dx.doi.org/10.1016/0092-8674(80)90520-6
   PubMed Web of Science ®Google Scholar
• Chatterjee N, Rolling J, Mahowald A, Bazinet C. Neurotransmitter transporter-like: a male germline-specific SLC6 transporter required for Drosophila spermiogenesis. PLoS One 2011; 6; e16275; PMID:21298005
   PubMed Web of Science ®Google Scholar
• Higuchi M, Miura C, Iwai T, Miura T. Trypsin regulates meiotic initiation in the Japanese eel (Anguilla japonica) by promoting the uptake of taurine into germ cells during spermatogenesis. Biol Rep 2013; 89:58; PMID:23926282; http://dx.doi.org/10.1095/biolreprod.113.109777
   PubMedGoogle Scholar
• Farmer M, Robbins M, Medhurst A, Campbell D, Ellington K, Duckworth M, Brown A, Middlemiss D, Price G, Pangalos M. Cloning and characterization of human NTT5 and v7-3: two orphan transporters of the Na+/Cl--dependent neurotransmitter transporter gene family. Genomics 2000; 70:241-52; PMID:11112352; http://dx.doi.org/10.1006/geno.2000.6387
   PubMedGoogle Scholar
• Iyer G, Krahe R, Goodwin L, Doggett N, Siciliano M, Funanage V, Proujansky R. Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28. Genomics 1996; 34:143-6; PMID:8661037; http://dx.doi.org/10.1006/geno.1996.0254
   PubMedGoogle Scholar
• Baliova M, Jursky F. Calcium dependent modification of distal C-terminal sequences of glycine transporter GlyT1. Neurochem Int 2010; 57:254-61; PMID:20542070; http://dx.doi.org/10.1016/j.neuint.2010.06.003
   PubMedGoogle Scholar
• Baliova M, Knab A, Franekova V, Jursky F. Modification of the cytosolic regions of GABA transporter GAT1 by calpain. Neurochem Int 2009; 55:288-94; PMID:19576516; http://dx.doi.org/10.1016/j.neuint.2009.03.012
   PubMedGoogle Scholar
• Laflamme B, Wolfner M. Identification and function of proteolysis regulators in seminal fluid. Mol Rep Dev 2013; 80:80-101; PMID:23109270; http://dx.doi.org/10.1002/mrd.22130
   PubMedGoogle Scholar
• Odet F, Verot A, Le Magueresse-Battistoni B. The mouse testis is the source of various serine proteases and serine proteinase inhibitors (SERPINs): Serine proteases and SERPINs identified in Leydig cells are under gonadotropin regulation. Endocrinology 2006; 147:4374-83; PMID:16740973
   PubMed Web of Science ®Google Scholar